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Ac-D-His-Phe-GlyNH2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1402723-39-0 Structure
  • Basic information

    1. Product Name: Ac-D-His-Phe-GlyNH2
    2. Synonyms:
    3. CAS NO:1402723-39-0
    4. Molecular Formula:
    5. Molecular Weight: 400.437
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1402723-39-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Ac-D-His-Phe-GlyNH2(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ac-D-His-Phe-GlyNH2(1402723-39-0)
    11. EPA Substance Registry System: Ac-D-His-Phe-GlyNH2(1402723-39-0)
  • 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: 1402723-39-0(Hazardous Substances Data)

1402723-39-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1402723-39-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,2,7,2 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1402723-39:
(9*1)+(8*4)+(7*0)+(6*2)+(5*7)+(4*2)+(3*3)+(2*3)+(1*9)=120
120 % 10 = 0
So 1402723-39-0 is a valid CAS Registry Number.

1402723-39-0Downstream Products

1402723-39-0Relevant articles and documents

Opioid activity profiles of oversimplified peptides lacking in the protonable N-terminus

De Marco, Rossella,Tolomelli, Alessandra,Spampinato, Santi,Bedini, Andrea,Gentilucci, Luca

, p. 10292 - 10296 (2013/01/16)

Recently, we described cyclopeptide opioid agonists containing the D-Trp-Phe sequence. To expand the scope of this atypical pharmacophore, we tested the activity profiles of the linear peptides Ac-Xaa-Phe-Yaa (Xaa = L/D-Trp, D-His/Lys/Arg; Yaa = H, GlyNH2). Ac-D-Trp-PheNH2 appeared to be the minimal binding sequence, while Ac-D-Trp-Phe-GlyNH 2 emerged as the first noncationizable short peptide (partial) agonist with high μ-opioid receptor affinity and selectivity. Conformational analysis suggested that 5 adopts in solution a β-turn conformation.

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