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IMPPAT Phytochemical information:
Aristolochic acid I methyl ester
Summary
Physicochemical
Drug-likeness
ADMET
Descriptors
Summary
IMPPAT Phytochemical identifier:
IMPHY008671
Phytochemical name:
Aristolochic acid I methyl ester
Synonymous chemical names:
methyl aristolochate, methylaristolochate
External chemical identifiers:
CID:96709
,
ChEMBL:CHEMBL1684823
Chemical structure information
SMILES:
COC(=O)c1cc2OCOc2c2c1c(cc1c2cccc1OC)[N+](=O)[O-]
InChI:
InChI=1S/C18H13NO7/c1-23-13-5-3-4-9-10(13)6-12(19(21)22)15-11(18(20)24-2)7-14-17(16(9)15)26-8-25-14/h3-7H,8H2,1-2H3
InChIKey:
RZUABJWVTLHGHJ-UHFFFAOYSA-N
DeepSMILES:
COC=O)cccOCOc5cc9cccc6cccc6OC)))))))))[N+]=O)[O-]
Functional groups:
c1cOCO1, cC(=O)OC, cOC, c[N+](=O)[O-]
Molecular scaffolds
Scaffold Graph/Node/Bond level:
c1ccc2c(c1)ccc1ccc3c(c12)OCO3
Scaffold Graph/Node level:
C1CCC2C(C1)CCC1CCC3OCOC3C12
Scaffold Graph level:
C1CCC2C(C1)CCC1CCC3CCCC3C12
Chemical classification
ClassyFire Kingdom:
Organic compounds
ClassyFire Superclass:
Benzenoids
ClassyFire Class:
Phenanthrenes and derivatives
ClassyFire Subclass:
Aristolochic acids and derivatives
NP Classifier Biosynthetic pathway:
Alkaloids
NP Classifier Superclass:
Tyrosine alkaloids
NP Classifier Class:
Aporphine alkaloids
NP-Likeness score:
0.426
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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