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947669-91-2

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947669-91-2 Usage

Uses

WWL70 is a selective inhibitor of ABHD6.

Check Digit Verification of cas no

The CAS Registry Mumber 947669-91-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,7,6,6 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 947669-91:
(8*9)+(7*4)+(6*7)+(5*6)+(4*6)+(3*9)+(2*9)+(1*1)=242
242 % 10 = 2
So 947669-91-2 is a valid CAS Registry Number.

947669-91-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(4-carbamoylphenyl)phenyl] N-methyl-N-[(3-pyridin-4-ylphenyl)methyl]carbamate

1.2 Other means of identification

Product number -
Other names WWL70

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:947669-91-2 SDS

947669-91-2Downstream Products

947669-91-2Relevant academic research and scientific papers

A functional proteomic strategy to discover inhibitors for uncharacterized hydrolases

Li, Weiwei,Blankman, Jacqueline L.,Cravatt, Benjamin F.

, p. 9594 - 9595 (2007)

Hydrolytic enzymes constitute one of the largest and most diverse protein classes in Nature and play key roles in nearly all physiological and pathological processes. The mammalian serine hydrolase superfamily contains a remarkable number of uncharacterized members, with at least 40-50% of these enzymes lacking experimentally verified endogenous substrates and products. Assignment of metabolic and cellular functions to these enzymes requires the development of pharmacological tools to selectively perturb their activity. We describe herein a functional proteomic strategy to systematically develop potent and selective inhibitors for uncharacterized serine hydrolases and its application to the brain-enriched enzyme α/β-hydrolase-6. We anticipate that the methods described herein will facilitate the development of selective chemical probes to annotate the metabolic and (patho)physiological functions of many of the uncharacterized serine hydrolases that currently populate eukaryotic and prokaryotic proteomes. Copyright

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