6
3
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T10140 |
4-Diethylaminobenzaldehyde
|
Dehydrogenase | Metabolism |
4-Diethylaminobenzaldehyde 是醛脱氢酶(ALDHs)的可逆抑制剂,对 ALDH1 的 Ki 为 4 nM,具有较强的抗雄激素作用 ,IC50为1.71 μM。 | |||
T14843 |
Bifluranol
BX341 |
Androgen Receptor | Endocrinology/Hormones |
Bifluranol (BX341) 具有抗雄激素活性,在体内实验中显示出显著的抗前列腺活性,可用于治疗良性前列腺增生 (BPH)。 | |||
T30161 |
EN3356
AS N001,ASN-001 |
P450 | Metabolism |
EN3356 是一种可口服且具有选择性的类固醇 17-α- 羟化酶/C17,20 裂解酶(CYP17A1 或 CYP17)抑制剂,是一种非甾体类裂解酶选择性化合物,具有潜在的抗雄激素和抗肿瘤活性。 | |||
T25961 |
Piperophos
Rilof |
||
Piperophos is an organophosphate with anti-androgenic activities. | |||
T81662 |
N-Nitrosodicyclohexylamine
NDCHA |
Androgen Receptor | Endocrinology/Hormones |
N-Nitrosodicyclohexylamine (NDCHA) 是一种N-亚硝基化合物,具有抗雄激素活性。它通过与雄激素受体 (AR) 竞争性结合来抑制 5α-二氢睾酮的作用,并能降低 AR 蛋白水平。 | |||
T73671 |
7β-Hydroxy-epi-androsterone
|
||
7β-Hydroxy-epi-androsterone (7β-Hydroxy-EpiA) 是一种与ERβ结合的内源性雄激素衍生物,具有抗炎和神经保护特性。该化合物来源于dehydroepiandrosterone。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T7957 |
2-Isopropyl Thioxanthone
|
Others | Others |
2-Isopropyl Thioxanthone 具有潜在的抗雌激素和抗雄激素特性。 | |||
T1284 |
Megestrol acetate
SC10363,醋酸甲地孕酮,BDH1298 |
Glucocorticoid Receptor; Estrogen/progestogen Receptor; Progesterone Receptor; HIV Protease; Autophagy | Autophagy; Endocrinology/Hormones; Microbiology/Virology; Others; Proteases/Proteasome |
Megestrol acetate (BDH1298) 是具有口服活性的合成孕激素。它还具有抗雄激素特性,可用于治疗厌食症和恶病质。 | |||
TN4604 | Myricanone | BCL; HSP; NF-κB; ROS; Caspase; STAT | Apoptosis; Cytoskeletal Signaling; Immunology/Inflammation; JAK/STAT signaling; Metabolism; NF-κB; Proteases/Proteasome; Stem Cells |
Myricanone has antioxidant, and anticancer activities, it has apoptosis-promoting ability by triggering caspase activation, and suppression of cell proliferation by down-regulation of NF-κB and STAT3 signalling cascades. Myricanone shows in vitro testost |