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Chemical Structure Cat. No. Product Name CAS No.
Luxdegalutamide Chemical Structure
BCP49650 Luxdegalutamide 2750830-09-0
Luxdegalutamide is an orally active and potent proteolysis targeting chimera (PROTAC) protein degrader. Luxdegalutamide degrades wild-type androgen receptor (AR) but also relevant AR LBD mutants, including the most prevalent AR L702H, H875Y, and T878A mutations.
Protirelin Acetate Chemical Structure
BCP40636 Protirelin Acetate 120876-23-5
Protirelin Acetate is a thyrotropin-releasing hormone, stimulating the release of thyrotropin and prolactin from the anterior pituitary.
GPR81 agonist 1 Chemical Structure
BCP36389 GPR81 agonist 1 1620992-67-7
GPR81 agonist 1 is a potent and highly selective GPR81 agonist, with EC50s of 58 nM and 50 nM for human and mouse GPR81, respectively.
Masofaniten Chemical Structure
BCP49523 Masofaniten 2416716-62-4
Masofaniten is an antiandrogen and an antineoplastic.
LPCN-1144 Chemical Structure
BCP49389 LPCN-1144 LPCN-1144
LPCN 1144 is an oral prodrug of bioidentical testosterone that is absorbed through intestinal lymphatics and intended for the treatment of hypogonadism in males.
AC-0176 Chemical Structure
BCP49348 AC-0176 AC-0176
AC176 is an investigational medicinal product that is a potent orally bioavailable Androgen Receptor (AR) degrader.
OP-1250 Chemical Structure
BCP49307 OP-1250 OP-1250
OP-1250 is a novel oral compound developed to completely antagonize the estrogen receptor (ER) and block the ER-mediated cancer cell growth and proliferation signal.
Onapristone Chemical Structure
BCP49272 Onapristone 96346-61-1
Onapristone is a progesterone receptor antagonist potentially for the treatment of breast cancer, advanced prostate cancer, and inducer of vaginal bleeding.
Nalbuphine hydrochloride Chemical Structure
BCP49247 Nalbuphine hydrochloride 23277-43-2
Nalbuphine Hydrochloride is the hydrochloride salt form of nalbuphine, a synthetic phenanthrene opioid with opiate agonist and antagonist effects, used to treat moderate to severe pain and provide preoperative and postoperative analgesia and sedation.
TERN-501 Chemical Structure
BCP49228 TERN-501 TERN-501
TERN 501 is an orally administered, small molecule therapeutic, being developed as a thyroid hormone receptor beta (THR-β) agonist, for the treatment of.
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