Summary
IMPPAT Phytochemical identifier: IMPHY012468
Phytochemical name: Ajmaline
Synonymous chemical names:ajmaline, raugalline
External chemical identifiers:CID:6100671, ZINC:ZINC000000898188, FDASRS:1PON08459R, MolPort-006-069-263
Chemical structure information
SMILES:
CC[C@H]1[C@@H]2C[C@@H]3N([C@@H]1O)[C@@H]1[C@H]2[C@@H](O)[C@]2([C@H]3N(C)c3c2cccc3)C1InChI:
InChI=1S/C20H26N2O2/c1-3-10-11-8-14-17-20(12-6-4-5-7-13(12)21(17)2)9-15(16(11)18(20)23)22(14)19(10)24/h4-7,10-11,14-19,23-24H,3,8-9H2,1-2H3/t10-,11-,14-,15-,16-,17-,18+,19+,20+/m0/s1InChIKey:
CJDRUOGAGYHKKD-RQBLFBSQSA-NDeepSMILES:
CC[C@H][C@@H]C[C@@H]N[C@@H]6O))[C@@H][C@H]6[C@@H]O)[C@][C@H]7NC)cc5cccc6))))))))C5Functional groups:
CO, C[C@@H](O)N(C)C, cN(C)C
Molecular scaffolds
Scaffold Graph/Node/Bond level:
c1ccc2c(c1)NC1C3CC4CCN3C3CC21CC43Scaffold Graph/Node level:
C1CCC2C(C1)NC1C3CC4CCN3C3CC21CC43Scaffold Graph level:
C1CCC2C(C1)CC1C3CC4CCC3C3CC21CC43
Chemical classification
ClassyFire Kingdom: Organic compoundsClassyFire Superclass: Alkaloids and derivativesClassyFire Class: Ajmaline-sarpagine alkaloids
NP Classifier Biosynthetic pathway: Alkaloids
NP Classifier Superclass: Tryptophan alkaloids
NP Classifier Class: Corynanthe type
NP-Likeness score: 2.375
Chemical structure download