MMS

MIMOSINE

Created: 2002-08-22
Last modified:  2020-06-05

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Chemical Details

Formal Charge0
Atom Count24
Chiral Atom Count1
Bond Count24
Aromatic Bond Count6
2D diagram of MMS

Chemical Component Summary

NameMIMOSINE
Synonyms3-HYDROXY-4-OXO-1(4H)-PYRIDINEALANINE
Systematic Name (OpenEye OEToolkits)(2S)-2-amino-3-(3-hydroxy-4-oxo-pyridin-1-yl)propanoic acid
FormulaC8 H10 N2 O4
Molecular Weight198.176
TypeNON-POLYMER

Chemical Descriptors

TypeProgram Version Descriptor
SMILESACDLabs10.04O=C(O)C(N)CN1C=CC(=O)C(O)=C1
SMILESCACTVS3.341N[CH](CN1C=CC(=O)C(=C1)O)C(O)=O
SMILESOpenEye OEToolkits1.5.0C1=CN(C=C(C1=O)O)CC(C(=O)O)N
Canonical SMILESCACTVS3.341 N[C@@H](CN1C=CC(=O)C(=C1)O)C(O)=O
Canonical SMILESOpenEye OEToolkits1.5.0 C1=CN(C=C(C1=O)O)C[C@@H](C(=O)O)N
InChIInChI1.03 InChI=1S/C8H10N2O4/c9-5(8(13)14)3-10-2-1-6(11)7(12)4-10/h1-2,4-5,12H,3,9H2,(H,13,14)/t5-/m0/s1
InChIKeyInChI1.03 WZNJWVWKTVETCG-YFKPBYRVSA-N

Drug Info: DrugBank

DrugBank IDDB01055 
NameMimosine
Groups experimental
DescriptionMimosine is an antineoplastic alanine-substituted pyridine derivative isolated from _Leucena glauca_.
Synonyms
  • Leucaenine
  • Leucenine
  • (S)-2-amino-3-(3-hydroxy-4-oxo-4H-pyridin-1-yl)propanoate
  • Leucaenol
  • (L)-Mimosine
Categories
  • Alanine
  • Amino Acids
  • Amino Acids, Peptides, and Proteins
  • Pyridines
  • Pyridones
CAS number500-44-7

Drug Targets

NameTarget SequencePharmacological ActionActions
Serine hydroxymethyltransferase, cytosolicMTMPVNGAHKDADLWSSHDKMLAQPLKDSDVEVYNIIKKESNRQRVGLEL...unknowninhibitor
C-C motif chemokine 2MKVSAALLCLLLIAATFIPQGLAQPDAINAPVTCCYNFTNRKISVQRLAS...unknowninhibitor
TyrosinaseMLLAVLYCLLWSFQTSAGHFPRACVSSKNLMEKECCPPWSGDRSPCGQLS...unknowninhibitor
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 6971294, 440473
ChEMBL CHEMBL245416
ChEBI CHEBI:77689, CHEBI:77848, CHEBI:29063