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1-acetyl-2-phenyl-indol-3-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83894-24-0

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83894-24-0 Usage

Physical state

Yellowish-brown crystalline solid

Usage

Organic synthesis, pharmaceutical research

Properties

a. Potent antioxidant
b. Anti-inflammatory

Mechanism of action

Inhibits cyclooxygenase enzyme, reducing production of inflammatory mediators

Potential effects

Anticancer (induces apoptosis in cancer cells)

Research significance

Valuable tool for developing new therapeutic agents and drugs

Check Digit Verification of cas no

The CAS Registry Mumber 83894-24-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,8,9 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 83894-24:
(7*8)+(6*3)+(5*8)+(4*9)+(3*4)+(2*2)+(1*4)=170
170 % 10 = 0
So 83894-24-0 is a valid CAS Registry Number.

83894-24-0Downstream Products

83894-24-0Relevant academic research and scientific papers

N-ARYLSULFONYL-3-AMINOALKOXYINDOLES

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Page 56, (2008/06/13)

The present invention describes substituted 3-Aminoalkoxyindoles, compounds of the general formula (I), its stereoisomers, its radioisotopes, its geometric forms, its N-oxides, its polymorphs, its pharmaceutically acceptable salts, its pharmaceutically acceptable solvates, its useful bio-active metabolites and any suitable combination of the above. The invention also discloses the processes for preparing such compounds of the general formula (I), its stereoisomers, its radioisotopes, its geometric forms, its N-oxides, its polymorphs, its pharmaceutically acceptable salts, its pharmaceutically acceptable solvates, its useful bio-active metabolites and also includes any suitable combination of the above. Further described are various methods of administering these compounds of general formula (I), i.e. pharmaceutically acceptable dosage forms, their composition and their use in either therapy or diagnosis.

N-ARYLALKYL-3-AMINOALKOXYINDOLES AND THEIR USE AS 5-HT LIGANDS

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Page 49, (2010/02/07)

The present invention describes substituted 3-Aminoalkoxyindoles, as compounds of the general formula (I), its stereoisomers, its radioisotopes, its geometric forms, its N-oxides, its polymorphs, its pharmaceutically acceptable salts, its pharmaceutically acceptable solvates, its useful bioactive metabolites and any suitable combination of the above. The invention also discloses the processes for preparing such compounds of the general formula (I), its stereoisomers, its radioisotopes, its geometric forms, its N-oxides, its polymorphs, its pharmaceutically acceptable salts, its pharmaceutically acceptable solvates, its useful bio-active metabolites and also includes any suitable combination of the above. Further described are various methods of administering these compounds of general formula (I), i.e. pharmaceutically acceptable dosage forms, their composition and their use in either therapy or diagnosis.

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