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Merck
모든 사진(1)

문서

870432P

Avanti

C18:1 anandamide

Avanti Research - A Croda Brand 870432P, powder

동의어(들):

9Z-octadecenoylethanolamide

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About This Item

실험식(Hill 표기법):
C20H39NO2
CAS Number:
Molecular Weight:
325.53
UNSPSC 코드:
12352211
NACRES:
NA.25

형태

powder

포장

pkg of 1 × 5 mg (870432P-5mg)

제조업체/상표

Avanti Research - A Croda Brand 870432P

지질 유형

bioactive lipids

배송 상태

dry ice

저장 온도

−20°C

SMILES string

O=C(CCCCCCC/C=C\CCCCCCCC)NCCO

일반 설명

Anandamide is an endocannabinoid. It acts as a ligand for cannabinoid (CB) receptors CB1 and CB2 in the brain and peripheral tissues. It is synthesized from glycerophospho-N-arachidonoylethanolamine (GP-NArE) precursor by the reaction catalyzed by glycerophosphodiesterase 1.

생화학적/생리학적 작용

Anandamide plays a vital role in various processes including inflammation, pain, and appetite.

포장

5 mL Clear Glass Sealed Ampule (870432P-5mg)

법적 정보

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


시험 성적서(COA)

제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.

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문서 라이브러리 방문

Mohammed K Hankir et al.
Frontiers in neuroscience, 10, 620-620 (2017-01-31)
Brain μ-opioid receptors (MORs) stimulate high-fat (HF) feeding and have been implicated in the distinct long term outcomes on body weight of bariatric surgery and dieting. Whether alterations in fat appetite specifically following these disparate weight loss interventions relate to
Selective blockade of 2-arachidonoylglycerol hydrolysis produces cannabinoid behavioral effects
Long J, et al.
Nature Chemical Biology, 5(1), 37-37 (2009)
Identification of biosynthetic precursors for the endocannabinoid anandamide in the rat brain
Astarita G, et al.
Journal of Lipid Research, 49(1), 48-57 (2008)
Mohammad Younus et al.
Langmuir : the ACS journal of surfaces and colloids, 32(35), 8942-8950 (2016-08-16)
Oleoylethanolamide (OEA) is an endogenous lipid with neuroprotective properties and the fortification of its concentration in the brain can be beneficial in the treatment of many neurodegenerative disorders. However, OEA is rapidly eliminated by hydrolysis in vivo, limiting its therapeutic
Gabriel M Simon et al.
The Journal of biological chemistry, 283(14), 9341-9349 (2008-01-30)
Anandamide (AEA) is an endogenous ligand of cannabinoid receptors and a well characterized mediator of many physiological processes including inflammation, pain, and appetite. The biosynthetic pathway(s) for anandamide and its N-acyl ethanolamine (NAE) congeners remain enigmatic. Previously, we proposed an

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