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  • 1367362-24-0 Structure
  • Basic information

    1. Product Name: C23H28N2O6
    2. Synonyms:
    3. CAS NO:1367362-24-0
    4. Molecular Formula:
    5. Molecular Weight: 428.485
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1367362-24-0.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: C23H28N2O6(CAS DataBase Reference)
    10. NIST Chemistry Reference: C23H28N2O6(1367362-24-0)
    11. EPA Substance Registry System: C23H28N2O6(1367362-24-0)
  • 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: 1367362-24-0(Hazardous Substances Data)

1367362-24-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1367362-24-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,7,3,6 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1367362-24:
(9*1)+(8*3)+(7*6)+(6*7)+(5*3)+(4*6)+(3*2)+(2*2)+(1*4)=170
170 % 10 = 0
So 1367362-24-0 is a valid CAS Registry Number.

1367362-24-0Relevant articles and documents

Discovery of a new class of ghrelin receptor antagonists

Mihalic, Jeffrey T.,Kim, Yong-Jae,Lizarzaburu, Mike,Deignan, Jeff,Wanska, Malgorzata,Yu, Ming,Fu, Jiasheng,Chen, Xi,Zhang, Alex,Connors, Richard,Liang, Lingming,Lindstrom, Michelle,Ma, Ji,Tang, Liang,Dai, Kang,Li, Leping,Chen, Xiaoqi

, p. 2046 - 2051 (2012/04/17)

A series of benzodiazepine antagonists of the human ghrelin receptor GHSR1a were synthesized and their antagonism and metabolic stability were evaluated. The potency of these analogs was determined using a functional aequorin (Euroscreen) luminescent assay measuring the intracellular Ca2+ concentration, and their metabolic stability was measured using an in vitro rat and human S9 hepatocyte assay. These efforts led to the discovery of a potent ghrelin antagonist with good rat pharmacokinetic properties.

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