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  • 36261-62-8 Structure
  • Basic information

    1. Product Name: H-MET-GLN-OH
    2. Synonyms: L-MET-L-GLN OH;H-MET-GLN-OH;Met-Gln-OH;N2-L-Methionyl-L-glutamine;Nα-L-Methionyl-L-glutamine
    3. CAS NO:36261-62-8
    4. Molecular Formula: C10H19N3O4S
    5. Molecular Weight: 277.34
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 36261-62-8.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. CAS DataBase Reference: H-MET-GLN-OH(CAS DataBase Reference)
    10. NIST Chemistry Reference: H-MET-GLN-OH(36261-62-8)
    11. EPA Substance Registry System: H-MET-GLN-OH(36261-62-8)
  • 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: 36261-62-8(Hazardous Substances Data)

36261-62-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36261-62-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,2,6 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 36261-62:
(7*3)+(6*6)+(5*2)+(4*6)+(3*1)+(2*6)+(1*2)=108
108 % 10 = 8
So 36261-62-8 is a valid CAS Registry Number.

36261-62-8Downstream Products

36261-62-8Relevant articles and documents

Slow-binding inhibition of peptide deformylase by cyclic peptidomimetics as revealed by a new spectrophotometric assay

Nguyen, Kiet T.,Hu, Xubo,Pei, Dehua

, p. 178 - 191 (2007/10/03)

A new spectrophotometric/fluorimetric assay for peptide deformylase (PDF) has been developed by coupling the PDF reaction with that of dipeptidyl peptidase I (DPPI) and using N-formyl-Met-Lys-AMC as substrate. Removal of the N-terminal formyl group by PDF renders the dipeptide an efficient substrate of DPPI, which subsequently removes the dipeptidyl units to release 7-amino-4-methylcoumarin as the chromophore/fluorophore. The PDF reaction is conveniently monitored on a UV-Vis spectrophotometer or a fluorimeter in a continuous fashion. The utility of the assay was demonstrated by determining the catalytic activity of PDF and the inhibition constants of PDF inhibitors. These studies revealed the slow-binding behavior of a previously reported macrocyclic PDF inhibitor. This method offers several advantages over the existing PDF assays and should be particularly useful for screening PDF inhibitors in the continuous fashion.

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