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870706P

Avanti

06:0 Coenzyme A

Avanti Research™ - A Croda Brand 870706P, powder

Synonim(y):

hexanoyl Coenzyme A (ammonium salt)

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About This Item

Wzór empiryczny (zapis Hilla):
C27H55N10O17P3S
Numer CAS:
799812-81-0
Masa cząsteczkowa:
916.77
Kod UNSPSC:
12352211
NACRES:
NA.25

Postać

powder

opakowanie

pkg of 1 × 5 mg (870706P-5mg)

producent / nazwa handlowa

Avanti Research™ - A Croda Brand 870706P

Zastosowanie

lipidomics

typ lipidu

coenzymes

Warunki transportu

dry ice

temp. przechowywania

−20°C

ciąg SMILES

O[C@@](C(NCCC(NCCSC(CCCCC)=O)=O)=O)(C(C)(COP([O-])(OP([O-])(OC[C@H]([C@H]1OP([O-])(O)=O)O[C@H]([C@@H]1O)N2C3=C(C(N)=NC=N3)N=C2)=O)=O)C)[H].[NH4+].[NH4+].[NH4+]

InChI

1S/C27H46N7O17P3S.3H3N/c1-4-5-6-7-18(36)55-11-10-29-17(35)8-9-30-25(39)22(38)27(2,3)13-48-54(45,46)51-53(43,44)47-12-16-21(50-52(40,41)42)20(37)26(49-16)34-15-33-19-23(28)31-14-32-24(19)34;;;/h14-16,20-22,26,37-38H,4-13H2,1-3H3,(H,29,35)(H,30,39)(H,43,44)(H,45,46)(H2,28,31,32)(H2,40,41,42);3*1H3/t16-,20?,21+,22+,26-;;;/m1.../s1

Klucz InChI

MXEFXWIYODKXEJ-WSHYHEJESA-N

Zastosowanie

06:0 Coenzyme A has been used as an internal standard in ultra-high performance liquid chromatography–tandem mass spectrometry for quantitative analysis of fatty-acyl-Coenzyme A species in biological samples.

Działania biochem./fizjol.

06:0 Coenzyme A, also known as hexanoyl coenzyme A, is a derivate of short-chain fatty acid hexanoate. It might be an intermediate of fatty acid metabolism. It acts as a source of N-acyl chain in the synthesis of N-hexanoyl-L-homoserine lactone (HHL) by LuxI homologue RhlI(VsmI). Hexanoyl coenzyme A also acts as a precursor for the synthesis of olivetolic acid (OLA), a polyketide metabolite. N-hexanoyl-CoA is preferred over N-octanoyl-CoA as an acyl donor substrate by GOAT (ghrelin O-acyltransferase).

Opakowanie

5 mL Amber Glass Screw Cap Vial (870706P-5mg)

Informacje prawne

Avanti Research is a trademark of Avanti Polar Lipids, LLC
This page may contain text that has been machine translated.

Kod klasy składowania

11 - Combustible Solids

Klasa zagrożenia wodnego (WGK)

WGK 3

Certyfikaty analizy (CoA)

Poszukaj Certyfikaty analizy (CoA), wpisując numer partii/serii produktów. Numery serii i partii można znaleźć na etykiecie produktu po słowach „seria” lub „partia”.

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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

László Abrankó et al.
Journal of chromatography. A, 1534, 111-122 (2018-01-02)
Fatty acyl-Coenzyme A species (acyl-CoAs) are key biomarkers in studies focusing on cellular energy metabolism. Existing analytical approaches are unable to simultaneously detect the full range of short-, medium-, and long-chain acyl-CoAs, while chromatographic limitations encountered in the analysis of
Futoshi Taura et al.
FEBS letters, 583(12), 2061-2066 (2009-05-21)
Alkylresorcinol moieties of cannabinoids are derived from olivetolic acid (OLA), a polyketide metabolite. However, the polyketide synthase (PKS) responsible for OLA biosynthesis has not been identified. In the present study, a cDNA encoding a novel PKS, olivetol synthase (OLS), was
Y Jiang et al.
Molecular microbiology, 28(1), 193-203 (1998-05-21)
In Pseudomonas aeruginosa, synthesis of the quorum-sensing signal molecules N-butanoyl-L-homoserine lactone (BHL) and N-hexanoyl-L-homoserine lactone (HHL) requires the Luxl homologue Rhll(Vsml). By using thin-layer chromatography in conjunction with high-performance liquid chromatography (HPLC) and mass spectrometry, we show that purified Rhll
Hideko Ohgusu et al.
Biochemical and biophysical research communications, 386(1), 153-158 (2009-06-09)
Ghrelin is a peptide hormone in which serine 3 is modified by n-octanoic acid through GOAT (ghrelin O-acyltransferase). However, the enzymological properties of GOAT remain to be elucidated. We analyzed the in vitro activity of GOAT using the recombinant enzyme.
Jake M Stout et al.
The Plant journal : for cell and molecular biology, 71(3), 353-365 (2012-02-23)
The psychoactive and analgesic cannabinoids (e.g. Δ(9) -tetrahydrocannabinol (THC)) in Cannabis sativa are formed from the short-chain fatty acyl-coenzyme A (CoA) precursor hexanoyl-CoA. Cannabinoids are synthesized in glandular trichomes present mainly on female flowers. We quantified hexanoyl-CoA using LC-MS/MS and

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