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Cat. No. | Product Name | Target | Signaling Pathways |
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T24840 |
STS-E412
STS E412,STSE412 |
Others | Others |
STS-E412 是一种具有组织保护性和选择性的 EPOR/CD131 受体激活剂,可用于研究神经系统疾病。 | |||
T2577 |
Dienogest
地诺孕素,STS 557 |
Apoptosis; Estrogen/progestogen Receptor; Progesterone Receptor; Autophagy | Apoptosis; Autophagy; Endocrinology/Hormones; Others |
Dienogest (STS 557) 是一种孕酮受体激动剂,作用于子宫内膜异位,有口服的子宫内膜活性。 | |||
T10665 |
Calcium-Sensing Receptor Antagonists I
|
Others | Others |
Calcium-Sensing Receptor Antagonists I functions as an antagonist to the parathyroid hormone receptors that sense calcium. | |||
T11413 |
Glucagon receptor antagonists-1
|
Others | Others |
Glucagon receptor antagonist -1 is a highly effective glucagon receptor antagonist. | |||
T15584 |
Integrin Antagonists 27
|
Others | Others |
Integrin Antagonists 27 is a small molecule integrin αvβ3 antagonist. It has a binding affinity of 18 nM and as a novel anticancer agent. | |||
TP2421 |
Ysdspstst peptide
|
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Ysdspstst peptide is a biochemical. | |||
T25973 |
Poststatin
|
||
Poststatin is a prolyl endopeptidase inhibitor produced by Streptomyces viridochromogenes MH534-30F3. | |||
T126527 |
Poststerone
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||
Poststerone 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T126527。 | |||
T11416 | Glucagon receptor antagonists-5 | Others | Others |
Glucagon receptor antagonists-5 is an orally bioavailable indazole-based glucagon receptor antagonist (Ki: 32 nM). It has potential for the treatment of type 2 diabetes mellitus (T2DM). | |||
T11415 |
Glucagon receptor antagonists-3
|
Others | Others |
Glucagon receptor antagonist -3 is a highly effective glucagon receptor antagonist. | |||
T11414 |
Glucagon receptor antagonists-2
|
Others | Others |
Glucagon receptor antagonist -2 is a highly effective glucagon receptor antagonist. | |||
T72470 |
Estrone O-sulfamate
Estrone 3-O-sulfamate |
Others | Others |
Estrone O-sulfamate (Estrone 3-O-sulfamate) 是一种高效的的类固醇硫酸酯酶 (STS) 抑制剂。Estrone O-sulfamate 是一种胎盘微粒体抑制剂 (P.M.) ,IC50 值分别为 18 nM。Estrone O-sulfamate 在 MCF-7 细胞中对 STS 显示出抑制作用,IC50 值分别为 0.83 nM。Estrone O-sulfamate 可用于研究癌症。 | |||
T81089 | Steroid sulfatase-IN-7 | ||
Steroid sulfatase-IN-7是一种具有高度选择性的不可逆STS抑制剂,表现出0.05 nM的强效对人胎盘STS抑制能力,常被用于癌症方面的科学研究。 | |||
T81090 | Steroid sulfatase-IN-6 | ||
Steroid sulfatase-IN-6 (Compound 10c) 是一种针对类固醇硫酸酯酶 (STS) 的不可逆抑制剂,对人胎盘 STS 的 Ki 值达到 0.4 nM。该化合物适用于肿瘤疾病研究。 | |||
T62237 | Steroid sulfatase-IN-4 | ||
Steroid sulfatase-IN-4 (Compound 16) 是一种类固醇硫酸酯酶 (STS) 的不可逆抑制剂,能够作用于人 STS (IC50: 25 nM)。Steroid sulfatase-IN-4 能够用于研究子宫内膜异位。 | |||
T61686 |
Steroid sulfatase-IN-3
|
||
Steroid sulfatase-IN-3 (compound 1q) is a highly effective Steroid sulfatase (STS) inhibitor, exhibiting an IC 50 value of 25.8 nM. This compound also demonstrates antiproliferative properties against T-47D estrogen-dependent breast cancer cells, with an IC 50 of 1.04 μM [1]. | |||
T61212 | Steroid sulfatase-IN-2 | ||
Steroid sulfatase-IN-2 is an active inhibitor of steroid sulfatase (STS), demonstrating an IC50 value of 109.5 nM. Its potential application lies in hormone-dependent cancer research, specifically estrogen-dependent breast and endometrial cancer [1]. | |||
T81091 | Steroid sulfatase-IN-5 | ||
Steroid sulfatase-IN-5 (compound 10b) 是一种高效的STS抑制剂,具有0.32 nM的IC50值。该化合物还能显著抑制T-47D细胞增殖,其IC50为35.7 μM,常用于乳腺癌相关的研究领域。 | |||
T62236 | Steroid sulfatase/17β-HSD1-IN-3 | ||
Steroid sulfatase/17β-HSD1-IN-3 (compound 19) 是一种双重的类固醇硫酸酯酶 (STS) 和 17β-羟基类固醇脱氢酶 1 型 (17β HSD1) 抑制剂。Steroid sulfatase/17β-HSD1-IN-3 对 hSTS 的活性具有不可逆的抑制作用 (IC50: 27 nM)。Steroid sulfatase/17β-HSD1-IN-3 能够用于研究子宫内膜异位症及其他雌激素依赖性疾病。 | |||
T61979 | Steroid sulfatase/17β-HSD1-IN-4 | ||
Steroid sulfatase/17β-HSD1-IN-4 (compound 37) 是一种类固醇硫酸酯酶 (STS) 和 17β-羟基类固醇脱氢酶 1 型 (17β HSD1) 双重抑制剂。Steroid sulfatase/17β-HSD1-IN-4 对 hSTS 的活性抑制作用不可逆,IC50为 63 nM。Steroid sulfatase/17β-HSD1-IN-4 在子宫内膜异位症及其他雌激素依赖性疾病方面有研究价值。 | |||
T81092 | Steroid sulfatase/17β-HSD1-IN-5 | ||
Steroid sulfatase/17β-HSD1-IN-5 是一种不可逆抑制剂,针对类固醇硫酸酯酶(STS),同时也是17β-羟甾类固醇脱氢酶1型(17β-HSD1)的可逆且选择性抑制剂,表现出对17β-HSD1的IC50为43 nM,对17β-HDS1为6.2 μM。该化合物主要用于研究代谢性疾病,特别是子宫内膜异位症。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6680 |
Staurosporine
Antibiotic AM-2282,星形孢菌素,AM-2282,CGP 41251,星孢菌素 |
Apoptosis; PKA; Antibacterial; Antibiotic; Src; PKC; Antifungal | Angiogenesis; Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling; Microbiology/Virology; Tyrosine Kinase/Adaptors |
Staurosporine (AM-2282) 是一种蛋白激酶抑制剂,对 PKC、PKA、c-Fgr、Phosphorylase kinase 和 TAOK2 均有抑制活性 (IC50=6/15/2/3/3000 nM),具有 ATP 竞争性和非选择性。Staurosporine 也可以诱导凋亡。 | |||
T36857 |
Estrone sulfate sodium
雌酮3-硫酸钠,Estrone 3-sulfate (sodium salt),17β-Estrone 3-sulfate |
Endogenous Metabolite | Metabolism |
Estrone sulfate sodium (17β-Estrone 3-sulfate) 是一种主要的循环血浆雌激素,无生物活性,通过类固醇硫酸酯酶(STS) 转化为生物活性雌激素雌酮。 | |||
TN5091 |
Tagitinin A
|
PPAR; Antifection | DNA Damage/DNA Repair; Metabolism; Microbiology/Virology |
Tagitinin A is a plant insecticidal compound, it has phytotoxic activity, it shows significant inhibition of wheat coleoptile growth, seed germination, and the growth of STS and weeds. Tagitinin A is also a PPARα/γ dual agonist , it exerts anti-diabetic e |