119
19
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TP1830 |
SV40 large T antigen NLS
|
||
SV40 large T antigen NLS is from Large T antigen residue 47 to 55, enables protein import into cell nucleus. This peptide is generated from Large T antigen residue 47 to 55. | |||
TP1830L |
SV40 large T antigen NLS acetate
|
Others | Others |
SV40 large T antigen NLS acetate 是从大 T 抗原残基 47 到 55,使蛋白质进入细胞核。 | |||
TP2183 |
Large T antigen - rhesus polyomavirus 560-568
|
Others | Others |
Large T antigen - rhesus polyomavirus 560-568 has a peptide sequence of Ser-Glu-Phe-Leu-Leu-Glu-Lys-Arg-Ile. T antigen is required for viral DNA replication, transcription, and virion assembly. | |||
T10096L |
Voruciclib
|
CDK | Cell Cycle/Checkpoint |
Voruciclib 是一种具有口服活性和选择性 CDK 抑制剂,Ki 为 0.626 nM-9.1 nM。它在多种弥漫性大 B 细胞淋巴瘤模型中抑制 MCL-1 的表达。它有效阻断 MCL-1 的转录调节子 CDK9。 | |||
T16040 |
Mepazine
甲哌啶嗪,Pecazine |
Apoptosis; MALT | Apoptosis; Immunology/Inflammation |
Mepazine (Pecazine) 是一种有效的特异性 MALT1 抑制剂。 Mepazine 抑制 GSTMALT1 全长和 GSTMALT1 325-760,IC50 为 0.83 μM 和 0.42 μM。 Mepazine 增强细胞凋亡并影响细胞活力。 | |||
T9203 |
JH-X-119-01
|
IRAK | Immunology/Inflammation; NF-κB |
JH-X-119-01 是白介素 1 受体相关激酶 1 的选择性抑制剂。它能够改善 LPS 诱导的小鼠败血症。它可以抑制 IRAK1(IC50:9 nM),在浓度达到 10 μM 时,也不会对 IRAK4 产生抑制作用。 | |||
T3549 |
Avadomide
CC 122 |
Apoptosis; E1/E2/E3 Enzyme; Ligand for E3 Ligase | Apoptosis; PROTAC; Ubiquitination |
Avadomide (CC 122) 是口服有效的cereblon 调节剂,可以调节 cereblon E3 连接酶活性,诱导弥漫性大 B 细胞淋巴瘤细胞凋亡,具有抗肿瘤和免疫调节活性。 | |||
T14367 |
AZ1495
|
IRAK; CDK; Haspin Kinase | Cell Cycle/Checkpoint; Immunology/Inflammation; NF-κB |
AZ1495 是一种口服有活性的白介素-1受体相关激酶 4(IRAK4)抑制剂,能够作用于 IRAK4 (IC50:5 nM)和 IRAK1 (IC50:23 nM)。可用于研究突变型 MYD88L265P 弥漫性 B 细胞淋巴瘤 (DLBCL) 。 | |||
T5354 |
IRAK4-IN-7
CA-4948 |
IRAK | Immunology/Inflammation; NF-κB |
IRAK4-IN-7 (CA-4948) 是白介素 1 受体相关激酶 4 (IRAK4) 的选择性抑制剂,口服有活性。它可用于研究癌症以及炎症疾病。 | |||
T67940 |
WAY-329738
|
||
WAY-329738具有抗真菌活性,可用来治疗真菌感染。 | |||
TP1309 |
Gastric mucin
|
Antibacterial; Antibiotic | Microbiology/Virology |
Gastric mucin 是一种能保护胃肠道免受酸、蛋白酶、致病微生物和机械创伤影响的糖蛋白。 | |||
T4294 |
NS 11021
NS11021 |
Potassium Channel | Membrane transporter/Ion channel |
NS 11021 (NS11021) 是特异性 Ca2+激活的大电导 K+(KCa1.1)通道激活剂。当浓度高于0.3 μM 时,它通过平行移动通道激活曲线产生更多负电位,以浓度依赖的方式激活 KCa1.1。 | |||
T14125 |
Adarotene
ST1926 |
Apoptosis | Apoptosis |
Adarotene (ST1926) 是一种细胞凋亡诱导剂,通过产生 DNA 损伤,来阻止人类肿瘤细胞的增殖。 | |||
T12186 |
Navitoclax-piperazine
ABT-263-piperazine |
BCL; Ligands for Target Protein for PROTAC | Apoptosis; PROTAC |
Navitoclax-piperazine (ABT-263-piperazine) 是一种特大型 B 细胞淋巴瘤(BCL-XL)抑制剂。它和 E3 泛素连接酶的 VHL 配体可用来合成 PROTAC DT2216。 | |||
T7512 |
BMS-191011
BMS-A |
Potassium Channel | Membrane transporter/Ion channel |
BMS-191011 (BMS-A) 是一种大电导 Ca2+激活的钾通道 (Ca2+-activated potassium (maxi-K) channel) 激活剂,在中风模型中有研究价值。 | |||
T35366 |
4-Nitroquinoline 1-oxide
4-Nitroquinoline 1-oxide,4Nqo,NQO,4-NQO,4-Nitroquinoline-N-oxide,NQNO,4-硝基喹啉-N-氧化物 |
Others | Others |
4-Nitroquinoline 1-oxide (4-NQO) 是一种化学致癌物,可通过形成大量嘌呤加合物来诱导细菌、真菌和动物的突变。 | |||
T77135 |
Tafasitamab
MOR00208,XmAb5574,Tafasitamab-cxix |
Apoptosis; Immunology/Inflammation related | Apoptosis; Immunology/Inflammation |
Tafasitamab (XmAb5574) 是一种 Fc 修饰的人源化单克隆抗体,靶向人 B 细胞表面抗原 CD19 ,可用于研究弥漫性大B细胞淋巴瘤。 | |||
T60008 |
BCL6-IN-6
|
BCL | Apoptosis |
BCL6-IN-6 是 Bcl-6 的抑制剂,可用于关于弥漫性大 B 细胞淋巴瘤的研究。 BCL6-IN-6 阻断 Bcl-6 与其辅阻遏物的相互作用,并以剂量依赖性方式重新激活 Bcl-6 靶基因。 | |||
T8411 |
C-215
|
Others | Others |
C-215 是MmpL3抑制剂。它在 HTS 中被鉴定为对结核分枝杆菌具有独立的甘油活性,对哺乳动物细胞的非特异性毒性较低,对结核分枝杆菌的IC90=16 μM,并且能够有效抑制在巨噬细胞中生长的结核分枝杆菌。 | |||
T5458 |
Darusentan
Lu-135252,达卢生坦 |
Endothelin Receptor | GPCR/G Protein |
Darusentan (Lu-135252) 是内皮素受体 A (ET-A) 受体选择性拮抗剂,能够作用于 ET-A 受体(Ki:1.4 nM)及ET-B 受体(Ki:184 nM),对 ETA 受体的选择性大于 ETB 受体的100以上。它在大鼠主动脉血管平滑肌细胞膜中竞争结合放射性标记的内皮素(Ki:13 nM)。 | |||
T77367 |
Urelumab
BMS-663513,BMS-66513 |
Others | Others |
Urelumab(BMS-66513) 是一种人源化的 IgG4 单克隆抗体,常被当作 CD137 激动剂使用。Urelumab 具有潜在的抗肿瘤活性,可增强 T 细胞和自然杀伤细胞对肿瘤细胞的杀伤作用,并增强 Rituximab 的细胞毒性。Urelumab 可用于研究弥漫性大B细胞淋巴瘤 (DLBCL)合滤泡性淋巴瘤 (FL) 等实体瘤相关疾病。 | |||
T9223 |
RO-0335
|
Reverse Transcriptase | Microbiology/Virology |
RO-0335 是新高效二苯醚非核苷逆转录酶抑制剂。它 (IC50= 1.1 nM) 可以抑制Wt HIV-1病毒,对 92% 的 NNRTI 耐药临床分离株具有保留活性 (IC50<100 nM)。 | |||
TP2325L |
Endotoxin Inhibitor acetate(147396-10-9 free base)
|
Others | Others |
Endotoxin Inhibitor acetate(147396-10-9 free base) 对细菌生理活性有很强的阻断作用,从而产生具有二硫键和大量赖氨酸的抗菌毒素抑制剂序列。内毒素抑制剂醋酸盐在酸性条件下更可能发挥生理活性 | |||
T9969 |
EZM0414
|
Histone Methyltransferase | Chromatin/Epigenetic |
EZM0414 是一种有效、选择性、口服生物利用度高的SETD2抑制剂,在 SETD2 生化分析中,IC50值为18 nM;在细胞分析中,IC50值为34 nM。EZM0414可用于复发或难治性多发性骨髓瘤和弥漫性大 B 细胞淋巴瘤的研究。 | |||
T14021 |
20-HETE
20-hydroxy Arachidonic Acid |
Others | Others |
20-HETE (20-hydroxy Arachidonic Acid) is a CYP450 metabolite and a potent vasoconstrictor and it is an endogenous inhibitor of the large-conductance Ca2+-activated K+ channel in renal arterioles. 20-HETE increases NADPH oxidase, ROS, and NF-κB activity, a | |||
T13665 |
DT2216
|
Apoptosis; Ligand for E3 Ligase; PROTACs | Apoptosis; PROTAC |
DT2216 抑制各种 Bcl-XL 依赖性白血病和癌细胞,但对血小板的毒性显着降低。DT2216 是一种选择性 B 细胞淋巴瘤,极大 (BCL-XL),蛋白水解靶向嵌合体 (PROTAC)。DT2216 靶向 bcl-XL 到 Von Hippel-Lindau (VHL) E3 连接酶进行降解。 | |||
T11820 |
LAT1-IN-1
2-氨基-2-去甲菠烷羧酸,BCH |
Apoptosis; Others | Apoptosis; Others |
LAT1-IN-1 (BCH) 是 L 型氨基酸转运蛋白 1 的选择性竞争性抑制剂,显着抑制细胞对氨基酸的摄取和 mTOR 磷酸化,从而诱导抑制癌症生长和细胞凋亡。 | |||
T22694 |
CRANAD 2
|
Others | Others |
CRANAD 2 是一种特异性近红外 (NIR) 荧光探针,可用于检测 Aβ 斑块。它可透过血脑屏障,且对 Aβ 聚集体有高亲和性,其 Kd=38 nM。 | |||
T2331 |
Solithromycin
索利霉素,OP-1068,CEM-101 |
Antibacterial; Antibiotic | Microbiology/Virology |
Solithromycin (OP-1068) 是口服可生物利用的抗菌剂,抑制肺炎链球菌、葡萄球菌、金黄色葡萄球菌和流感嗜血杆菌的细胞活力、蛋白质合成和生长速率, IC50 值分别为 7.5 ng/mL、40 ng/mL 和 125 ng/mL。它可与核糖体的大 50S 亚基结合抑制蛋白质生物合成。 | |||
T15286 |
Flindokalner
BMS-204352 |
Potassium Channel | Membrane transporter/Ion channel |
Flindokalner (BMS-204352) 是一种钾离子通道调节剂。它是大电导钙激活 K 通道正向调节剂。它是在 HEK293 细胞中表达的所有神经元 Kv7通道亚型的正调节剂。它在 Kv7.1 通道 (Ki=3.7 μM) 处显示负调节活性,并充当 GABAA 受体的负调节剂。它在体内显示出抗焦虑功效。 | |||
T60013 |
GA-017
|
Others | Others |
GA-017是一种有效的选择性 LATS1和 LATS2(大型肿瘤抑制激酶 1/2) 抑制剂,其 IC50值分别为 4.10 和 3.92 nM。GA-017 是细胞增殖的激活剂。GA-017 促进 YAP/TAZ 激活和核转位。GA-017 在 3D 培养条件下促进细胞生长。GA-017 增强小鼠肠道类器官的离体形成。 | |||
T0782 |
Benzthiazide
Aquatag,苄噻嗪,Lemazide,Dihydrex |
Carbonic Anhydrase | Metabolism |
Benzthiazide (Lemazide) 是长效利尿剂及抗高血压剂。它也是碳酸酐酶 9 的抑制剂,他对 CA9,CA2 和 CA1 的 Ki 分别为 8.0,8.8 和 10 nM。它对肿瘤细胞增殖具有抑制作用。 | |||
T4612 |
NS309
|
EGFR; Potassium Channel; HER | Angiogenesis; JAK/STAT signaling; Membrane transporter/Ion channel; Tyrosine Kinase/Adaptors |
NS309 是选择性钙依赖性钾离子通道 SK/IK 的激活剂,在 BK 通道上没有激活作用。 | |||
T4260 |
Capmatinib 2HCl
INC-280 2HCl,INCB28060盐酸盐,INCB28060 2HCl |
c-Met/HGFR | Tyrosine Kinase/Adaptors |
Capmatinib 2HCl (INC-280 2HCl) 是一种新型的 ATP 竞争性 c-MET 激酶抑制剂,IC50 为 0.13 nM。它具有皮摩尔酶效,对 c-MET 具有高度特异性,选择性超过 10, 000 倍一大组人类激酶。该抑制剂在 c-MET 依赖性肿瘤细胞系中有效阻断 c-MET 磷酸化和其关键下游效应子的激活。因此,它在体外有效抑制 c-MET 依赖性肿瘤细胞增殖和迁移,并有效诱导细胞凋亡。 | |||
T24137 |
HENA
|
||
HENA is a novel activator of large conductance, voltage- and Ca2+-gated K+ (BK) channels. | |||
T23012 |
MNI caged kainic acid
|
Others | Others |
Generates large inward currents at resting membrane potential | |||
T28195 |
NS004
NS 004,NS-004 |
||
NS004 is a large-conductance K+ channel opener, it inhibits mitochondrial function in glioma cells. | |||
T26119 |
Romifidine
Romifidinum |
||
Romifidine is used as a sedative in veterinary medicine mainly in large animals such as horses. It acts as an agonist at the α2 adrenergic receptor subtype. | |||
T26062 |
Reprimun
|
||
Reprimun has a large spectrum antibiotic activity that contains an oxyminomethyl rifamycin-SV derivative as the active substance. | |||
T25400 |
EZH2-IN-3
EZH2 inhibitor 3,EZH2-inhibitor-3 |
||
EZH2-IN-3 is an inhibitor of EZH2 and EZH1 with selective impact on diffuse large B cell lymphoma cell growth. | |||
T70144 |
ORP-101
|
||
ORP-101 is a new chemical entity designed with intent to create a large stable molecule and to confer partial μ agonist and full κ-antagonist receptor pharmacology. | |||
T71060 | IST-622 | ||
IST-622 is a unique topoisomerase inhibitor, showing significant growth-inhibitory effects against large-cell lung cancer (Lu-116) and gastric adenocarcinoma (St-4). | |||
T69033 |
Magnesium Oxaloacetate
|
||
Magnesium Oxaloacetate is an inhibitor of the amebicidal activity of activated murine macrophages, helping the parasite to survive within the mouse large intestine and increasing the survival of C. elegans exposed to H2O2. | |||
T33558 |
N,N'-Ethylenediamine disuccinic acid
L-Ethylenediaminedisuccinic acid,EDDS,EDSS |
||
N, N'-Ethylenediamine disuccinic acid, as an aminopolycarboxylic acid, can be used as a biodegradable chelating agent similar to EDTA and used on a large scale in numerous applications. | |||
T70691 |
ITP-2
|
||
ITP-2 is a selective activator of hERG channels. ITP-2 causes large depolarizing shifts in the midpoint of voltage-dependent inactivation and hyperpolarizing shifts in the voltage-dependence of activation. | |||
T29030 |
U-101958 Maleate
U101958,U-101958,U 101958 |
||
U-101958 Maleate is a ligand of dopamine D4 receptor. U-101958 Maleate also binds to a large sigma1 receptor-like component in SK-N-MC neuroblastoma cells and human cerebellum with high affinity. | |||
T40650 | Dihydroisopimaric acid | ||
Dihydroisopimaric acid activates BK channels alphabeta1, which are large conductance Ca 2+ activated K + channels. This compound directly measures the opening of BKalphabeta1 under a whole-cell voltage clamp. | |||
T27165 |
Diazaborine
Diazaborine compound 2b18,Pkf 84.474,Pkf 84474,Pkf-84474,SA-84474 |
||
Diazaborine inhibits maturation of rRNAs for the large ribosomal subunit. Diazaborine blocks ribosome biogenesis by inhibiting the AAA-ATPase Drg1. Diazaborine treatment causes, within minutes, a rapid redistribution of the protein from the nucleolus to t | |||
T19038 |
NIR-H2O2
|
Others | Others |
NIR-H2O2 is a cell-permeable near-infrared (NIR) fluorescent turn-on sensor. It responds to H2O2 with a large turn-on NIR fluorescence signal upon excitation in the NIR region. | |||
T30842 |
Cgp 6809
Cgp6809,Cgp-6809 |
||
Cgp 6809 is a new methylnitrosoureido-sugar derivative that has been shown to be active against a broad spectrum of transplantable tumours in mice and rats. CGP 6809 is a promising new agent for clinical trials, especially for large bowel and epidermoid l |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T22291 |
Chitin
Chitin (From shrimp and crab shells) |
Others | Others |
Chitin 是一种大型的结构多糖,存在于真菌的细胞壁、昆虫的外骨骼以及鱼类和无脊椎动物的某些坚硬结构中。 | |||
TN7211 |
Tetrahydroharmine
Leptaflorine |
MAO | Metabolism; Neuroscience |
Tetrahydroharmine (Leptaflorine) 是一种天然产物,存在于植物Banisteriopsis caapi cultivar Da Vine 的茎和枝中。四氢骆驼蓬碱是一种Monoamine oxidase A 抑制剂。 | |||
T1571 |
Estriol
NSC-12169,Oestriol,雌三醇 |
Estrogen Receptor/ERR; Estrogen/progestogen Receptor; MRP; Endogenous Metabolite | Endocrinology/Hormones; Immunology/Inflammation; Metabolism |
Estriol (Oestriol) 是G 蛋白偶联雌激素受体拮抗剂,能够作用于雌激素受体阴性乳腺癌细胞。 | |||
T4766 |
3-Methylglutaric acid
|
Endogenous Metabolite | Metabolism |
3-Methylglutaric acid 是亮氨酸代谢物,是一种与两种亮氨酸途径 HMGCL、AUH 酶缺陷显著相关的 C6 二元羧酸有机酸。 | |||
T5S1708 |
Dendrobine
|
Others; Influenza Virus | Microbiology/Virology; Others |
Dendrobine 是从石斛中分离的一种生物碱,对甲型流感病毒具有抗病毒活性。 | |||
T8948 |
Ferroheme
protoheme,Hematin,heme |
Others | Others |
Ferroheme (protoheme) 是一种亚铁离子和卟啉的复合物,也是脂肪酸结合大鼠肝脏脂肪酸结合蛋白的同位异构抑制剂。 | |||
T5222 |
N-(5-Aminopentyl)acetamide
Monoacetylcadaverine,N-(5-氨基戊基)乙酰胺,N-Acetylcadaverine,N-Acetyl-1,5-pentanediamine |
Others; Endogenous Metabolite | Metabolism; Others |
N-(5-Aminopentyl)acetamide (N-Acetylcadaverine) 是用作多胺尸胺的乙酰化形式。尸胺是有机体中的氨基酸分解产生的,大剂量时有毒。 | |||
T4781 |
N-Acetyl-L-phenylalanine
N-Ac-Phenylalanine,N-乙酰-L-苯丙氨酸 |
Others; Endogenous Metabolite | Metabolism; Others |
N-Acetyl-L-phenylalanine (N-Ac-Phenylalanine) 是一种大肠杆菌中的主要酰基氨基酸,由 L-苯丙氨酸和乙酰辅酶 A 合成。 | |||
T5004 |
Hyaluronic acid sodium
透明质酸钠,Sodium Hyaluronate |
Others | Others |
Hyaluronic acid sodium (Sodium Hyaluronate) 是一种生物聚合物,由二糖的重复单元组成,应用领域广泛。 | |||
T19281L |
Dihydroxyacetone phosphate hemimagnesium salt hydrate
Dihydroxyacetone phosphate hemimagnesium salt hydrate(57-04-5 free base) |
Others | Others |
Dihydroxyacetone phosphate hemimagnesium salt hydrate 也称为磷酸二羟基丙酮或 3-羟基-2-氧代丙基磷酸。 Dihydroxyacetone phosphate hemimagnesium salt hydrate 存在于从细菌到人类的所有生物中。在人类体内, Dihydroxyacetone phosphate hemimagnesium salt hydrate参与许多酶促反应。 Dihydroxyacetone phosphate hemimagnesium salt hydrate 已被研究用于治疗淋巴瘤、大细胞淋巴瘤、弥漫性淋巴瘤。 | |||
T5074 |
Cholesteryl palmitate
|
Others; Endogenous Metabolite | Metabolism; Others |
Cholesteryl palmitate 是一种慢性间质性肺炎的有用预后生物标志物。 | |||
T2864 |
Lycopene
番茄红素,ψ,ψ-Carotene |
Reactive Oxygen Species; ROS | Immunology/Inflammation; Metabolism; NF-κB |
Lycopene (ψ,ψ-Carotene) 是一种番茄及其产品和其他红色水果和蔬菜中天然存在的类胡萝卜素,具有抗氧化活性。 | |||
T4827 |
Trimethylammonium chloride
三甲胺盐酸盐,Trimethylamine hydrochloride |
Others; Endogenous Metabolite | Metabolism; Others |
Trimethylammonium chloride (Trimethylamine hydrochloride) 是动植物分解的产物。它是造成鱼腥味的主要物质,通常与脏鱼、细菌性阴道感染和口臭有关。它也与服用大剂量胆碱有关。三甲胺尿是一种遗传性疾病,身体无法从食物中代谢三甲胺。食用富含胆碱的食物后,患者的汗液、尿液和呼吸中会出现特有的鱼腥味。三甲胺尿症是一种常染色体隐性遗传病,涉及三甲胺氧化酶缺乏症。三甲氨基尿症在罗德岛红鸡中也有发现,这种鸡产的蛋有腥味。尿液中的 Trimethylammonium chloride 是食用豆类的生物标志物。 | |||
T8098 |
γ-Hexalactone
γ-caprolactone,gamma-己内酯,γ-己内酯 |
Others | Others |
γ-Hexalactone (γ-caprolactone) 是一种存在成熟水果中的 gamma 内酯。它会导致 DNA 损伤,可用作对氧磷酶 1 的底物 (PON1)。 | |||
TN1228 |
25S-Inokosterone
|
TNF | Apoptosis |
25S-Inokosterone exhibits potent inhibition against TNF-expression levels in A23187 plus phorbol-myrisrate acetate-induced RBL-2H3 cells. 25S-Inokosterone has excellent anti-atopy activity, thus 25S-Inokosterone could be used to a large range of functional anti-atopy cosmetics. | |||
T25579 |
Kijanimicin
Kijanimicin sodium salt |
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Kijanimicin is an antitumor and antibiotic. It is a unique, large acid enol antibiotic and possesses an unusual in vitro spectrum of activity against some Gram-positive and anaerobic microorganisms. It has also shown interesting activity against malaria i | |||
TN1227 |
25R-Inokosterone
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TNF | Apoptosis |
25R-Inokosterone exhibits potent inhibition against TNF-expression levels in A23187 plus phorbol-myrisrate acetate-induced RBL-2H3 cells. 25R-Inokosterone has excellent anti-atopy activity, thus 25R-Inokosterone could be used to a large range of functional anti-atopy cosmetics. | |||
T5S2073 | Senkyunolide A | Others | Others |
Senkyunolide A 是用于川芎和当归的质量评价和化学鉴别的有用标准化合物,适用于大量样品的分析。 Senkyunolide A 在大鼠离体主动脉的各种收缩剂的收缩中具有血管舒张活性。 | |||
TN4040 | Eupatoriochromene | Antifection | Microbiology/Virology |
Eupatoriochromene retard seed germination , reduced radicle and hypocotyl growth of weed and crop plant seedlings and increased adventitious root formation of mung bean cuttings. Eupatoriochromene has insecticidal activity, it exhibits toxicity againstCul |