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Key Documents

M186

Sigma-Aldrich

R(+)-Methanandamide

5 mg/mL in absolute ethanol, ≥96% (HPLC)

Synonym(s):

AM-356, R(+)-Arachidonyl-1′-hydroxy-2′-propylamide

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About This Item

Empirical Formula (Hill Notation):
C23H39NO2
CAS Number:
Molecular Weight:
361.56
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:

Quality Level

Assay

≥96% (HPLC)

optical activity

[α]/D +8.7°, c = 4 in chloroform(lit.)

drug control

regulated under CDSA - not available from Sigma-Aldrich Canada

storage condition

desiccated
protect from light
under inert gas

concentration

5 mg/mL in absolute ethanol

storage temp.

−20°C

SMILES string

CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(=O)N[C@H](C)CO

InChI

1S/C23H39NO2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-23(26)24-22(2)21-25/h7-8,10-11,13-14,16-17,22,25H,3-6,9,12,15,18-21H2,1-2H3,(H,24,26)/b8-7-,11-10-,14-13-,17-16-/t22-/m1/s1

InChI key

SQKRUBZPTNJQEM-FQPARAGTSA-N

Gene Information

Biochem/physiol Actions

R(+)-Methanandamide is metabolically stable congener of anandamide that has higher affinity for the cannabinoid receptor. Of the analogs tested, (R)-methanandamide exhibited the highest affinity for the cannabinoid receptor with a Ki of 20 +/- 1.6 nM, 4-fold lower than that of anandamide (Ki = 78 +/- 2 nM). (R)-methanandamide exhibits high stability to aminopeptidase hydrolysis. Experiments with mice have demonstrated that (R)-methanandamide also posseses cannabimimetric properties in vivo, as established by the four tests of hypothermia, hypokinesia, ring immobility, and antinociception.

Features and Benefits

This compound is featured on the Cannabinoid Receptors page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Pictograms

FlameExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

57.2 °F

Flash Point(C)

14 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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V Abadji et al.
Journal of medicinal chemistry, 37(12), 1889-1893 (1994-06-10)
Four chiral congeners of arachidonylethanolamide (anandamide) have been synthesized and evaluated for (a) their ability to bind to the cannabinoid receptor in rat forebrain membranes and (b) their pharmacological potency as measured by the compounds' ability to inhibit electrically-evoked contractions
Raffaele Nuzzi et al.
Frontiers in neuroscience, 11, 494-494 (2017-09-21)
Glaucoma is a common degenerative disease affecting
María Gracia Gervasi et al.
PloS one, 6(2), e16993-e16993 (2011-02-25)
Anandamide (AEA), a major endocannabinoid, binds to cannabinoid and vanilloid receptors (CB1, CB2 and TRPV1) and affects many reproductive functions. Nanomolar levels of anandamide are found in reproductive fluids including mid-cycle oviductal fluid. Previously, we found that R(+)-methanandamide, an anandamide
María de Los Ángeles Nuñez-Lumbreras et al.
Frontiers in behavioral neuroscience, 14, 611780-611780 (2021-02-09)
Cannabinoid receptors 1 and 2 (CB1 and CB2, respectively) play an important role in maintaining the integrity of the blood-brain barrier (BBB). On the other hand, BBB dysfunction is a common feature in drug-resistant epilepsy. The focus of the present
Ana Inés Salazar et al.
Molecular human reproduction, 23(7), 500-508 (2017-05-02)
What is the role of the endocannabinoid system (eCS) on the lipopolysaccharide (LPS) effects on uterine explants from 7-day pregnant mice in a murine model of endotoxin-induced miscarriage? We found evidence for cannabinoid receptor type2 (CB2) involvement in LPS-induced increased

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