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1337988-14-3

C37H48N4O14S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1337988-14-3 Structure

  • Basic information

    1. Product Name: C37H48N4O14S
    2. Synonyms: C37H48N4O14S
    3. CAS NO:1337988-14-3
    4. Molecular Formula:
    5. Molecular Weight: 804.873
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1337988-14-3.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: C37H48N4O14S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C37H48N4O14S(1337988-14-3)
    11. EPA Substance Registry System: C37H48N4O14S(1337988-14-3)

  • 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: 1337988-14-3(Hazardous Substances Data)

1337988-14-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1337988-14-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,7,9,8 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1337988-14:
(9*1)+(8*3)+(7*3)+(6*7)+(5*9)+(4*8)+(3*8)+(2*1)+(1*4)=203
203 % 10 = 3
So 1337988-14-3 is a valid CAS Registry Number.

1337988-14-3Downstream Products

1337988-14-3Relevant articles and documents

Mannich reaction derivatives of novobiocin with modulated physiochemical properties and their antibacterial activities

Tambo-Ong, Arlyn,Chopra, Sidharth,Glaser, Bryan T.,Matsuyama, Karen,Tran, Tran,Madrid, Peter B.

, p. 5697 - 5700 (2011/10/18)

Synthetic derivatives of the natural product antibiotic novobiocin were synthesized in order to improve their physiochemical properties. A Mannich reaction was used to introduce new side chains at a solvent-exposed position of the molecule, and a diverse panel of functional groups was evaluated at this position. Novobiocin and the new derivatives were tested for their binding to gyrase B and their antibacterial activities against Staphylococcus aureus, Mycobacterium tuberculosis, Francisella tularensis and Escherichia coli. While the new derivatives still bound the gyrase B protein potently (0.07-1.8 μM, IC50), they had significantly less antibacterial activity. Two compounds were identified with increased antibacterial activity against M. tuberculosis, with a minimum inhibitory concentration of 2.5 μg/ml.

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