20
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T10320 | Androgen receptor antagonist 1 | Others | |
Androgen receptor antagonist 1 is an orally available full androgen receptor antagonist (IC50: 59 nM). It can be used in the synthesis of PROTAC AR degraders, which results in 24% and 47 % AR protein degradation in LNCaP... | |||
T0380 | Bicalutamide | ICI-176334 | Androgen Receptor , Autophagy |
Bicalutamide (ICI-176334), a synthetic, nonsteroidal antiandrogen, competitively binds to cytosolic androgen receptors in target tissues, thereby inhibiting the receptor binding of androgens. | |||
T9035 | Testosterone undecanoate | Others , Androgen Receptor | |
Testosterone undecanoate is a metabolite of Testosterone, which is a promising androgen for male hormonal contraception. | |||
T22263 | Bavdegalutamide | ARV-110 | Androgen Receptor |
Bavdegalutamide (ARV-110) is a PROTAC degrader of androgen receptor (AR). Bavdegalutamide can be used in studies about prostate cancer. Bavdegalutamide shows oral activity and selectivity and facilitates the ubiquitinati... | |||
T60988 | Androgen receptor antagonist 4 | ||
Androgen receptor antagonist 4 (Compound AT2) has anticancer activities. Androgen receptor antagonist 4 potently antagonizes the activity of AR transcriptional, inhibits downstream target gene of AR, and blocks the DHT-i... | |||
T80633 | Androgen receptor degrader-1 | Androgen Receptor | |
Androgen Receptor Degrader-1 (Compound 18) is a potent agent for androgen receptor degradation, applicable in cancer research [1]. | |||
T60987 | Androgen receptor antagonist 3 | ||
Androgen receptor antagonist 3 (Compound C18) has anticancer activities that is an antagonist of androgen receptor (AR) (IC 50 = 2.4 μM) [1]. | |||
T12928 | SK33 | Androgen Receptor | |
SK33 is a potent and tissue selective anti-androgen agent. SK33 reduces androgen receptor (AR) transcriptional activity. | |||
T79024 | Androgen receptor-IN-5 | Androgen Receptor | |
Androgen receptor-IN-5 is a potent inhibitor of the androgen receptor with anticancer properties. It additionally suppresses the synthesis of IL-17A, IL-17F, and INF-γ. | |||
T83119 | Androgen receptor antagonist 9 | Androgen Receptor | |
Androgen Receptor Antagonist 9 (compound 28) serves as an antagonist to the androgen receptor [1]. | |||
T63324 | Androgen receptor antagonist 5 | ||
Androgen receptor antagonist 5 is a potent antagonist of the androgen receptor (AR) (IC50: 6.17 μM). Androgen receptor antagonist 5 inhibited the proliferation of prostate cancer cells LNCaP and showed antitumor effect i... | |||
T80647 | Androgen receptor degrader-2 | Androgen Receptor | |
Androgen Receptor Degrader-2 (Compound 9) is a potent degrader of androgen receptors, with potential application in cancer research [1]. | |||
T79891 | Androgen receptor degrader-3 | Androgen Receptor | |
Androgen Receptor Degrader-3 (ARD-3) is a compound that inhibits androgen receptor signaling and promotes the degradation of the receptor, with potential applications in prostate cancer research [1]. | |||
T6829 | EPI-001 | EPI001,EPI 001 | Apoptosis , Androgen Receptor , PPAR |
EPI-001 is an androgen receptor N-terminal domain antagonist with IC50 of ~6 μM and a selective PPAR-gamma modulator. | |||
T14116 | ACP-105 | Androgen Receptor | |
ACP-105 is a novel and potent nonsteroidal selective androgen receptor modulator (SARM) with partial agonist activity relative to the natural androgen testosterone. | |||
T13272 | UT-155 | Androgen Receptor | |
UT-155 is a selective and potent antagonist of the androgen receptor (AR) (Ki: 267 nM for UT-155 binding to AR-LBD). | |||
T12323 | ORM-15341 | Androgen Receptor | |
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) | |||
T14008 | 2,2,5,7,8-Pentamethyl-6-Chromanol | PMC | Androgen Receptor |
2,2,5,7,8-Pentamethyl-6-Chromanol (PMC) is the anti-oxidant moiety of vitamin E (α-tocopherol), which has potent androgen receptor (AR) signaling modulation and anti-cancer activity against prostate cancer cell lines. | |||
T20625 | Prochloraz | Sporgon,Prelude | Estrogen Receptor/ERR , AhR , Androgen Receptor , Antifungal |
Prochloraz (Prelude) is a broad-spectrum contact imidazole fungicide. Prochloraz inhibits human placental microsomal aromatase in vitro (IC50 = 40 nM). Prochloraz also acts as an estrogen receptor (IC50s = 25 μM) and and... | |||
T7690 | 2-hydroxy Flutamide | Androgen Receptor | |
2-hydroxy Flutamide is competitive inhibition of androgen receptor (AR) for the treatment of prostate cancer |