2-METHYLBIPHENYL

CC1=CC=CC=C1C2=CC=CC=C2

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

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

PubMed

Title	Date	PubMed
Replacement of imidazolyl by pyridyl in biphenylmethylenes results in selective CYP17 and dual CYP17/CYP11B1 inhibitors for the treatment of prostate cancer.	2010-08-12	20684610
Isopropylidene substitution increases activity and selectivity of biphenylmethylene 4-pyridine type CYP17 inhibitors.	2010-07-08	20550118
New Ras CAAX mimetics: design, synthesis, antiproliferative activity, and RAS prenylation inhibition.	2009-09-15	19666221
Inhibition of nucleoside transport by new analogues of 4-nitrobenzylthioinosine: replacement of the ribose moiety by substituted benzyl groups.	2004-10-21	15481982
Analysis of electron transfer in substituted biphenylmethane.	2003-12	14976015

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 19:00:14 GMT 2025` Edited by `admin` on `Mon Mar 31 19:00:14 GMT 2025`
Record UNII	X937MQ8S1T
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

NSC-5321

Preferred Name

English

2-METHYLBIPHENYL

Systematic Name

English

1,1'-BIPHENYL, 2-METHYL-

Systematic Name

English

O-METHYLBIPHENYL

Common Name

English

2-METHYL-1,1'-BIPHENYL

Systematic Name

English

BIPHENYL, 2-METHYL-

Systematic Name

English

Code System Code Type Description

NSC

5321