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144029

2,6-Dimethylquinoline

Name: 2,6-Dimethylquinoline
Brand: ALDRICH

98%

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About This Item

Empirical Formula (Hill Notation):

C₁₁H₁₁N

CAS Number:

877-43-0

Molecular Weight:

157.21

NACRES:

NA.22

PubChem Substance ID:

24848622

UNSPSC Code:

12352100

EC Number:

212-891-5

MDL number:

MFCD00006762

Assay:

98%

Form:

solid

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Properties

assay

98%

form

solid

mp

57-59 °C (lit.)

SMILES string

Cc1ccc2nc(C)ccc2c1

InChI

1S/C11H11N/c1-8-3-6-11-10(7-8)5-4-9(2)12-11/h3-7H,1-2H3

InChI key

JJPSZKIOGBRMHK-UHFFFAOYSA-N

Gene Information

human ... CYP1A2(1544)

Description

Application

2,6-Dimethylquinoline was used to study the inhibition potencies (IC₅₀ values) of structurally diverse chemicals with recombinant human CYP2B6 enzyme for in vitro research purposes.

Biochem/physiol Actions

2,6-Dimethylquinoline is the chemical constituent present in roots of Peucedantu praeruptorum. It is a potential inhibitor of cytochrome P450 1A2 activity.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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[Studies on chemical constituents from roots of Peucedanum praeruptorum II].

Cun Zhang et al.

Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 31(16), 1333-1335 (2006-10-26)

To isolate and identify the chemical constituents from the roots of Peucedantu praeruptorum. The constituents were isolated by column chromatography on silica gel and ODS, and identified by NMR, MS spectroscopic methods. Eight compounds, (-) sclerodin (1), palmitic acid (2)

New potent and selective cytochrome P450 2B6 (CYP2B6) inhibitors based on three-dimensional quantitative structure-activity relationship (3D-QSAR) analysis.

L E Korhonen et al.

British journal of pharmacology, 150(7), 932-942 (2007-02-28)

The cytochrome P450 2B6 (CYP2B6) enzyme metabolises a number of clinically important drugs. Drug-drug interactions resulting from inhibition or induction of CYP2B6 activity may cause serious adverse effects. The aims of this study were to construct a three-dimensional structure-activity relationship

Prediction of Setschenow constants of N-heteroaromatics in NaCl solutions based on the partial charge on the heterocyclic nitrogen atom.

Bin Yang et al.

Environmental science and pollution research international, 23(4), 3399-3405 (2015-10-23)

The solubilities of 19 different kinds of N-heteroaromatic compounds in aqueous solutions with different concentrations of NaCl were determined at 298.15 K with a UV-vis spectrophotometry and titration method, respectively. Setschenow constants, Ks, were employed to describe the solubility behavior

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Global Trade Item Number

SKU	GTIN
144029-10G	04061833313053