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1380522-37-1

H-D-γ-Glu(OBzl)-L-Lys(Fmoc)-OMe*HCl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1380522-37-1 Structure

  • Basic information

    1. Product Name: H-D-γ-Glu(OBzl)-L-Lys(Fmoc)-OMe*HCl
    2. Synonyms:
    3. CAS NO:1380522-37-1
    4. Molecular Formula:
    5. Molecular Weight: 638.16
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1380522-37-1.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: H-D-γ-Glu(OBzl)-L-Lys(Fmoc)-OMe*HCl(CAS DataBase Reference)
    10. NIST Chemistry Reference: H-D-γ-Glu(OBzl)-L-Lys(Fmoc)-OMe*HCl(1380522-37-1)
    11. EPA Substance Registry System: H-D-γ-Glu(OBzl)-L-Lys(Fmoc)-OMe*HCl(1380522-37-1)

  • 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: 1380522-37-1(Hazardous Substances Data)

1380522-37-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1380522-37-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,0,5,2 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1380522-37:
(9*1)+(8*3)+(7*8)+(6*0)+(5*5)+(4*2)+(3*2)+(2*3)+(1*7)=141
141 % 10 = 1
So 1380522-37-1 is a valid CAS Registry Number.

1380522-37-1Relevant articles and documents

Synthesis of modified peptidoglycan precursor analogues for the inhibition of glycosyltransferase

Dumbre, Shrinivas,Derouaux, Adeline,Lescrinier, Eveline,Piette, Andre,Joris, Bernard,Terrak, Mohammed,Herdewijn, Piet

, p. 9343 - 9351 (2012/07/14)

The peptidoglycan glycosyltransferases (GTs) are essential enzymes that catalyze the polymerization of glycan chains of the bacterial cell wall from lipid II and thus constitute a validated antibacterial target. Their enzymatic cavity is composed of a donor site for the growing glycan chain (where the inhibitor moenomycin binds) and an acceptor site for lipid II substrate. In order to find lead inhibitors able to fill this large active site, we have synthesized a series of substrate analogues of lipid I and lipid II with variations in the lipid, the pyrophosphate, and the peptide moieties and evaluated their biological effect on the GT activity of E. coli PBP1b and their antibacterial potential. We found several compounds able to inhibit the GT activity in vitro and cause growth defect in Bacillus subtilis. The more active was C16-phosphoglycerate-MurNAc-(l-Ala-d-Glu)-GlcNAc, which also showed antibacterial activity. These molecules are promising leads for the design of new antibacterial GT inhibitors.

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