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A1651

Sigma-Aldrich

Adenosine 3′-phosphate 5′-phosphosulfate lithium salt hydrate

≥60%

Sinônimo(s):

3′-Phosphoadenosine 5′-phosphosulfate lithium salt, APPS, Active sulfate, PAPS

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About This Item

Fórmula empírica (Notação de Hill):
C10H15N5O13P2S · xLi+ · yH2O
Número CAS:
Peso molecular:
507.26 (free acid basis)
Beilstein:
8181191
Código UNSPSC:
41106305
eCl@ss:
32160414
NACRES:
NA.51

forma

powder

Nível de qualidade

concentração

≥60%

Condições de expedição

dry ice

temperatura de armazenamento

−70°C

InChI

1S/C10H15N5O13P2S.4Li.H2O/c11-8-5-9(13-2-12-8)15(3-14-5)10-6(16)7(27-29(17,18)19)4(26-10)1-25-30(20,21)28-31(22,23)24;;;;;/h2-4,6-7,10,16H,1H2,(H,20,21)(H2,11,12,13)(H2,17,18,19)(H,22,23,24);;;;;1H2/q;4*+1;/p-4/t4-,6-,7-,10-;;;;;/m1...../s1

chave InChI

UGODCLHJOJPPHP-AZGWGOJFSA-J

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Aplicação

3′-Phosphoadenosine 5′-phosphosulfate (PAPS) is used as a universal sulfonate donor for in vivo sulfonation by sulfotransferases. PAPS is used for the sulfation of glycans. PAPS is also useful to study the distribution and function of its biological transporter(s).
Adenosine 3′-phosphate 5′-phosphosulfate lithium salt has been used in a study that cloned and characterized a mammalian lithium-sensitive bisphosphate 3′-nucleotidase inhibited by inositol 1,4-bisphosphate. Adenosine 3′-phosphate 5′-phosphosulfate lithium salt has also been used in a study to assess the golgi-resident PAP-specific 3′-phosphatase-coupled sulfotransferase assays.

Qualidade

Major impurities appear to be adenosine 3′,5′-diphosphate, sulfate and ammonia substitution products.

Atenção

Rapid decomposition occurs when exposed to room temperature: up to 17% per day at 37 °C. We ship on dry ice to minimize decomposition in transit.

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

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves


Certificados de análise (COA)

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Paul A Dawson
Seminars in cell & developmental biology, 22(6), 653-659 (2011-03-23)
Sulfate (SO(4)(2-)) is an important nutrient for human growth and development, and is obtained from the diet and the intra-cellular metabolism of sulfur-containing amino acids, including methionine and cysteine. During pregnancy, fetal tissues have a limited capacity to produce sulfate
Xianxuan Zhou et al.
Glycobiology, 21(6), 771-780 (2011-01-13)
Heparan sulfate (HS) belongs to a major class of glycans that perform central physiological functions. Heparin is a specialized form of HS and is a clinically used anticoagulant drug. Heparin is a natural product isolated from pig intestine. There is
Saveria Pastore et al.
The Journal of investigative dermatology, 127(3), 660-667 (2006-10-14)
ATP is abundantly released from stressed or damaged cells in response to mechanical stimulation, bacteria, or noxious agents. In this study, we have investigated the possible involvement of P2 receptors (receptor for extracellular nucleotides) in the expression and release of
J P Horwitz et al.
Biochimica et biophysica acta, 480(2), 376-381 (1977-02-09)
A practical synthesis of 3'-phosphoadenosine 5'-phosphosulfate (IV) in yields of 68-72% from adenosine 2',3'-cyclic phosphate 5'-phosphate (II) is described. Reaction of II with triethylamine-N-sulfonic acid affords adenosine 2',3'-cyclic phosphate 5'-phosphosulfate (III) which, on treatment with ribonuclease-T2, provides IV. Spleen phosphodiesterase
Emanuel Smeds et al.
Glycobiology, 20(10), 1274-1282 (2010-06-18)
The signaling of various molecules involved in development and regulation of cell growth are regulated by heparan sulfate (HS). Specific binding of HS to ligand proteins depends on the HS sulfation pattern, where the spacing and number of O-sulfate groups

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