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94455

Sigma-Aldrich

Adenosine 3′-phosphate 5′-phosphosulfate triethylammonium salt

≥90.0% (HPLC)

Synonym(s):

3′-Phosphoadenosine-5′-phosphosulfate triethylammonium salt

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About This Item

Empirical Formula (Hill Notation):
C10H15N5O13P2S · xC6H15N
CAS Number:
Molecular Weight:
507.26 (free acid basis)
UNSPSC Code:
12352204
PubChem Substance ID:
NACRES:
NA.32

Assay

≥90.0% (HPLC)

form

powder or crystals

solubility

water: soluble

storage temp.

−20°C

SMILES string

CCN(CC)CC.Nc1ncnc2n(cnc12)[C@@H]3O[C@H](COP(O)(=O)OS(O)(=O)=O)[C@@H](OP(O)(O)=O)[C@H]3O

InChI

1S/C10H15N5O13P2S.C6H15N/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;1-4-7(5-2)6-3/h2-4,6-7,10,16H,1H2,(H,20,21)(H2,11,12,13)(H2,17,18,19)(H,22,23,24);4-6H2,1-3H3/t4-,6-,7-,10-;/m1./s1

InChI key

IIAWHKVLRMAJSN-MCDZGGTQSA-N

Related Categories

General description

Adenosine 3′-phosphate 5′-phosphosulfate or 3′-Phosphoadenosine-5′-phosphosulfate (PAPS) is produced by the action of PAPS synthase in the cytoplasm and nucleus in animal cells. It is also found in the cytoplasm and plastids of plant cells.

Application

Adenosine 3′-phosphate 5′-phosphosulfate triethylammonium salt has been used in the determination of human 3-O-sulfotransferase-1 (3-OST-1) and aryl-sulfotransferase (AST-IV) enzyme activity.

Biochem/physiol Actions

3′-Phosphoadenosine-5′-phosphosulfate (PAPS) acts as a sulfate donor and serves as a substrate for sulfotransferases (STs).

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

94455-1MG:
94455-25MG:
94455-BULK:
94455-VAR:
94455-5MG:


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Zhengqi Zha et al.
International journal of biological macromolecules, 201, 47-58 (2022-01-10)
Heparosan, with a linear chain of disaccharide repeating units of → 4) β-D-glucuronic acid (GlcA) (1 → 4)-α-D-N-acetylglucosamine (GlcNAc) (1→, is a potential starting chemical for heparin synthesis. However, the chemoenzymatic synthesis of single-site sulfated heparosan and its antitumor activity have not been studied.

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