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200706-56-5 | Methanone, di-1H-indol-2-yl-
CAS No: 200706-56-5 Catalog No: AG002CXL MDL No:
Product Description
Catalog Number:
AG002CXL
Chemical Name:
Methanone, di-1H-indol-2-yl-
CAS Number:
200706-56-5
Molecular Formula:
C17H12N2O
Molecular Weight:
260.2900
IUPAC Name:
bis(1H-indol-2-yl)methanone
InChI:
InChI=1S/C17H12N2O/c20-17(15-9-11-5-1-3-7-13(11)18-15)16-10-12-6-2-4-8-14(12)19-16/h1-10,18-19H
InChI Key:
GQJIQKLWZMQQGO-UHFFFAOYSA-N
SMILES:
O=C(c1cc2c([nH]1)cccc2)c1cc2c([nH]1)cccc2
Properties
Complexity:
349
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
260.095g/mol
Formal Charge:
0
Heavy Atom Count:
20
Hydrogen Bond Acceptor Count:
1
Hydrogen Bond Donor Count:
2
Isotope Atom Count:
0
Molecular Weight:
260.296g/mol
Monoisotopic Mass:
260.095g/mol
Rotatable Bond Count:
2
Topological Polar Surface Area:
48.6A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
4.2
Literature
| Title | Journal |
|---|---|
| Stent-based release of a selective PDGF-receptor blocker from the bis-indolylmethanon class inhibits restenosis in the rabbit animal model. | Vascular pharmacology 20100101 |
| Novel bis(1H-indol-2-yl)methanones as potent inhibitors of FLT3 and platelet-derived growth factor receptor tyrosine kinase. | Journal of medicinal chemistry 20060601 |
| Bis(1H-2-indolyl)-1-methanones as inhibitors of the hematopoietic tyrosine kinase Flt3. | Leukemia 20020801 |
| Bis(1H-2-indolyl)methanones as a novel class of inhibitors of the platelet-derived growth factor receptor kinase. | Journal of medicinal chemistry 20020227 |
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