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货号 产品名 纯度
A1176943 现货 UT-155

99%
A1249543 现货 VPC-13566

99%
A2328208 现货 Androgen receptor degrader-1

99%
A478291 现货 (R)-Bicalutamide/(R)-比卡鲁胺

99%
A573327 现货 LY2452473

99%
A1167310 现货 Ralaniten

99%
A1339048 现货 UT-34

99%
A1448575 现货 VPC-14449

99%
A1489661 现货 Masofaniten

98%
A1365651 现货 Apalutamide-d4

99%
A1487533 现货 JNJ-63576253

99%
A593783 现货 Monobutyl phthalate

Monobutyl phtalate is a metabolite of di(n-butyl)phthalate. It affects the expressions of EMT-related proteins and enhances the migration and invasion of MLTC-1 cells.

99%
A112189 现货 Triptophenolide/雷酚内酯

Triptophenolide is a colorless crystalline plate isolated from ethyl acetate extracts of Tripterygium wilfordii.

99%
A754229 现货 Hydroxyflutamide/羟基氟他胺

Hydroxyflutamide is a derivative of the synthetic steroid ethisterone, that suppresses the production of gonadotrophins, and has some weak androgenic effects.

99%
A516990 现货 Brassicasterol/油菜甾醇

98%
A155014 现货 3,3'-Diindolylmethane/3,3'-亚甲基二吲哚

3,3'-Diindolylmethane is an AR structurally similar androgen receptor antagonist.

99%
A1228867 现货 ARCC-4

ARCC-4 is a PROTAC, acting as an androgen receptor degrader. ARCC-4 is a low-nanomolar androgen receptor degrader able to degrade about 95% of cellular androgen receptors. ARCC-4 inhibits prostate tumor cell proliferation, degrades clinically relevant androgen receptor point mutants and unlike enzalutamide, retains antiproliferative effect in a high androgen environment. Thus, ARCC-4 exemplifies how protein degradation can address the drug resistance hurdles of enzalutamide.

99%
A526563 现货 N-desmethyl Enzalutamide

N-Desmethyl enzalutamide is a major metabolite of Enzalutamide, Enzalutamide (MDV3100) is an androgen-receptor (AR) antagonist with IC50 of 36 nM.

99%
A517338 现货 ORM-15341

ORM-15341 is a potent and full antagonist for human AR (hAR) with IC50 values of 38 nM as shown by transactivation assays in AR-HEK293 cells stably expressing full-length hAR and an androgen-responsive luciferase reporter gene construct.

99%
A136293 现货 Apalutamide

ARN-509 can compeitively and selectively inhibit androgen receptor with IC50 value of 16 nM.

99%
产品名 Androgen Receptor 其他靶点 纯度
Cyproterone acetate ++++

Androgen Receptor, IC50: 7.1 nM

98%
Apalutamide +++

Androgen Receptor, IC50: 16 nM

98%
AZD3514 +

Androgen Receptor, Ki: 2.2 μM

99%
Darolutamide ++++

Androgen receptor, Ki: 11 nM

98%
Flutamide +++

Androgen Receptor, Ki: 55 nM

98%
Galeterone ++

Androgen Receptor, IC50: 384 nM

98%
Enzalutamide +++

Androgen Receptor, IC50: 36 nM

98%
Megestrol 98%
Bicalutamide ++

Androgen Receptor, IC50: 0.16 μM

99%
EPI-001 +

Androgen Receptor, IC50: ~6 μM

98%
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。
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