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1392327-82-0

C20H19N3O is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1392327-82-0 Structure

  • Basic information

    1. Product Name: C20H19N3O
    2. Synonyms:
    3. CAS NO:1392327-82-0
    4. Molecular Formula:
    5. Molecular Weight: 317.39
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1392327-82-0.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: C20H19N3O(CAS DataBase Reference)
    10. NIST Chemistry Reference: C20H19N3O(1392327-82-0)
    11. EPA Substance Registry System: C20H19N3O(1392327-82-0)

  • 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: 1392327-82-0(Hazardous Substances Data)

1392327-82-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1392327-82-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,2,3,2 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1392327-82:
(9*1)+(8*3)+(7*9)+(6*2)+(5*3)+(4*2)+(3*7)+(2*8)+(1*2)=170
170 % 10 = 0
So 1392327-82-0 is a valid CAS Registry Number.

1392327-82-0Downstream Products

1392327-82-0Relevant articles and documents

Benzoylbenzimidazole-based selective inhibitors targeting Cryptosporidium parvum and Toxoplasma gondii calcium-dependent protein kinase-1

Zhang, Zhongsheng,Ojo, Kayode K.,Johnson, Steven M.,Larson, Eric T.,He, Penqing,Geiger, Jennifer A.,Castellanos-Gonzalez, Alejandro,White Jr., A. Clinton,Parsons, Marilyn,Merritt, Ethan A.,Maly, Dustin J.,Verlinde, Christophe L.M.J.,Van Voorhis, Wesley C.,Fan, Erkang

, p. 5264 - 5267 (2012/09/07)

Calcium-dependent protein kinase-1 (CDPK1) from Cryptosporidium parvum (CpCDPK1) and Toxoplasma gondii (TgCDPK1) have become attractive targets for discovering selective inhibitors to combat infections caused by these protozoa. We used structure-based design to improve a series of benzoylbenzimidazole-based compounds in terms of solubility, selectivity, and potency against CpCDPK1 and TgCDPK1. The best inhibitors show inhibitory potencies below 50 nM and selectivity well above 200-fold over two human kinases with small gatekeeper residues.

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