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抑制剂 & 化合物

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Cat. No.	Product Name	Target	Signaling Pathways
T0272	Nilutamide 尼鲁米特,RU23908	Androgen Receptor	Endocrinology/Hormones
	Nilutamide (RU23908) 是一种非甾体抗雄激素药物，有用于转移性前列腺癌的潜力。
T3521	γ-Secretase-IN-1 Compound E	Beta Amyloid; Gamma-secretase	Neuroscience; Proteases/Proteasome; Stem Cells
	γ-Secretase-IN-1 是一种高效的 γ-secretase 抑制剂，对T-47D 细胞显示部分抗增殖活性且抑制 β-amyloid(40)，β-amyloid(42)，和Notch γ-分泌酶裂解。
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].
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。
T36860	C22 Sphingomyelin (d18:1/22:0) C22 Sphingomyelin (d18:1/22:0)
	C22 Sphingomyelin is a naturally occurring form of sphingomyelin . Plasma levels of C22 sphingomyelin positively correlate with hepatic steatosis severity in patients with chronic hepatitis C virus (HCV). C22 Sphingomyelin levels are decreased in T-47D mammary epithelial cells and increased in MDA-MB-231 breast cancer cells relative to C16 sphingomyelin .
T14144	AGN-195183	Others	Others
	AGN 195183 is a potent and selective agonist of RARα(Kd=3 nM) with improved binding selectivity relative to AGN 193836; no activity on RARβ/γ. IC50 value: 3 nM (Kd); 200 nM (EC80, RAR Trans.) Target: RARα agonist Compound 4(AGN-195183) inhibited the growt

化合物

Nilutamide

Cat.No: T0272

Synonym: 尼鲁米特,RU23908

Target: Androgen Receptor

γ-Secretase-IN-1

Cat.No: T3521

Synonym: Compound E

Target: Beta Amyloid, Gamma-secretase

Steroid sulfatase-IN-3

Cat.No: T61686

Synonym:

Target:

Steroid sulfatase-IN-5

Cat.No: T81091

Synonym:

Target:

C22 Sphingomyelin (d18:1/22:0)

Cat.No: T36860

Synonym: C22 Sphingomyelin (d18:1/22:0)

Cat. No.	Product Name	Target	Signaling Pathways
TN1768	Iriflophenone	Estrogen Receptor/ERR; Estrogen/progestogen Receptor	Endocrinology/Hormones
	Iriflophenone 是从 Aquilaria sinensis 中分离得到，能诱导 MCF-7 和 T-47D 人乳腺癌细胞增殖。
TN4457	Lucidal	Others	Others
	Lucialdehyde C (Lucidal) exhibits potent cytotoxicity against LLC, T-47D, Sarcoma 180, and Meth-A tumor cells with ED(50) values of 10.7, 4.7, 7.1, and 3.8 microg/ml, respectively.
TN4455	Lucialdehyde B	Integrase; HSV	Microbiology/Virology
	Lucialdehyde B exhibits potent inhibitory activity against herpes simplex virus. It shows cytotoxic effects on Lewis lung carcinoma (LLC), T-47D, Sarcoma 180, and Meth-A tumor cell lines.