310
29
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T7856 |
Naphthol AS-E
色酚 AS-E,nAS-E |
Epigenetic Reader Domain; Histone Acetyltransferase | Chromatin/Epigenetic |
Naphthol AS-E (nAS-E) 是一种具有细胞渗透性的KIX-KID 相互作用的抑制剂,可用于癌症研究。它直接结合 CBP 的 KIX 域,Kd 为 8.6 µM,阻断 KIX 域和 KID 域的相互作用,IC50为 2.26 µM。 | |||
T69959 |
NAS-181 free base
|
||
NAS-181 free base is a 5-HT(1B) receptor antagonist. | |||
T23055 |
NAS181
NAS-181 |
Others | Others |
rat 5-HT1B receptor antagonist | |||
T62585 |
NAS-181
|
||
NAS-181 是一种选择性大鼠 5-羟色胺 1B (r5-HT1B) 的有效拮抗剂 (Ki: 47 nM)。NAS-181 可以加强大鼠脑区 5-HTP 的积累。 | |||
T0889 |
Saccharin
O-Sulfobenzimide,O-Benzoic sulfimide,Saccharimide,Benzoic sulfimide,糖精 |
Others; Antibacterial | Microbiology/Virology; Others |
Saccharin (O-Sulfobenzimide) 是一种口服有效的人造甜味剂,具有抑菌和微生物调节特性。 | |||
T69958 | Tofacitinib maleate | ||
Tofacitinib, also known as tasocitinib, CP-690550, is a Janus kinase (JAK) inhibitor. Tofacitinib modulates the signaling pathway at the point of JAKs, preventing the phosphorylation and activation of STATs. JAK enzymes transmit cytokine signaling through pairing of JAKs (e.g., JAK1/JAK3, JAK1/JAK2, JAK1/TyK2, JAK2/JAK2). Tofacitinib inhibited the in vitro activities of JAK1/JAK2, JAK1/JAK3, and JAK2/JAK2 combinations with IC50 of 406, 56, and 1377 nM, respectively. | |||
TP1053L |
Protein Kinase C 19-31 acetate
Protein Kinase C 19-31 acetate(121545-65-1 free base),PKC (19-31) acetate |
PKC | Chromatin/Epigenetic; Cytoskeletal Signaling |
Protein Kinase C 19-31 acetate(121545-65-1 free base) 是一种蛋白激酶 C (PKC) 的肽抑制剂,源自 PKCa 的假底物调节结构域(残基 19-31),在 25 位用丝氨酸取代野生型丙氨酸作为蛋白激酶 C 底物肽,用于测试蛋白激酶 C 活性。 | |||
T11580 |
Heme Oxygenase-1-IN-1
HO-1-IN-1 |
Reactive Oxygen Species | Immunology/Inflammation; Metabolism; NF-κB |
Heme Oxygenase-1-IN-1 (HO-1-IN-1) 是一种血红素加氧酶 1 (HO-1) 抑制剂,IC50=250 nM。 | |||
T78554 | Tyrosinase-IN-12 | Tyrosinase | Proteases/Proteasome |
Tyrosinase-IN-12(Non-competitive tyrosinase inhibitor) 是一种有效的非竞争性酪氨酸酶抑制剂,IC50 值为 49.33 ± 2.64 µM,Ki 值为31.25 ± 0.25 µM。Tyrosinase-IN-12 具有显著的抗氧化和自由基清除活性,减少活性氧 (ROS) 的产生(IC50:25.39 ± 0.77 µM)。Tyrosinase-IN-12 可用于研究食品和水果中物质的褐变。 | |||
TP1051L |
Protein Kinase C Peptide Substrate acetate
Protein Kinase C Peptide Substrate acetate(120253-69-2 free base) |
Others | Others |
Protein Kinase C Peptide Substrate acetate(120253-69-2 free base) 以依赖于第二信使和特定衔接蛋白的方式靶向特定细胞间隔物,以响应激活 g 蛋白偶联受体、酪氨酸激酶受体或酪氨酸激酶偶联受体的细胞外信号。 | |||
T82174 |
hRIO2 kinase ligand-1
|
Others | Others |
hRIO2 kinase ligand-1 是一种有效的 hRIO2 激酶的配体(Kd:520 nM)。 | |||
T11184 |
EML4-ALK kinase inhibitor 1
EML4 ALK kinase inhibitor 1,EML4-ALK kinase inhibitor 1 |
ALK | Angiogenesis; Tyrosine Kinase/Adaptors |
EML4-ALK kinase inhibitor 1 (EML4 ALK kinase inhibitor 1) 是有效的、具有口服活性的类棘皮细胞微管相关蛋白4-间变性淋巴瘤激酶 (EML4-ALK) 的抑制剂,其 IC50 值为 1 nM。 | |||
T8591 |
RNase L-IN-2
5-(3-hydroxyphenyl)-8-thia-4,6-diazatricyclo[7.4.0.0,2,7]trideca-1(9),2(7),5-trien-3-one |
Others | Others |
RNase L-IN-2 是 RNase L 的激活剂,EC50 为 22 uM;对多种类型的 RNA 病毒(包括人类病原体人类副流感病毒 3 型)具有广谱抗病毒活性,在有效浓度下没有细胞毒性。 | |||
T8936 |
Proteinase K
proteinase K for tritirachium album,Protease K,蛋白酶 K |
Others | Others |
Proteinase K (proteinase K for tritirachium album) 是一种非特异性丝氨酸蛋白酶,可用于蛋白消化。它在有 SDS 或尿素存在的情况下,在很大 pH 值 (4-12)、盐浓度和温度单位内均有活性。 | |||
T9229 |
Pim-1/2 kinase inhibitor 1
|
Pim | Chromatin/Epigenetic; JAK/STAT signaling |
Pim-1/2 kinase inhibitor 1 是一种具有口服活性的 Pim-1/2 激酶抑制剂。Pim-1/2 kinase inhibitor 1 能阻断 Pim 激酶磷酸化肽的能力,并且抑制4E-BP1和p27Kip1的Pim 蛋白激酶定向磷酸化。Pim-1/2 kinase inhibitor 1 可用于癌症,尤其是前列腺癌的研究。 | |||
TP1115 |
L-Asparaginase
L-ASNase |
Others | Others |
L-Asparaginase (L-ASNase) 是催化 L-天冬酰胺转化的水解酶,从血浆中去除 L-天冬酰胺,导致 RNA 和 DNA 合成抑制,随后引起细胞凋亡。它用于急性淋巴细胞白血病的研究。 | |||
T9040 |
Aurora kinase inhibitor-2
IUN-70219,Aurora Kinase Inhibitor II |
Aurora Kinase | Cell Cycle/Checkpoint; Chromatin/Epigenetic |
Aurora kinase inhibitor-2 (IUN-70219) 是一种可渗透细胞的苯胺喹唑啉,可抑制极光激酶的活性,对Aurora A 和Aurora B 的IC50分别为 390 nM 和 240 nM。 | |||
T11421 |
Glutaminase-IN-1
CB839 derivative |
transporter | Metabolism |
Glutaminase-IN-1 (CB839 derivative),是一种新型 1,3,4-硒二氮基肾型谷氨酰胺酶(KGA) 的变构抑制剂,在侵袭性 H22 肝癌异种移植模型中显示出抗肿瘤活性。 | |||
T0393 |
Anastrozole
阿那曲唑,ZD1033 |
Aromatase | Endocrinology/Hormones |
Anastrozole (ZD1033) 是芳香酶的选择性抑制剂,能够抑制胎盘芳香化酶(IC50:15 nM)。 | |||
T2346L |
Enasidenib mesylate
AG221 mesylate,AG 221 mesylate,恩西地平甲磺酸盐,AG-221 mesylate |
Dehydrogenase | Metabolism |
Enasidenib mesylate (AG-221 mesylate) 是一种具有有效性和选择性的 IDH2 突变酶抑制剂,可促进白血病成髓细胞的分化,可用于治疗急性髓系白血病。 | |||
T77500 |
Casein kinase 1δ-IN-6
|
Casein Kinase | Metabolism; Stem Cells |
Casein kinase 1δ-IN-6 是一种有效且具有选择性的蛋白激酶 CK-1δ 抑制剂,其 IC50 为 23 nM。Casein kinase 1δ-IN-6 在体外和体内实验中均显示出神经保护和抗炎活性。Casein kinase 1δ-IN-6 可用于研究神经退行性疾病。 | |||
T4692 |
Protein kinase inhibitors 1 hydrochlorid
Protein kinase inhibitors 1 hydrochlorid (1365986-44-2(free base)) |
Others | Others |
Protein kinase inhibitors 1 hydrochlorid (Protein kinase inhibitors 1 hydrochlorid (1365986-44-2(free base))) 是一种新型 HIPK2 抑制剂,IC50 为 74 nM,Kd 为 9.5 nM。 | |||
T22831 |
Protein kinase inhibitor H-7 dihydrochloride
H-7 dihydrochloride |
PKC | Chromatin/Epigenetic; Cytoskeletal Signaling |
Protein kinase inhibitor H-7 dihydrochloride(H-7 dihydrochloride0) 是一种有效的蛋白激酶 C(PKC)抑制剂。Protein kinase inhibitor H-7 dihydrochloride(100 μM)显著抑制 TPA (皮肤肿瘤启动子,12-O-tetradecanoylphorbol-13-acetate) 和磷脂酶 C 促使的 ODC (鸟氨酸脱羧酶),抑制 PMA 诱导的混杂细胞溶解活性。 | |||
T6335 |
Tie2 kinase inhibitor 1
Tie2 kinase inhibitor |
Tie-2 | Tyrosine Kinase/Adaptors |
Tie2 kinase inhibitor 1 (Tie2 kinase inhibitor) 是Tie2激酶选择性抑制剂9IC50:250 nM),具有抗癌作用。 | |||
T0488 |
Finasteride
非那雄胺,MK-906 |
Reductase | Endocrinology/Hormones; Metabolism |
Finasteride (MK-906) 是 5α-还原酶的竞争性抑制剂,对 II 型 5α-还原酶的IC50为 4.2 nM,对 II 型 5α-还原酶的亲和力是 I 型酶的 100 倍。它可用于研究前列腺增生和雄激素性脱发。 | |||
T6488 |
Epinastine hydrochloride
Alesion,Epinastine HCl,WAL-801CL HCl,依匹斯汀盐酸盐,Elestat |
5-HT Receptor; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Epinastine hydrochloride (WAL-801CL HCl) 是抗组胺剂和肥大细胞稳定剂,是一种可口服的选择性组胺 H1 受体拮抗剂,可抑制 IL-8 释放,具有抗过敏作用。 | |||
T8864 |
Thymidylate Kinase Inhibitor, YMU1
|
Others | Others |
YMU1 是一种选择性抑制剂,特异性作用于人胸苷酸激酶 (IC50: 610 nM) 。 | |||
T9564 |
IRE1α kinase-IN-1
|
IRE1 | Cell Cycle/Checkpoint |
IRE1α kinase-IN-1 是IRE1α 的选择性抑制剂(IC50为 77 nM),对 IRE1α 的选择性高于 IRE1β 亚型 100 倍。它抑制内质网诱导的 IRE1α 寡聚和自磷酸化,并抑制 IRE1α RNase 活性 (IC50=80 nM)。 | |||
T9940 |
Protein kinase G inhibitor-2
|
Others | Others |
Protein kinase G inhibitor-2 具有抗菌、抗病毒和抗肿瘤活性。 | |||
T10276L |
AKT Kinase Inhibitor HCl
AKT Kinase Inhibitor HCl(842148-40-7 Free base) |
Akt | Cytoskeletal Signaling; PI3K/Akt/mTOR signaling |
AKT Kinase Inhibitor HCl 是一种 Akt 抑制剂,具有抗肿瘤活性。 | |||
T64376 |
Casein kinase 1δ-IN-9
|
NADPH | Metabolism |
Casein kinase 1δ-IN-9是一种醌还原酶2(Quinone reductase 2)抑制剂,IC50为0.6μM。 | |||
T12187L |
Naspm trihydrochloride
1-Naphthylacetyl spermine trihydrochloride |
iGluR | Membrane transporter/Ion channel; Neuroscience |
Naspm trihydrochloride (1-Naphthylacetyl spermine trihydrochloride) 是Joro 蜘蛛毒素的合成类似物,具有拮抗CP-AMPA 受体的活性。 | |||
T3964 |
Glutaminase C-IN-1
Compound 968,Glutaminase Inhibitor Compound 968 |
Glutaminase | Proteases/Proteasome |
Glutaminase C-IN-1 (Compound 968) 是一种 Glutaminase C 变构抑制剂。 | |||
T31792 |
Filaminast
UNII-CDD69JC61J,Way-pda-641,WAY-PDA 641,CDD69JC61J |
PDE | Metabolism |
Filaminast (UNII-CDD69JC61J) 是磷酸二酯酶4抑制剂(PDE4抑制剂)和罗利普兰的类似物,罗利普兰被用作抗哮喘药物。 | |||
T1848 |
Dynasore
Dynamin Inhibitor I |
Dynamin; Virus Protease; Autophagy; HSV | Autophagy; Cytoskeletal Signaling; Microbiology/Virology |
Dynasore (Dynamin Inhibitor I) 是一种可渗透细胞的化学物质,可逆且非竞争性地抑制 dynamin 1/2 的 GTPase 活性。 它还抑制线粒体动力蛋白 Drp1,对其他小 GTPase 没有影响。 | |||
T4191 |
Multi-kinase inhibitor 1
Multi-kinase inhibitor I |
Others; Bcr-Abl; PDGFR; c-Kit | Angiogenesis; Cytoskeletal Signaling; Others; Tyrosine Kinase/Adaptors |
Multi-kinase inhibitor 1 (Multi-kinase inhibitor I) 是多激酶抑制剂。它有用于导致与酪氨酸激酶活性异常或失控有关的疾病或失调的潜力,特别是与c-Kit,PDGF-R,Bcr-abl 活性相关的疾病。 | |||
T62560 |
Sirpiglenastat
DRP-104 |
Glutaminase | Proteases/Proteasome |
Sirpiglenastat (DRP-104) 是一种谷氨酰胺 (glutamine) 拮抗剂,是DON的前药,具有抗肿瘤活性,通过抑制谷氨酰胺代谢和刺激先天性和适应性免疫系统来发挥作用。 | |||
T10687 |
Casein Kinase II Inhibitor IV
|
Casein Kinase | Metabolism; Stem Cells |
Casein Kinase II Inhibitor IV 是一种小分子诱导剂,可诱导表皮角质形成细胞分化。 | |||
T3118 |
Dimethylenastron
|
Kinesin | Cytoskeletal Signaling |
Dimethylenastron 是一种驱动蛋白Eg5抑制剂,IC50值为 200 nM。它可阻止具有单极纺锤体的细胞,所有染色体都以单极纺锤体方式附着在该纺锤体上。 | |||
T79860 |
TIE-2/VEGFR-2 kinase-IN-5
|
VEGFR; Tie-2 | Angiogenesis; Tyrosine Kinase/Adaptors |
TIE-2/VEGFR-2 kinase-IN-5 是一种高效的 TIE-2 和 VEGFR-2 酪氨酸激酶受体抑制剂,具有的抗血管生成活性,常用于血管生成相关的生物医学研究领域。 | |||
T2129 |
Zaprinast
|
PDE | Metabolism |
Zaprinast 是一种 cGMP 选择性的磷酸二酯酶(PDE)抑制剂,是一种 GPR35激动剂,对大鼠 GPR35 有很强的激活作用,对人 GPR35 有一定的激活作用。它通过抗增殖和促凋亡作用,减少血管的重构。 | |||
T77501 |
TAO Kinase inhibitor 2
|
Serine/threonin kinase | Cell Cycle/Checkpoint; Metabolism |
TAO Kinase inhibitor 2 是 TAO 激酶 抑制剂 ,IC50为50-500 nM。TAO Kinase inhibitor 2 对 KIAA1361 和 JIK 具有抑制作用,IC50s 为 50-500 nM。 | |||
T10276 |
AKT Kinase Inhibitor
|
Akt | Cytoskeletal Signaling; PI3K/Akt/mTOR signaling |
AKT Kinase Inhibitor 是一种具有抗肿瘤活性的 Akt 抑制剂,以剂量依赖的方式选择性抑制细胞增殖。 | |||
T4048 |
Monastrol
(±)-Monastrol |
Apoptosis; Kinesin | Apoptosis; Cytoskeletal Signaling |
Monastrol ((±)-Monastrol) 是一种具有高效性和细胞渗透性的有丝分裂驱动蛋白Eg5的抑制剂,IC50值为 14 μM。 | |||
T78362 |
Transglutaminase
TG |
||
Transglutaminase (TG) 是一种硫醇酶,促使蛋白质分子间交联,通过催化谷氨酰胺残基的γ-羧酰胺基团与其他化合物的一级ε-胺基团形成异肽键。该酶在包括凝血、抗菌免疫反应和光合作用在内的多种生理过程中发挥作用。 | |||
T6409 |
ALK kinase inhibitor-1
SAR348830 |
Others | Others |
SAR348830 是间变性淋巴瘤激酶ALK 抑制剂。 | |||
T15654 |
Ketohexokinase inhibitor 1
PF-06835919 |
Others | Others |
Ketohexokinase inhibitor 1 是一种酮己糖激酶抑制剂(对 KHK-C 和 KHK-A 的 IC50:分别为 8.4 nM 和 66 nM)。 | |||
T74671 |
ROS kinases-IN-2
|
ROS Kinase | Tyrosine Kinase/Adaptors |
ROS kinases-IN-2 是一种有效的 ROS kinase 抑制剂,在 10 μM 时测得抑制率为 21.53%。ROS kinases-IN-2 具有潜在的抗癌活性,可用于研究异常细胞生长。 | |||
T77648 |
Casein kinase 1δ-IN-14
WAY-637081 |
Others | Others |
Casein kinase 1δ-IN-14(WAY-637081) 可用于研究动脉粥样硬化相关心血管疾病。 | |||
T83627 |
Pim-1 kinase inhibitor 8
|
Pim; PKC | Chromatin/Epigenetic; Cytoskeletal Signaling; JAK/STAT signaling |
Pim-1 kinase inhibitor 8 是一种高效的 Pim-1 kinase 抑制剂,具有抗癌活性,可有效抑制细胞迁移。Pim-1 kinase inhibitor 8 对 MCF-7 和 HepG2 细胞有细胞毒性,是研究乳腺癌的候选化合物。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T19529 | Proteinase | Others | Others |
Proteinase 是一种催化蛋白质分解的酶。它们通过水解作用来裂解蛋白质内的肽键,将蛋白质分解成更小的多肽或单个氨基酸。Proteinase 参与许多生物功能,包括消化进食的蛋白质、旧蛋白质的分解,以及细胞信号传递。它们同时促进新的蛋白质产物的形成 | |||
T3667 |
Kalii Dehydrographolidi Succinas
Ddhads,穿琥宁,Dehydroandrographolide Succinate Potasium Salt |
Others | Others |
Kalii Dehydrographolidi Succinas (Dehydroandrographolide Succinate Potasium Salt) 从中药穿心莲中提取得到,具有免疫刺激、抗感染和抗炎作用,对病毒性肺炎和病毒性上呼吸道感染具有潜在的研究价值。 | |||
T13827 |
Pronase E (Activity ≥ 7000 U/g)
Pronase,Pronase E |
Others | Others |
Pronase E 是一种蛋白水解酶混合物,从灰色链霉菌 (Streptomyces griseus) 中获得,能够将蛋白质消化成单个氨基酸。 | |||
T41044 |
Naringinase
|
Glucosidase | Metabolism |
Naringinase 是一种在自然界中广泛存在的水解酶复合物,具有 α-L-鼠李糖苷酶和 β-D-葡萄糖苷酶的活性,主要用于糖苷的水解。 | |||
TQ0036 |
Anemarrhenasaponin I
|
Others | Others |
Anemarrhenasaponin I 是一种对血小板聚集有显著的抑制作用的传统中药。 | |||
T21205 |
Ponasterone A
坡那甾酮A,AI3-44686 |
Others | Others |
Ponasterone A (AI3-44686) 是一种蜕皮激素,能够高度亲和蜕皮激素受体。它能够使报告基因能够快速打开和关闭,是细胞和转基因动物中基因表达的有效调节剂。 | |||
TN1377 |
α-Spinasterol
Α-波菜甾醇,alpha-Spinasterol,菠甾醇 |
COX; Antibacterial; TRP/TRPV Channel | Immunology/Inflammation; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience |
α-Spinasterol 是一种从Spinacia oleracea 分离的瞬时受体电位香草酸 1 拮抗剂,具有抗菌、抗炎、抗抑郁、抗氧化和抗伤害作用。它抑制COX-1和COX-2活性,IC50值分别为 16.17 μM 和 7.76 μM。 | |||
TN6931 |
Anemarrhenasaponin Ia
知母皂苷IA,(2S,3R,4S,5S,6R)-2-{[(2R,3R,4S,5R,6R)-4,5-dihydroxy-2-{[(1R,3R,4R,7S,9S,12S,13S,16S,18R)-3-hydroxy-6-methoxy-7,9,13-trimethyl-6-(3-methylbutyl)-5-oxapentacyclo[10.8.0.02,?.0?,?.013,1?]icosan-16-yl]oxy}-6-(hydroxymethyl)oxan-3-yl]oxy}-6-(hydroxymethyl)oxan |
Others | Others |
Anemarrhenasaponin Ia ((2S,3R,4S,5S,6R)-2-{[(2R,3R,4S,5R,6R)-4,5-dihydroxy-2-{[(1R,3R,4R,7S,9S,12S,13S,16S,18R)-3-hydroxy-6-methoxy-7,9,13-trimethyl-6-(3-methylbutyl)-5-oxapentacyclo[10.8.0.02,?.0?,?.013,1?]icosan-16-yl]oxy}-6-(hydroxymethyl)oxan-3-yl]oxy}-6-(hydroxymethyl)oxan) 具有抗炎活性。Anemarrhenasaponin Ia 具有抗炎作用,从知母根茎中分离得到。 Anemarrhenasaponin Ia 抑制 N-甲酰-甲硫氨酰-亮氨酰-苯丙氨酸 (fMLP) 诱导的超氧化物的进一步产生。 | |||
T64812 |
Collagenase Type I
Collagenase I,Collagenase Type I (From microorganisms) |
Others | Others |
Collagenase Type I 是一种蛋白水解酶,能分解胶原蛋白中的肽键(胶原蛋白是结缔组织的主要结构蛋白)。Collagenase 已被探索作为一种潜在的治疗选择来分解突出的椎间盘物质,从而减少对附近神经的压迫。Collagenase 可能有助于过度疤痕组织的分解和重组,潜在地改善组织功能和外观。Collagenase 具有治疗椎间盘突出、瘢痕疙瘩、脂肪团、脂肪瘤以及佩罗尼氏病和手掌纤维瘤病等方面的潜力。 | |||
T81116 | Spinasaponin E | ||
Spinasaponin E 是一种具有研究潜力的化合物,适用于探索炎性疾病的治疗机制。 | |||
TN2038 | Panasenoside | Others | Others |
Panasenoside is a natural product | |||
TN4490 | Manassantin B | ERK; BCL; p38 MAPK; TNF; NF-κB; JNK; STAT; Antifection | Apoptosis; JAK/STAT signaling; MAPK; Microbiology/Virology; NF-κB; Stem Cells |
Manassantin B is a potent inhibitor of NF-κB activation by the suppression of transciptional activity of RelA/p65 subunit of NF-κB. It also possesses anti-EBV lytic replication activity. Manassantin B inhibits interleukin-6-induced signal transducer and activator of transcription 3 activation in Hep3B cells, it has potential as a potent anti-inflammatory drug for use in pathological processes such as sepsis or acute lung injury. Manassantin B exerts antifibrotic activity in HSC-T6 cells, in pa... | |||
T11150 |
Ecteinascidin 770
Ecteinascidine 770,Et-770 |
Others | Others |
Ecteinascidin 770 (ET-770) inhibits U373MG cells and is a 1,2,3, 4-tetrahydroisoquinoline alkaloid with strong anticancer activity.IC50 is 4.83 nM. | |||
T75684 | Monascorubrin | ||
Monascorubrin 是一种从红曲菌菌丝体中纯化获得的化合物,对枯草芽孢杆菌和拟假丝酵母显示出显著的抗生素活性。 | |||
TN3391 |
alpha-Spinasterol acetate
|
Others | Others |
alpha-Spinasterol has a significant therapeutic potential to modulate the development and/or progression of diabetic nephropathy. | |||
TMA1799 | alpha-Spinasterol glucoside | Others | Others |
alpha-Spinasterol glucoside 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TMA1799,CAS号为 1745-36-4。 | |||
TN3815 | Delta 7-avenasterol | ||
Delta 7-avenasterol has antioxidant activity. | |||
TN4489 | Manassantin A | ERK; cAMP; TNF; NF-κB; MAPK; COX; HIF; Prostaglandin Receptor; JNK; STAT | Angiogenesis; Apoptosis; Chromatin/Epigenetic; GPCR/G Protein; Immunology/Inflammation; JAK/STAT signaling; MAPK; Neuroscience; NF-κB; Stem Cells |
Manassantin A is a high potent HIF-1 inhibitor, it protects the gastric mucosa from ethanol-induced acute gastric injury, and suggest that these protective effects might be associated with COX/PGE2 stimulation, inhibition of iNOS production and NF-κB act | |||
TN1382 | Anemarrhenasaponin III | Others | Others |
Anemarrhenasaponin III is a natural product | |||
T75476 | Monaschromone | ||
Monaschromone 是一种聚酮代谢物,可显著抑制灰霉病菌、茄病菌、稻瘟病菌和索比内蒂菌的生长,MIC 值在 6.25 至 12.5 μM 之间。 | |||
T75574 | Monascorubramine | ||
Monascorubramine,一种由Talaromyces属的红曲素 (Monascus) 产生的微生物着色剂,在不同pH值条件下表现出不同的色调和色度值。 | |||
TN3814 |
Delta 5-avenasterol
|
Others | Others |
Delta 5-avenasterol has antioxidant activity. | |||
TN5766 |
Nandinaside A
|
||
Nandinaside A 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN5766,CAS号为 1813517-23-5。 | |||
T82533 | Donasine | ||
Donasine是一种退热效果的吲哚生物碱天然产物,可从芦竹根茎中提取。 | |||
T82300 | Gluconasturtiin | ||
Gluconasturtiin 作为P. maculipennis幼虫的摄食诱导剂,但其高浓度会对幼虫产生毒害效应。 | |||
T31371 |
Nasunin
Violanin,Delphanin |
||
Delphanin, also known as Nasunin, is an anthocyanin isolated as purple colored crystals from eggplant peels. | |||
T12093 |
Monascin
|
Others | Others |
Monascin is a kind of azaphilonoid pigments extracted from Monascus pilosus-fermented rice (red-mold rice),exhibits anti-tumor-initiating activity and anti-inflammatory activity . | |||
T11364 |
Ganoderic acid TR
|
Others | Others |
Ganoderic acid TR is a broad-spectrum inhibitor against influenza neuraminidases (NAs), particularly H1N1 and H5N1 neuraminidases. The IC50 values of 4.6 and 10.9 μM, respectively. | |||
TN4105 | Ganoderic acid T-Q | Others | Others |
Ganoderic acid T-Q and TR are two inhibitors of H5N1 and H1N1 NAs. |