Details
Stereochemistry | ACHIRAL |
Molecular Formula | C13H12 |
Molecular Weight | 168.2344 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC=CC=C1C2=CC=CC=C2
InChI
InChIKey=ALLIZEAXNXSFGD-UHFFFAOYSA-N
InChI=1S/C13H12/c1-11-7-5-6-10-13(11)12-8-3-2-4-9-12/h2-10H,1H3
Molecular Formula | C13H12 |
Molecular Weight | 168.2344 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Analysis of electron transfer in substituted biphenylmethane. | 2003 Dec |
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Inhibition of nucleoside transport by new analogues of 4-nitrobenzylthioinosine: replacement of the ribose moiety by substituted benzyl groups. | 2004 Oct 21 |
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New Ras CAAX mimetics: design, synthesis, antiproliferative activity, and RAS prenylation inhibition. | 2009 Sep 15 |
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Replacement of imidazolyl by pyridyl in biphenylmethylenes results in selective CYP17 and dual CYP17/CYP11B1 inhibitors for the treatment of prostate cancer. | 2010 Aug 12 |
|
Isopropylidene substitution increases activity and selectivity of biphenylmethylene 4-pyridine type CYP17 inhibitors. | 2010 Jul 8 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:00:24 GMT 2023
by
admin
on
Fri Dec 15 18:00:24 GMT 2023
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Record UNII |
X937MQ8S1T
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Record Status |
Validated (UNII)
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Record Version |
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