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Arachidonoyl Cyclopropylamide

Arachidonoyl Cyclopropylamide

2800-39200 INR

Product Details:

  • Usage R&D FORMULATION
  • Molecular Weight 343.6 Kilograms (kg)
  • Melting Point REFER C.O.A ,MSDS
  • Physical Form Powder
  • Molecular Formula C23H37NO
  • Taste Bitter
  • Other Names N-cyclopropyl-5Z,8Z,11Z,14Z-eicosatetraenamide
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Arachidonoyl Cyclopropylamide Price And Quantity

  • 2800-39200 INR
  • 1 Pack

Arachidonoyl Cyclopropylamide Product Specifications

  • 12 Months
  • REFER C.O.A ,MSDS
  • Stimulus
  • Other
  • C23H37NO
  • POWDER
  • C23H37NO
  • Bitter
  • Crystal
  • N-cyclopropyl-5Z,8Z,11Z,14Z-eicosatetraenamide
  • R&D FORMULATION
  • WHITE
  • Powder
  • 98%
  • REFER C.O.A ,MSDS
  • 343.6 Kilograms (kg)
  • High Purity
  • 229021-64-1
  • REFER C.O.A ,MSDS
  • TETRA HYDROXI STEAROL

Arachidonoyl Cyclopropylamide Trade Information

  • NEW DELHI
  • Days after Acceptance (DA), Cheque, Cash Advance (CA)
  • 10 Pack Per Day
  • 10-15 Days
  • Yes
  • Within a certain price range free samples are available
  • 5MG 10MG 50MG 100MG
  • Asia
  • All India

Product Description

DESCRIPTION

Synonyms

  • ACPA

Arachidonoyl cyclopropylamide (ACPA) is a potent and selective cannabinoid (CB) receptor 1 agonist with Ki values of 2.2 and 715 nM for CB1 and CB2receptors, respectively.1 In whole animal experiments, ACPA induces hypothermia in mice with the same efficacy as arachidonoyl ethanolamide (AEA; Item No. 90050), in spite of its higher affinity for the CB1 receptor. These data have been interpreted to indicate that ACEA may be a substrate for fatty acid amide hydrolase (FAAH), and thus only transiently available in whole animal experiments.2

DESCRIPTION

Synonyms

  • ACPA

Arachidonoyl cyclopropylamide (ACPA) is a potent and selective cannabinoid (CB) receptor 1 agonist with Ki values of 2.2 and 715 nM for CB1 and CB2receptors, respectively.1 In whole animal experiments, ACPA induces hypothermia in mice with the same efficacy as arachidonoyl ethanolamide (AEA; Item No. 90050), in spite of its higher affinity for the CB1 receptor. These data have been interpreted to indicate that ACEA may be a substrate for fatty acid amide hydrolase (FAAH), and thus only transiently available in whole animal experiments.2

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