Summary

IMPPAT Phytochemical identifier: IMPPAT3_PHYID003565

Phytochemical name: Lysergamide

Synonymous chemical names:
Ergine, ergine, lysergic acid amide

External chemical identifiers:
CID:CID_442072, ChEMBL:CHEMBL227213, ChEBI:CHEBI:4819, ZINC:ZINC000056727892, FDASRS:073830XH10, SureChEMBL:SCHEMBL183540

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Chemical structure information

SMILES:
CN1C[C@@H](C=C2[C@H]1Cc1c[nH]c3c1c2ccc3)C(=O)N

InChI:
InChI=1S/C16H17N3O/c1-19-8-10(16(17)20)5-12-11-3-2-4-13-15(11)9(7-18-13)6-14(12)19/h2-5,7,10,14,18H,6,8H2,1H3,(H2,17,20)/t10-,14-/m1/s1

InChIKey:
GENAHGKEFJLNJB-QMTHXVAHSA-N

DeepSMILES:
CNC[C@@H]C=C[C@H]6Ccc[nH]cc5c9ccc6)))))))))))))C=O)N

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

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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: 1.003

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Chemical structure download