Summary

IMPPAT Phytochemical identifier: IMPHY011760

Phytochemical name: Ergometrinine

Synonymous chemical names:
ergometrinine, ergonovinine

External chemical identifiers:
CID:5486180, ChEMBL:CHEMBL1555758, FDASRS:5EXN22NGMW, SureChEMBL:SCHEMBL918411

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Chemical structure information

SMILES:
OC[C@@H](NC(=O)[C@@H]1CN(C)[C@H]2C(=C1)c1cccc3c1c(C2)c[nH]3)C

InChI:
InChI=1S/C19H23N3O2/c1-11(10-23)21-19(24)13-6-15-14-4-3-5-16-18(14)12(8-20-16)7-17(15)22(2)9-13/h3-6,8,11,13,17,20,23H,7,9-10H2,1-2H3,(H,21,24)/t11-,13-,17+/m0/s1

InChIKey:
WVVSZNPYNCNODU-PLQHRBFRSA-N

DeepSMILES:
OC[C@@H]NC=O)[C@@H]CNC)[C@H]C=C6)cccccc6cC%10)c[nH]5))))))))))))))))C

Functional groups:
CN(C)C, CNC(C)=O, CO, cC(C)=CC, c[nH]c

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Molecular scaffolds

Scaffold Graph/Node/Bond level:
C1=C2c3cccc4[nH]cc(c34)CC2NCC1

Scaffold Graph/Node level:
C1CNC2CC3CNC4CCCC(C2C1)C34

Scaffold Graph level:
C1CCC2C(C1)CC1CCC3CCCC2C31

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Chemical classification

ClassyFire Kingdom: Organic compounds

ClassyFire Superclass: Alkaloids and derivatives

ClassyFire Class: Ergoline and derivatives

ClassyFire Subclass: Lysergic acids and derivatives

NP Classifier Biosynthetic pathway: Alkaloids

NP Classifier Superclass: Tryptophan alkaloids

NP Classifier Class: Ergot alkaloids

NP-Likeness score: 0.862

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Chemical structure download