Summary
IMPPAT Phytochemical identifier: IMPHY009328
Phytochemical name: Norisocorydine
Synonymous chemical names:nor-isocorydine, norisocorydine
External chemical identifiers:CID:12313549, ChEMBL:CHEMBL465212, ChEBI:175177, FDASRS:4JS4P60W6G
Chemical structure information
SMILES:
COc1ccc2c(-c3c(OC)c(OC)cc4c3[C@H](C2)NCC4)c1OInChI:
InChI=1S/C19H21NO4/c1-22-13-5-4-10-8-12-15-11(6-7-20-12)9-14(23-2)19(24-3)17(15)16(10)18(13)21/h4-5,9,12,20-21H,6-8H2,1-3H3/t12-/m0/s1InChIKey:
OHDQLTAYHMLRBA-LBPRGKRZSA-NDeepSMILES:
COccccc-ccOC))cOC))ccc6[C@H]C%10)NCC6))))))))))c6OFunctional groups:
CNC, cO, cOC
Molecular scaffolds
Scaffold Graph/Node/Bond level:
c1ccc2c(c1)CC1NCCc3cccc-2c31Scaffold Graph/Node level:
C1CCC2C(C1)CC1NCCC3CCCC2C31Scaffold Graph level:
C1CCC2C(C1)CC1CCCC3CCCC2C31
Chemical classification
ClassyFire Kingdom: Organic compoundsClassyFire Superclass: Alkaloids and derivativesClassyFire Class: Aporphines
NP Classifier Biosynthetic pathway: Alkaloids
NP Classifier Superclass: Tyrosine alkaloids
NP Classifier Class: Aporphine alkaloids, Isoquinoline alkaloids
NP-Likeness score: 1.705
Chemical structure download