IMPPAT Phytochemical information: 
Pentanoic acid, 2-hydroxy-2-(1-hydroxyethyl)-3-methyl-, (hexahydro-1H-pyrrolizin-1-yl)methyl ester

Pentanoic acid, 2-hydroxy-2-(1-hydroxyethyl)-3-methyl-, (hexahydro-1H-pyrrolizin-1-yl)methyl ester
Summary

IMPPAT Phytochemical identifier: IMPHY007858

Phytochemical name: Pentanoic acid, 2-hydroxy-2-(1-hydroxyethyl)-3-methyl-, (hexahydro-1H-pyrrolizin-1-yl)methyl ester

Synonymous chemical names:
curassavine

External chemical identifiers:
CID:155104
Chemical structure information

SMILES:
CCC(C(C(=O)OCC1CCN2C1CCC2)(C(O)C)O)C

InChI:
InChI=1S/C16H29NO4/c1-4-11(2)16(20,12(3)18)15(19)21-10-13-7-9-17-8-5-6-14(13)17/h11-14,18,20H,4-10H2,1-3H3

InChIKey:
VBLBKKUAYMFOAG-UHFFFAOYSA-N

DeepSMILES:
CCCCC=O)OCCCCNC5CCC5)))))))))))CO)C))O))C

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: 1.049


Chemical structure download