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Chemistry

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Also known as: Palmidrol, 544-31-0, N-(2-hydroxyethyl)hexadecanamide, Palmitoyl ethanolamide, Impulsin, Palmitamide mea
Molecular Formula
C18H37NO2
Molecular Weight
299.5  g/mol
InChI Key
HXYVTAGFYLMHSO-UHFFFAOYSA-N
FDA UNII
6R8T1UDM3V

Palmitoylethanolamide
Palmitoyl ethanolamide is a metabolite found in the aging mouse brain.
1 2D Structure

Palmitoylethanolamide

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
N-(2-hydroxyethyl)hexadecanamide
2.1.2 InChI
InChI=1S/C18H37NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-18(21)19-16-17-20/h20H,2-17H2,1H3,(H,19,21)
2.1.3 InChI Key
HXYVTAGFYLMHSO-UHFFFAOYSA-N
2.1.4 Canonical SMILES
CCCCCCCCCCCCCCCC(=O)NCCO
2.2 Other Identifiers
2.2.1 UNII
6R8T1UDM3V
2.3 Synonyms
2.3.1 MeSH Synonyms

1. Impulsin

2. Mimyx

3. N-(2-hydroxyethyl)palmitate

4. N-palmitoylethanolamine

5. Palmidrol

6. Palmitylethanolamide

2.3.2 Depositor-Supplied Synonyms

1. Palmidrol

2. 544-31-0

3. N-(2-hydroxyethyl)hexadecanamide

4. Palmitoyl Ethanolamide

5. Impulsin

6. Palmitamide Mea

7. N-palmitoylethanolamine

8. Loramine P 256

9. Hydroxyethylpalmitamide

10. Palmitic Acid Monoethanolamide

11. N-(2-hydroxyethyl)palmitamide

12. Palmitoyl-ea

13. Palmitylethanolamide

14. Palmidrolum

15. Hexadecanamide, N-(2-hydroxyethyl)-

16. Palmidrol [inn]

17. Monoethanolamine Palmitic Acid Amide

18. Levagen

19. Anandamide (16:0)

20. N-palmitoyl Ethanolamine

21. Palmitic Monoethanolamide

22. Palmdrol Prodes

23. N-hexadecanoylethanolamine

24. Palmitinsaeure-beta-hydroxyethylamid

25. Nsc 23320

26. Hexadecanoyl Ethanolamide

27. Nsc-23320

28. N-hexadecanoyl-ethanolamine

29. N(2-hydroxyethyl)palmitide

30. Am 3112

31. 6r8t1udm3v

32. N(2-hydroxyethyl) Palmitide

33. N-(2-hydroxyethyl)-palmitide

34. Chebi:71464

35. Fsd-201

36. Palmidrol (inn)

37. Ncgc00015793-03

38. Am 3112;loramine P 256;mackpeart Dr 14v

39. Dsstox_cid_22254

40. Dsstox_rid_79975

41. Dsstox_gsid_42254

42. Mimyx

43. Palmidrolum [inn-latin]

44. Cas-544-31-0

45. Sr-01000076055

46. Einecs 208-867-9

47. Unii-6r8t1udm3v

48. N-(2-hydroxyethyl) Hexadecanamide

49. Hexadecanamide,n-(2-hydroxyethyl)-

50. Mackpeart Dr 14v

51. Mfcd00020562

52. Anandamide C16:0

53. 2-palmitoylaminoethanol

54. Palmdrol Prodes (tn)

55. Tocris-0879

56. N-palmitoyl Ethanolamide

57. N-hexadecyl-ethanolamine

58. Palmidrol [mi]

59. Lopac-p-0359

60. Palmidrol [mart.]

61. Palmitoylethanolamide-[d4]

62. Palmityoletanolamide (pea)

63. 2-palmitamidoethanol

64. Palmidrol [who-dd]

65. Cbiol_002043

66. Lopac0_000905

67. Bspbio_001454

68. Kbiogr_000174

69. Kbioss_000174

70. Mls002153421

71. Schembl120518

72. Palmitamide Mea [inci]

73. Bml2-b10

74. Chembl417675

75. Gtpl3622

76. Am-3112

77. Dtxsid4042254

78. Palmidrol

79. N-palmitoylethanolamine

80. Schembl19511663

81. Bdbm29083

82. Kbio2_000174

83. Kbio2_002742

84. Kbio2_005310

85. Kbio3_000347

86. Kbio3_000348

87. Bio1_000329

88. Bio1_000818

89. Bio1_001307

90. Bio2_000174

91. Bio2_000654

92. Hms1361i16

93. Hms1791i16

94. Hms1989i16

95. Hms2234l19

96. Hms3264c10

97. Hms3266n08

98. Hms3374k03

99. Hms3402i16

100. Hms3411b14

101. Hms3649l03

102. Hms3675b14

103. Pharmakon1600-01506156

104. Bcp29005

105. Cs-d1253

106. Nsc23320

107. Zinc8035017

108. Tox21_110222

109. Ana(16:0)

110. Lmfa08040013

111. Nae(16:0)

112. Nsc760371

113. S4708

114. Stl454872

115. Akos002676363

116. Tox21_110222_1

117. Ccg-204987

118. Db14043

119. Lp00905

120. Nsc-760371

121. Sdccgsbi-0050880.p002

122. Idi1_033924

123. S10398

124. Ncgc00015793-01

125. Ncgc00015793-02

126. Ncgc00015793-04

127. Ncgc00015793-05

128. Ncgc00015793-06

129. Ncgc00015793-07

130. Ncgc00015793-08

131. Ncgc00015793-09

132. Ncgc00015793-10

133. Ncgc00015793-12

134. Ncgc00024840-01

135. Ncgc00024840-02

136. Ncgc00024840-05

137. Ncgc00024840-06

138. Ncgc00024840-07

139. Ncgc00024840-08

140. Ncgc00024840-09

141. As-14094

142. Hy-20685

143. Palmitoylethanolamide [nflis-drug]

144. Smr000058371

145. Hexadecanoic Acid (2-hydroxy-ethyl)-amide

146. B6485

147. Eu-0100905

148. Ft-0778178

149. P2670

150. D08328

151. P 0359

152. Ab00918319_06

153. A904411

154. Q2159860

155. Sr-01000076055-1

156. Sr-01000076055-3

157. Sr-01000076055-7

158. Brd-k68095457-001-04-4

159. Z2687203832

2.4 Create Date
2005-03-25
3 Chemical and Physical Properties
Molecular Weight 299.5 g/mol
Molecular Formula C18H37NO2
XLogP36.2
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count16
Exact Mass299.282429423 g/mol
Monoisotopic Mass299.282429423 g/mol
Topological Polar Surface Area49.3 Ų
Heavy Atom Count21
Formal Charge0
Complexity219
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count1
4 Pharmacology and Biochemistry
4.1 MeSH Pharmacological Classification

Cannabinoid Receptor Agonists

Compounds that interact with and stimulate the activity of CANNABINOID RECEPTORS. (See all compounds classified as Cannabinoid Receptor Agonists.)


Analgesics

Compounds capable of relieving pain without the loss of CONSCIOUSNESS. (See all compounds classified as Analgesics.)


Anti-Inflammatory Agents, Non-Steroidal

Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions. They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects. (See all compounds classified as Anti-Inflammatory Agents, Non-Steroidal.)


Antiviral Agents

Agents used in the prophylaxis or therapy of VIRUS DISEASES. Some of the ways they may act include preventing viral replication by inhibiting viral DNA polymerase; binding to specific cell-surface receptors and inhibiting viral penetration or uncoating; inhibiting viral protein synthesis; or blocking late stages of virus assembly. (See all compounds classified as Antiviral Agents.)


API Reference Price

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02-Apr-2021
06-Jul-2024
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Drugs in Development

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Details:

SCI-110 contains dronabinol with the endocannabinoid palmitoylethanolamide. It is developed for Tourette Syndrome to stimulate cannabinoid receptors across the CNS.


Lead Product(s): Tetrahydrocannabinol,Palmitoylethanolamide

Therapeutic Area: Neurology Brand Name: SCI-110

Study Phase: Phase IIProduct Type: Small molecule

Sponsor: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable September 30, 2024

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01

SciSparc

Israel
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AES 2024
Not Confirmed

SciSparc

Israel
arrow
AES 2024
Not Confirmed

Details : SCI-110 contains dronabinol with the endocannabinoid palmitoylethanolamide. It is developed for Tourette Syndrome to stimulate cannabinoid receptors across the CNS.

Brand Name : SCI-110

Molecule Type : Small molecule

Upfront Cash : Not Applicable

September 30, 2024

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Details:

SCI-110 contains dronabinol with the endocannabinoid palmitoylethanolamide. It is developed for Tourette Syndrome to stimulate cannabinoid receptors across the CNS.


Lead Product(s): Tetrahydrocannabinol,Palmitoylethanolamide

Therapeutic Area: Neurology Brand Name: SCI-110

Study Phase: Phase IIProduct Type: Small molecule

Sponsor: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable September 23, 2024

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