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(S)-Boc-dMP, a member of peptide synthesis reagents, is a derivative of dMP, a crucial intermediate in the synthesis of various peptide and peptidomimetic compounds. Characterized by a tert-butoxycarbonyl (Boc) protecting group on the amino group, it facilitates selective deprotection and subsequent coupling reactions in peptide synthesis. (S)-Boc-dMP is pivotal in the construction of peptide libraries and combinatorial chemistry applications, serving as an essential tool in medicinal chemistry and drug discovery for creating diverse and complex peptide structures for biological and pharmaceutical research.

943318-67-0

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943318-67-0 Usage

Uses

Used in Medicinal Chemistry:
(S)-Boc-dMP is used as a building block for the synthesis of complex peptide structures, enabling researchers to explore new therapeutic agents and drug candidates.
Used in Drug Discovery:
(S)-Boc-dMP is utilized as a key component in the development of novel pharmaceuticals, contributing to the advancement of treatments for various diseases and conditions.
Used in Peptide Synthesis:
(S)-Boc-dMP is employed as a reagent in the synthesis of peptides, allowing for the selective deprotection of the amino group and facilitating coupling reactions, which are essential for the assembly of peptide chains.
Used in Combinatorial Chemistry:
(S)-Boc-dMP is used as a versatile building block in combinatorial chemistry, allowing for the rapid generation of diverse peptide libraries for high-throughput screening and lead optimization in drug development.
Used in Biological Research:
(S)-Boc-dMP is applied as a tool in biological research to study the structure, function, and interactions of peptides, providing insights into their roles in biological processes and potential applications in medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 943318-67-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,3,3,1 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 943318-67:
(8*9)+(7*4)+(6*3)+(5*3)+(4*1)+(3*8)+(2*6)+(1*7)=180
180 % 10 = 0
So 943318-67-0 is a valid CAS Registry Number.

943318-67-0SDS

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 1,2-Pyrrolidinedicarboxylic acid, 5,5-dimethyl-, 1-(1,1-dimethylethyl) ester, (2S)-

1.2 Other means of identification

Product number -
Other names BOC-(R)-5,5-DIMETHYLTHIAZOLIDINE-4-CARBOXYLIC ACID

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:943318-67-0 SDS

943318-67-0Downstream Products

943318-67-0Relevant academic research and scientific papers

The neuroprotective activity of GPE tripeptide analogues does not correlate with glutamate receptor binding affinity

Alonso De Diego, Sergio A.,Gutierrez-Rodriguez, Marta,Perez de Vega, M. Jesus,Gonzalez-Muniz, Rosario,Herranz, Rosario,Martin-Martinez, Mercedes,Cenarruzabeitia, Edurne,Frechilla, Diana,Rio, Joaquin Del,Jimeno, M. Luisa,Garcia-Lopez, M. Teresa

, p. 3396 - 3400 (2007/10/03)

The influence of several modifications on the GPE tripeptide structure upon the binding to GluRs and on their neuroprotective effects has been studied. The results indicated that the prevention of neuronal death showed by GPE and some analogues is not dir

Vanilloid receptor ligands and their use in treatments

-

Page/Page column 63, (2008/06/13)

Compounds having the general structure and compositions containing them, for the treatment of acute, inflammatory and neuropathic pain, dental pain, general headache, migraine, cluster headache, mixed-vascular and non-vascular syndromes, tension headache, general inflammation, arthritis, rheumatic diseases, osteoarthritis, inflammatory bowel disorders, inflammatory eye disorders, inflammatory or unstable bladder disorders, psoriasis, skin complaints with inflammatory components, chronic inflammatory conditions, inflammatory pain and associated hyperalgesia and allodynia, neuropathic pain and associated hyperalgesia and allodynia, diabetic neuropathy pain, causalgia, sympathetically maintained pain, deafferentation syndromes, asthma, epithelial tissue damage or dysfunction, herpes simplex, disturbances of visceral motility at respiratory, genitourinary, gastrointestinal or vascular regions, wounds, burns, allergic skin reactions, pruritus, vitiligo, general gastrointestinal disorders, gastric ulceration, duodenal ulcers, diarrhea, gastric lesions induced by necrotising agents, hair growth, vasomotor or allergic rhinitis, bronchial disorders or bladder disorders.

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