AT5

3-[(2S,4S,5R)-5,6-DICHLORO-2,4-DIMETHYL-1-OXOHEXYL]-4-HYDROXY-5,6-DIMETHOXY-2(1H)-PYRIDINONE

Created: 2005-07-21
Last modified:  2020-06-05

Find related ligands:

Chemical Details

Formal Charge0
Atom Count44
Chiral Atom Count3
Bond Count44
Aromatic Bond Count6
2D diagram of AT5

Chemical Component Summary

Name3-[(2S,4S,5R)-5,6-DICHLORO-2,4-DIMETHYL-1-OXOHEXYL]-4-HYDROXY-5,6-DIMETHOXY-2(1H)-PYRIDINONE
SynonymsATPENIN A5; AA5
Systematic Name (OpenEye OEToolkits)3-[(2S,4S,5R)-5,6-dichloro-2,4-dimethyl-hexanoyl]-4-hydroxy-5,6-dimethoxy-1H-pyridin-2-one
FormulaC15 H21 Cl2 N O5
Molecular Weight366.237
TypeNON-POLYMER

Chemical Descriptors

TypeProgram Version Descriptor
SMILESACDLabs10.04O=C(C1=C(O)C(OC)=C(OC)NC1=O)C(C)CC(C)C(Cl)CCl
SMILESCACTVS3.341COC1=C(OC)C(=C(C(=O)N1)C(=O)[CH](C)C[CH](C)[CH](Cl)CCl)O
SMILESOpenEye OEToolkits1.5.0CC(CC(C)C(=O)C1=C(C(=C(NC1=O)OC)OC)O)C(CCl)Cl
Canonical SMILESCACTVS3.341 COC1=C(OC)C(=C(C(=O)N1)C(=O)[C@@H](C)C[C@H](C)[C@@H](Cl)CCl)O
Canonical SMILESOpenEye OEToolkits1.5.0 C[C@@H](C[C@H](C)C(=O)C1=C(C(=C(NC1=O)OC)OC)O)[C@H](CCl)Cl
InChIInChI1.03 InChI=1S/C15H21Cl2NO5/c1-7(9(17)6-16)5-8(2)11(19)10-12(20)13(22-3)15(23-4)18-14(10)21/h7-9H,5-6H2,1-4H3,(H2,18,20,21)/t7-,8-,9-/m0/s1
InChIKeyInChI1.03 OVULNOOPECCZRG-CIUDSAMLSA-N

Drug Info: DrugBank

DrugBank IDDB04631 
NameAtpenin A5
Groups experimental
Synonyms
  • 3-[(2S,4S,5R)-5,6-dichloro-2,4-dimethyl-1-oxohexyl]-4-hydroxy-5,6-dimethoxy-2(1H)-pyridinone
  • Atpenin A5
CategoriesPyridines
CAS number119509-24-9

Drug Targets

NameTarget SequencePharmacological ActionActions
Succinate dehydrogenase iron-sulfur subunitMRLEFSIYRYNPDVDDAPRMQDYTLEADEGRDMMLLDALIQLKEKDPSLS...unknown
Succinate dehydrogenase cytochrome b556 subunitMIRNVKKQRPVNLDLQTIRFPITAIASILHRVSGVITFVAVGILLWLLGT...unknown
Succinate dehydrogenase hydrophobic membrane anchor subunitMVSNASALGRNGVHDFILVRATAIVLTLYIIYMVGFFATSGELTYEVWIG...unknown
Succinate dehydrogenase flavoprotein subunitMKLPVREFDAVVIGAGGAGMRAALQISQSGQTCALLSKVFPTRSHTVSAQ...unknown
Drug Info/Drug Targets: DrugBank 3.0: a comprehensive resource for 'omics' research on drugs. Knox C, Law V, Jewison T, Liu P, Ly S, Frolkis A, Pon A, Banco K, Mak C, Neveu V, Djoumbou Y, Eisner R, Guo AC, Wishart DS. Nucleic Acids Res. 2011 Jan; 39 (Database issue):D1035-41. | PMID:21059682

Related Resource References

Resource NameReference
PubChem 54676868, 197273
ChEMBL CHEMBL1081615