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1892-55-3

1892-55-3 | 5H-Pyrido[3,2-a]phenoxazin-5-one

CAS No: 1892-55-3 Catalog No: AG002I2I MDL No:

Product Description

Catalog Number:
AG002I2I
Chemical Name:
5H-Pyrido[3,2-a]phenoxazin-5-one
CAS Number:
1892-55-3
Molecular Formula:
C15H8N2O2
Molecular Weight:
248.2362
IUPAC Name:
pyrido[3,2-a]phenoxazin-5-one
InChI:
InChI=1S/C15H8N2O2/c18-11-8-13-15(9-4-3-7-16-14(9)11)17-10-5-1-2-6-12(10)19-13/h1-8H
InChI Key:
ZCWXAKLJKGJBRM-UHFFFAOYSA-N
SMILES:
O=c1cc2oc3ccccc3nc2c2c1nccc2

Properties

Complexity:
469  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
248.059g/mol
Formal Charge:
0
Heavy Atom Count:
19  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
248.241g/mol
Monoisotopic Mass:
248.059g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
51.6A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.2  

Literature

Title Journal
Antitumor agents. 5. synthesis, structure-activity relationships, and biological evaluation of dimethyl-5H-pyridophenoxazin-5-ones, tetrahydro-5h-benzopyridophenoxazin-5-ones, and 5h-benzopyridophenoxazin-5-ones with potent antiproliferative activity. Journal of medicinal chemistry 20060824
Antitumor agents. 3. Design, synthesis, and biological evaluation of new pyridoisoquinolindione and dihydrothienoquinolindione derivatives with potent cytotoxic activity. Journal of medicinal chemistry 20040212
Antitumor agents 4. Characterization of free radicals produced during reduction of the antitumor drug 5H-pyridophenoxazin-5-one: an EPR study. Biochemistry 20031021
Antitumor agents. 1. Synthesis, biological evaluation, and molecular modeling of 5H-pyrido[3,2-a]phenoxazin-5-one, a compound with potent antiproliferative activity. Journal of medicinal chemistry 20021121
Antitumor agents. 2. Synthesis, structure-activity relationships, and biological evaluation of substituted 5H-pyridophenoxazin-5-ones with potent antiproliferative activity. Journal of medicinal chemistry 20021121

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