IMPPAT: Indian Medicinal Plants, Phytochemistry And Therapeutics
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IMPPAT Phytochemical information:
Tussilagine
Summary
Physicochemical
Drug-likeness
ADMET
Descriptors
Summary
IMPPAT Phytochemical identifier:
IMPHY003764
Phytochemical name:
Tussilagine
Synonymous chemical names:
tussilagine
External chemical identifiers:
CID:185071
,
ChEBI:9782
,
FDASRS:N9VOG4YJ1H
Chemical structure information
SMILES:
COC(=O)[C@H]1[C@@H]2CCCN2C[C@@]1(C)O
InChI:
InChI=1S/C10H17NO3/c1-10(13)6-11-5-3-4-7(11)8(10)9(12)14-2/h7-8,13H,3-6H2,1-2H3/t7-,8+,10+/m0/s1
InChIKey:
LADVYSUMGRTFSZ-QXFUBDJGSA-N
DeepSMILES:
COC=O)[C@H][C@@H]CCCN5C[C@@]8C)O
Functional groups:
CN(C)C, CO, COC(C)=O
Molecular scaffolds
Scaffold Graph/Node/Bond level:
C1CC2CCCN2C1
Scaffold Graph/Node level:
C1CC2CCCN2C1
Scaffold Graph level:
C1CC2CCCC2C1
Chemical classification
ClassyFire Kingdom:
Organic compounds
ClassyFire Superclass:
Organoheterocyclic compounds
ClassyFire Class:
Pyrrolizidines
NP Classifier Biosynthetic pathway:
Alkaloids
NP Classifier Superclass:
Ornithine alkaloids
NP Classifier Class:
Pyrrolizidine alkaloids
NP-Likeness score:
1.454
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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