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Merck
모든 사진(2)

주요 문서

O8382

Sigma-Aldrich

17-Octadecynoic acid

≥95% (GC)

동의어(들):

17-ODYA, Alkynyl Stearic Acid, Octadec-17-ynoic acid

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크기 선택

5 MG
₩621,891
25 MG
₩1,479,363

₩621,891


구입 가능 여부는 고객센터에 문의하십시오.

벌크 견적 요청

크기 선택

보기 변경
5 MG
₩621,891
25 MG
₩1,479,363

About This Item

실험식(Hill 표기법):
C18H32O2
CAS Number:
Molecular Weight:
280.45
MDL number:
UNSPSC 코드:
12352106
PubChem Substance ID:
NACRES:
NA.77

₩621,891


구입 가능 여부는 고객센터에 문의하십시오.

벌크 견적 요청

분석

≥95% (GC)

양식

powder

solubility

chloroform: 10 mg/mL to clear, colorless to faintly yellow

SMILES string

C#CCCCCCCCCCCCCCCCC(O)=O

InChI

1S/C18H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h1H,3-17H2,(H,19,20)

InChI key

DZIILFGADWDKMF-UHFFFAOYSA-N

관련 카테고리

애플리케이션

17-Octadecynoic acid has been used in lipid synthesis.[1]

생화학적/생리학적 작용

17-Octadecynoic acid (7-ODYA) is an irreversible inhibitor of cytochrome P450 isozymes, that participates in long-chain fatty acid metabolism.[2]
Suicide substrate inhibitor that selectively and irreversibly inhibits cytochrome P450 epoxygenases and ω-hydrolases.

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)


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문서 라이브러리 방문

H Dong et al.
British journal of pharmacology, 120(4), 695-701 (1997-02-01)
1. The nature and cellular mechanisms that are responsible for endothelium-dependent relaxations resistant to indomethacin and NG-nitro-L-arginine methyl ester (L-NAME) were investigated in phenylephrine (PE) precontracted isolated carotid arteries from the rabbit. 2. In the presence of the cyclo-oxygenase inhibitor
Jacob S Yount et al.
Current protocols in chemical biology, 3(2), 65-79 (2011-05-01)
Protein fatty-acylation is the covalent addition of a lipid chain at specific amino acids. This modification changes the inherent hydrophobicity of a protein, often targeting it to cellular membrane compartments. Acylation may also regulate protein activity, stability, and protein-protein interactions.
Hanane Issa et al.
PloS one, 12(2), e0171955-e0171955 (2017-02-16)
Protein mycoloylation is a recently identified, new form of protein acylation. This post-translational modification consists in the covalent attachment of mycolic acids residues to serine. Mycolic acids are long chain, α-branched, β-hydroxylated fatty acids that are exclusively found in the
Corinne Ivaldi et al.
PloS one, 7(5), e37187-e37187 (2012-05-23)
S-palmitoylation is a reversible post-translational modification important for controlling the membrane targeting and function of numerous membrane proteins with diverse roles in signalling, scaffolding, and trafficking. We sought to identify novel palmitoylated proteins in B lymphocytes using acyl-biotin exchange chemistry
J C Komen et al.
FEBS letters, 580(16), 3794-3798 (2006-06-20)
Patients suffering from Refsum disease have a defect in the alpha-oxidation pathway which results in the accumulation of phytanic acid in plasma and tissues. Our previous studies have shown that phytanic acid is also a substrate for the omega-oxidation pathway.

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