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Chemistry

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Also known as: Tyrosol, 501-94-0, 4-hydroxyphenethyl alcohol, 4-(2-hydroxyethyl)phenol, 4-hydroxyphenylethanol, 4-hydroxybenzeneethanol

Molecular Formula

C₈H₁₀O₂

Molecular Weight

138.16 g/mol

InChI Key

YCCILVSKPBXVIP-UHFFFAOYSA-N

FDA UNII

1AK4MU3SNX

Tyrosol is a metabolite found in or produced by Saccharomyces cerevisiae.

1 2D Structure

2-(4-Hydroxyphenyl)Ethanol

2 Identification

2.1 Computed Descriptors

2.1.1 IUPAC Name

4-(2-hydroxyethyl)phenol

2.1.2 InChI

InChI=1S/C8H10O2/c9-6-5-7-1-3-8(10)4-2-7/h1-4,9-10H,5-6H2

2.1.3 InChI Key

YCCILVSKPBXVIP-UHFFFAOYSA-N

2.1.4 Canonical SMILES

C1=CC(=CC=C1CCO)O

2.2 Other Identifiers

2.2.1 UNII

1AK4MU3SNX

2.3 Synonyms

2.3.1 MeSH Synonyms

1. 2-(4-hydroxyphenyl)ethyl Acetate

2. 4-hydroxybenzeneethanol

3. 4-hydroxyphenylethanol

4. Beta-(4-hydroxyphenyl)ethanol

5. N-tyrosol

6. P-hydroxyphenylethanol

7. P-tyrosol

8. Para-hydroxyphenylethanol

9. Tyrosol

10. Tyrosol Acetate

2.3.2 Depositor-Supplied Synonyms

1. Tyrosol

2. 501-94-0

3. 4-hydroxyphenethyl Alcohol

4. 4-(2-hydroxyethyl)phenol

5. 4-hydroxyphenylethanol

6. 4-hydroxybenzeneethanol

7. P-hydroxyphenethyl Alcohol

8. Benzeneethanol, 4-hydroxy-

9. P-tyrosol

10. 4-hydroxyphenylethyl Alcohol

11. 2-(4-hydroxyphenyl)ethyl Alcohol

12. P-thyrosol

13. Mfcd00002902

14. Nsc 59876

15. 2-(p-hydroxyphenyl)ethanol

16. Metoprolol Impurity 07

17. 4-hydroxy-benzeneethanol

18. 1ak4mu3snx

19. P-hydroxyphenylethyl Alcohol

20. 4-(2-hydroxy-ethyl)-phenol

21. Chembl53566

22. Chebi:1879

23. Nsc-59876

24. P-hydroxyphenylethanol

25. Tyrosol C

26. Smr000857159

27. P-hpea

28. 4-hydroxyphenethylalcohol

29. Einecs 207-930-8

30. Unii-1ak4mu3snx

31. Beta-(4-hydroxyphenyl)ethanol

32. 4-tyrosol

33. Yrl

34. Tyrosol ,(s)

35. 4-hydroxybenzenethanol

36. 4-(hydroxyethyl)phenol

37. P-hydroxy-benzeneethanol

38. Tyrosol [mi]

39. B-(p-hydroxyphenyl)ethanol

40. Bmse000173

41. B-(4-hydroxyphenyl)ethanol

42. 4-hydroxyphenylmethylcarbinol

43. 2-(p-hydroxyphenyl) Ethanol

44. Schembl43838

45. (4-hydroxyphenethyl) Alcohol

46. 2-(4-hydroxyphenyl) Ethanol

47. 2-(4-hydroxyphenyl)-ethanol

48. Beta-(p-hydroxyphenyl)ethanol

49. Mls001332423

50. Mls001332424

51. Phenethyl Alcohol, P-hydroxy-

52. Ethanol, 2-(4-hydroxyphenyl)

53. Dtxsid8060111

54. Schembl10620528

55. .beta.-(p-hydroxyphenyl)ethanol

56. 2-(4-hydroxyphenyl)-1-ethanol

57. Ethanol, 2-(4-hydroxyphenyl)-

58. .beta.-(4-hydroxyphenyl)ethanol

59. Hms2230e12

60. Zinc164581

61. 2-(4-hydroxyphenyl)ethanol, 98%

62. Bcp34277

63. Hy-n0474

64. Nsc59876

65. Str02735

66. Hydroxyphenethyl Alcohol, P-

67. Bdbm50339585

68. S3773

69. Akos000280287

70. Ac-2493

71. Ccg-266147

72. Cs-w019782

73. Ks-5274

74. Ncgc00246994-01

75. Sy001653

76. Db-019455

77. Am20060146

78. Ft-0608647

79. H0720

80. N1496

81. A14486

82. C06044

83. 2-(4-hydroxyphenyl)ethanol, Analytical Standard

84. Nsc 59876; P-hpea;4-hydroxyphenethyl Alcohol

85. Q402607

86. Metoprolol Tartrate Impurity G [ep Impurity]

87. Metoprolol Succinate Impurity G [ep Impurity]

88. Tyrosol (constituent Of Rhodiola Rosea) [dsc]

89. F0001-1309

90. 947d0361-23c6-4863-8346-22ab05108ac5

91. 4-hydroxy-benzeneethanol;4-hydroxyphenylethanol;beta-(4-hydroxyphenyl)ethanol

2.4 Create Date

2005-03-26

3 Chemical and Physical Properties

Molecular Formula	C₈H₁₀O₂
Molecular Weight	138.16 g/mol
XLogP3	0.4
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	2
Exact Mass	138.068079557 g/mol
Monoisotopic Mass	138.068079557 g/mol
Topological Polar Surface Area	40.5 Å²
Heavy Atom Count	10
Formal Charge	0
Complexity	85.3
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
Covalently Bonded Unit Count	1

4 Pharmacology and Biochemistry

4.1 MeSH Pharmacological Classification

Anti-Arrhythmia Agents

Agents used for the treatment or prevention of cardiac arrhythmias. They may affect the polarization-repolarization phase of the action potential, its excitability or refractoriness, or impulse conduction or membrane responsiveness within cardiac fibers. Anti-arrhythmia agents are often classed into four main groups according to their mechanism of action: sodium channel blockade, beta-adrenergic blockade, repolarization prolongation, or calcium channel blockade. (See all compounds classified as Anti-Arrhythmia Agents.)

Antioxidants

Naturally occurring or synthetic substances that inhibit or retard oxidation reactions. They counteract the damaging effects of oxidation in animal tissues. (See all compounds classified as Antioxidants.)

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