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201730-11-2

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201730-11-2 Usage

Uses

(S)-3,4-DCPG is a potent and selective mGluR-8a agonist.

Biological Activity

Potent, selective mGlu 8a agonist (EC 50 = 31 nM). Displays > 100-fold selectivity over mGlu 1-7 and displays little or no activity at NMDA and kainate receptors. Increases c-Fos expression in stress-related brain areas following systemic administration in mice in vivo . Also potent anticonvulsant in mice in vivo .

Check Digit Verification of cas no

The CAS Registry Mumber 201730-11-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,7,3 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 201730-11:
(8*2)+(7*0)+(6*1)+(5*7)+(4*3)+(3*0)+(2*1)+(1*1)=72
72 % 10 = 2
So 201730-11-2 is a valid CAS Registry Number.

201730-11-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(S)-amino(carboxy)methyl]phthalic acid

1.2 Other means of identification

Product number -
Other names HMS3267L19

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:201730-11-2 SDS

201730-11-2Upstream product

201730-11-2Downstream Products

201730-11-2Relevant articles and documents

Structure-activity relationships of new agonists and antagonists of different metabotropic glutamate receptor subtypes

Sekiyama,Hayashi,Nakanishi,Jane,Tse,Birse,Watkins

, p. 1493 - 1503 (1996)

1. We investigated the agonist and antagonist activities of 22 new phenylglycine and phenylalanine derivatives for metabotropic glutamate receptors (mGluRs) by examining their effects on the signal transduction of mGluR1, mGluR2 and

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