General Information of the Compound
Compound ID
CP0415143
Compound Name
3-carboxamido coumarin, 1
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Synonyms
2-Oxo-2H-chromene-3-carboxylic acid cyclohexylamide
3-carboxamido coumarin, 1
4021-23-2
AC1LF7K7
AC1Q5N8P
AKOS000533315
BAS 00837943
BDBM29152
CCG-15837
CHEMBL472080
CTK1C9968
ChemDiv2_003298
DTXSID70352366
EU-0035943
HMS1378F20
MCULE-8945496486
MolPort-001-028-458
N-cyclohexyl(2-oxochromen-3-yl)carboxamide
N-cyclohexyl-2-oxo-2H-chromene-3-carboxamide
N-cyclohexyl-2-oxochromene-3-carboxamide
Oprea1_254332
Oprea1_273725
SR-01000410421
SR-01000410421-1
ST50185340
STK408165
ZINC130287
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Structure
Formula
C16H17NO3
Molecular Weight
271.316
Canonical SMILES
O=C(NC1CCCCC1)c1cc2ccccc2oc1=O
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InChI
InChI=1S/C16H17NO3/c18-15(17-12-7-2-1-3-8-12)13-10-11-6-4-5-9-14(11)20-16(13)19/h4-6,9-10,12H,1-3,7-8H2,(H,17,18)
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InChIKey
KUWSPPXPGQEHSQ-UHFFFAOYSA-N
Physicochemical Property
logP
2.8555
Rotatable Bonds
2
Heavy Atom Count
20
Polar Areas
59.31
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
3
Complexity
20

"RO5" indicates the cutoff set by lipinski's rule of five:

(1) Molecular weight less than 500 Dalton;

(2) xlogp less than 5;

(3) No more than 5 hbonddonor (Hydrogen Bond Donor Count);

(4) No more than 10 hbondacc (Hydrogen Bond Acceptor Count);

(5) No more than 10 rotbonds (Rotatable Bond Count).

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PubChem ID
CID: 724217
SID: 103800148
ChEMBL ID
CHEMBL472080
Map of Molecular Bioactivity Related to the Compound
Map of Molecular Bioactivity Related to the Compound

Compound
Cell Line
Protein

Bioactivity Value:

<= 0.1 μM
> 0.1 μM and <= 10 μM
> 10 μM
Imprecise Activity
Table of Molecular Bioactivities Related to the Compound
Protein ID: PT01362, Amine oxidase [flavin-containing] B
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000023 BTI-Tn-5B1-4 Trichoplusia ni (Cabbage looper)  1
1
IC50 = 500 nM
   TI
   LI
   LO
   TS
Clinical Information about the Compound
Drug 1 ( N-cyclohexyl-2-oxo-2H-chromene-3-carboxamide )
Drug Name N-cyclohexyl-2-oxo-2H-chromene-3-carboxamide
Target(s)
Monoamine oxidase type B (MAO-B)
Inhibitor