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Details

Stereochemistry ACHIRAL
Molecular Formula C30H33NO4
Molecular Weight 471.5873
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CHF-4227

SMILES

COC1=CC=C(C=C1)C2=C(CC3=CC=C(OCCN4CCCCC4)C=C3)C5=CC=C(O)C=C5OC2

InChI

InChIKey=ZUDXUNPSRMREOJ-UHFFFAOYSA-N
InChI=1S/C30H33NO4/c1-33-25-12-7-23(8-13-25)29-21-35-30-20-24(32)9-14-27(30)28(29)19-22-5-10-26(11-6-22)34-18-17-31-15-3-2-4-16-31/h5-14,20,32H,2-4,15-19,21H2,1H3

HIDE SMILES / InChI

Molecular Formula C30H33NO4
Molecular Weight 471.5873
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Single and multiple ascending dose studies of a novel tissue-selective oestrogen receptor modulator, CHF 4227, in healthy postmenopausal women.
2007-09
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
A new selective estrogen receptor modulator, CHF 4227.01, preserves bone mass and microarchitecture in ovariectomized rats.
2005-12
Pharmacological actions of a novel, potent, tissue-selective benzopyran estrogen.
2002-10
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:03:39 GMT 2025
Edited
by admin
on Mon Mar 31 22:03:39 GMT 2025
Record UNII
1O98089Q9M
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2H-1-BENZOPYRAN-7-OL, 3-(4-METHOXYPHENYL)-4-((4-(2-(1-PIPERIDINYL)ETHOXY)PHENYL)METHYL)-
Preferred Name English
CHF-4227
Common Name English
Code System Code Type Description
FDA UNII
1O98089Q9M
Created by admin on Mon Mar 31 22:03:39 GMT 2025 , Edited by admin on Mon Mar 31 22:03:39 GMT 2025
PRIMARY
PUBCHEM
9912639
Created by admin on Mon Mar 31 22:03:39 GMT 2025 , Edited by admin on Mon Mar 31 22:03:39 GMT 2025
PRIMARY
CAS
444643-64-5
Created by admin on Mon Mar 31 22:03:39 GMT 2025 , Edited by admin on Mon Mar 31 22:03:39 GMT 2025
PRIMARY
EPA CompTox
DTXSID50196184
Created by admin on Mon Mar 31 22:03:39 GMT 2025 , Edited by admin on Mon Mar 31 22:03:39 GMT 2025
PRIMARY
ChEMBL
CHEMBL3545355
Created by admin on Mon Mar 31 22:03:39 GMT 2025 , Edited by admin on Mon Mar 31 22:03:39 GMT 2025
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY