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Adenosine 5'-[γ-thio]triphosphate TetralithiuM Salt

Product Name
Adenosine 5'-[γ-thio]triphosphate TetralithiuM Salt
CAS No.
93839-89-5
Chemical Name
Adenosine 5'-[γ-thio]triphosphate TetralithiuM Salt
Synonyms
ATP-γ-S;Ado-5'-PPP[S];ATP-ALPHA-S, NA;ATP-GAMMA-S LI4;ATP-GAMMA-S, 4LI;ADO-5'-PPP[S] 4LI;S tetralithium salt;ATPgammaS tetralithi;ATP-GAMMA-S SODIUM SALT;ATPγS tetralithium salt
CBNumber
CB5702961
Molecular Formula
C10H12Li4N5O12P3S
Formula Weight
546.98
MOL File
93839-89-5.mol
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Adenosine 5'-[γ-thio]triphosphate TetralithiuM Salt Property

Melting point:
>192°C (dec.)
storage temp. 
-20°C
solubility 
H2O: 25 mg/mL
form 
powder
color 
white
Water Solubility 
Soluble to 50 mM in water
BRN 
6265083
Stability:
Moisture Sensitive
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
3-10-21
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P321Specific treatment (see … on this label).

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

P362Take off contaminated clothing and wash before reuse.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
A1388
Product name
Adenosine 5′-[γ-thio]triphosphate tetralithium salt
Purity
≥75%, powder
Packaging
1mg
Price
$118
Updated
2024/03/01
Sigma-Aldrich
Product number
119123
Product name
Adenosine5ʹ-O-(3-Thiotriphosphate),Solution,TetralithiumSalt-CAS93839-89-5-Calbiochem
Purity
Aphosphatase-resistantATPanalogue.
Packaging
100μL
Price
$370
Updated
2024/03/01
Sigma-Aldrich
Product number
11162306001
Product name
ATP-γ-S
Purity
=90% (HPLC), solution, pkg of 200?μL (20 μmol)
Packaging
200μL
Price
$477
Updated
2024/03/01
Cayman Chemical
Product number
14957
Product name
Adenosine 5'-(γ-thio)-triphosphate (lithium salt)
Purity
≥90%
Packaging
1mg
Price
$31
Updated
2024/03/01
Cayman Chemical
Product number
14957
Product name
Adenosine 5'-(γ-thio)-triphosphate (lithium salt)
Purity
≥90%
Packaging
5mg
Price
$108
Updated
2024/03/01
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Adenosine 5'-[γ-thio]triphosphate TetralithiuM Salt Chemical Properties,Usage,Production

Chemical Properties

White Solid

Uses

Adenosine 5’[γ-thio]triphosphate Tetralithium Salt is used as a reagent in the synthesis of DNA N-acetylglucosamine analogs.

Uses

Adenosine 5′-[γ-thio]triphosphate tetralithium salt has been used to treat the pollen grains to determine the inhibitory effect of adenosine triphosphate (ATP) or its hydrolysis product. It has also been used to select thiophosphorylate target protein.

Uses

ATP-γ-S is a substrate and inhibitor of ATP-dependent enzyme systems. It is hydrolyzed very slowly by phosphatases and most ATPases. Once thiophosphorylated, proteins are resistant to protein phosphatases.

Biological Activity

atpγs tetralithium salt is an analogue of atp, acting as a potent agonist of g protein-coupled p2y2 and p2y11 receptors (pec50 = 5.52 for p2y11) [1].the p2y receptors consist of 8 human subtypes, i.e. p2y1, p2y2, p2y4, p2y6, p2y11, p2y12, p2y13, and p2y14, coupled to g protein-dependent and -independent signaling pathways, including ion channels. the p2y receptors are involved in controlling levels of extracellular nucleotides and nucleosides, and intracellular signaling pathways [1].in pc 12 cells, preincubation of the cells with norepinephrine (ne) and atpγs tetralithium salt (1 μm) resulted in a persistent increase in uptake of ne, whilst similar pretreatment with atp did not show this increase. in the presence of atp, the activation effect produced by atpγs tetralithium salt on ne uptake was blocked [2]. in tea3a1 cells, atpγs tetralithium salt (0 ~ 200 μm) increased ca2+ influx in a dose-dependent manner, with ed50 value of about 50 μm. a maximum level of ca2+ influx was observed when cells were treated with atpγs tetralithium salt at concentrations above 100 μm. similar dose-dependent increases in the production of prostaglandin e2 (pge2) were also observed after atpγs tetralithium salt treatment [3].[1]. jacobson k a, ivanov a a, de castro s, et al. development of selective agonists and antagonists of p2y receptors. purinergic signal, 2009, 5(1): 75-89.[2]. hardwick j c, ehrlich y h, hendley e d. extracellular atp stimulates norepinephrine uptake in pc12 cells. journal of neurochemistry, 1989, 53(5):1512-1518.[3]. liu p, lalor d, bowser s s, et al. regulation of arachidonic acid release and prostaglandin e2 production in thymic epithelial cells by atpgammas and transforming growth factor-alpha. cellular immunology, 1998, 188(2): 81-88.

Biochem/physiol Actions

Adenosine 5′-[γ-thio]triphosphate (ATP-γ-S) is widely used as a non-hydrolyzed ATP analogue for studies on the effects of ATP binding to ATP sites in a wide range of processes including extracellular functions. ATP- γ-S is a P2 purinergic agonist which increases the activity of Ca2+-activated K+ channels. ATP- γ-S can substitute for ATP in kinase reactions yielding thiophosphorylated proteins that are resistant to protein phosphatases and modulate the ATP-dependent steps in the binding of ubiquitin conjugates to the 26S proteasome. ATP-γ -S differentially modulates Toll-like receptor 4-mediated cell survival and death.

storage

Store at -20°C

Adenosine 5'-[γ-thio]triphosphate TetralithiuM Salt Preparation Products And Raw materials

Raw materials

Preparation Products

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Adenosine 5'-[γ-thio]triphosphate TetralithiuM Salt Suppliers

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93839-89-5, Adenosine 5'-[γ-thio]triphosphate TetralithiuM SaltRelated Search:


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  • Adenosine 5'-[γ-thio]triphosphate TetralithiuM Salt
  • 93839-89-5
  • C10H12N5O12P3S4Li
  • C10H12Li4N5O12P3S
  • Enzymes, Inhibitors, and Substrates
  • Cofactors
  • Phosphate Donors
  • Nucleotides
  • Nucleosides, Nucleotides, Oligonucleotides
  • Biochemicals and Reagents
  • BioChemical