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M5281635

Relugolix , ≥98% , 737789-87-6

CAS NO.:737789-87-6

Empirical Formula: C29H27F2N7O5S

Molecular Weight: 623.63

MDL number:

Pack Size Price Stock Quantity
1mg RMB624.80 In Stock
5mg RMB1071.20 In Stock
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Update time: 2022-07-08

PRODUCT Properties

Melting point: 228 °C (decomp)(Solv: ethyl acetate (141-78-6); tetrahydrofuran (109-99-9))
Density  1.442±0.06 g/cm3(Predicted)
storage temp.  Store at -20°C
solubility  DMSO:20.0(Max Conc. mg/mL);32.1(Max Conc. mM)
Ethanol:1.0(Max Conc. mg/mL);1.6(Max Conc. mM)
form  A crystalline solid
pka 13.17±0.70(Predicted)
color  White to off-white
InChIKey AOMXMOCNKJTRQP-UHFFFAOYSA-N
SMILES N(C1=CC=C(C2SC3=C(C=2CN(C)C)C(=O)N(C2=NN=C(OC)C=C2)C(=O)N3CC2=C(F)C=CC=C2F)C=C1)C(NOC)=O

Description and Uses

Relugolix (TAK-385) is a potent, orally active, nonpeptidic gonadotropin-releasing hormone (GnRH) antagonist. It possesses high affinity and potent antagonistic activity for human receptor (binding IC50=0.33 nM) and monkey receptor (IC50=0.32 nM) compared with TAK-013 (HY-100209). Relugolix is used for the study of sex-hormone-dependent diseases, such as including endometriosis, uterine fibroids and prostate cancer et al.

Relugolix is a highly selective, oral, nonpeptide GnRH antagonist being investigated as a possible prostate cancer treatment

Safety

Symbol(GHS) 
GHS08
Signal word  Warning
Hazard statements  H361-H371
Precautionary statements  P201-P202-P281-P308+P313-P405-P501-P260-P264-P270-P309+P311-P405-P501

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