U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C17H18F2O2
Molecular Weight 292.3204
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BIFLURANOL

SMILES

CC[C@H]([C@H](C)C1=CC(F)=C(O)C=C1)C2=CC=C(O)C(F)=C2

InChI

InChIKey=RDVXUHOSYIBGBT-ZWNOBZJWSA-N
InChI=1S/C17H18F2O2/c1-3-13(12-5-7-17(21)15(19)9-12)10(2)11-4-6-16(20)14(18)8-11/h4-10,13,20-21H,3H2,1-2H3/t10-,13-/m1/s1

HIDE SMILES / InChI

Molecular Formula C17H18F2O2
Molecular Weight 292.3204
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Bifluranol (brand name Prostarex), a fluorinated bibenzyl anti-androgen was developed as a nonsteroidal estrogen and was studied for the treatment of benign prostatic hyperplasia. Besides, was shown that bifluranol inhibited 17 alpha-hydroxylase/C17-C20 lyase.

Approval Year

PubMed

PubMed

TitleDatePubMed
Comparison of the novel bibenzyl bifluranol with diethystilboestrol: effect of aromatic fluorine substitution on metabolism [proceedings].
1978 Jun
Anti-prostatic activity of bifluranol, a fluorinated bibenzyl.
1980
Bifluranol, a novel fluorinated bibenzyl anti-androgen, its chemistry and disposition in different animal species.
1981 May

Sample Use Guides

In Vivo Use Guide
Thirty five patients with bladder outflow obstruction received either Bifluranol 1.5 mg orally, t.d.s. or placebo in a double‐blind trial.
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:35:14 GMT 2023
Edited
by admin
on Fri Dec 15 15:35:14 GMT 2023
Record UNII
47602X79JF
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BIFLURANOL
INN   MI  
INN  
Official Name English
BX 341
Code English
BX-341
Code English
BIFLURANOL [MI]
Common Name English
bifluranol [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C242
Created by admin on Fri Dec 15 15:35:14 GMT 2023 , Edited by admin on Fri Dec 15 15:35:14 GMT 2023
Code System Code Type Description
SMS_ID
100000085904
Created by admin on Fri Dec 15 15:35:14 GMT 2023 , Edited by admin on Fri Dec 15 15:35:14 GMT 2023
PRIMARY
FDA UNII
47602X79JF
Created by admin on Fri Dec 15 15:35:14 GMT 2023 , Edited by admin on Fri Dec 15 15:35:14 GMT 2023
PRIMARY
INN
3795
Created by admin on Fri Dec 15 15:35:14 GMT 2023 , Edited by admin on Fri Dec 15 15:35:14 GMT 2023
PRIMARY
MESH
C017070
Created by admin on Fri Dec 15 15:35:14 GMT 2023 , Edited by admin on Fri Dec 15 15:35:14 GMT 2023
PRIMARY
MERCK INDEX
m1025
Created by admin on Fri Dec 15 15:35:14 GMT 2023 , Edited by admin on Fri Dec 15 15:35:14 GMT 2023
PRIMARY Merck Index
PUBCHEM
12850912
Created by admin on Fri Dec 15 15:35:14 GMT 2023 , Edited by admin on Fri Dec 15 15:35:14 GMT 2023
PRIMARY
NCI_THESAURUS
C77332
Created by admin on Fri Dec 15 15:35:14 GMT 2023 , Edited by admin on Fri Dec 15 15:35:14 GMT 2023
PRIMARY
ChEMBL
CHEMBL2105524
Created by admin on Fri Dec 15 15:35:14 GMT 2023 , Edited by admin on Fri Dec 15 15:35:14 GMT 2023
PRIMARY
DRUG CENTRAL
3026
Created by admin on Fri Dec 15 15:35:14 GMT 2023 , Edited by admin on Fri Dec 15 15:35:14 GMT 2023
PRIMARY
EPA CompTox
DTXSID30865725
Created by admin on Fri Dec 15 15:35:14 GMT 2023 , Edited by admin on Fri Dec 15 15:35:14 GMT 2023
PRIMARY
CHEBI
135219
Created by admin on Fri Dec 15 15:35:14 GMT 2023 , Edited by admin on Fri Dec 15 15:35:14 GMT 2023
PRIMARY
EVMPD
SUB05830MIG
Created by admin on Fri Dec 15 15:35:14 GMT 2023 , Edited by admin on Fri Dec 15 15:35:14 GMT 2023
PRIMARY
CAS
34633-34-6
Created by admin on Fri Dec 15 15:35:14 GMT 2023 , Edited by admin on Fri Dec 15 15:35:14 GMT 2023
PRIMARY
WIKIPEDIA
Bifluranol
Created by admin on Fri Dec 15 15:35:14 GMT 2023 , Edited by admin on Fri Dec 15 15:35:14 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY