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Ostarine (MK-2866, GTx-024)
Catalog No. A10253 Androgen Receptor ModulatorsOstarine (MK-2866,GTX-024)是一种雄激素受体调节剂(SARM)。 了解更多 -
(R)-Bicalutamide
Catalog No. A10008 Androgen Receptor 拮抗剂(R)-Bicalutamide是一种活性的竞争性非甾体雄激素受体拮抗剂，对MDA 453细胞的IC50为0.17μM。 了解更多 -
Bicalutamide (Casodex)
Catalog No. A10142 Androgen Receptor 拮抗剂Bicalutamide (Casodex)是一种口服非甾体抗雄激素，用于治疗前列腺癌和多毛症。 了解更多 -
Andarine (GTX-007)
Catalog No. A10076 -
Cyproterone acetate
Catalog No. A11409 Androgen Receptor 拮抗剂Cyproterone acetate是17-羟孕酮的合成衍生物，可作为雄激素受体拮抗剂以及具有弱孕激素和糖皮质激素活性的弱孕激素受体激动剂。 了解更多 -
Eprosartan
Catalog No. A11121 -
Betamethasone dipropionate
Catalog No. A10130 Glucocorticoid Receptor 激动剂Betamethasone Dipropionate是糖皮质激素类固醇，具有抗炎和免疫抑制特性。 了解更多 -
Azilsartan (TAK-536)
Catalog No. A11775 -
Tamoxifen Citrate
Catalog No. A10885 Estrogen receptor 拮抗剂Tamoxifen Citrate是哺乳动物甾醇异构酶的选择性和有效抑制剂。 了解更多 -
Prednisone (Adasone)
Catalog No. A10752 -
Acolbifene (EM 652, SCH57068)
Catalog No. A12771 estrogen receptor modulatorAcolbifene (EM 652,SCH57068)是第四代选择性的estrogen receptor拮抗剂，LC50 值为 22±3 nM。用于预防高乳腺癌女性的乳腺癌。 盐酸阿科比芬与体内雌激素受体结合，阻断雌激素对乳房的作用。 它是选择性雌激素受体调节剂（SERM）的一种。 了解更多 -
PD 123319 ditrifluoroacetate
Catalog No. A13201 angiotensin AT2 receptor 拮抗剂PD 123319 ditrifluoroacetate是一种有效的，选择性的非肽血管紧张素AT2受体拮抗剂。大鼠肾上腺组织和大脑的IC50值分别为34和210 nM。 了解更多 -
AZD5423
Catalog No. A13249 -
(Glp1)-Apelin-13
Catalog No. A13215 -
Tasosartan
Catalog No. A10891 -
Lonaprisan
Catalog No. A14130 progesterone receptor 拮抗剂Lonaprisan是米非司酮相关类固醇的口服生物可利用的五氟乙基衍生物，具有抗孕激素活性。 了解更多 -
LCZ696 (Valsartan)
Catalog No. A14206 angiotensin receptor-neprilysin 抑制剂LCZ696 (Valsartan)是一种生物利用型双效血管紧张素受体-中性溶血素抑制剂（ARNi），用于治疗高血压和心力衰竭。 了解更多 -
Ospemifene
Catalog No. A14261 -
N-desMethyl EnzalutaMide
Catalog No. A13964 -
Nestoron
Catalog No. A15184 -
Tanaproget
Catalog No. A15256 Progesterone receptor 激动剂Tanaproget是一种新型的非甾体孕激素受体激动剂，与参考甾体孕激素相比，它可以更高的相对亲和力与各种物种的PR结合。 了解更多 -
Toremifene
Catalog No. A15265 -
ODM-201
Catalog No. A15797 -
AZD9496
Catalog No. A15822 -
EXP-3174
Catalog No. A15451 -
RU43044
Catalog No. A14340 -
GSK-2881078
Catalog No. A12645 androgen receptor modulatorGSK-2881078是一种选择性雄激素受体调节剂（SARM），正在针对肌肉萎缩以改善其身体功能的受试者的肌肉生长和力量进行评估。 了解更多 -
(E/Z)-4-hydroxy Tamoxifen
Catalog No. A12532 Estrogen receptor 拮抗剂(E/Z)-4-hydroxy Tamoxifen是他莫昔芬的活性代谢产物，是一种选择性雌激素受体（ER）调节剂，广泛用于乳腺癌的治疗和化学预防治疗。 了解更多 -
GDC-0810 (Brilanestrant)
Catalog No. A15958 Estrogen receptor degraderGDC-0810 (Brilanestrant)是一种口服可生物利用的选择性雌激素受体降解剂（SERD），在耐他莫昔芬的乳腺癌异种移植物中表现出强大的活性。 了解更多 -
Medroxyprogesterone Acetate
Catalog No. A11625 progesterone receptor 激动剂Medroxyprogesterone acetate是一种孕激素，是人激素黄体酮的合成变异体，也是一种强效的黄体酮受体激动剂。 了解更多 -
Azilsartan Medoxomil
Catalog No. A16420 angiotensin II receptor type 1 拮抗剂Azilsartan medoxomil是一种口服给药的1型血管紧张素II受体拮抗剂，IC50为0.62 nM。 了解更多 -
Beclometasone
Catalog No. A18177 glucocorticoid receptor agonistBeclometasone, also known as Beclomethasone, is an anti-inflammatory, synthetic glucocorticoid. It is used topically as an anti-inflammatory agent and in aerosol form for the treatment of asthma. 了解更多 -
PROTAC ERRα ligand 2
Catalog No. A18939 ERRα inverse agonistPROTAC ERRα ligand 2 is an estrogen-related receptor α (ERRα) inverse agonist with an IC50 of 5.67 nM. PROTAC ERRα ligand 2 (IC50=5.67 nM) displays a ~11-fold improved potency than XCT790 (IC50=61.3 nM). 了解更多 -
PROTAC ER Degrader-3
Catalog No. A18519 PROTAC ER Degrader-3 is an intermediate for synthesis of PAC. PAC, consists the ADCs linker and PROTACs, conjugated to an antibody. PAC extracts from patent WO2017201449A1, compound LP2. PAC conjugated to an antibody is a more marked estrogen receptor-alpha (ERα) degrader compared to PROTAC (without Ab). 了解更多 -
(R)-Elagolix
Catalog No. A21184 GnRHR antagonistElagolix is a highly potent, selective, orally-active, short-duration, non-peptide antagonist of the gonadotropin-releasing hormone receptor (GnRHR) (KD = 54 pM). 了解更多
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