10000+
1000+
26
7
174
26
Cat. No. | Product Name | ||
---|---|---|---|
L9410 | 共价抑制剂库 | 1920 compounds | |
1920 种小分子的独特集合,包含已发现的共价抑制剂以及包含某些共价反应基团常见弹头的分子,如氯乙酰基,2-氯丙酰基,丙烯酰基,1-丙-2-炔基,1-丁-2-炔基,酮羰基,二硫键等,可以用于共价抑制剂药物研发; | |||
LF9000 | 半胱氨酸靶向共价抑制剂库 | 3400 compounds | |
It contains over 3,400 potential covalent modifiers. | |||
L1100 | 蛋白酶抑制剂库 | 343 compounds | |
343 种已知的小分子蛋白酶抑制剂的特有集合,可用于高通量筛选和高内涵筛选; | |||
L1400 | MAPK 抑制剂库 | 365 compounds | |
365 种与MAPK 信号通路相关的生物活性小分子化合物的特有集合,可用于高通量筛选和高内涵筛选; | |||
L2200 | 酪氨酸激酶分子库 | 1016 compounds | |
1016 种酪氨酸激酶抑制剂的独特集合,可用于高通量筛选和高内涵筛选; | |||
L9400 | PPI抑制剂库 | 485 compounds | |
485 种已知活性的 PPI 相关的抑制剂,可用于高通量、高内涵筛选; | |||
LF9100 | 丝氨酸靶向共价抑制剂库 | 2700 compounds | |
Over 2,700 small-molecule screening compounds in the library. | |||
L9100 | 磷酸酶抑制剂化合物库 | 79 compounds | |
79 种已知活性的磷酸酶抑制剂的集合,可用于化合物筛选、化学基因组学、药理分析等方面; | |||
L1600 | 激酶抑制剂库 | 2720 compounds | |
2720 种激酶抑制剂/调节剂的独特集合,用于特定靶向激酶,可用于高通量筛选和高内涵筛选; | |||
L7600 | 趋化因子抑制剂库 | 59 compounds | |
59 种趋化因子或其受体抑制剂的独特集合,可用于高通量筛选和高内涵筛选; | |||
L2000 | 抑制剂库 | 8328 compounds | |
8328 个小分子抑制剂的独特集合,主要用于细胞信号研究、新药筛选、高通量筛选和高内涵筛选; | |||
L2010 | 高选择性抑制剂库 | 575 compounds | |
575种具有高选择性的抑制剂集合 | |||
L3600 | 细胞因子抑制剂库 | 604 compounds | |
604 个与细胞因子紧密相关的化合物集合,是高通量、高内涵筛选的良好载体; | |||
L1610 | FDA 上市激酶抑制剂库 | 263 compounds | |
263种靶向激酶的上市药物集合,用于特定靶向激酶,可用于高通量筛选和高内涵筛选; | |||
DO2200 | 共价抑制剂库CD | 12000 compounds | |
数量多:超过12000种共价结合化合物,并且数量在持续增加; | |||
DF4100 | Smart共价抑制剂库 | 1787 compounds | |
ChemDiv’s Smart Library of Covalent Inhibitors contains 1152 compounds | |||
L2300 | 离子通道库 | 1147 compounds | |
1147 种与离子通道相关的生物活性小分子化合物的特有集合,用于离子通道相关的疾病和药物研究,可用于高通量筛选和高内涵筛选; | |||
L5400 | 抗心血管疾病化合物库 | 1408 compounds | |
1408 种心血管疾病相关的生物活性小分子化合物的特有集合,用于高通量、高内涵筛选; | |||
L1110 | 微管靶向化合物库 | 142 compounds | |
142 种靶向微管的分子集合,用于高通量筛选和高内涵筛选; | |||
L6730 | 抗病毒中药单体化合物库 | 268 compounds | |
268 种具有抗病毒活性的中药单体集合,是药物开发、药理研究的有效工具; | |||
L6120 | 黄酮类天然产物库 | 514 compounds | |
514 种黄酮类天然产物的独特集合,可用于高通量筛选和高内涵筛选; | |||
L2520 | 糖代谢化合物库 | 702 compounds | |
702 种糖代谢相关的化合物,可用于高通量和高内涵筛选; | |||
L4700 | 免疫/炎症分子化合物库 | 4720 compounds | |
4720 种具有抗炎症活性的化合物的特有集合,可用于高通量筛选和高内涵筛选; | |||
L9420 | 外泌体相关化合物库 | 76 compounds | |
76 种外泌体相关的化合物,可以用于高通量和高内涵筛选; | |||
L4020 | NO PAINS 化合物库 | 9384 compounds | |
TargetMol NO PAINS 化合物库包含 9384 个剔除了PAINS 的小分子活性化合物,可用于新药研发,信号通路研究,老药新用等研究。 | |||
L6740 | 抗结直肠癌中药单体化合物库 | 382 compounds | |
382 种抗结直肠癌相关的中药单体集合,是药物开发、药理研究的有效工具; |
Cat. No. | Product Name | Form | Specificity Of Inhibition |
---|---|---|---|
C0002 |
Phosphatase Inhibitor Cocktail I (100× ddH2O)
磷酸酶抑制剂 Cocktail I (100× ddH2O) |
Solution (100× in ddH2O) | |
C0048 |
Deacetylase Inhibitor Cocktail (100× in 70% DMSO)
去乙酰化酶抑制剂 Cocktail(100× in 70% DMSO) |
Solution (100× in 70% DMSO) | |
C0001 |
Protease Inhibitor Cocktail (EDTA-Free, 100× in DMSO)
蛋白酶抑制剂 Cocktail (EDTA-Free, 100× in DMSO) |
Solution (EDTA-Free,100× in DMSO) | |
C0004 |
Phosphatase Inhibitor Cocktail III (2 Tubes, 100x)
磷酸酶抑制剂 Cocktail III (2 Tubes, 100x) |
2 Tube Solution (100×) | |
C0003 |
Phosphatase Inhibitor Cocktail II (100× DMSO)
磷酸酶抑制剂 Cocktail II (100× DMSO) |
Solution (100× in DMSO) | |
C0051 |
Penicillin-Streptomycin Solution (100×), Sterile
青霉素-链霉素双抗溶液(100×),灭菌 |
Solution in bottle | |
C0052 |
Penicillin-Streptomycin-Amphotericin B Solution (100×), Sterile
青霉素-链霉素-两性霉素B三抗溶液(100×),灭菌 |
Solution in bottle |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T10599 |
BRAF inhibitor
|
Raf | MAPK |
BRAF inhibitor 是B-Raf 抑制剂。 | |||
T2072 |
BET bromodomain inhibitor
|
Epigenetic Reader Domain | Chromatin/Epigenetic |
BET bromodomain inhibitor 是 BET 的一种有效抑制剂。 | |||
T13098 |
TBOPP
|
Others | Others |
TBOPP 是DOCK1的选择性抑制剂(IC50:8.4 μM)。它以高亲和力与DOCK1DHR-2 结构域结合 (Kd 为 7.1 μM) ,对多种肿瘤均具有抗肿瘤活性。 | |||
T15352 |
FTBMT
|
GPR | Endocrinology/Hormones; GPCR/G Protein |
FTBMT 是一种选择性的GPR52激动剂(EC50:75 nM),具有抗精神病和促进认知的作用。 | |||
T19821 |
Methoxyfenozide
|
Others | Others |
Methoxyfenozide 是一种二酰基肼类杀虫剂,其与鳞翅类蜕皮激素受体 (EcRs) 结合 (Kd=0.5 nM) 比对二萜 EcRs 结合 (Kd=124 nM) 的选择性高。 | |||
TQ0013 |
BTTAA
|
Others | Others |
BTTAA 是 Cu(I)-稳定配体,能够的有效与泛素 Glu18AzF 反应。 | |||
T19561 |
Simetryn
|
Others | Others |
Simetryn 是一种稻田除草剂,可作为一种化学应激源,延缓蝌蚪的生长和发育,而不会破坏甲状腺功能,即使在 96 小时 LC50 值的 1/100 时也是如此。 | |||
T18934 |
Calmagite
|
Others | Others |
Calmagite 是络合指示剂,可用于多种样品中的钙和镁的检测。 | |||
T18919 |
Bathophenanthroline
|
Others | Others |
Bathophenanthroline 是一种能够通过染色法测量水,血清和尿液样中铁浓度的试剂。 | |||
T15051 |
Dansylamide
|
Others | Others |
Dansylamide 是活性荧光染料,可标记丹磺酰基团,常用于生物化学实验。 | |||
T6606 |
Nicaraven
|
Others | Others |
Nicaraven 是新型的、化学合成的羟基自由基清除剂。 | |||
T6969 |
Imidacloprid
|
Others | Others |
Imidacloprid 是一种新烟碱类农药,广泛用于控制蔬菜,谷物,茶叶和棉花的害虫。 | |||
T19356 |
HTBA
|
Others | Others |
HTBA 是一种用于测定尿肌酐的低成本酶促纸基分析试剂 (enz-PAD)。 | |||
T9751 |
Transfluthrin
|
Others | Others |
Transfluthrin 是一种挥发性拟除虫菊酯类杀虫剂,针对昆虫电压门控钠通道 (VGSC)。 | |||
T40477 |
Dichlormid
|
Others | Others |
Dichlormid 是一种除草剂剂。它上调 ZmMRP1 和 ZmGST27 的表达并增加 ZmGT1。 | |||
T5560 |
Dicyclanil
|
Others | Others |
Dicyclanil 是一种化学结构与环丙嗪相似的昆虫生长调节剂。 | |||
T15140 |
DLinDMA
|
Others | Others |
DLinDMA 是一种稳定的核酸脂质颗粒 (SNALPs) 中的关键脂质成分,是一种可电离的阳离子脂质。它可用于siRNA 递送的研究。 | |||
T7421 |
Melperone
|
Others | Others |
Melperone 是一种丁酰苯,是一种具有睡眠诱导作用的抗精神病试剂,常用于研究精神类疾病。 | |||
T11950 |
MAT2A inhibitor 2
|
Others; Methionine Adenosyltransferase (MAT) | Chromatin/Epigenetic; Others |
MAT2A inhibitor 2 是一种甲硫氨酸腺苷转移酶2A 的抑制剂。 | |||
T15146 |
DNA2 inhibitor C5
|
Others | Others |
DNA2 inhibitor C5 是竞争性特异性的DNA2 核酸酶活性抑制剂(IC50:20 μM)。它能够抑制DNA 依赖性 ATPase、 DNA2 的核酸酶、解旋酶和 DNA 结合活性。它可用于研究奥正癌症。 | |||
T2554 |
Etofibrate
|
Others | Others |
Etofibrate 是烟酸和氯贝酸的醚二醇-1,2 二酯。它是动物和人类中一种有效的降血脂剂。 | |||
T15106 |
DFHBI
|
Others | Others |
DFHBI 是类似于绿色荧光蛋白发色团的小分子。 Spinach-DFHBI 复合物在体外和活细胞中都具有明亮的荧光,而pinach 和 DFHBI 在未结合时基本不发荧光。 | |||
T7099 |
Gefarnate
|
Others | Others |
Gefarnate 是一种胃炎和胃溃疡的研究药物,目前也用于研究干眼症。 | |||
T14529 |
Bentiromide
|
Others | Others |
Bentiromide 是一种可被胰腺分泌的胰凝乳蛋白酶分解的多肽。Bentiromide 通过胰凝乳蛋白酶功能的体外试验确认胰腺外分泌功能。 | |||
T40626 |
Curdlan
|
Others | Others |
Curdlan 是一种多糖,由细菌产生。 | |||
T5161 |
Gadodiamide
|
Others | Others |
Gadodiamide 是一种含钆造影剂,可用于医学成像。 | |||
T39635 |
Obafistat
|
NADPH | Metabolism |
Obafistat 是醛酮还原酶 AKR1C3 的有效抑制剂,抑制人 AKR1C3 的IC50为 1.2 nM。 | |||
T17040 |
Terbutryn
|
Others | Others |
Terbutryn 是选择性除草剂和三嗪化合物,能够被根部和叶子吸收,抑制光合作用的发生。 | |||
T14527 |
Benfluralin
|
Others | Others |
Benfluralin 是一种除草剂,是一种农用化学品,可用作芽前除草剂。 用于控制一系列粮食和非粮食作物中的草和其他杂草。 | |||
T18981 |
DMA
|
Others | Others |
DMA 是一种荧光试剂 (λex=340 nm, λem=478 nm)。 | |||
T14353 |
Auxinole
|
Others | Others |
Auxinole 是TIR1/AFB 受体植物激素拮抗剂。它可与 TIR1 结合,阻断 TIR1-IAA-Aux/IAA 复合物的形成,抑制 auxin 应答基因的表达。 | |||
T15136 |
DiZPK
|
Others | Others |
DiZPK 是吡咯赖氨酸的类似物,可用作光交联剂。 | |||
T38655 |
Trifludimoxazin
|
Others | Others |
Trifludimoxazin 可用作除草剂,是一种原卟啉原氧化酶的抑制剂。 | |||
T19586 |
TOPS
|
Others | Others |
TOPS 是一种高度溶于水的苯胺衍生物,在诊断和生物实验中有广泛运用。 | |||
T15447 |
Guacetisal
|
Others | Others |
Guacetisal 是从乙酰水杨酸与愈创木酚的酯化反应中提取的,可用于治疗慢性支气管炎的相关研究。 | |||
T11050 |
Dipyrocetyl
|
Others | Others |
Dipycecetyl 是止痛及抗炎剂。 | |||
T40515 |
Metamitron
|
Others | Others |
Metamitron 是一种光合电子传递链抑制剂,可用作化学稀释剂。 | |||
T38585 |
Tetrachlorocatechol
|
Others | Others |
Tetrachlorocatechol (TCC) 是一种氯化邻苯二酚化合物,是五氯苯酚的代谢产物。在纸浆生产的氯漂白过程中显著生成,并常见于牢固纸浆厂废水中检测到[1] [2]。TCC作为最有毒的氯化邻苯二酚之一而著称。 | |||
T19533 |
Pyraclonil
|
Others | Others |
Pyraclonil 作为一种除草剂,有效地控制了敏感型(S)和多重抗药性(MHR)E. indica群体。Pyraclonil 作为丙啶类光 敏色素原氧化酶(PPO)抑制剂发挥作用。 | |||
T8455 |
Spinorphin
|
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Spinorphin 是一种脑非肽降解酶抑制剂,能够抑制氨基肽酶、二肽基氨基肽酶III、血管紧张素转换酶和脑非肽酶。它可用于研究疼痛的缓解。 | |||
T5123 |
Pirozadil
|
Others | Others |
Pirozadil 是降血脂药。 | |||
T19060 |
SPQ
|
Others | Others |
SPQ 可用于测量膜氯化物传输机制。 | |||
T16537 |
Pimonidazole
|
Others | Others |
Pimonidazole 是缺氧标记物,能够与大分子的共价结合或被还原形成还原性代谢物后在缺氧细胞中积累,可用于定性和定量评估肿瘤缺氧。它可用于瘤内缺氧和细胞增殖的补充性研究。 | |||
T19353 |
HDAOS
|
Others | Others |
HDAOS 是一种新型Trinder's 试剂,是苯胺衍生物,具有高水溶性,被广泛用于诊断检测和生化试验。 | |||
T18913 |
ADOS
|
Others | Others |
ADOS 是一种显色试剂。 | |||
T3592 |
MQAE
|
Others | Others |
MQAE 是荧光氯离子指示剂,相较于36Cl 同位素示踪法和微电极法,它更加灵敏,更有选择性。 | |||
T19508 |
Peroxidase
|
Others | Others |
Peroxidase 来自辣根,在先天免疫、氧化活性氧、激素生物合成和多种疾病的发病机制等方面具有重要作用。 | |||
T40505 |
Pendimethalin
|
Others | Others |
Pendimethalin 是一种特异性除草剂,防除一年生禾本科和某些一年生阔叶杂草。 | |||
T9416 |
Dansylglycine
|
Others | Others |
Dansylglycine 是一种荧光探针,用于特异性测定髓过氧化物酶和嗜酸性粒细胞过氧化物酶的卤化活性。 | |||
T12094 |
Monobehenin
|
Others; Antibacterial | Microbiology/Virology; Others |
Monobehenin 对细菌生物膜的形成有很强的抑制作用。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN1453 |
Bruceantinol
|
Anti-infection | Microbiology/Virology |
Bruceantinol 是一种quassinol 化合物,分离自Brucea javanica 的 CH3OH 提取物。它能够将系统性寄主植物中灭活。有效的抑制浓度为 10 μM。 | |||
T39049 |
Yubeinine
|
Others | Others |
Yubeinine 是一种生物碱类天然产物,可以起到气管松弛作用。 | |||
TN1455 |
Bryodulcosigenin
|
Immunology/Inflammation related | Immunology/Inflammation |
Bryodulcosigenin 是一种 Bryoniadioica 根的提取物,具有抗炎活性。 | |||
T8194 |
Isoflavone
|
Antioxidant | oxidation-reduction |
Isoflavone 是大豆植物雌激素和生物活性成分,存在于大豆、青豆、花生、鹰嘴豆和苜蓿等几种重要的豆类作物中。 | |||
T3S0693 |
Blinin
|
Others | Others |
Blinin 是一种二萜,分离自植物 Conyza blinii 中。 | |||
T8195 |
Lotusine
|
Others | Others |
Lotusine 是一种提取自Nelumbo nucifera Gaertn 的绿色种胚中的纯生物碱。它能够作用于心肌中动作电位及心脏浦肯野纤维缓慢内向电流。 | |||
TN1028 |
Militarine
|
Others | Others |
Militarine 是一种糖苷化合物,分离自 Bletilla striata,能够抑制植物生长。 | |||
TN3548 |
Bulleyanin
|
Others | Others |
Bulleyanin 是从 isodon species (Labiatae) 中分离出来的一种物质。 | |||
T5747 |
ISOBERGAPTEN
|
Others | Others |
Isobergapten 是一种化感抑制剂,分离自Hevacleum laciniatum 种子。 | |||
TN1785 |
Isomagnolone
|
Others | Others |
Isomagnolone 是一种分离自八角茴香中的天然产物,具有抗炎作用。 | |||
TN2058 |
Persicogenin
|
Anti-infection | Microbiology/Virology |
Persicogenin 是分离自 Rhus retinorrhoea 中,具有抗癌作用。 | |||
T14961 |
Chrysene
䓛,屈 |
Others | Others |
Chrysene 是高分子量 (HMW) 多环芳烃,有极强的顽固性和致癌性。 | |||
T3S0860 |
Gitogenin
|
UGT | Metabolism |
Gitogenin 是一种从Tribulus longipetalus 整株中分离出来的天然类固醇,是一种 UDP-葡萄糖醛酸转移酶 1A4 (UGT1A4) 和 α-葡萄糖苷酶的选择性抑制剂,其IC50分别为 0.69 µM (使用三氟拉嗪为底物) 和 37.2 μM,对人类主要细胞色素 P450 亚型的活性无抑制作用。 | |||
T5813 |
BYAKANGELICIN
|
Reductase | Endocrinology/Hormones; Metabolism |
Byakangelicin 是发现于当归根中的一种活性化合物,可作为调节剂,改善各种活性化合物 (Umb,Cur 和 Dox) 的脑积累,增强研究效果。它提高所有PXR 靶基因 (如MDR1) 的表达,并广泛的诱导药物-药物相互作用。它可抑制性激素的作用,可能会增加内源激素的分解代谢。 | |||
T3873 |
griffonilide
|
Others | Others |
Griffonilide 是一种提取自Semiaquilegia adoxoides 根中的丁烯内酯类化合物,常与紫草甙一起出现。它是一种传统抗癌药草。 | |||
T3931 |
Isobavachin
|
Others | Others |
Isobavachin 是一种分离自Psoralea morisiana 中的抗氧化剂,在A 环的8号位置有一个prenyl 基团,具有潜在的促进神经元的分化和其蛋白异戊烯化作用。 | |||
T8208 |
androsin
|
Others | Others |
Androsin 分离于印度胡黄连中,具有抗哮喘作用。 | |||
T19431 |
Moluccanin
|
Others | Others |
Moluccanin 是来自 Aleurites moluccana 的香豆素类。 | |||
TN1982 |
Neoglycyrol
|
Others | Others |
Neoglycyrol 是分离自甘草的根中的化合物。它是由传统专利药通脉养心丸中筛选得到,具有潜在心肌保护作用。 | |||
T6S1676 |
Cimigenoside
|
Others; Gamma-secretase | Neuroscience; Others; Proteases/Proteasome; Stem Cells |
Cimigenoside 是升麻属中的一种成分,是一种 γ-分泌酶抑制剂,通过 γ-分泌酶/Notch 轴抑制人类乳腺癌细胞的增殖或转移。 | |||
TN6723 |
Lactiflorin
|
Others | Others |
Lactiflorin 是一种具有肾脏保护作用的单萜苷。 | |||
T8077 |
Dihydrojasmone
|
Others | Others |
Dihydrojasmone 是一种重要的香料成分,是佛手柑油的成分。 | |||
T14291 |
Anisindione
|
Others | Others |
Anisindione 是合成的抗凝血剂,对活性促凝因子II,VII,IX 和X 的形成具有抑制作用。 | |||
T5S1331 |
Herbacetin
|
c-Met/HGFR; Akt | Cytoskeletal Signaling; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors |
Herbacetin 是一种亚麻籽中的天然类黄酮,具有多种药理活性,如抗氧化、抗炎、抗癌作用。 它是鸟氨酸脱羧酶Ornithine decarboxylase (ODC)变构抑制剂,能够直接与 ODC 上的 Asp44,Asp243 和 Glu384 结合。其中鸟氨酸脱羧酶是多胺生物合成中的限速酶。 | |||
T5777 |
Phaseoloidin
|
Others | Others |
Phaseoloidin 是来自烟草细毛虫的高纯酸苷,有助于植物抵抗鳞翅目草食动物。它能够抑制Manduca sexta 和Spodoptera littoralis 的幼虫生长。它具有抗补体特性。 | |||
TWS1563 |
Incensole
|
Others | Others |
Incensole 是一种 14-membered 二萜类化合物,分离自烯属植物的香精油和乳香树脂中。它能够激活脑中离子通道,并可以缓解焦虑或抑郁,从而显示出抗炎和抗抑郁的特性。 | |||
T8203 |
Gentianose
|
Others | Others |
Gentianose 是一种碳水化合储备物,来源于多年生黄龙胆贮藏根中。 | |||
T3S1729 |
Dihydrolycorine
|
Others | Others |
Dihydrolycorine 是分离自Lycoris radiate 草药中,是一种真核细胞中蛋白质合成的抑制剂。 | |||
Fr13711 |
Tropinone
|
Others | Others |
Tropinone 是一种可用作合成 Atropine 中间体的生物碱。 | |||
TN6712 |
yibeissine
|
Others | Others |
Yibeissine 是一种甾体生物碱,分离自贝母球茎中。 | |||
TQ0096 |
Scabertopin
|
Others | Others |
Scabertopin 是一种从地胆草中分离得到倍半萜内酯,具有抗癌和抑菌活性。 | |||
TN1829 |
Kakkalide
|
Dehydrogenase | Metabolism |
Kakkalide 是提取自葛根花中的一种异黄酮。它可以抑制活性氧相关炎症,并改善内皮细胞胰岛素抵抗作用。 | |||
T8212 |
Dichotomitin
|
Others | Others |
Dichotomitin 是一种提取自Belamcanda chinensis 根茎中的异黄酮。 | |||
T3S1850 |
Bayogenin
|
Others | Others |
Bayogenin 是紫花苜蓿皂苷,一定程度上能够抑制糖原磷酸化酶的活性。 | |||
T3S2019 |
Lathyrol
|
Others | Others |
Lathyrol 是一种具有抗癌功能的天然产物。 | |||
T16943 |
Stigmastanol
|
Endogenous Metabolite | Metabolism |
Stigmastanol 是分离自Hypericum riparium 的 6-氨基衍生物。Hypericum riparium 是属于杜仲科的药用植物。 | |||
T13350 |
Wushanicaritin
|
Others | Others |
Wushanicaritin 在 DPPH 自由基清除活性测试中显示出显著的抗氧化活性 ,其IC50值为35.3 μM,具有抗肿瘤作用和抗炎活性。 | |||
TJS0851 |
Plantagoside
|
Others | Others |
Plantagoside 是α-mannosidase 的非竞争性特异性抑制剂(IC50:5 μM),分离自Plantago asiatica 种子中。 | |||
T5789 |
XYLOTRIOSE
|
Others | Others |
Xylotriose 是双歧杆菌促生因子,是天然的低聚木糖。 | |||
T7032 |
Eupatorin
|
Others; P450 | Metabolism; Others |
Eupatorin 是天然存在的黄酮,可捕获 G2-M 细胞周期,激活多个 caspase、细胞色素 C 的释放、多聚 (ADP-核糖) 聚合酶的裂解,促使凋亡细胞死亡。 | |||
TN1002 |
Blumeatin
|
ROS | Immunology/Inflammation |
Blumeatin 是从Blumea balsamiferaDC 中分离得到,对 CCl4 和硫代乙酰胺 (TAA) 所致的肝损伤表现出保护活性。 | |||
TN1833 |
Karacoline
|
NF-κB | NF-κB |
Karacoline 是发现于植物Aconitum kusnezoffii 中的一种二萜生物碱,通过 NF-κB 信号通路,抑制椎间盘退变中细胞外基质的降解。 | |||
TN1111 |
Arnidiol
|
Immunology/Inflammation related | Immunology/Inflammation |
Arnidiol 是一种五环三萜烯,从Barleria Longiflora LinnF. 中提取得到。 | |||
T8169 |
Decursinol
|
Others | Others |
Decursinol 是一种分离自Angelica gigas 的根中的、口服具有活性的抗伤害药物。它具有抗肿瘤和抗转移作用。 | |||
TN2197 |
Secoisolariciresinol
|
TNF | Apoptosis |
Secoisolariciresinol 是一种属于苯丙素类的木脂素。 | |||
T6S2252 |
Sweroside
|
Others | Others |
Sweroside 是分离自Lonicera japonica 中,具有细胞保护、抗骨质疏松和保护肝脏活性。 | |||
T6S0525 |
Farrerol
|
ERK; p38 MAPK; Akt | Cytoskeletal Signaling; MAPK; PI3K/Akt/mTOR signaling |
Farrerol 是一种杜鹃花的生物活性成分,具有抗氧化、抗肿瘤、抗炎、神经保护和肝保护等多种功能。 | |||
TN1075 |
Adynerin
|
Others | Others |
Adynerin 是一种发现于夹竹桃中的天然类固醇。 | |||
T5733 |
Xylotetraose
|
Others | Others |
Xylotetraose 是木聚糖的水解产物,可用于酶生化分析。Xylan 是由木糖单元组成的多糖,主要包含由纤维素连接的 β-D- 木糖单位。 | |||
TN1626 |
Eugenin
|
Others | Others |
Eugenin 是一种色酮,分离自滨海前胡,能够抗血小板聚集。 | |||
------------------------ 更多 ------------------------ |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-04815 |
C1 inhibitor Protein, Rat, Recombinant (His)
serpin peptidase inhibitor, clade G (C1 inhibit... |
Rat | HEK293 Cells |
C1 inhibitor Protein, Rat, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 54.7 kDa and the accession number is A6HMR4. | |||
TMPH-03529 |
Chemotaxis inhibitory Protein, S. aureus (strain MRSA252), Recombinant (His)
CHIPS,Chemotaxis inhibitory protein,chp |
Staphylococcus aureus | P. pastoris (Yeast) |
Involved in countering the first line of host defense mechanisms. Specifically inhibits the response of human neutrophils and monocytes to complement anaphylatoxin C5a and formylated peptides, like N-formyl-methionyl-leucyl-phenylalanine (fMLP). Acts by binding directly to the C5a receptor (C5aR) and formylated peptide receptor (FPR), thereby blocking the C5a- and fMLP-induced calcium responses. Prevents phagocytosis of the bacterium. Chemotaxis inhibitory Protein, S. aureus (strain MRSA252), Re... | |||
TMPH-03528 |
Chemotaxis inhibitory Protein, S. aureus (strain NCTC 8325/PS47), Recombinant (His & Myc)
chp,Chemotaxis inhibitory protein,CHIPS |
Staphylococcus aureus | E. coli |
Involved in countering the first line of host defense mechanisms. Specifically inhibits the response of human neutrophils and monocytes to complement anaphylatoxin C5a and formylated peptides, like N-formyl-methionyl-leucyl-phenylalanine (fMLP). Acts by binding directly to the C5a receptor (C5aR) and formylated peptide receptor (FPR), thereby blocking the C5a- and fMLP-induced calcium responses. Prevents phagocytosis of the bacterium. Chemotaxis inhibitory Protein, S. aureus (strain NCTC 8325/PS... | |||
TMPY-01183 |
C1 inhibitor Protein, Human, Recombinant (His)
serpin peptidase inhibitor, clade G (C1 inhibit... |
Human | HEK293 Cells |
C1 inhibitor Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 54.3 kDa and the accession number is E9KL26. | |||
TMPH-00554 |
Trypsin inhibitor DE-3 Protein, Erythrina caffra, Recombinant (His)
Trypsin inhibitor DE-3 |
Erythrina caffra | P. pastoris (Yeast) |
Inhibition of trypsin. | |||
TMPH-02787 |
Muellerian-inhibiting factor/AMH Protein, Mouse, Recombinant (His)
Anti-Muellerian hormone,Amh,Muellerian-inhibiting s... |
Mouse | P. pastoris (Yeast) |
Muellerian-inhibiting factor/AMH Protein, Mouse, Recombinant (His) is expressed in Yeast. | |||
TMPH-00520 |
Host-nuclease inhibitor protein gam Protein, Enterobacteria phage lambda, Recombinant (His & Myc)
Host-nuclease inhibitor protein gam,gam |
Escherichia phage lambda | E. coli |
Binds to host RecBCD nuclease and inhibits it thereby protecting the viral DNA against recBCD mediated degradation. | |||
TMPH-02788 |
Muellerian-inhibiting factor/AMH Protein, Mouse, Recombinant (E. coli, His)
Amh,Anti-Muellerian hormone,Muellerian-inhibiting s... |
Mouse | E. coli |
Muellerian-inhibiting factor/AMH Protein, Mouse, Recombinant (E. coli, His) is expressed in E. coli. | |||
TMPJ-00779 |
TNF alpha Protein, Rabbit, Recombinant
TNF-a,Tumor Necrosis Factor,TNF-α,TNF α,Cachectin,肿瘤坏死因子,Tum... |
Rabbit | E. coli |
Tumor necrosis factor alpha (TNFα) is the prototypic ligand of the TNF superfamily. TNFα forms a homotrimer and functions by activating two types of receptors TNF-R1 (TNF receptor type 1,p55R) and TNF-R2 (TNF receptor type 2,p75R). TNFα is a pleiotropic cytokine that is capable to promote inflammation, to induce apoptotic cell death, and to inhibit tumorigenesis and viral replication. TNFα is a potent lymphoid factor that exerts cytotoxic effects on a wide range of tumor cells and certain other ... | |||
TMPJ-00603 |
TL1A/TNFSF15 Protein, Mouse, Recombinant
TNFSF15,Tumor Necrosis Factor Ligand Superfamily Member 15,V... |
Mouse | E. coli |
Tumor Necrosis Factor Ligand Superfamily Member 15 (TNFSF15) is a new member of the tumor necrosis factor family. TNFSF15 is predominantly an endothelial cell-specific gene, and recombinant TNFSF15 is a potent inhibitor of endothelial cell proliferation, angiogenesis and tumor growth. TNFSF15 exerts two activities on endothelial cells: early G1 arrest of G0/G1-cells responding to growth stimuli and programmed cell death of proliferating cells. These activities are highly specific to endothelial ... | |||
TMPY-01009 |
TGFBI Protein, Human, Recombinant (His)
CDG2,CSD,EBMD,CSD1,CDGG1,CSD3,transforming growth factor, be... |
Human | HEK293 Cells |
TGFBI is an RGD-containing protein that binds to type I, II and IV collagens. The RGD motif is found in many extracellular matrix proteins modulating cell adhesion and serves as a ligand recognition sequence for several integrins. TGFBI plays a role in cell-collagen interactions and may be involved in endochondral bone formation in cartilage. TGFBI is induced by transforming growth factor-beta and acts to inhibit cell adhesion. Mutations in TGFBI are associated with multiple types of corneal dys... | |||
TMPY-01442 |
DMBT1 Protein, Human, Recombinant (His)
GP340,deleted in malignant brain tumors 1,muclin |
Human | HEK293 Cells |
Deleted in malignant brain tumors 1 protein, also known as glycoprotein 34, surfactant pulmonary-associated D-binding protein, DMBT1 and GP34, is a secreted protein which belongs to theDMBT1 family. DMBT1 contains 2CUB domains, 14SRCR domains and 1ZP domain. It is highly expressed in alveolar and macrophage tissues. In some macrophages, expression is detected on the membrane, and in other macrophages, it is strongly expressed in the phagosome/phagolysosome compartments. Defects in DMBT1 are invo... | |||
TMPY-04548 |
CDK4 Protein, Human, Recombinant (GST)
CMM3,PSK-J3,cyclin-dependent kinase 4 |
Human | Baculovirus Insect Cells |
CDK4 is a member of the Ser/Thr protein kinase family. It is highly similar to the gene products of S. cerevisiae cdc28 and S. pombe cdc2. It is a catalytic subunit of the protein kinase complex that is important for cell cycle G1 phase progression. The activity of CDK4 is restricted to the G1-S phase, which is controlled by the regulatory subunits D-type cyclins and CDK inhibitor p16(INK4a). CDK4 was shown to be responsible for the phosphorylation of retinoblastoma gene product. CDK4 is the ser... | |||
TMPH-02268 |
AGTR2 Protein, Human, Recombinant (His & SUMO)
AT2 receptor,Angiotensin II type-2 receptor,Type-2 angiotens... |
Human | E. coli |
Receptor for angiotensin II. Cooperates with MTUS1 to inhibit ERK2 activation and cell proliferation. | |||
TMPH-01589 |
KIR2DS3 Protein, Human, Recombinant (His)
KIR2DS3,Natural killer-associated transcript 7,Killer cell i... |
Human | P. pastoris (Yeast) |
Receptor on natural killer (NK) cells for HLA-C alleles. Does not inhibit the activity of NK cells. | |||
TMPH-01588 |
KIR2DS1 Protein, Human, Recombinant (His)
KIR2DS1,CD158 antigen-like family member H,Killer cell immun... |
Human | P. pastoris (Yeast) |
Receptor on natural killer (NK) cells for some HLA-C alleles such as w6. Does not inhibit the activity of NK cells. | |||
TMPH-02213 |
Tomoregulin-1 Protein, Human, Recombinant (E. coli, His)
H7365,TMEFF1,Tomoregulin-1,Transmembrane protein with EGF-li... |
Human | E. coli |
May inhibit NODAL and BMP signaling during neural patterning. May be a tumor suppressor in brain cancers. | |||
TMPH-00546 |
Epstein-Barr virus (strain GD1) BARF1 Protein (His)
33 kDa early protein,BARF1,p33,Secreted protein BARF1 |
EBV | E. coli |
Plays diverse functions in immunomodulation and oncogenicity, maybe by acting as a functional receptor for human CSF1. May inhibit interferon secretion from mononuclear cells. Exhibits oncogenic activity in vitro. | |||
TMPH-00892 |
A1AR Protein, Human, Recombinant (His)
Adenosine receptor A1,ADORA1 |
Human | E. coli |
Receptor for adenosine. The activity of this receptor is mediated by G proteins which inhibit adenylyl cyclase. A1AR Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-10xHis tag. The predicted molecular weight is 39.3 kDa and the accession number is P30542. | |||
TMPH-00819 |
Pro-hevein Protein, Hevea brasiliensis, Recombinant (His)
HEV1,Pro-hevein,Major hevein |
Hevea brasiliensis | E. coli |
N-acetyl-D-glucosamine / N-acetyl-D-neuraminic acid binding lectin. Can inhibit fungal growth. Pro-hevein Protein, Hevea brasiliensis, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 24.1 kDa and the accession number is P02877. | |||
TMPY-01363 |
Serpin A11 Protein, Mouse, Recombinant (His)
serpin peptidase inhibitor, clade A (α-1 antiprotei... |
Mouse | HEK293 Cells |
Serpins are the largest and most diverse family of serine protease inhibitors which are involved in a number of fundamental biological processes such as blood coagulation, complement activation, fibrinolysis, angiogenesis, inflammation and tumor suppression and are expressed in a cell-specific manner. Serpins are a group of proteins with similar structures that were first identified as a set of proteins able to inhibit proteases. The acronym serpin was originally coined because many serpins inhi... | |||
TMPH-00547 |
Epstein-Barr virus (strain B95-8) BARF1 Protein (His & Myc)
33 kDa early protein,p33,Secreted protein BARF1 |
EBV | E. coli |
Plays diverse functions in immunomodulation and oncogenicity, maybe by acting as a functional receptor for human CSF1. May inhibit interferon secretion from mononuclear cells. Exhibits oncogenic activity in vitro. | |||
TMPH-01201 |
DRD2 Protein, Human, Recombinant (His & Myc)
Dopamine D2 receptor,D(2) dopamine receptor,DRD2 |
Human | E. coli |
Dopamine receptor whose activity is mediated by G proteins which inhibit adenylyl cyclase. Positively regulates postnatal regression of retinal hyaloid vessels via suppression of VEGFR2/KDR activity, downstream of OPN5. | |||
TMPH-01590 |
KIR2DS3 Protein, Human, Recombinant (His & Myc)
KIR2DS3,Natural killer-associated transcript 7,Killer cell i... |
Human | E. coli |
Receptor on natural killer (NK) cells for HLA-C alleles. Does not inhibit the activity of NK cells. KIR2DS3 Protein, Human, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 31.7 kDa and the accession number is Q14952. | |||
TMPH-01587 |
KIR2DS1 Protein, Human, Recombinant (E. coli, His)
CD158 antigen-like family member H,MHC class I NK cell recep... |
Human | E. coli |
Receptor on natural killer (NK) cells for some HLA-C alleles such as w6. Does not inhibit the activity of NK cells. KIR2DS1 Protein, Human, Recombinant (E. coli, His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 28.8 kDa and the accession number is Q14954. | |||
TMPY-01855 |
Serpin A10 Protein, Mouse, Recombinant (His)
serpin peptidase inhibitor, clade A (alpha-1 antipr... |
Mouse | HEK293 Cells |
Protein Z-dependent protease inhibitor, also known as PZ-dependent protease inhibitor, SERPINA1 and ZPI, is a secreted protein that belongs to the serpin family. It is expressed by the liver and secreted in plasma. SERPINA1 / Serpin-A1 inhibits factor Xa activity in the presence of protein Z, calcium and phospholipid. Serpins are a group of proteins with similar structures that were first identified as a set of proteins able to inhibit proteases. The acronym serpin was originally coined because ... | |||
TMPH-00430 |
VxXIIC Protein, Conus vexillum, Recombinant (His & Myc & SUMO)
Alpha-conotoxin VxXXC,VxXIIC |
Conus vexillum | E. coli |
Alpha-conotoxins act on postsynaptic membranes, they bind to the nicotinic acetylcholine receptors (nAChR) and thus inhibit them. This toxin specifically blocks mammalian neuronal nAChR of the alpha-7/CHRNA7, alpha-3-beta-2/CHRNA3-CHRNB2 and alpha-4-beta-2/CHRNA4-CHRNB2 subtypes. VxXXA and VxXXB inhibit alpha-7/CHRNA7 and alpha-3-beta-2/CHRNA3-CHRNB2 nAChR more efficiently than VxXXC. VxXXB is the most effective at inhibiting alpha-4-beta-2/CHRNA4-CHRNB2 nAChR, followed by VxXXC and VxXXA. VxXII... | |||
TMPH-02408 |
SPI Protein, Lentinula edodes, Recombinant (His)
Serine protease inhibitor |
Lentinula edodes | E. coli |
Serine protease inhibitor. Active against beta-trypsin and alpha-chymotrypsin with dissociation constants of 0.35 nM and 40 nM respectively. Inhibits factor XIa, but not other enzymes involved in coagulation and fibrinolysis. Does not inhibit subtilisin, lysyl endopeptidase, arginyl endopeptidase or papain. | |||
TMPK-01480 |
HLA-A*02:01&B2M&Survivin (LMLGEFLKL) Monomer Protein, Human, MHC (His & Avi), Biotinylated
IAP4,Survivin,API4,BIRC5,MHC,MHC I,EPR-1,survivin variant 3 ... |
Human | HEK293 Cells |
Survivin (also known as BIRC5) is an evolutionarily conserved eukaryotic protein that is essential for cell division and can inhibit cell death. Normally it is only expressed in actively proliferating cells, but is upregulated in most, if not all cancers; consequently, it has received significant attention as a potential oncotherapeutic target. | |||
TMPH-02358 |
Influenza B (strain B/Lee/1940) Non-structural protein 1 (His)
NS1A,Non-structural protein 1,NS |
Influenza B | E. coli |
Binds and inhibits the conjugation of the ubiquitin-like G1P2/ISG15 protein to its target proteins. Since G1P2/ISG15 is an early antiviral protein, NS1 may inhibit the host antiviral response. Prevents EIF2AK2/PKR activation, either by binding double strand RNA or by interacting directly with EIF2AK2/PKR. Also binds poly(A) and U6 snRNA. | |||
TMPH-02693 |
GNAI2 Protein, Mouse, Recombinant (His)
Guanine nucleotide-binding protein G(i) subunit alpha-2,Gnai... |
Mouse | E. coli |
Guanine nucleotide-binding proteins (G proteins) are involved as modulators or transducers in various transmembrane signaling systems. The G(i) proteins are involved in hormonal regulation of adenylate cyclase: they inhibit the cyclase in response to beta-adrenergic stimuli. May play a role in cell division. | |||
TMPY-03498 |
ING4 Protein, Human, Recombinant (His)
inhibitor of growth family, member 4,p29ING4,my036 |
Human | E. coli |
ING4 is similar to ING1, a tumor suppressor protein that can interact with TP53, inhibit cell growth, and induce apoptosis. ING4 contains a PHD-finger, which is a common motif in proteins involved in chromatin remodeling. ING4 protein can bind TP53 and EP3/p3, a component of the histone acetyltransferase complex, suggesting its involvement in the TP53-dependent regulatory pathway. ING4 is a component of the HBO1 complex which has a histone H4-specific acetyltransferase activity, a reduced activi... | |||
TMPJ-00697 |
NOL3 Protein, Human, Recombinant (GST)
Nop30,Myp,NOP,Apoptosis Repressor With CARD,Nucleolar Protei... |
Human | E. coli |
Nucleolar Protein 3 is encoded by NOL3 gene; multiple transcript variants encoding different isoforms have been found for this gene. So far, Nucleolar protein 3 has show to have two Isoforms. Isoform 1 may be involved in RNA splicing.Isoform 2 may inhibit apoptosis.It has been shown to down-regulate the enzyme activities of caspase 2, caspase 8 and tumor protein p53. | |||
TMPK-01517 |
HLA-A*02:01&B2M&Survivin (LMLGEFLKL) Monomer Protein, Human, MHC (His & Avi)
survivin variant 3 alpha,MHC I,BIRC5,EPR-1,IAP4,Survivin,API... |
Human | HEK293 Cells |
Survivin (also known as BIRC5) is an evolutionarily conserved eukaryotic protein that is essential for cell division and can inhibit cell death. Normally it is only expressed in actively proliferating cells, but is upregulated in most, if not all cancers; consequently, it has received significant attention as a potential oncotherapeutic target. | |||
TMPH-01654 |
MAGEA1 Protein, Human, Recombinant (His)
Antigen MZ2-E,MAGE-1 antigen,Cancer/testis antigen 1.1,Melan... |
Human | P. pastoris (Yeast) |
May be involved in transcriptional regulation through interaction with SNW1 and recruiting histone deactelyase HDAC1. May inhibit notch intracellular domain (NICD) transactivation. May play a role in embryonal development and tumor transformation or aspects of tumor progression. Antigen recognized on a melanoma by autologous cytolytic T-lymphocytes. MAGEA1 Protein, Human, Recombinant (His) is expressed in yeast with N-6xHis tag. The predicted molecular weight is 36.3 kDa and the accession number... | |||
TMPH-03315 |
IGFBP-1 Protein, Rat, Recombinant
Insulin-like growth factor-binding protein 1,Igfbp1 |
Rat | E. coli |
IGF-binding proteins prolong the half-life of the IGFs and have been shown to either inhibit or stimulate the growth promoting effects of the IGFs on cell culture. They alter the interaction of IGFs with their cell surface receptors. Promotes cell migration. IGFBP-1 Protein, Rat, Recombinant is expressed in E. coli expression system. The predicted molecular weight is 26.9 kDa and the accession number is P21743. | |||
TMPH-00837 |
BjaIT Protein, Hottentotta judaicus, Recombinant (His & Myc)
Alpha-insect toxin BjaIT,Bj-alpha-IT |
Hottentotta judaicus | E. coli |
Alpha toxins bind voltage-independently at site-3 of sodium channels (Nav) and inhibit the inactivation of the activated channels, thereby blocking neuronal transmission. This toxin is active against insects (para/tipE). BjaIT Protein, Hottentotta judaicus, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 14.4 kDa and the accession number is Q56TT9. | |||
TMPK-01516 |
HLA-A*02:01&B2M&Survivin (LMLGEFLKL) Tetramer Protein, Human, MHC (His & Avi)
IAP4,survivin variant 3 alpha,BIRC5,Survivin,EPR-1,API4,MHC ... |
Human | HEK293 Cells |
Survivin (also known as BIRC5) is an evolutionarily conserved eukaryotic protein that is essential for cell division and can inhibit cell death. Normally it is only expressed in actively proliferating cells, but is upregulated in most, if not all cancers; consequently, it has received significant attention as a potential oncotherapeutic target. | |||
TMPY-02712 |
Serpin B3 Protein, Human, Recombinant (His)
T4-A,HsT1196,serpin peptidase inhibitor, clade B (o... |
Human | Baculovirus Insect Cells |
SERPINB3, also known as SCCA-1, belongs to the serpin family. Serpins are a group of proteins with similar structures that were first identified as a set of proteins able to inhibit proteases. The acronym serpin was originally coined because many serpins inhibit chymotrypsin-like serine proteases. SERPINB3 is expressed in some hepatocellular carcinoma (at protein level). Its expression is closely related to cellular differentiation in both normal and malignant squamous cells. It seems to also be... | |||
TMPH-02188 |
Tenascin-X Protein, Human, Recombinant (His & Myc)
TNXB,Tenascin-X,Hexabrachion-like protein |
Human | E. coli |
Appears to mediate interactions between cells and the extracellular matrix. Substrate-adhesion molecule that appears to inhibit cell migration. Accelerates collagen fibril formation. May play a role in supporting the growth of epithelial tumors. Tenascin-X Protein, Human, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 81.5 kDa and the accession number is P22105. | |||
TMPY-01841 |
Serpin I2 Protein, Human, Recombinant (His)
PI14,TSA2004,PANCPIN,MEPI,Serpin I2,serpin peptidase inh... |
Human | HEK293 Cells |
Serpins are the largest and most diverse family of serine protease inhibitors which are involved in some fundamental biological processes such as blood coagulation, complement activation, fibrinolysis, angiogenesis, inflammation and tumor suppression and are expressed in a cell-specific manner. Serpins are a group of proteins with similar structures that were first identified as a set of proteins able to inhibit proteases. The acronym serpin was originally coined because many serpins inhibit chy... | |||
TMPY-01843 |
SEMA6A Protein, Human, Recombinant (His)
HT018,VIA,sema domain, transmembrane domain (TM), and cytopl... |
Human | HEK293 Cells |
SEMA6A, the first identified class 6 semaphorin, is contributed to regulate vascular development and adult angiogenesis. SEMA6A could inhibit proliferation, migration, and invasion in different glioma cell lines. That SEMA6A may be a potential prognostic biomarker in the treatment of GBM. Among different semaphorins tested by reverse transcriptase-polymerase chain reaction in human immune cells, the expression of class 6 transmembrane semaphorin SEMA6A was restricted to dendritic cells (DCs). | |||
TMPY-04417 |
DAPK1 Protein, Human, Recombinant (aa 1-363, His & GST)
DAPK,death-associated protein kinase 1,ROCO3 |
Human | Baculovirus Insect Cells |
Death-associated protein kinase 1, also known as DAP kinase 1, DAPK1 and DAPK, is a cytoplasm protein which belongs to theprotein kinase superfamily, CAMK Ser / Thr protein kinase family and DAP kinase subfamily. DAPK1 contains tenANK repeats, onedeath domain and oneprotein kinase domain. DAPK1 is a calcium / calmodulin-dependent serine/threonine kinase which acts as a positive regulator of apoptosis. DAPK1 gene is a candidate tumor suppressor (TSG) and the abnormal methylation of DAPK1 g... | |||
TMPH-01672 |
Human metapneumovirus (strain CAN97-83) Matrix protein (His & Myc)
M,Matrix protein,M protein |
HMPV | E. coli |
Plays a crucial role in virus assembly into filaments and budding. Early in infection, localizes in the nucleus where it may inhibit host cell transcription. Later in infection, traffics to the cytoplasm through the action of host CRM1 to associate with inclusion bodies, the site of viral transcription and replication. During virus assembly and budding, acts as a bridge between the nucleocapsid and the lipid bilayer. | |||
TMPH-01673 |
Human metapneumovirus (strain CAN97-83) Matrix protein (His)
M,Matrix protein,M protein |
HMPV | P. pastoris (Yeast) |
Plays a crucial role in virus assembly into filaments and budding. Early in infection, localizes in the nucleus where it may inhibit host cell transcription. Later in infection, traffics to the cytoplasm through the action of host CRM1 to associate with inclusion bodies, the site of viral transcription and replication. During virus assembly and budding, acts as a bridge between the nucleocapsid and the lipid bilayer. | |||
TMPK-00610 |
SIRP alpha V2 Protein, Human, Recombinant (hFc)
PTPNS1,MYD-1,MFR,SHPS1,SIRPalpha2,SIRPα2,SIRPA,SIRP α V2/CD1... |
Human | HEK293 Cells |
Signal regulatory protein α (SIRPα) is a regulatory membrane glycoprotein from SIRP family expressed mainly by myeloid cells and also by stem cells or neurons.SIRPα acts as inhibitory receptor and interacts with a broadly expressed transmembrane protein CD47 also called the "don´t eat me" signal.Cancer cells highly expressed CD47 that activate SIRP α and inhibit macrophage-mediated destruction. SIRP alpha V2 Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with C-hFc tag.... | |||
TMPH-02650 |
FCMR/FAIM3 Protein, Mouse, Recombinant (His & SUMO)
Fas apoptotic inhibitory molecule 3,Immunoglobulin ... |
Mouse | E. coli |
May play a role in the immune system processes. Protects cells from FAS-, TNF alpha- and FADD-induced apoptosis without increasing expression of the inhibitors of apoptosis BCL2 and BCLXL. Seems to activate an inhibitory pathway that prevents CASP8 activation following FAS stimulation, rather than blocking apoptotic signals downstream. May inhibit FAS-induced apoptosis by preventing CASP8 processing through CFLAR up-regulation. | |||
TMPJ-01016 |
INHBC Protein, Human, Recombinant (N-His)
Activin Beta-C Chain,INHBC,Inhibin β C Chain,Activin β-C Cha... |
Human | E. coli |
Inhibins/activins are involved in regulating a number of diverse functions such as hypothalamic and pituitary hormone secretion, gonadal hormone secretion, germ cell development and maturation, erythroid differentiation, insulin secretion, nerve cell survival, embryonic axial development or bone growth, depending on their subunit composition. Inhibins appear to oppose the functions of activins,Inhibins and activins inhibit and activate, respectively, the secretion of follitropin by the pituitary... | |||
TMPK-00489 |
TL1A/TNFSF15 Protein, Cynomolgus/Rhesus macaque, Recombinant (His)
TNFSF15,TNF superfamily member 15,TL1,VEGI192A,TL1A,VEGI-251... |
Cynomolgus,Rhesus | HEK293 Cells |
TNF superfamily member 15 (TNFSF15), a cytokine largely produced by vascular endothelial cells and a specific inhibitor of the proliferation of these same cells, can inhibit VEGF-induced vascular permeability in vitro and in vivo, and that death receptor 3 (DR3), a cell surface receptor of TNFSF15, mediates TNFSF15-induced dephosphorylation of VEGFR2. TNFSF15 Protein, Cynomolgus/Rhesus macaque, Recombinant (His) is expressed in HEK293 mammalian cells with N-His tag. The predicted molecular weigh... | |||
TMPJ-01313 |
HIV-1 gp120 Protein (His)
Envelope glycoprotein gp120,Surface protein gp120,Glycoprote... |
HIV | HEK293 Cells |
Envelope glycoprotein gp160 is single-pass type I membrane protein. The mature envelope protein (Env) consists of a homotrimer of non-covalently associated gp120-gp41 heterodimers. It is cleaved into the following 2 chains: glycoprotein 120 and transmembrane protein gp41. The resulting complex protrudes from the virus surface as a spike. The 17 amino acids long immunosuppressive region is present in many retroviral envelope proteins. Synthetic peptides derived from this relatively conserved sequ... | |||
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Cat. No. | Product Name | Target | Signaling Pathways |
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T14687 |
Deucravacitinib
BMS-986165 |
Tyrosine Kinases; JAK; IFNAR; Interleukin | Angiogenesis; Chromatin/Epigenetic; Immunology/Inflammation; JAK/STAT signaling; Stem Cells; Tyrosine Kinase/Adaptors |
Deucravacitinib (BMS-986165) 是一种高选择性、口服生物可利用的变构 TYK2 抑制剂,用于治疗自身免疫性疾病。它通过稳定调节 JH2 结构域来阻断受体介导的 Tyk2 激活,可抑制IL-12/23和 I 型IFN 途径。它选择性结合 TYK2 假激酶 (JH2) 结构域,IC50为1.0 nM。 | |||
T22301 |
L-838417 D9
CTP354,CTP354 (C-21191),C-21191 |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
L-838417 D9 (C-21191) 是 L-838417 的氘代物。其中L-838417 是亚型选择性GABAA 正变构调节剂,在 α2, α3 和 α5 亚型中作为部分激动剂。 | |||
T9087 |
Creatine-d3 hydrate
CREATINE-(METHYL-D3) MONOHYDRATE,肌氨酸酐-甲基-D3 一水合物 |
Endogenous Metabolite | Metabolism |
Creatine-d3 hydrate (CREATINE-(METHYL-D3) MONOHYDRATE) 是一种氘标记的肌酸水合物。其中肌酸水合物在肌肉和脑细胞的能量代谢中起着关键作用。 | |||
T40376 |
L-Phenylalanine-15N
L-苯丙氨酸 15N,(S)-2-Amino-3-phenylpropionic acid-15N,L-Phenylalanine-15N |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
L-Phenylalanine-15N ((S)-2-Amino-3-phenylpropionic acid-15N) 是 15N 标记的 L-Phenylalanine。L-Phenylalanine 是从大肠杆菌中分离出来的一种必需氨基酸。 L-Phenylalanine 广泛用于食品香精和药物的生产。 | |||
T13446 |
(S)-Rivastigmine D6 tartrate
酒石酸卡巴拉汀 D6,(R)-卡巴拉汀酒石盐酸-D6,(R)-Rivastigmine D6 tartrate |
AChE | Neuroscience |
(S)-Rivastigmine D6 tartrate 是一种 (S)-Rivastigmine 氘代化合物。 | |||
T38118 |
Zanamivir-13C,15N2
Zanamivir-13C,15N2 |
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Zanamivir-13C,15N2is intended for use as an internal standard for the quantification of zanamivir by GC- or LC-MS. Zanamivir is a sialic acid analog that inhibits neuraminidase release of newly replicated influenza virus particles.1It has been shown to selectively inhibit the growth of influenza A and B viruses in plaque reduction assays with IC50values ranging from 5 to 14 nM and to directly inhibit influenza A and B virus neuraminidases with IC50values ranging from 0.6 to 7.9 nMin vitro. Intra... | |||
TMID-0132 |
Levonorgestrel-d6
|
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Levonorgestrel-d6 是 Levonorgestrel 的氘代化合物。Levonorgestrel 的 CAS 号为 797-63-7。Levonorgestrel 是一种合成孕激素,可作用于孕酮受体。它是一种宫内节育器,可以抑制卵子受精。 | |||
TMIJ-0466 |
Acephate-d3 (acetyl-d3)
|
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Acephate-d3 (acetyl-d3) 是 Acephate 的氘代化合物。Acephate 的 CAS 号为 30560-19-1。Acephate 是能产生胆碱毒性的抗胆碱酯酶杀虫剂。它能够有效抑制蟑螂的AChE,但对大鼠 AChE 的抑制作用较弱。 | |||
T85097 |
1-Palmitoyl-d9-2-hydroxy-sn-glycero-3-PE
16:0 Lyso-PE-d9,16:0 LPE-d9,1-Palmitoyl-d9-2-hydroxy-sn-glycero-3-Phosphoethanolamine,1-Hexadecanoyl-d9-sn-glycero-3-Phosphoethanolamine |
Others | Others |
1-Palmitoyl-d9-2-hydroxy-sn-glycero-3-PE serves as an internal standard for quantifying 1-palmitoyl-2-hydroxy-sn-glycero-3-PE, a lysophospholipid naturally found to inhibit L. donovani promastigotes growth (GI50= 8 µM). Its levels are reduced in mice after alcohol-induced liver damage, in hepatocellular carcinoma mouse xenografts, and in humans following a rigorous three-day exercise regimen of 2.5 hours running daily and 14 hours post-regimen. This compound is also applied in measuring saturate... | |||
TMIH-0089 |
Androstenedione-d7
|
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Androstenedione-d7 是 Androstenedione 的氘代化合物。Androstenedione 的 CAS 号为 560-62-3。9-hydroxy-4-androstene-3,17-dione 是一种类固醇激素,具有抗肿瘤活性,可以抑制多种癌症细胞的生长,包括乳腺癌、前列腺癌和肺癌细胞。 | |||
TMIJ-0147 |
Gefitinib-d6
|
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Gefitinib-d6 是 Gefitinib 的氘代化合物。Gefitinib 的 CAS 号为 184475-35-2。Gefitinib 是一种有口服活性的EGFR酪氨酸激酶抑制剂,可诱导细胞自噬,有抗肿瘤活性。它选择性抑制 EGF 刺激的肿瘤细胞生长,并阻断 EGF 刺激的肿瘤细胞中EGFR自磷酸化。 | |||
TMIJ-0117 |
rac-Clopidogrel-d4 Hydrogen Sulfate
|
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rac-Clopidogrel-d4 Hydrogen Sulfate 是 rac-Clopidogrel Hydrogen Sulfate 的氘代化合物。rac-Clopidogrel Hydrogen Sulfate 的 CAS 号为 135046-48-9。(±) Clopidogrel hydrogen sulfate是一种在药理学和结构上类似于ticlopidine的抗血小板药物,用于抑制脑血管疾病、外周血管疾病和冠状动脉疾病等各种疾病中的血栓。 | |||
TMID-0083 |
Arbidol-d6 Hydrochloride
|
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Arbidol-d6 Hydrochloride 是 Arbidol Hydrochloride 的氘代化合物。Arbidol Hydrochloride 的 CAS 号为 131707-23-8。Umifenovir hydrochloride 是一种口服有效的广谱抗病毒药物,对多种包膜和非包膜病毒均有活性。它被用作抗流感病毒剂,可通过阻断病毒与宿主细胞膜的融合来抑制包膜病毒的细胞侵袭。它是一种 SARS-CoV-2 抑制剂,具有抗炎活性。 | |||
TMIJ-0157 |
Cefoperazone-d5
|
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Cefoperazone-d5 是 Cefoperazone 的氘代化合物。Cefoperazone 的 CAS 号为 62893-19-0。Cefoperazone是一种半合成的头孢菌素,有抗菌活性。 | |||
TMIJ-0518 |
L-Kynurenine-d4-1
|
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L-Kynurenine-d4-1 是 L-Kynurenine 的氘代化合物。L-Kynurenine 的 CAS 号为 2922-83-0。L-Kynurenine是L-色氨酸的代谢物,是芳香烃受体激动剂,可抑制同种异体 T 细胞增殖并增加恶性 U87 神经胶质瘤细胞侵入胶原基质。 | |||
TMID-0071 |
L-Kynurenine-d4
|
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L-Kynurenine-d4 是 L-Kynurenine 的氘代化合物。L-Kynurenine 的 CAS 号为 2922-83-0。L-Kynurenine是L-色氨酸的代谢物,是芳香烃受体激动剂,可抑制同种异体 T 细胞增殖并增加恶性 U87 神经胶质瘤细胞侵入胶原基质。 | |||
TMIJ-0099 |
Minodronic acid-d4
|
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Minodronic acid-d4 是 Minodronic acid 的氘代化合物。Minodronic acid 的 CAS 号为 180064-38-4。Minodronic acid(YM-529) 是一种 P2X2/3 受体拮抗剂, 具有抗癌活性,可直接或间接的抑制癌细胞增殖,诱导细胞凋亡。Minodronic-acid 对各种类型的癌细胞的转移具有抑制作用。Minodronic-acid 可用于研究骨质疏松。 | |||
TMIH-0163 |
Clidinium Bromide-d5
|
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Clidinium Bromide-d5 是 Clidinium Bromide 的氘代化合物。Clidinium Bromide 的 CAS 号为 3485-62-9。Clidinium bromide 是季胺抗毒蕈碱剂,可通过减少胃酸和减慢肠道速度,缓解痉挛和腹部疼痛的症状。 | |||
TMID-0078 |
Irinotecan-d10 Hydrochloride
|
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Irinotecan-d10 Hydrochloride 是 Irinotecan Hydrochloride 的氘代化合物。Irinotecan Hydrochloride 的 CAS 号为 100286-90-6。Irinotecan Hydrochloride 是喜树碱半合成衍生物的盐酸盐,是一种拓扑异构酶 I 抑制剂,可研究结肠癌和直肠癌。 | |||
TMID-0299 |
Zonisamide-d4
|
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Zonisamide-d4 是 Zonisamide 的氘代化合物。Zonisamide 的 CAS 号为 68291-97-4。Zonisamide 是锌酶碳酸酐酶 (carbonic anhydrase) 的有效抑制剂,对人类线粒体同工酶 hCA II 和 hCA V 作用的Ki值分别为 35.2 nM 和 20.6 nM。Zonisamide 具有抗癫痫活性,在癫痫、癫痫发作和帕金森病的研究中具有价值。 | |||
T70882 |
Orlistat-d3
|
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Orlistat-d3 is intended for use as an internal standard for the quantification of orlistat by GC- or LC-MS. Orlistat is a digestive lipase inhibitor. It inhibits diacylglycerol lipase α (DAGLα), DAGLβ, α/β-hydrolase domain-containing protein 12 (ABHD12), ABHD16A, and platelet-activating factor acetylhydrolase (PAF-AH; IC50s = 0.06, 0.1, 0.08, 0.03, and 0.05 µM, respectively), as well as pancreatic lipase and hormone-sensitive lipase (IC50s = 0.65 and 2.1 µg/ml, respectively) but does not inhibit... | |||
TMIJ-0268 |
Relugolix-d6
|
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Relugolix-d6 是 Relugolix 的氘代化合物。Relugolix 的 CAS 号为 737789-87-6。Relugolix 是口服有活性的非肽性促性腺激素释放激素的拮抗剂。同 TAK-013 相比,它对人和猴子的受体具有高亲和力和强拮抗活性,它们的IC50值分别为0.33 nM和0.32 nM。它可用于研究性激素依赖性疾病,如子宫肌瘤、子宫内膜异位症、前列腺癌等。 | |||
TMIH-0549 |
Tafamidis-d3
|
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Tafamidis-d3 是 Tafamidis 的氘代化合物。Tafamidis 的 CAS 号为 594839-88-0。Tafamidis 是选择性的transthyretin (TTR)稳定剂,对野生型 WT-TTR 、突变型同源四聚体 V30M-TTR、V122I-TTR 的活性相当,它们的EC50值为2.7-3.2 μM。它对淀粉样蛋白的生成具有抑制作用。 | |||
TMIH-0025 |
13C-d3-AOH1996
|
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13C-d3-AOH1996 是 AOH1996 的 13C 和氘代化合物。AOH1996 的 CAS 号为 2089314-64-5。AOH1996 是一种具有口服活性的复制体组分 PCNA (增殖细胞核抗原) 配体,靶向转录-复制冲突 (TRC)。AOH1996 可干扰 PCNA 与其结合蛋白的相互作用,导致 DNA 复制应激,诱导细胞凋亡 (apoptosis)。AOH1996 通过稳定 PCNA 和 RNA 聚合酶 II 的相互作用从而导致蛋白酶体依赖的 rpb1 降解和致命的 DNA 损伤。AOH1996 与 DNA 损伤剂具有协同作用,可抑制肿瘤细胞生长。 | |||
TMIH-0091 |
AOH-d3
|
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AOH-d3 是 AOH 的氘代化合物。AOH 的 CAS 号为 2089314-64-5。AOH1996 是一种具有口服活性的复制体组分 PCNA (增殖细胞核抗原) 配体,靶向转录-复制冲突 (TRC)。AOH1996 可干扰 PCNA 与其结合蛋白的相互作用,导致 DNA 复制应激,诱导细胞凋亡 (apoptosis)。AOH1996 通过稳定 PCNA 和 RNA 聚合酶 II 的相互作用从而导致蛋白酶体依赖的 rpb1 降解和致命的 DNA 损伤。AOH1996 与 DNA 损伤剂具有协同作用,可抑制肿瘤细胞生长。 | |||
T38297 |
Ribavirin-13C5
Ribavirin-13C5 |
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Ribavirin-13C5is intended for use as an internal standard for the quantification of ribavirin by GC- or LC-MS. Ribavirin is an antiviral guanosine nucleoside analog.1,2Upon entry into cells, ribavirin is metabolized to an active triphosphate form that induces viral RNA chain termination and inhibits viral polymerases. It reduces replication in a panel of seven RNA and four DNA viruses in Vero cells (EC50s = 2-95 μg/ml).3Ribavirin also reduces replication of severe acute respiratory syndrome coro... |