DTY

D-TYROSINE

Created: 1999-07-08
Last modified:  2023-11-03

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Chemical Details

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

Chemical Component Summary

NameD-TYROSINE
Systematic Name (OpenEye OEToolkits)(2R)-2-amino-3-(4-hydroxyphenyl)propanoic acid
FormulaC9 H11 N O3
Molecular Weight181.189
TypeD-PEPTIDE LINKING

Chemical Descriptors

TypeProgram Version Descriptor
SMILESACDLabs10.04O=C(O)C(N)Cc1ccc(O)cc1
SMILESCACTVS3.341N[CH](Cc1ccc(O)cc1)C(O)=O
SMILESOpenEye OEToolkits1.5.0c1cc(ccc1CC(C(=O)O)N)O
Canonical SMILESCACTVS3.341 N[C@H](Cc1ccc(O)cc1)C(O)=O
Canonical SMILESOpenEye OEToolkits1.5.0 c1cc(ccc1C[C@H](C(=O)O)N)O
InChIInChI1.03 InChI=1S/C9H11NO3/c10-8(9(12)13)5-6-1-3-7(11)4-2-6/h1-4,8,11H,5,10H2,(H,12,13)/t8-/m1/s1
InChIKeyInChI1.03 OUYCCCASQSFEME-MRVPVSSYSA-N

Drug Info: DrugBank

DrugBank IDDB03839 
NameD-Tyrosine
Groups experimental
DescriptionA non-essential amino acid. In animals it is synthesized from PHENYLALANINE. It is also the precursor of EPINEPHRINE; THYROID HORMONES; and melanin.
Synonyms
  • (R)-3-(p-Hydroxyphenyl)alanine
  • (R)-2-Amino-3-(p-hydroxyphenyl)propionic acid
  • D-Tyrosin
  • D-Tyrosine
  • D-Tyr
CAS number556-02-5

Drug Targets

NameTarget SequencePharmacological ActionActions
Monocarboxylate transporter 10MVLSQEEPDSARGTSEAQPLGPAPTGAAPPPGPGPSDSPEAAVEKVEVEL...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 71098, 6919035
ChEMBL CHEMBL1076637
ChEBI CHEBI:58570, CHEBI:28479
CCDC/CSD FAZHET01, SEDDEM, DLTYRS, RODSUA, FAPLIS