Summary

IMPPAT Phytochemical identifier: IMPHY004136

Phytochemical name: Julifloricine

Synonymous chemical names:
julifloricine, juliflorine, juliprosopine

External chemical identifiers:
CID:128344

---

Chemical structure information

SMILES:
OC1CCC(NC1C)CCCCCCCCCCC1=CC(C2N(C1)CCC2)CCCCCCCCCCC1CCC(C(N1)C)O

InChI:
InChI=1S/C40H75N3O2/c1-32-39(44)27-25-36(41-32)22-17-13-9-5-3-7-11-15-20-34-30-35(38-24-19-29-43(38)31-34)21-16-12-8-4-6-10-14-18-23-37-26-28-40(45)33(2)42-37/h30,32-33,35-42,44-45H,3-29,31H2,1-2H3

InChIKey:
JOTBJXJGDRSICD-UHFFFAOYSA-N

DeepSMILES:
OCCCCNC6C)))CCCCCCCCCCC=CCCNC6)CCC5)))))CCCCCCCCCCCCCCCN6)C))O

Functional groups:
CC=C(C)C, CN(C)C, CNC, CO

---

Molecular scaffolds

Scaffold Graph/Node/Bond level:
C1=C(CCCCCCCCCCC2CCCCN2)CN2CCCC2C1CCCCCCCCCCC1CCCCN1

Scaffold Graph/Node level:
C(CCCCCC1CCCCN1)CCCCC1CC(CCCCCCCCCCC2CCCCN2)C2CCCN2C1

Scaffold Graph level:
C(CCCCCC1CC(CCCCCCCCCCC2CCCCC2)C2CCCC2C1)CCCCC1CCCCC1

---

Chemical classification

ClassyFire Kingdom: Organic compounds

ClassyFire Superclass: Alkaloids and derivatives

NP Classifier Biosynthetic pathway: Alkaloids

NP Classifier Superclass: Lysine alkaloids

NP Classifier Class: Indolizidine alkaloids, Piperidine alkaloids

NP-Likeness score: 1.301

---

Chemical structure download