Summary

IMPPAT Phytochemical identifier: IMPHY006883

Phytochemical name: (+)-Minovincine

Synonymous chemical names:
minovincine

External chemical identifiers:
CID:11121714, ZINC:ZINC000038275862

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Chemical structure information

SMILES:
COC(=O)C1=C2Nc3c([C@]42[C@H]2[C@@](C1)(CCCN2CC4)C(=O)C)cccc3

InChI:
InChI=1S/C21H24N2O3/c1-13(24)20-8-5-10-23-11-9-21(19(20)23)15-6-3-4-7-16(15)22-17(21)14(12-20)18(25)26-2/h3-4,6-7,19,22H,5,8-12H2,1-2H3/t19-,20-,21-/m1/s1

InChIKey:
DAWIIFABKVMRDV-NJDAHSKKSA-N

DeepSMILES:
COC=O)C=CNcc[C@@]5[C@H][C@@]C9)CCCN6CC9))))))C=O)C)))))cccc6

Functional groups:
CC(C)=O, CN(C)C, cNC(C)=C(C)C(=O)OC

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Molecular scaffolds

Scaffold Graph/Node/Bond level:
C1=C2Nc3ccccc3C23CCN2CCCC(C1)C23

Scaffold Graph/Node level:
C1CCC2C(C1)NC1CCC3CCCN4CCC12C34

Scaffold Graph level:
C1CCC2C(C1)CC1CCC3CCCC4CCC12C34

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Chemical classification

ClassyFire Kingdom: Organic compounds

ClassyFire Superclass: Alkaloids and derivatives

ClassyFire Class: Aspidospermatan-type alkaloids

NP Classifier Biosynthetic pathway: Alkaloids

NP Classifier Superclass: Tryptophan alkaloids

NP Classifier Class: Aspidosperma type

NP-Likeness score: 1.611

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Chemical structure download