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219829-00-2 | Imidazo[1',5':1,6]pyrrolo[3',4':4,5]pyrido[2,3-b]indole-1,3(2H,8H)-dione
CAS No: 219829-00-2 Catalog No: AG007OJD MDL No:
Product Description
Catalog Number:
AG007OJD
Chemical Name:
Imidazo[1',5':1,6]pyrrolo[3',4':4,5]pyrido[2,3-b]indole-1,3(2H,8H)-dione
CAS Number:
219829-00-2
Molecular Formula:
C15H8N4O2
Molecular Weight:
276.2496
IUPAC Name:
8-hydroxy-2,4,9,19-tetrazapentacyclo[10.7.0.02,6.07,11.013,18]nonadeca-1(19),3,5,7,11,13,15,17-octaen-10-one
InChI:
InChI=1S/C15H8N4O2/c20-14-11-9-5-16-6-19(9)13-10(12(11)15(21)18-14)7-3-1-2-4-8(7)17-13/h1-6,20H,(H,18,21)
InChI Key:
KUWAFJHRXZRHJH-UHFFFAOYSA-N
SMILES:
O=c1[nH]c(=O)c2c1c1c3ccccc3[nH]c1n1c2cnc1
Properties
Complexity:
648
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
276.065g/mol
Formal Charge:
0
Heavy Atom Count:
21
Hydrogen Bond Acceptor Count:
4
Hydrogen Bond Donor Count:
2
Isotope Atom Count:
0
Molecular Weight:
276.255g/mol
Monoisotopic Mass:
276.065g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
79.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0
Literature
| Title | Journal |
|---|---|
| A broad activity screen in support of a chemogenomic map for kinase signalling research and drug discovery. | The Biochemical journal 20130415 |
| Comprehensive assay of kinase catalytic activity reveals features of kinase inhibitor selectivity. | Nature biotechnology 20111101 |
| Synthesis, checkpoint kinase 1 inhibitory properties and in vitro antiproliferative activities of new pyrrolocarbazoles. | Bioorganic & medicinal chemistry 20080415 |
| A systematic interaction map of validated kinase inhibitors with Ser/Thr kinases. | Proceedings of the National Academy of Sciences of the United States of America 20071218 |
| Inhibition of Chk1 by the G2 DNA damage checkpoint inhibitor isogranulatimide. | Molecular cancer therapeutics 20041001 |
| High-throughput assay for G2 checkpoint inhibitors and identification of the structurally novel compound isogranulatimide. | Cancer research 19981215 |
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