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Home > Indoles and Oxindole > 128533-02-8
128533-02-8 | Dibenz[cd,f]indol-4(5H)-one, 2-hydroxy-1-methoxy-5-methyl-
CAS No: 128533-02-8 Catalog No: AG000Y6C MDL No:
Product Description
Catalog Number:
AG000Y6C
Chemical Name:
Dibenz[cd,f]indol-4(5H)-one, 2-hydroxy-1-methoxy-5-methyl-
CAS Number:
128533-02-8
Molecular Formula:
C17H13NO3
Molecular Weight:
279.2900
IUPAC Name:
14-hydroxy-15-methoxy-10-methyl-10-azatetracyclo[7.6.1.02,7.012,16]hexadeca-1(16),2,4,6,8,12,14-heptaen-11-one
InChI:
InChI=1S/C17H13NO3/c1-18-12-7-9-5-3-4-6-10(9)15-14(12)11(17(18)20)8-13(19)16(15)21-2/h3-8,19H,1-2H3
InChI Key:
WRFZNTLPRUIGKH-UHFFFAOYSA-N
SMILES:
COc1c(O)cc2c3c1c1ccccc1cc3n(c2=O)C
Properties
Complexity:
440
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
279.09g/mol
Formal Charge:
0
Heavy Atom Count:
21
Hydrogen Bond Acceptor Count:
3
Hydrogen Bond Donor Count:
1
Isotope Atom Count:
0
Molecular Weight:
279.295g/mol
Monoisotopic Mass:
279.09g/mol
Rotatable Bond Count:
1
Topological Polar Surface Area:
49.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.1
Literature
| Title | Journal |
|---|---|
| KO-202125, a sauristolactam derivate, induces apoptosis to prevent KB human oral squamous carcinoma cells through inhibition of cyclooxygenase-2 expression. | European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP) 20100101 |
| Synthesis of aristolactam analogues and evaluation of their antitumor activity. | Bioorganic & medicinal chemistry letters 20090601 |
| Total synthesis of aristolactams via a one-pot suzuki-miyaura coupling/aldol condensation cascade reaction. | Organic letters 20080821 |
| [Advance of chemical constituents and bioactivity of Saururuaceae plants]. | Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica 20030301 |
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