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Details

Stereochemistry ACHIRAL
Molecular Formula C26H24N2O6S
Molecular Weight 492.544
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BGC-20-1531 free base

SMILES

COC1=CC=C(N=C1)C2=CC=C(OCC3=C(C)OC(=C3)C(=O)NS(=O)(=O)C4=CC=CC=C4C)C=C2

InChI

InChIKey=IXDVRRPNWPOPGV-UHFFFAOYSA-N
InChI=1S/C26H24N2O6S/c1-17-6-4-5-7-25(17)35(30,31)28-26(29)24-14-20(18(2)34-24)16-33-21-10-8-19(9-11-21)23-13-12-22(32-3)15-27-23/h4-15H,16H2,1-3H3,(H,28,29)

HIDE SMILES / InChI

Molecular Formula C26H24N2O6S
Molecular Weight 492.544
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
3.0 nM [Ki]
Target ID: P35408
Gene ID: 5734.0
Gene Symbol: PTGER4
Target Organism: Homo sapiens (Human)
PubMed

PubMed

TitleDatePubMed
The pharmacological effect of BGC20-1531, a novel prostanoid EP4 receptor antagonist, in the prostaglandin E2 human model of headache.
2011-10
BGC20-1531, a novel, potent and selective prostanoid EP receptor antagonist: a putative new treatment for migraine headache.
2009-01
Substance Class Chemical
Created
by admin
on Wed Apr 02 05:46:28 GMT 2025
Edited
by admin
on Wed Apr 02 05:46:28 GMT 2025
Record UNII
Z49JYU6T3P
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-Furancarboxamide, 4-[[4-(5-methoxy-2-pyridinyl)phenoxy]methyl]-5-methyl-N-[(2-methylphenyl)sulfonyl]-
Preferred Name English
BGC-20-1531 free base
Common Name English
N-[[4-[[4-(5-Methoxypyridin-2-yl)phenoxy]methyl]-5-methylfuran-2-yl]carbonyl]-2-methylbenzenesulfonamide
Systematic Name English
4-[[4-(5-Methoxy-2-pyridinyl)phenoxy]methyl]-5-methyl-N-[(2-methylphenyl)sulfonyl]-2-furancarboxamide
Systematic Name English
4-((4-(5-Methoxypyridin-2-yl)phenoxy)methyl)-5-methyl-n-(2-methylphenyl)sulfonyl-furan-2-carboximidic acid
Systematic Name English
Code System Code Type Description
PUBCHEM
18444613
Created by admin on Wed Apr 02 05:46:28 GMT 2025 , Edited by admin on Wed Apr 02 05:46:28 GMT 2025
PRIMARY
FDA UNII
Z49JYU6T3P
Created by admin on Wed Apr 02 05:46:28 GMT 2025 , Edited by admin on Wed Apr 02 05:46:28 GMT 2025
PRIMARY
EPA CompTox
DTXSID001351969
Created by admin on Wed Apr 02 05:46:28 GMT 2025 , Edited by admin on Wed Apr 02 05:46:28 GMT 2025
PRIMARY
CAS
736183-35-0
Created by admin on Wed Apr 02 05:46:28 GMT 2025 , Edited by admin on Wed Apr 02 05:46:28 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT