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Technical details about Glycyltyrosine, learn more about the structure, uses, toxicity, action, side effects and more

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2D Structure
1. Also known as: 658-79-7, Gly-tyr, N-glycyl-l-tyrosine, H-gly-tyr-oh, Glycyltyrosine, L-tyrosine, glycyl-
Molecular Formula
C11H14N2O4
Molecular Weight
238.24  g/mol
InChI Key
XBGGUPMXALFZOT-VIFPVBQESA-N
FDA UNII
A226496H4O

1 2D Structure

2D Structure

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
(2S)-2-[(2-aminoacetyl)amino]-3-(4-hydroxyphenyl)propanoic acid
2.1.2 InChI
InChI=1S/C11H14N2O4/c12-6-10(15)13-9(11(16)17)5-7-1-3-8(14)4-2-7/h1-4,9,14H,5-6,12H2,(H,13,15)(H,16,17)/t9-/m0/s1
2.1.3 InChI Key
XBGGUPMXALFZOT-VIFPVBQESA-N
2.1.4 Canonical SMILES
C1=CC(=CC=C1CC(C(=O)O)NC(=O)CN)O
2.1.5 Isomeric SMILES
C1=CC(=CC=C1C[C@@H](C(=O)O)NC(=O)CN)O
2.2 Other Identifiers
2.2.1 UNII
A226496H4O
2.3 Synonyms
2.3.1 MeSH Synonyms

1. Gly-tyr

2. Glycyl-tyrosine

3. Glycyltyrosine

2.3.2 Depositor-Supplied Synonyms

1. 658-79-7

2. Gly-tyr

3. N-glycyl-l-tyrosine

4. H-gly-tyr-oh

5. Glycyltyrosine

6. L-tyrosine, Glycyl-

7. Glycyl-tyrosine

8. (s)-2-(2-aminoacetamido)-3-(4-hydroxyphenyl)propanoic Acid

9. Glycyl-l-tyrosine 2-hydrate

10. Chembl53400

11. Chebi:73517

12. (2s)-2-[(2-aminoacetyl)amino]-3-(4-hydroxyphenyl)propanoic Acid

13. A226496h4o

14. L-tyrosine, Glycyl-, Monomer

15. Gy Dipeptide

16. Nsc-83260

17. Unii-a226496h4o

18. G-y Dipeptide

19. Einecs 211-525-1

20. Gly-l-tyr

21. Nsc 83260

22. Gly-l-tyr-oh

23. L-glycyl-l-tyrosine

24. Nsc 118362

25. Glycine Tyrosine Dipeptide

26. Glycine-tyrosine Dipeptide

27. Schembl479126

28. Glycyltyrosine [who-dd]

29. (2s)-2-(2-aminoacetamido)-3-(4-hydroxyphenyl)propanoic Acid

30. Dtxsid701316223

31. Bcp24671

32. Glycyl-l-tyrosine [usp-rs]

33. Gy

34. Zinc1730678

35. Bdbm50188508

36. Stl466189

37. Akos010366204

38. Ac-6976

39. Cs-w010308

40. Hy-w009592

41. S10390

42. Ds-13668

43. G0145

44. G-6370

45. 658g797

46. Q27140599

47. 2-(2-amino-acetylamino)-3-(4-hydroxy-phenyl)-propionic Acid

48. (s)-2-(2-amino-acetylamino)-3-(4-hydroxy-phenyl)-propionic Acid

49. G-y

50. Melanin Synthesized From Gly-tyr Substrate Catalyzed By Tyrosinase For 22 Hrs, >10 Kd Fraction

51. Melanin Synthesized From Gly-tyr Substrate Catalyzed By Tyrosinase For 3 Hrs, Hcl Insoluble Portion (precipitate)

52. Melanin Synthesized From Gly-tyr Substrate Catalyzed By Tyrosinase, Brominated With N-bromosuccinimide

53. Melanin Synthesized From Gly-tyr Substrate Catalyzed By Tyrosinase, Sulfonated Using Sulfur Trioxide/dmf Complex For 1.5-7 Hours

2.4 Create Date
2005-06-24
3 Chemical and Physical Properties
Molecular Weight 238.24 g/mol
Molecular Formula C11H14N2O4
XLogP3-3.3
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count5
Rotatable Bond Count5
Exact Mass238.09535693 g/mol
Monoisotopic Mass238.09535693 g/mol
Topological Polar Surface Area113 Ų
Heavy Atom Count17
Formal Charge0
Complexity275
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count1
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