321527-77-9 Usage
Chemical structure
1H-Indole-1-carboxylic acid derivative with a benzoyl group at the 7th position, a 1,1-dimethylethyl ester group at the carboxylic acid, and a methoxy group at the 5th position. The compound also has a 2,3-dihydro structure.
Pharmaceutical potential
The compound has shown potential as an antitumor agent and has been studied for its potential use in the treatment of various types of cancers.
Anti-inflammatory and analgesic properties
The compound is also being researched for its potential as an anti-inflammatory and analgesic agent.
Versatility
1H-Indole-1-carboxylic acid, 7-benzoyl-2,3-dihydro-5-methoxy-, 1,1-dimethylethyl ester has shown promise as a versatile and potent pharmaceutical compound with a wide range of potential applications in the field of medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 321527-77-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,1,5,2 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 321527-77:
(8*3)+(7*2)+(6*1)+(5*5)+(4*2)+(3*7)+(2*7)+(1*7)=119
119 % 10 = 9
So 321527-77-9 is a valid CAS Registry Number.
321527-77-9Relevant articles and documents
Synthesis, structure-activity relationships, and pharmacological profile of 9-amino-4-oxo-1-phenyl-3,4,6,7-tetrahydro[1,4]diazepino[6,7,1-hi]indoles: Discovery of potent, selective phosphodiesterase type 4 inhibitors
Burnouf,Auclair,Avenel,Bertin,Bigot,Calvet,Chan,Durand,Fasquelle,Féru,Gilbertsen,Jacobelli,Kebsi,Lallier,Maignel,Martin,Milano,Ouagued,Pascal,Pruniaux,Puaud,Rocher,Terrasse,Wrigglesworth,Doherty
, p. 4850 - 4867 (2007/10/03)
The synthesis, structure-activity relationships, and biological properties of a novel series of potent and selective phosphodiesterase type 4 (PDE4) inhibitors are described. These new aminodiazepinoindoles displayed in vitro PDE4 activity with submicromo
