Welcome to LookChem.com Sign In|Join Free
  • or
BOC-ALA-ALA-D-TRP-PHE-D-PRO-PRO-NLE-NH2 is a synthetic peptide composed of a specific sequence of amino acids, including both Land D-amino acids, with a tert-butyloxycarbonyl (BOC) protecting group. The sequence is characterized by the presence of alanine (ALA), tryptophan (D-TRP), phenylalanine (PHE), proline (D-PRO), and leucine (NLE), terminated with an amino group (NH2) on the C-terminus. This peptide may hold potential in pharmaceutical research for the development of peptide-based drugs or as a molecular probe in biological studies.

141663-86-7

Post Buying Request

141663-86-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

141663-86-7 Usage

Uses

Used in Pharmaceutical Research:
BOC-ALA-ALA-D-TRP-PHE-D-PRO-PRO-NLE-NH2 is used as a peptide-based drug candidate for its potential therapeutic properties. The unique sequence of amino acids and the presence of D-amino acids may contribute to its biological activity, making it a valuable compound for the development of new medications.
Used in Biological Studies:
BOC-ALA-ALA-D-TRP-PHE-D-PRO-PRO-NLE-NH2 is used as a molecular probe in biological research to investigate its interactions with various biological targets, such as receptors, enzymes, or other proteins. The peptide's specific sequence and the presence of the BOC protecting group may provide insights into its binding properties and potential applications in understanding biological processes.
Used in Drug Development:
BOC-ALA-ALA-D-TRP-PHE-D-PRO-PRO-NLE-NH2 is used as a lead compound in drug development, where its unique properties can be further optimized and modified to enhance its therapeutic potential. The peptide's sequence and structure can be altered to improve its stability, bioavailability, and target specificity, leading to the discovery of novel drugs with improved efficacy and safety profiles.
Used in Peptide Synthesis:
BOC-ALA-ALA-D-TRP-PHE-D-PRO-PRO-NLE-NH2 is used as a model compound in the study of peptide synthesis techniques, particularly those involving the use of protecting groups such as BOC. Understanding the synthesis and properties of this peptide can contribute to the development of more efficient and reliable methods for the production of peptide-based drugs and other bioactive compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 141663-86-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,6,6 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 141663-86:
(8*1)+(7*4)+(6*1)+(5*6)+(4*6)+(3*3)+(2*8)+(1*6)=127
127 % 10 = 7
So 141663-86-7 is a valid CAS Registry Number.

141663-86-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Boc-Ala-Ala-D-Trp-Phe-D-Pro-Pro-NleNH2

1.2 Other means of identification

Product number -
Other names BOC-ALA-ALA-D-TRP-PHE-D-PRO-PRO-NLE-NH2

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:141663-86-7 SDS

141663-86-7Upstream product

141663-86-7Downstream Products

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 141663-86-7