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首页 > 产品展示 > Endocrinology & Hormones
目录号 产品名称 产品描述
R10065 Losartan potassium Losartan is an angiotensin II receptor antagonist, competes with the binding of
R10075 Apalutamide (ARN-509) Apalutamide (ARN-509) 是有效,竞争性的 雄激素受体 (AR) 拮抗剂,IC50 为 16 nM。
R10110 LCZ696;Sacubitril/Valsartan LCZ696 (Sacubitril/Valsartan) 是由 Valsartan (an ARB) 和 Sacubitril (AHU377) 组成,摩尔比
R10111 Enzalutamide; MDV3100 Enzalutamide (MDV3100) 是一种雄激素受体 (androgen receptor (AR)) 拮抗剂,在LNCaP前列腺细胞中抑制AR 的
R10184 GW9508 GW9508 is a potent and selective agonist for FFA1 (GPR40) with pEC50 of 7.32, 10
R10194 OC000459 OC000459 is a potent and selective D prostanoid receptor 2 (DP2) antagonist with
R10244 Fasiglifam (TAK-875) Fasiglifam (TAK-875) 是一种有效的,可口服的,具有选择性的 GPR40 激动剂,EC50 值为 72 nM。
R10245 Ostarine; MK2866 Andarine is a selective non-steroidal androgen receptor (AR) agonist with Ki of
R10415 AZD1981 AZD1981 is a potent, selective CRTh2 (DP2) receptor antagonist with IC50 of 4 nM
R10453 ExemestaneF; CE24304 Exemestane is an aromatase inhibitor, inhibits human placental and rat ovarian a
R10500 Fluticasone propionate Fluticasone Propionate is a synthetic glucocorticoid, used to treat non-allergic
R10510 Fulvestrant; Faslodex; ICI182780; ZD9238; ZM182780 Fulvestrant is an estrogen receptor (ER) antagonist with IC50 of 0.94 nM in a ce
R10515 Dutasteride; GG 745; GI198745 Dutasteride is a dual 5-α reductase inhibitor that inhibits conversion of testos
R10549 Azilsartan medoxomil; TAK491 Azilsartan Medoxomil is a potent angiotensin II type 1 (AT1) receptor antagonist
R10674 APD668 APD668 is a potent GPR119 agonist with EC50 of 2.7 nM and 33 nM for hGPR119 and
R10893 JNJ38431055; APD-597 APD597是GPR119激动剂, 作用于hGPR119, EC50为46 nM, 可用于治疗2型糖尿病。 
R10912 Darolutamide; ODM-201; BAY-1841788 Darolutamide (ODM-201;BAY-1841788) 是有效的雄激素受体 (AR) 拮抗剂, 在体内试验中的 IC50 值为26 nM。
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