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
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
Molecular Formula | C17H18F2O2 |
Molecular Weight | 292.3204 |
Charge | 0 |
Count |
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Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
PubMed
Title | Date | PubMed |
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Comparison of the novel bibenzyl bifluranol with diethystilboestrol: effect of aromatic fluorine substitution on metabolism [proceedings]. | 1978 Jun |
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Anti-prostatic activity of bifluranol, a fluorinated bibenzyl. | 1980 |
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Bifluranol, a novel fluorinated bibenzyl anti-androgen, its chemistry and disposition in different animal species. | 1981 May |
Sample Use Guides
In Vivo Use Guide
Sources: https://doi.org/10.1002/pros.2990070403
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
Edited
Fri Dec 15 15:35:14 GMT 2023
by
admin
on
Fri Dec 15 15:35:14 GMT 2023
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Record UNII |
47602X79JF
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Record Status |
Validated (UNII)
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Record Version |
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C242
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100000085904
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47602X79JF
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3795
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C017070
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m1025
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12850912
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C77332
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CHEMBL2105524
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DTXSID30865725
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SUB05830MIG
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34633-34-6
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Bifluranol
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Related Record | Type | Details | ||
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ACTIVE MOIETY |