Home   >  
∨

Classified by application

All Products

Signaling Pathways

Research Areas

Nature products

Antibodies

Peptides

Catalysts

Impurities

Intermediate

Raw Materials

Hormone Pathay

Chemical Structure Cat. No. Product Name CAS No.
Eprotirome Chemical Structure
 BCP35042 Eprotirome 355129-15-6
Eprotirome is a thyroid hormone analog with hypocholesterolemic properties.
G15 Chemical Structure
 BCP34886 G15 1161002-05-6
G-15 is a cell-permeable non-steroidal antagonist of GPER (Ki = 20 nM).
Almestrone Chemical Structure
 BCP34841 Almestrone 10448-96-1
Almestrone is a synthetic, steroidal estrogen.
Mestranol Chemical Structure
 BCP34710 Mestranol 72-33-3
Mestranol is the 3-methyl ether of ethinylestradiol.
DL-Thyroxine Chemical Structure
 BCP34411 DL-Thyroxine 300-30-1
Thyroxine is an iodothyronine compound having iodo substituents at the 3-, 3'-, 5- and 5'-positions. It has a role as a mitogen. It is an iodothyronine, a 2-halophenol, an iodophenol, a tyrosine derivative and a non-proteinogenic alpha-amino acid. It is a tautomer of a thyroxine zwitterion.
LY-2795050 Chemical Structure
 BCP33958 LY-2795050 1346133-08-1
LY2795050 is a nobel kappa opioid receptor selective antagonist.
11α-Hydroxyprogesterone Chemical Structure
 BCP25704 11α-Hydroxyprogesterone 80-75-1
11alpha-hydroxyprogesterone is a 11alpha-hydroxy steroid that is pregn-4-ene-3,20-dione substituted by a hydroxy group at position 11.
Tamoxifen Chemical Structure
 BCP33248 Tamoxifen 10540-29-1
Tamoxifen is a selective estrogen receptor modulator (SERM) which blocks estrogen action in breast cells and can activate estrogen activity in other cells, such as bone, liver, and uterine cells. Tamoxifen is a potent Hsp90 activator and enhances the Hsp90 molecular chaperone ATPase activity. Tamoxifen activates autophagy and induces apoptosis.
Estradiol hemihydrate Chemical Structure
 BCP33020 Estradiol hemihydrate 35380-71-3
Estradiol Hemihydrate is the hemihydrate form of estradiol, the most potent, naturally produced estrogen.
H3B-5942 Chemical Structure
 BCP32835 H3B-5942 2052128-15-9
H3B-5942 is a selective and irreversible estrogen receptor covalent antagonist, inactivates both ERα WT and ERα mutation. The Ki values are 1 nM and 0.41 nM, respectively.
123下一页末页共 332 条记录 1 / 34 页 
0086-15971444841