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Glycine, N-[3,5-bis(trifluoromethyl)benzoyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

217655-97-5

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217655-97-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 217655-97-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,7,6,5 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 217655-97:
(8*2)+(7*1)+(6*7)+(5*6)+(4*5)+(3*5)+(2*9)+(1*7)=155
155 % 10 = 5
So 217655-97-5 is a valid CAS Registry Number.

217655-97-5SDS

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 2-[[3,5-bis(trifluoromethyl)benzoyl]amino]acetic acid

1.2 Other means of identification

Product number -
Other names HMS1661O13

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:217655-97-5 SDS

217655-97-5Downstream Products

217655-97-5Relevant academic research and scientific papers

Design, synthesis and prostate cancer cell-based studies of analogs of the Rho/MKL1 transcriptional pathway inhibitor, CCG-1423

Evelyn, Chris R.,Bell, Jessica L.,Ryu, Jenny G.,Wade, Susan M.,Kocab, Andrew,Harzdorf, Nicole L.,Hollis Showalter,Neubig, Richard R.,Larsen, Scott D.

scheme or table, p. 665 - 672 (2010/06/21)

We recently identified bis(amide) CCG-1423 (1) as a novel inhibitor of RhoA/C-mediated gene transcription that is capable of inhibiting invasion of PC-3 prostate cancer cells in a Matrigel model of metastasis. An initial structure-activity relationship study focusing on bioisosteric replacement of the amides and conformational restriction identified two compounds, 4g and 8, with improved selectivity for inhibition of RhoA/C-mediated gene transcription and attenuated cytotoxicity relative to 1. Both compounds were also capable of inhibiting cell invasion with equal efficacy to 1 but with less attendant cytotoxicity.

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