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Palmidrol

DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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ACTIVE PHARMA INGREDIENTS

6 API Suppliers, 1 NDC API, 6 Listed Suppliers, $ API Reference Price

6 API Suppliers
1 NDC API
6 Listed Suppliers
$ API Reference Price

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Synopsis

ACTIVE PHARMA INGREDIENTS

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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

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 Formula	C₁₈H₃₇NO₂
Molecular Weight	299.5 g/mol
XLogP3	6.2
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	16
Exact Mass	299.282429423 g/mol
Monoisotopic Mass	299.282429423 g/mol
Topological Polar Surface Area	49.3 Å²
Heavy Atom Count	21
Formal Charge	0
Complexity	219
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

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 SUPPLIERS

01

Laboratorium Ofichem B.V

Netherlands

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

Antibody Engineering

Not Confirmed

Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.

Contact Supplier

Netherlands

Virtual Booth

Digital Content

USDMF CEP/COS JDMF EU-WC NDC

KDMF VMF Others AUDIT

02

ASolution Pharmaceuticals

India

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

Antibody Engineering

Not Confirmed

ASolution Pharmaceuticals: Your Partner for cGMP Development & Manufacturing Services – Supplying APIs, FDFs, and Specialty Molecules.

Contact Supplier

India

Virtual Booth

Digital Content

USDMF CEP/COS JDMF EU-WC NDC KDMF VMF Others AUDIT

03

Allastir

India

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

Antibody Engineering

Not Confirmed

Not Confirmed

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API Reference Price

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