Androgen Receptor
Androgen Receptor(雄激素受体)
AR (androgen receptor) is a member of steroid hormone receptor and ligand-activated transcription factor. It plays a crucial role in prostate cellular proliferation and male sexual differentiation.
Androgen Receptor 相关产品(148)
- GC1755717 alpha-propionateCAS: 19608-29-8纯度: >98.50%
A peripherally selective androgen receptor antagonist
- GC26431Pentacosafluorotridecanoic AcidCAS: 72629-94-8纯度: >97.00%
Perfluorotridecanoic Acid (Perfluorinated Compound (PFC)) is a perfluorinated alkyl acid (PFAA) and a possible organic pollutant.
- GC30101GLPG0492 R enantiomerCAS: 1215085-93-0纯度: >99.50%
GLPG0492Renantiomer是GLPG0492的R型对映体,GLPG0492是新型选择性SARM
- GC30710(R)-UT-155CAS: 2031161-54-1纯度: >98.00%
(R)-UT-155(compound11)是一种选择性的、雄激素受体降解物(SARD)配体。活性低于S型异构体。
- GC31254Androst-4-ene-3,17-diol, dipropanoate, (3β,17β)- (Androst-4-ene-3β,17β-diol, dipropionate)CAS: 56699-31-1
Androst-4-ene-3,17-diol,dipropanoate,(3β,17β)-是睾酮代谢物4-雄烯二醇的二丙酸酯。
- GC31742Ailanthone (δ13-Dehydrochaparrinone)CAS: 981-15-7纯度: >99.50% / >98.00%
Ailanthone (δ13-Dehydrochaparrinone)是一种源自传统中药植物臭椿( Ailanthus altissima )的苦木素类化合物,是全长雄激素受体(AR)(IC 50 =69nM)及其组成型活性截短剪接变体(AR-Vs)(IC 50 =309nM)的强效抑制剂。
- GC32907N-desmethyl Enzalutamide (N-desmethyl MDV 3100)CAS: 1242137-16-1纯度: >99.00%
N-desMethyl EnzalutaMide (N-desmethyl MDV 3100) is the active metabolite of Enzalutamide, which is an oral androgen receptor inhibitor for treatment of castration-resistant prostate cancer.
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC16840 | ARN-509 | 956104-40-8 | >99.50% | |
ARN-509是一种合成的双芳基硫代乙内酰脲化合物,抑制雄激素受体(AR),IC 50 值为16nM。 | ||||
| GC17160 | 2-hydroxy Flutamide | 52806-53-8 | - | |
An active metabolite of the antiandrogen flutamide | ||||
| GC17491 | CITCO | 338404-52-7 | >99.50% | |
An agonist of human CAR | ||||
| GC17557 | 17 alpha-propionate | 19608-29-8 | >98.50% | |
A peripherally selective androgen receptor antagonist | ||||
| GC17679 | GSK2881078 | 1539314-06-1 | >99.00% | |
A selective androgen receptor modulator | ||||
| GC18496 | Leelamine (hydrochloride) | 16496-99-4 | - | |
An inhibitor of pyruvate dehydrogenase kinase | ||||
| GC19305 | RAD140 | 1182367-47-0 | >99.00% | |
An androgen receptor modulator | ||||
| GC19458 | 6β-hydroxy Testosterone | 62-99-7 | >97.00% | |
CYP3A metabolite of testosterone | ||||
| GC26431 | Pentacosafluorotridecanoic Acid | 72629-94-8 | >97.00% | |
Perfluorotridecanoic Acid (Perfluorinated Compound (PFC)) is a perfluorinated alkyl acid (PFAA) and a possible organic pollutant. | ||||
| GC30086 | GLPG0492 | 1215085-92-9 | >99.50% | |
A selective androgen receptor modulator | ||||
| GC30101 | GLPG0492 R enantiomer | 1215085-93-0 | >99.50% | |
GLPG0492Renantiomer是GLPG0492的R型对映体,GLPG0492是新型选择性SARM | ||||
| GC30710 | (R)-UT-155 | 2031161-54-1 | >98.00% | |
(R)-UT-155(compound11)是一种选择性的、雄激素受体降解物(SARD)配体。活性低于S型异构体。 | ||||
| GC31254 | Androst-4-ene-3,17-diol, dipropanoate, (3β,17β)- (Androst-4-ene-3β,17β-diol, dipropionate) | 56699-31-1 | - | |
Androst-4-ene-3,17-diol,dipropanoate,(3β,17β)-是睾酮代谢物4-雄烯二醇的二丙酸酯。 | ||||
| GC31380 | LY2452473 | 1029692-15-6 | >98.00% | |
LY2452473是一种选择性雄激素受体(AR)调节剂(SARM)。 | ||||
| GC31441 | DJ-V-159 | 2253744-53-3 | >99.50% | |
DJ-V-159 is an agonist for G protein-coupled receptor family C group 6 member A (GPRC6A). | ||||
| GC31442 | YK11 | 1370003-76-1 | >98.00% | |
A partial agonist of the androgen receptor | ||||
| GC31577 | Bifluranol (BX341) | 34633-34-6 | >98.50% | |
Bifluranol (BX341) (BX341) 是一种抗雄激素。 | ||||
| GC31738 | ACP-105 | 899821-23-9 | >99.00% | |
ACP-105 is an orally available and potent selective androgen receptor modulator (SARM) with pEC50 of 9.0 and 9.4 for AR wild type and AR mutation T877A, respectively. | ||||
| GC31742 | Ailanthone (δ13-Dehydrochaparrinone) | 981-15-7 | >99.50% / >98.00% | |
Ailanthone (δ13-Dehydrochaparrinone)是一种源自传统中药植物臭椿( Ailanthus altissima )的苦木素类化合物,是全长雄激素受体(AR)(IC 50 =69nM)及其组成型活性截短剪接变体(AR-Vs)(IC 50 =309nM)的强效抑制剂。 | ||||
| GC32402 | ORM-15341 | 1297537-33-7 | >98.50% | |
ORM-15341 is a potent and full antagonist for human AR (hAR) with IC50 value of 38 nM and the inhibition constant (Ki) value of 8?nM. | ||||
| GC32403 | LGD-3303 | 917891-35-1 | >98.00% | |
LGD-3303是一种口服的非甾体选择性雄激素受体调节剂(SARM),与雄激素受体具有高亲和力(K i =0.9nM)。 | ||||
| GC32408 | LGD-4033 (Ligandrol) | 1165910-22-4 | - | |
An Analytical Reference Standard | ||||
| GC32907 | N-desmethyl Enzalutamide (N-desmethyl MDV 3100) | 1242137-16-1 | >99.00% | |
N-desMethyl EnzalutaMide (N-desmethyl MDV 3100) is the active metabolite of Enzalutamide, which is an oral androgen receptor inhibitor for treatment of castration-resistant prostate cancer. | ||||
| GC32908 | UT-155 | 2031161-35-8 | >99.50% | |
UT-155是一种选择性的、有效的雄激素受体(AR)拮抗剂,与AR-LBD结合的Ki值为267nM。 | ||||
