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H-PRO-PRO-GLY-PHE-SER-PRO-OH is a peptide composed of the amino acids proline (PRO), glycine (GLY), phenylalanine (PHE), and serine (SER). The sequence starts with a proline, followed by two prolines, then glycine, phenylalanine, serine, and ends with proline. This peptide is commonly used in research and pharmaceutical applications due to its ability to mimic the structure and function of natural proteins. It is also known for its potential therapeutic properties in the treatment of various diseases and conditions.

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  • (2S)-1-[(2S)-3-hydroxy-2-[[(2S)-3-phenyl-2-[[2-[[(2S)-1-[(2S)-pyrrolidine-2-carbonyl]pyrrolidine-2-carbonyl]amino]acetyl]amino]propanoyl]amino]propanoyl]pyrrolidine-2-carboxylic acid

    Cas No: 23828-06-0

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  • Suzhou Health Chemicals Co., Ltd.
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  • 23828-06-0 Structure
  • Basic information

    1. Product Name: H-PRO-PRO-GLY-PHE-SER-PRO-OH
    2. Synonyms: PRO-PRO-GLY-PHE-SER-PRO;BRADYKININ (2-7);H-PRO-PRO-GLY-PHE-SER-PRO-OH;L-PRO-PRO-GLY-PHE-SER-PRO;bradykinin fragment 2-7;L-Pro-L-Pro-Gly-L-Phe-L-Ser-L-Pro-OH;Pro-Pro-Gly-Phe-Ser-Pro-OH
    3. CAS NO:23828-06-0
    4. Molecular Formula: C29H40N6O8
    5. Molecular Weight: 600.66
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 23828-06-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: -15°C
    8. Solubility: N/A
    9. Water Solubility: Soluble in water at 1mg/ml
    10. CAS DataBase Reference: H-PRO-PRO-GLY-PHE-SER-PRO-OH(CAS DataBase Reference)
    11. NIST Chemistry Reference: H-PRO-PRO-GLY-PHE-SER-PRO-OH(23828-06-0)
    12. EPA Substance Registry System: H-PRO-PRO-GLY-PHE-SER-PRO-OH(23828-06-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 23828-06-0(Hazardous Substances Data)

23828-06-0 Usage

Uses

Used in Pharmaceutical Industry:
H-PRO-PRO-GLY-PHE-SER-PRO-OH is used as a research tool for studying protein structure and function, as well as for developing new drugs and therapies. Its ability to mimic natural proteins makes it a valuable asset in the development of peptide-based drugs and treatments.
Used in Research Applications:
H-PRO-PRO-GLY-PHE-SER-PRO-OH is used as a model compound for understanding the interactions between amino acids and their role in protein folding and stability. This knowledge can be applied to the design of new therapeutic agents and the study of protein-related diseases.
Used in Therapeutic Applications:
H-PRO-PRO-GLY-PHE-SER-PRO-OH has potential therapeutic properties and is being investigated for its use in the treatment of various diseases and conditions. Its ability to mimic natural proteins may allow it to target specific biological pathways and modulate cellular processes, offering new avenues for treatment and prevention of disease.

Check Digit Verification of cas no

The CAS Registry Mumber 23828-06-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,8,2 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 23828-06:
(7*2)+(6*3)+(5*8)+(4*2)+(3*8)+(2*0)+(1*6)=110
110 % 10 = 0
So 23828-06-0 is a valid CAS Registry Number.

23828-06-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name H-PRO-PRO-GLY-PHE-SER-PRO-OH

1.2 Other means of identification

Product number -
Other names bradykinin fragment 2-7

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:23828-06-0 SDS

23828-06-0Downstream Products

23828-06-0Relevant articles and documents

Use of Polar Picolyl Protecting Groups in Peptide Synthesis

Rizo, Josep,Albericio, Fernando,Romero, Guillermo,Garcia-Echeverria, Carlos,Claret, Josep,et al.

, p. 5386 - 5389 (1988)

Protection of serine and threonine side chains with the 4-picolyl group and aspartic and glutamic acids with the 3-picolyl group is described.Picolyl-protected peptide segments are markedly more polar than benzyl-protected analogues, which can facilitate their purification.

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