Pular para o conteúdo
Merck
Todas as fotos(2)

Documentos Principais

Visualizar Toda a Documentação

O8382

Sigma-Aldrich

17-Octadecynoic acid

≥95% (GC)

Sinônimo(s):

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

Faça loginpara ver os preços organizacionais e de contrato

Selecione um tamanho

5 MG
R$ 2.400,00
25 MG
R$ 9.600,00

R$ 2.400,00

Check Cart for Availability
Solicite uma grande encomenda
Todas as fotos(2)

Selecione um tamanho

Alterar visualização
5 MG
R$ 2.400,00
25 MG
R$ 9.600,00

About This Item

Fórmula empírica (Notação de Hill):
C18H32O2
Número CAS:
34450-18-5
Peso molecular:
280.45
Número MDL:
MFCD00077382
Código UNSPSC:
12352106
ID de substância PubChem:
24898058
NACRES:
NA.77

R$ 2.400,00

Check Cart for Availability
Solicite uma grande encomenda

Ensaio

≥95% (GC)

Formulário

powder

solubilidade

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

cadeia de caracteres SMILES

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)

chave InChI

DZIILFGADWDKMF-UHFFFAOYSA-N

Aplicação

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

Ações bioquímicas/fisiológicas

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.

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H319

Classificações de perigo

Eye Irrit. 2

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
0000287908
SLCP1113
SLCB5116
SLBN4823V
SLBN1738V

Não está vendo a versão correta?

Se precisar de uma versão específica, você pode procurar um certificado específico pelo número do lote ou da remessa.

Pesquise por COA

Já possui este produto?

Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.

Visite a Biblioteca de Documentos

Os clientes também visualizaram

Slide 1 of 8

1 of 8

5-Hexynoic acid 97%

Sigma-Aldrich

544000

5-Hexynoic acid

10,12-Pentacosadiynoic acid ≥97% (HPLC)

Sigma-Aldrich

76492

10,12-Pentacosadiynoic acid

5,7-Hexadecadiynoic acid 97%

Sigma-Aldrich

544027

5,7-Hexadecadiynoic acid

10-Undecyn-1-ol ≥95.0% (GC)

Sigma-Aldrich

94195

10-Undecyn-1-ol

10,12-Tricosadiynoic acid ≥98.0% (GC)

Sigma-Aldrich

91445

10,12-Tricosadiynoic acid

5,8,11,14-Eicosatetraynoic acid ≥97%

Sigma-Aldrich

E1768

5,8,11,14-Eicosatetraynoic acid

4-Pentynoic acid 95%

Sigma-Aldrich

232211

4-Pentynoic acid

2,4-Hexadiyne-1,6-diol ≥98.0% (GC)

Sigma-Aldrich

52490

2,4-Hexadiyne-1,6-diol

Sphingosine-1-phosphate lyase deficient cells as a tool to study protein lipid interactions
Gerl M J, et al.
Testing, 11(4), e0153009-e0153009 (2016)
Ossama A Hatoum et al.
American journal of physiology. Heart and circulatory physiology, 288(1), H48-H54 (2004-09-04)
The endothelium plays an important role in maintaining vascular homeostasis by synthesizing and releasing several mediators of vasodilation, which include prostacyclin (PGI(2)), nitric oxide, and endothelium-derived hyperpolarizing factor (EDHF). We have recently defined the role of nitric oxide and PGI(2)
Effects of intrarenal infusion of 17-octadecynoic acid on renal antihypertensive mechanisms in anesthetized rabbits
Evans R G, et al.
American Journal of Hypertension, 11(7), 803-812 (1998)
M H Wang et al.
The Journal of pharmacology and experimental therapeutics, 284(3), 966-973 (1998-03-13)
We characterized the inhibitory activity of several acetylenic and olefinic compounds on cytochrome P450 (CYP)-derived arachidonic acid omega-hydroxylation and epoxidation using rat renal cortical microsomes and recombinant CYP proteins. Among the acetylenic compounds, 6-(2-propargyloxyphenyl)hexanoic acid (PPOH) and N-methylsulfonyl-6-(2-propargyloxyphenyl)hexanamide were found
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
Exibir todos os documentos relacionados

Questions

Reviews

No rating value

Active Filters

Nossa equipe de cientistas tem experiência em todas as áreas de pesquisa, incluindo Life Sciences, ciência de materiais, síntese química, cromatografia, química analítica e muitas outras.

Entre em contato com a assistência técnica