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810705P

Avanti

16-NBD-16:0 Coenzyme A

Avanti Research™ - A Croda Brand 810705P, powder

동의어(들):

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

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모든 사진(2)

About This Item

실험식(Hill 표기법):
C43H77N14O20P3S
CAS Number:
1367862-09-6
Molecular Weight:
1235.14
UNSPSC 코드:
12352211
NACRES:
NA.25

분석

>99% (TLC)

양식

powder

포장

pkg of 1 × 1 mg (810705P-1mg)

제조업체/상표

Avanti Research™ - A Croda Brand 810705P

응용 분야

lipidomics

지질 유형

coenzymes

배송 상태

dry ice

저장 온도

−20°C

SMILES string

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+]

InChI

1S/C43H68N11O20P3S.3H3N/c1-43(2,25-70-77(67,68)74-76(65,66)69-24-30-37(72-75(62,63)64)36(57)42(71-30)53-27-50-35-39(44)48-26-49-40(35)53)38(58)41(59)47-21-19-31(55)46-22-23-78-32(56)16-14-12-10-8-6-4-3-5-7-9-11-13-15-20-45-28-17-18-29(54(60)61)34-33(28)51

InChI key

FBPTUXYEMIFLQO-DNLKZUPMSA-N

일반 설명

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.

애플리케이션

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

생화학적/생리학적 작용

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.

포장

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

법적 정보

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Storage Class Code

11 - Combustible Solids

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시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리 방문

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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