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Chemical Structure Cat. No. Product Name CAS No.
Drospirenone Chemical Structure
BCP27035 Drospirenone 67392-87-4
Drospirenone is a synthetic progestogen exhibiting antiandrogenic and antimineralocorticoid activity. This drug is used in oral contraceptives. Drospirenone binds to the progesterone receptor, the resulting complex becomes activated and binds to specific sites on DNA. This results in a suppression of LH activity and an inhibition of ovulation as well as an alteration in the cervical mucus and endometrium. This leads to an increased difficulty of sperm entry into the uterus and implantation.
Fispemifene Chemical Structure
BCP23860 Fispemifene 341524-89-8
Fispemifene is a selective estrogen receptor modulator (SERM) potentially for the treatment of hypogonadism.
CTOPA Chemical Structure
BCP24191 CTOPA 103429-31-8
CTOP is a potent and selective μ opioid receptor antagonist (Ki values are 0.96 and >10,000 nM for μ and δ receptors respectively).
Endoxifen hydrochloride Chemical Structure
BCP24689 Endoxifen hydrochloride 1197194-41-4
Endoxifen HCl, the active metabolite of Tamoxifen, ia a potent and selective estrogen receptor antagonist. Phase 2.
AC-262536 Chemical Structure
BCP49008 AC-262536 871032-12-1
AC-262536 is a selective and non-steroidal androgen receptor modulators (SARMs) with beneficial anabolic effects. AC-262536 exhibits potent agonist activity at the androgen receptor, with an affinity in the low nanomolar range (1-10 nM).
Bevenopran Chemical Structure
BCP48962 Bevenopran 676500-67-7
Bevenopran is a peripheral μ-opioid receptor antagonist.
ARV-766 Chemical Structure
BCP48951 ARV-766 2504913-62-4
ARV-766 is a PROTAC degrader of AR (androgen receptor) with anticancer activity.
Benazepril Chemical Structure
BCP25112 Benazepril 131064-74-9
Benazepril is used to treat high blood pressure (hypertension), congestive heart failure, and chronic renal failure.
Axelopran Chemical Structure
BCP47463 Axelopran 949904-48-7
Axelopran, also known as TD-1211, is a potent, selective, and peripherally-restricted μ-, κ-, and δ-opioid receptor antagonist, with similar affinity for the μ- and κ-opioid receptors and about an order of magnitude lower affinity for the δ-opioid recept
NCRW0005F05 Chemical Structure
BCP48739 NCRW0005F05 342779-66-2
NCRW0005-F05 is the first GPR139 antagonist (IC50 = 0.21 µM).
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