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IMPPAT Phytochemical information:
1,2,8-Trimethoxy-6-methyl-9H-carbazole
Summary
Physicochemical
Drug-likeness
ADMET
Descriptors
Summary
IMPPAT Phytochemical identifier:
IMPHY014450
Phytochemical name:
1,2,8-Trimethoxy-6-methyl-9H-carbazole
Synonymous chemical names:
murrayastine
External chemical identifiers:
CID:59053143
,
ChEMBL:CHEMBL4076427
,
ZINC:ZINC000014822167
Chemical structure information
SMILES:
COc1ccc2c(c1OC)[nH]c1c2cc(cc1OC)C
InChI:
InChI=1S/C16H17NO3/c1-9-7-11-10-5-6-12(18-2)16(20-4)15(10)17-14(11)13(8-9)19-3/h5-8,17H,1-4H3
InChIKey:
OLQWUZUMRBBFFC-UHFFFAOYSA-N
DeepSMILES:
COcccccc6OC)))[nH]cc5cccc6OC))))C
Functional groups:
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:
0.442
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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