172732-77-3 Usage
Chemical class
Indole derivatives
Physical appearance
Yellowish solid substance
Uses
Synthesis of pharmaceutical compounds and agrochemicals
Biological activities
Anti-inflammatory, antifungal, and anticancer properties
Mechanism of action
Inhibits tubulin polymerization
Potential use
Cancer therapy
Other activities
Antioxidant and neuroprotective activities
Significance
Target for further research in drug discovery and development.
Check Digit Verification of cas no
The CAS Registry Mumber 172732-77-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,7,3 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 172732-77:
(8*1)+(7*7)+(6*2)+(5*7)+(4*3)+(3*2)+(2*7)+(1*7)=143
143 % 10 = 3
So 172732-77-3 is a valid CAS Registry Number.
172732-77-3Relevant academic research and scientific papers
Method for treating sepsis
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, (2008/06/13)
A novel method of treating and/or preventing sepsis.
sPLA2 inhibitor ester
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, (2008/06/13)
The compound, ((3(2-amino-1,2-dioxoethyl)-2-methyl-1-(phenylmethyl)-1H-indol-4-yl)oxy)acetic acid N-morpholino ester, is disclosed together with its use as a highly bioavailable indole sPLA2inhibitor compound.
1H-INDOLE-3-GLYOXYLAMIDE SPLA2 INHIBITORS
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, (2008/06/13)
A class of novel 1H-indole-3-glyoxylamides is disclosed together with the use of such indole compounds for inhibiting sPLA2 mediated release of fatty adds for treatment of conditions such as septic shock
