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810705P

Avanti

16-NBD-16:0 Coenzyme A

Avanti Research™ - A Croda Brand 810705P, powder

Synonyme(s) :

{N-[(7-nitro-2-1,3-benzoxadiazol-4-yl)-methyl]amino} palmitoyl Coenzyme A (ammonium salt)

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About This Item

Formule empirique (notation de Hill):
C43H77N14O20P3S
Numéro CAS:
1367862-09-6
Poids moléculaire :
1235.14
Code UNSPSC :
12352211
Nomenclature NACRES :
NA.25

Pureté

>99% (TLC)

Forme

powder

Conditionnement

pkg of 1 × 1 mg (810705P-1mg)

Fabricant/nom de marque

Avanti Research™ - A Croda Brand 810705P

Application(s)

lipidomics

Type de lipide

coenzymes

Conditions d'expédition

dry ice

Température de stockage

−20°C

Chaîne SMILES 

O[C@@](C(NCCC(NCCSC(CCCCCCCCCCCCCCCNC1=CC=C([N+]([O-])=O)C2=NON=C12)=O)=O)=O)(C(C)(COP([O-])(OP([O-])(OC[C@H]([C@H]3OP([O-])(O)=O)O[C@H]([C@@H]3O)N4C5=C(C(N)=NC=N5)N=C4)=O)=O)C)[H].[NH4+].[NH4+].[NH4+]

Catégories apparentées

Description générale

NBD-palmitoyl-CoA ((N-[(7-nitro-2-1,3-benzoxadiazol-4-yl)-methyl]amino) palmitoyl Coenzyme A) is a fluorescent analog of palmitoyl-CoA.
Product can be used to fluorescently label palmitoylation sites on proteins.

Application

16-NBD-16:0 Coenzyme A ((N-[(7-nitro-2-1,3-benzoxadiazol-4-yl)-methyl]amino) palmitoyl Coenzyme A) has been used:
  • as a fluorescent substrate in fluorescent diacylglycerol acyltransferase (DGAT) assay
  • as a fluorescent analog to study the membrane translocation of lipids and to track palmitoyl-CoA uptake
  • as a component in wash buffer to measure autoacylation of the enzymes in palmitate transferase assay

Actions biochimiques/physiologiques

NBD-palmitoyl-CoA ((N-[(7-nitro-2-1,3-benzoxadiazol-4-yl)-methyl]amino) palmitoyl Coenzyme A) can be used as an economical alternative to radioactive tracers.

Conditionnement

5 mL Amber Glass Screw Cap Vial (810705P-1mg)

Informations légales

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Code de la classe de stockage

11 - Combustible Solids

Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Maurine E Linder et al.
Biochemistry, 42(15), 4311-4320 (2003-04-16)
Since its discovery more than 30 years ago, protein palmitoylation has been shown to have a role in protein-membrane interactions, protein trafficking, and enzyme activity. Until recently, however, the molecular machinery that carries out reversible palmitoylation of proteins has been
S J Moench et al.
Biochemistry, 33(19), 5783-5790 (1994-05-17)
Two tandem cysteine residues in the carboxyl-terminal region of rhodopsin have been shown to be covalently linked to palmitate via thioester bonds (Ovchinnikov, Y. A., et al. (1988) FEBS Lett. 230, 1-5). We have synthesized a fluorescent analogue of palmitoyl
Xiaochao Wei et al.
Cell host & microbe, 11(2), 140-152 (2012-02-22)
The intestinal mucus barrier prevents pathogen invasion and maintains host-microbiota homeostasis. We show that fatty acid synthase (FAS), an insulin-responsive enzyme essential for de novo lipogenesis, helps maintain the mucus barrier by regulating Mucin 2, the dominant mucin in the
Pamela J McFie et al.
Journal of lipid research, 52(9), 1760-1764 (2011-06-10)
Triacylglycerols (TG) are the major storage form of energy in eukaryotic organisms and are synthesized primarily by acyl CoA:1,2-diacylglycerol acyltransferase (DGAT) enzymes. In vitro DGAT activity has previously been quantified by measuring the incorporation of either radiolabeled fatty acyl CoA
Raffaello Verardi et al.
Structure (London, England : 1993), 25(9), 1337-1347 (2017-08-02)
DHHC enzymes catalyze palmitoylation, a major post-translational modification that regulates a number of key cellular processes. There are up to 24 DHHCs in mammals and hundreds of substrate proteins that get palmitoylated. However, how DHHC enzymes engage with their substrates
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