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IMPPAT Phytochemical information:
(1-methoxy-9H-carbazol-3-yl)methanol
Summary
Physicochemical
Drug-likeness
ADMET
Descriptors
Summary
IMPPAT Phytochemical identifier:
IMPHY003309
Phytochemical name:
(1-methoxy-9H-carbazol-3-yl)methanol
Synonymous chemical names:
koenoline
External chemical identifiers:
CID:375152
,
ChEMBL:CHEMBL503498
,
ChEBI:171730
,
SureChEMBL:SCHEMBL6052281
Chemical structure information
SMILES:
COc1cc(CO)cc2c1[nH]c1c2cccc1
InChI:
InChI=1S/C14H13NO2/c1-17-13-7-9(8-16)6-11-10-4-2-3-5-12(10)15-14(11)13/h2-7,15-16H,8H2,1H3
InChIKey:
KNKVHLASDDREQS-UHFFFAOYSA-N
DeepSMILES:
COcccCO))ccc6[nH]cc5cccc6
Functional groups:
CO, cOC, c[nH]c
Molecular scaffolds
Scaffold Graph/Node/Bond level:
c1ccc2c(c1)[nH]c1ccccc12
Scaffold Graph/Node level:
C1CCC2C(C1)NC1CCCCC12
Scaffold Graph level:
C1CCC2C(C1)CC1CCCCC12
Chemical classification
ClassyFire Kingdom:
Organic compounds
ClassyFire Superclass:
Organoheterocyclic compounds
ClassyFire Class:
Indoles and derivatives
ClassyFire Subclass:
Carbazoles
NP Classifier Biosynthetic pathway:
Alkaloids
NP Classifier Superclass:
Tryptophan alkaloids
NP Classifier Class:
Carbazole alkaloids
NP-Likeness score:
0.627
Chemical structure download
2D:
2D MOL
2D MOL2
2D SDF
3D:
3D MOL
3D MOL2
3D SDF
3D PDB
3D PDBQT
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