Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T8520 |
Tetrazole
1H-TETRAZOLE,1H-四唑 |
Antibacterial | Microbiology/Virology |
Tetrazole (1H-TETRAZOLE) 是羧酸的生物等排体,具有相当的抗菌性能。 | |||
T6716 |
Valsartan
Diovan,缬沙坦,Tareg,CGP 48933 |
RAAS | Endocrinology/Hormones |
Valsartan (CGP 48933) 是一种血管紧张素 II 受体拮抗剂,有用于高血压和心力衰竭的研究潜力。 | |||
T63376 |
CB 168
|
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CB 168是有效的靶向异亮基 tRNA 合成酶 (IleRS) 选择性氨基酰基氨基酰芳基四唑抑制剂。 | |||
T74273 |
Antifungal agent 52
|
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Antifungal agent 52 (compound 6c) 是四唑衍生物。Antifungal agent 52 抑制麦角固醇 的合成。Antifungal agent 52 对白色念珠菌表现出显着的抗真菌活性 Antifungal agent 52 影响白色念珠菌基底细胞膜通透性。 | |||
T78773 |
Tubulin inhibitor 38
|
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Tubulin inhibitor 38(化合物14)是一款强效的四唑基微管蛋白抑制剂,能够显著抑制细胞增殖。以100 nM浓度作用24小时后,该抑制剂能够引起有丝分裂停滞,特别是在G2/M期细胞周期阶段,进而诱导细胞凋亡。在HeLa、MCF7和U87 MG细胞系中,Tubulin inhibitor 38展现了较高的细胞毒性及选择性。 | |||
T38844 |
MK-8245 Trifluoroacetate
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MK-8245 trifluoroacetate is a liver-targeting inhibitor of stearoyl-CoA desaturase (SCD) with IC50 of 1 nM for human SCD1 and 3 nM for both rat SCD1 and mouse SCD1, with anti-diabetic and anti-dyslipidemic efficacy. IC50 value: 1 nM (hSCD1) Target: SCD1 in vitro: MK-8245, a phenoxy piperidine isoxazole derivative, has been identified as a potent and liver-specific SCD inhibitor. It contains a tetrazole acetic acid moiety, which is the key molecule for OATPs recognition and liver-targeting. MK... |