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Documentos Principais

A5763

Sigma-Aldrich

Adenosine 3′,5′-diphosphate disodium salt

≥96%

Sinônimo(s):

3′-phosphoadenosine 5′-phosphate, 3′-phosphorylated nucleotide, PAP, 3′-Phosphoadenosine 5′-phosphate

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10 MG
R$ 2.022,00
25 MG
R$ 4.457,00
100 MG
R$ 14.280,00

About This Item

Fórmula empírica (Notação de Hill):
C10H13N5Na2O10P2
Número CAS:
Peso molecular:
471.16
Número MDL:
Código UNSPSC:
41106305
eCl@ss:
32160414
ID de substância PubChem:
NACRES:
NA.51

R$ 2.022,00


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fonte biológica

synthetic (inorganic)

Nível de qualidade

Ensaio

≥96%

Formulário

powder

solubilidade

water: 25 mg/mL, clear, colorless to very faintly yellow

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

[Na].Nc1ncnc2n(cnc12)C3OC(COP(O)(O)=O)C(OP(O)(O)=O)C3O

InChI

1S/C10H15N5O10P2.Na.H/c11-8-5-9(13-2-12-8)15(3-14-5)10-6(16)7(25-27(20,21)22)4(24-10)1-23-26(17,18)19;;/h2-4,6-7,10,16H,1H2,(H2,11,12,13)(H2,17,18,19)(H2,20,21,22);;

chave InChI

ISROZYFZEAVMSP-UHFFFAOYSA-N

Descrição geral

3′-phosphoadenosine 5′-phosphate (PAP), a 3′-phosphorylated nucleotide is found in almost all organisms and is obtained as a by-product of sulfur and lipid metabolism.[1]

Aplicação

Adenosine 3′,5′-diphosphate disodium salt has been used:
  • to spot sample on cellulose high-performance thin-layer chromatography (HPTLC) plates in two-dimensional thin layer chromatography[2]
  • in enzyme activity assay to study the activities of HOS2/FIERY1 wild type
  • hos2 mutant and fiery1?2 mutant protein against 3′-phosphoadenosine 5′-phosphate (PAP)[3]
  • as a standard for the quantification of phosphoadenosines[4]

Ações bioquímicas/fisiológicas

3′-phosphoadenosine 5′-phosphate (PAP) is capable of blocking exoribonucleases (XRNs) activity in the nucleus and cytosol. It stimulates stomatal closure and can serve as a secondary messenger during abscisic acid (ABA) signaling.[5] It is capable of blocking RNA catabolism. Hence it may serve as a physiological modulator of poly (ADP-ribose) polymerase 1 (PARP1) activity.[1]
Adenosine 3′,5′-diphosphate (PAP) is used to study the kinetics and mechanisms of hydroxysteroid sulfotransferases such as SULT1A1, SULT2A1 of which it is product inhibitor.

Pictogramas

Exclamation mark

Palavra indicadora

Warning

Frases de perigo

Classificações de perigo

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves


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RISC is a 5? phosphomonoester-producing RNA endonuclease
Martinez J and Tuschl T
Genes & Development, 18(9), 975-980 (2004)
Hao Chen et al.
Plant, cell & environment, 33(12), 2180-2190 (2010-09-03)
The Arabidopsis FIERY1 (FRY1) locus was originally identified as a negative regulator of stress-responsive gene expression and later shown to be required for suppression of RNA silencing. In this study we discovered that the FRY1 locus also regulates lateral root
Zhihao Yu et al.
Biochemistry, 47(48), 12777-12786 (2008-11-11)
Most assimilatory bacteria, fungi, and plants species reduce sulfate (in the activated form of APS or PAPS) to produce reduced sulfur. In yeast, PAPS reductase reduces PAPS to sulfite and PAP. Despite the difference in substrate specificity and catalytic cofactor
Elie Toledano et al.
The Biochemical journal, 443(2), 485-490 (2012-01-14)
pAp (3'-5' phosphoadenosine phosphate) is a by-product of sulfur and lipid metabolism and has been shown to have strong inhibitory properties on RNA catabolism. In the present paper we report a new target of pAp, PARP-1 [poly(ADP-ribose) polymerase 1], a
A single amino acid substitution in the Arabidopsis FIERY1/HOS2 protein confers cold signaling specificity and lithium tolerance
Xiong L, et al.
The Plant Journal, 40(4), 536-545 (2004)

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