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H-GLY-D-TRP-OH is a unique chemical compound composed of glycine and D-tryptophan, which are linked by a peptide bond. Glycine, the simplest amino acid, is integral to the formation of proteins and other biological molecules, while D-tryptophan, an essential amino acid, is vital for protein synthesis and serves as a precursor for the neurotransmitter serotonin. The distinctive structure and properties of H-GLY-D-TRP-OH suggest potential applications in biochemistry, pharmaceuticals, and drug design.

50632-89-8

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50632-89-8 Usage

Uses

Used in Biochemistry:
H-GLY-D-TRP-OH is used as a research tool for studying the interactions and functions of amino acids in biological systems, particularly in the context of protein synthesis and neurotransmission.
Used in Pharmaceutical Industry:
H-GLY-D-TRP-OH is used as a potential therapeutic agent for the development of new drugs targeting various health conditions, leveraging its role in protein synthesis and neurotransmitter regulation.
Used in Drug Design:
H-GLY-D-TRP-OH is utilized as a structural component in the design of novel pharmaceutical compounds, taking advantage of its unique properties to create innovative and effective treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 50632-89-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,3 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 50632-89:
(7*5)+(6*0)+(5*6)+(4*3)+(3*2)+(2*8)+(1*9)=108
108 % 10 = 8
So 50632-89-8 is a valid CAS Registry Number.

50632-89-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name H-GLY-D-TRP-OH

1.2 Other means of identification

Product number -
Other names GLY-L-ARG-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:50632-89-8 SDS

50632-89-8Downstream Products

50632-89-8Relevant academic research and scientific papers

PROTECTION OF THE TRYPTOPHAN INDOLE RING IN PEPTIDE SYNTHESIS. USE OF A NEW DERIVATIVE, Nin-2,2,2-TRICHLOROETHOXYCARBONYLTRYPTOPHAN

Kiso, Yoshiaki,Inai, Masatoshi,Kitagawa, Kouki,Akita, Tadashi

, p. 739 - 742 (2007/10/02)

The 2,2,2-trichloroethoxycarbonyl (Troc) group attached at the Nin function of tryptophan by acylation with Troc-Cl in the presence of a catalytic amount of tetra-n-butylammonium hydrogensulfate can be quantitatively removed either by cadmium dust in acetic acid or under basic conditions, e. g., hydrazine hydrate and NaOH, but is resistant to strong acidic conditions.

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