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N-(tert-butoxycarbonyl)glycyltryptophan is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78700-53-5

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78700-53-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78700-53-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,7,0 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 78700-53:
(7*7)+(6*8)+(5*7)+(4*0)+(3*0)+(2*5)+(1*3)=145
145 % 10 = 5
So 78700-53-5 is a valid CAS Registry Number.

78700-53-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1H-indol-3-yl)-2-[[2-[(2-methylpropan-2-yl)oxycarbonylamino]acetyl]amino]propanoic acid

1.2 Other means of identification

Product number -
Other names Boc-Gly-Trp-OH

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:78700-53-5 SDS

78700-53-5Downstream Products

78700-53-5Relevant academic research and scientific papers

Design and synthesis of tryptophan containing peptides as potential analgesic and anti-inflammatory agents

Suhas,Gowda, D.Channe

, p. 535 - 540 (2012/09/22)

A new series of smaller peptides with tryptophan at C-terminal and varying N-protected amino acids/peptides were designed, synthesized and characterized by analytical and spectroscopic techniques. Analgesic and anti-inflammatory properties of these peptides were carried out in vivo using tail-flick method and carrageenan-induced paw edema method, respectively, at different doses and different time intervals. Most of the peptides synthesized displayed enhanced activity, and particularly tetra and hexapeptides 29-31 were found to be even more potent than the reference standards used. Moreover, some peptides have exhibited promising activity even after 24h of administration, whereas the reference standards were active only up to 3h. Further, the compounds did not present any ulcerogenic liability.

Water-soluble tripeptide Aβ (9-11) forms amyloid-like fibrils and exhibits neurotoxicity

Naskar, Jishu,Drew, Michael G. B.,Deb, Ishani,Das, Sumantra,Banerjee, Arindam

supporting information; experimental part, p. 2625 - 2628 (2009/05/30)

(Chemical Equation Presented) A water-soluble, hydrophilic tripeptide GYE, having sequence identity with the N-terminal segment of amyloid peptides Aβ(9-11), upon self-association exhibits amyloid-like fibrils and significant neurotoxicity towards the Neu

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