Glycyltyrosine

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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 Formula	C₁₁H₁₄N₂O₄
Molecular Weight	238.24 g/mol
XLogP3	-3.3
Hydrogen Bond Donor Count	4
Hydrogen Bond Acceptor Count	5
Rotatable Bond Count	5
Exact Mass	238.09535693 g/mol
Monoisotopic Mass	238.09535693 g/mol
Topological Polar Surface Area	113 Å²
Heavy Atom Count	17
Formal Charge	0
Complexity	275
Isotope Atom Count	0
Defined Atom Stereocenter Count	1
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
Covalently Bonded Unit Count	1

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

Glycyltyrosine

Glycyltyrosine

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ACTIVE PHARMA INGREDIENTS

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REF. STANDARDS & IMPURITIES

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