IMPPAT: Indian Medicinal Plants, Phytochemistry And Therapeutics
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IMPPAT Phytochemical information:
Julandine
Summary
Physicochemical
Drug-likeness
ADMET
Descriptors
Summary
IMPPAT Phytochemical identifier:
IMPHY001111
Phytochemical name:
Julandine
Synonymous chemical names:
julandine
External chemical identifiers:
CID:10407368
,
ZINC:ZINC000038795360
Chemical structure information
SMILES:
COc1ccc(cc1)C1=C(C[C@@H]2N(C1)CCCC2)c1ccc(c(c1)OC)OC
InChI:
InChI=1S/C24H29NO3/c1-26-20-10-7-17(8-11-20)22-16-25-13-5-4-6-19(25)15-21(22)18-9-12-23(27-2)24(14-18)28-3/h7-12,14,19H,4-6,13,15-16H2,1-3H3/t19-/m1/s1
InChIKey:
GZQPRQAGPHGFNW-LJQANCHMSA-N
DeepSMILES:
COcccccc6))C=CC[C@@H]NC6)CCCC6)))))))cccccc6)OC)))OC
Functional groups:
CN(C)C, cC(C)=C(c)C, cOC
Molecular scaffolds
Scaffold Graph/Node/Bond level:
c1ccc(C2=C(c3ccccc3)CN3CCCCC3C2)cc1
Scaffold Graph/Node level:
C1CCC(C2CC3CCCCN3CC2C2CCCCC2)CC1
Scaffold Graph level:
C1CCC(C2CC3CCCCC3CC2C2CCCCC2)CC1
Chemical classification
ClassyFire Kingdom:
Organic compounds
ClassyFire Superclass:
Phenylpropanoids and polyketides
ClassyFire Class:
Stilbenes
NP Classifier Biosynthetic pathway:
Alkaloids
NP Classifier Superclass:
Lysine alkaloids
NP Classifier Class:
Indolizidine alkaloids
NP-Likeness score:
0.314
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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