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Results for "

adenosine 5' succinate

" in TargetMol Product Catalog
  • Inhibitor Products
    42
    TargetMol | Activity
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    TargetMol | inventory
Adenosine 5'-succinate
T38416102029-71-0
Adenosine 5'-succinate is a compound closely related to adenosine monophosphate (AMP) that demonstrates strong inhibitory properties against taste receptor activation of transducin caused by Denatonium benzoate.
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Adenosine 5'-diphosphate
T172358-64-0
Adenosine 5'-diphosphate (ADP) induces human platelet aggregation and non-competitively blocks the stimulated human platelet adenylate cyclase.
  • $30
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TargetMol | Citations Cited
Adenosine receptor A1 antagonist 5
T2246685872-53-3In house
Adenosine receptor A1 antagonist 5 acts as an adenosine antagonist, is an oxypurine, acts as an insecticide and pest control agent, and has an inhibitory effect on elevated blood pressure.
  • $98
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Adenosine 5'-monophosphate monohydrate
T0853L18422-05-4
Adenosine 5'-monophosphate monohydrate (5'-AMP) , also known as 5'-adenylic acid, is a nucleotide that is used as a monomer in RNA. It is an ester of phosphoric acid and the nucleoside adenosine. Adenosine 5'-monophosphate monohydrate consists of a phosphate group, the sugar ribose, and the nucleobase adenine. As a substituent it takes the form of the prefix adenylyl-.
  • $48
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Adenosine 5’-methylenediphosphate (hydrate)
T35573
Adenosine 5’-methylenediphosphate is an inhibitor of ecto-5’-nucleotidase, also known as CD73, with a Kivalue of 37 nM.1It inhibits cAMP accumulation induced by adenosine 5’-monophosphate , adenosine 5’-diphosphate , or adenosine 5’-triphosphate but not adenosine in VA-13 human fibroblasts when used at a concentration of 100 μM. Adenosine 5’-methylenediphosphate reduces proliferation of U138MG glioma cells, as well as inhibits the invasion and migration of MHCC97H hepatocellular carcinoma (HCC) cells in a migration assay.2,3It increases tumor infiltration of CD3+CD8+T cells and reduces tumor growth in a K1735 murine melanoma model when administered at a dose of 400 μg/mouse.4 1.Bruns, R.F.Adenosine receptor activation by adenine nucleotides requires conversion of the nucleotides to adenosineNaunyn Schmiedebergs Arch. Pharmacol.315(1)5-13(1980) 2.Braganhol, E., Tamajusuku, A.S.K., Bernardi, A., et al.Ecto-5′-nucleotidase/CD73 inhibition by quercetin in the human U138MG glioma cell lineBiochim. Biophys. Acta1770(9)1352-1359(2007) 3.Shali, S., Yu, J., Zhang, X., et al.Ecto\5′\nucleotidase (CD73) is a potential target of hepatocellular carcinomaJ. Cell Physiol.234(7)10248-10259(2018) 4.Forte, G., Sorrentino, R., Montinaro, A., et al.Inhibition of CD73 improves B cell-mediated anti-tumor immunity in a mouse model of melanomaJ. Immunol.189(5)2226-2233(2021)
  • $57
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Adenosine 2',5'-diphosphate sodium
T39025154146-84-6
Adenosine 2',5'-diphosphate sodium is a competitive P2Y1 antagonist with non-selective antagonism at recombinant and human platelet P2X1 receptors.
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N7-Methyl-guanosine-5'-triphosphate-5'-adenosine diammonium
T7413575252-10-7
N7-Methylguanosine-5'-triphosphate-5'-adenosine (m7GpppA) diammonium, a dinucleotide cap analog, facilitates in vitro RNA transcription [1].
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N7-Methyl-guanosine-5'-triphosphate-5'-adenosine
T4072162828-63-1
N7-Methylguanosine-5'-triphosphate-5'-adenosine (m7GpppA) is a dinucleotide cap analog employed in the process of in vitro RNA transcription.
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Guanosine 5'-triphosphate-5'-adenosine
T3844910527-47-6
Guanosine 5'-triphosphate-5'-adenosine, known as a 5′ cap analog, serves as a fluorescent substrate analog.
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N6-Benzoyl-5’-O-(4,4’-dimethoxytrityl)-3’-O-(2-methoxyethyl)adenosine
TNU1260256224-00-7
Nucleoside Derivatives - 3’-Modified nucleosides; Protected nucleosides w/NH/OH open
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7-10 days
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Adenosine 5'-monophosphate disodium salt
T659794578-31-8
Adenosine 5'-monophosphate disodium salt (Adenosine Phosphate Disodium) is a purine nucleotide involved in ATP metabolism and is used to study the effects of ATP on cells and organisms. Adenosine 5'-monophosphate disodium salt has been shown to have a variety of biochemical and physiological effects. It has been shown to increase cell metabolism, gene expression, and protein synthesis.
  • $39
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2’,3’,5’-Tri-O-acetyl adenosine
TNU06407387-57-7
2',3',5'-Tri-O-acetyl adenosine is a Nucleoside.
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7-10 days
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2-Amino-3’,5’-di-O-acetyl-N6,N6-dimethyl-2’-O-methyl adenosine
TNU1364
2-Amino-3',5'-di-O-acetyl-N6,N6-dimethyl-2'-O-methyl adenosine is a Nucleoside Derivative - 6-Modified purine nucleoside; 2'-Modified nucleoside.
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7-10 days
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N6-Benzoyl-5’-O-(4,4’-dimethoxytrityl)-3’-O-methyl adenosine
TNU1121127212-38-8
Nucleoside Derivatives - 3’-Modified nucleosides; Protected nucleosides with NH2/OH open; Ready for phosphorylation
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7-10 days
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Adenosine 5′-monophosphoramidate sodium
T38415102029-68-5
Adenosine 5′-monophosphoramidate sodium is a derivative of adenosine used as an intermediate for nucleotide synthesis. It significantly influences the accumulation of cyclic AMP.
    7-10 days
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    Adenosine 3',5'-diphosphate sodium salt
    T3557275431-54-8
    Adenosine 3',5'-diphosphate sodium salt is an inhibitor of hydroxysteroid sulfotransferases, which are adenine nucleotides containing a phosphate group at the 3' and 5' positions of the pentose ribose.Adenosine 3',5'-diphosphate (sodium salt) is the product of 3'-phosphoadenosine 5'-phosphosulfonate (PAPS), a cofactor of sulfotransferases (SULTs). diphosphate disodium is the product of 3'-phosphoadenosine 5'-phosphosulfonate (PAPS), a cofactor for sulfotransferases (SULTs), which has been used to study the kinetic properties and structure of SULTs.
    • $146
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    Rp-Adenosine-5'-O-(1-thiotriphosphate) sodium
    T83807
    Rp-Adenosine-5'-O-(1-thiotriphosphate) (Rp-ATP-α-S), a sulfur-containing nucleotide derivative isomer and a purinergic P2Y1 receptor agonist, promotes calcium mobilization in HEK293 cells expressing the human P2Y1 receptor (EC50 = 75 nM). This compound exhibits binding affinity to washed isolated human platelets (Ki = 156 nM) and attenuates ADP-induced aggregation in human platelet-rich plasma (PRP; pA2 = 4.74), as well as inhibits cAMP production triggered by prostaglandin E1 (PGE1) in human PRP (pA2 = 5.26). Furthermore, it triggers relaxation in carbamoylcholine-constricted guinea pig taenia coli strips (EC50 = 56 nM). Rp-ATP-α-S also contributes to the synthesis of cyclic dinucleotides, recognized by bacterial riboswitches.
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    Adenosine 5’-monophosphate triethylammonium salt
    TNU1647
    Adenosine 5’-monophosphate triethylammonium salt is a useful organic compound for research related to life sciences and the catalog number is TNU1647.
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    7-10 days
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    8-Bromo-5’-O-(4-cyanobenzyl)-2’,3’-O-isopropylidene adenosine
    TNU07461134156-53-8
    5’-modified nucleoside; halo-nucleoside
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    7-10 days
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    N6-Bz-5’-O-DMTr-2’-O-hexadecanyl adenosine 3’-CED phosphoramidite
    TNU16522382942-35-8
    N6-Bz-5’-O-DMTr-2’-O-hexadecanyl adenosine 3’-CED phosphoramidite is a useful organic compound for research related to life sciences. The catalog number is TNU1652 and the CAS number is 2382942-35-8.
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    7-10 days
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    3’,5’-TIPS-N-Ac-Adenosine
    TNU1200828247-65-0
    3',5'-TIPS-N-Ac-Adenosine is a Nucleoside Derivative - Protected nucleoside with NH2/OH open.
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    7-10 days
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    5’-O-(4,4’-dimethoxytrityl)adenosine
    TNU059981352-25-2
    Nucleoside; Used for nucleoside modification
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    7-10 days
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    Adenosine 5'-diphosphate sodium salt
    T507920398-34-9
    Adenosine 5'-diphosphate sodium salt (ADP sodium salt) is an adenine nucleotide that is phosphorylated into ATP by ATPase. This phosphorylation is a key part of cellular homeostatis as it allows for energy storage and is involved in nucleic acid metabolism. ADP affects platelet activation through its interaction with ADP receptors P2Y1, P2Y12 and P2X1. Upon its conversion to adenosine by ecto-ADPases, platelet activation is inhibited via adenosine receptors.
    • $30
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    Adenosine-5'-diphosphate disodium salt
    T7192716178-48-6
    Adenosine 5'-diphosphate disodium salt has been shown to inhibit the binding of serotonin (5-hydroxytryptamine) to 5-HT2 receptors, which are present in heart tissue.
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    6-8 weeks
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    Sp-Adenosine-5'-O-(1-thiotriphosphate) sodium
    T83808
    Sp-Adenosine-5'-O-(1-thiotriphosphate) (Sp-ATP-α-S), an isomer of the ATP-α-S sulfur-containing nucleotide derivative and a purinergic P2Y1 receptor agonist, effectively increases calcium mobilization in HEK293 cells harboring the P2Y1 receptor with an EC50 of 9.4 nM for the human receptor. It also inhibits ADP-induced human isolated platelet aggregation with a Ki value of 4 μM and prompts relaxation in carbamoylcholine-tightened guinea pig taenia coli, achieving an EC50 of 426 nM.
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    Adenosine-5'-O-(3-thiotriphosphate) sodium
    T8382788453-52-5
    Adenosine-5'-O-(3-thiotriphosphate) (ATPγS), an agonist of the purinergic P2Y11 receptor, prompts inositol phosphate accumulation in CHO-K1 cells harboring the human or canine P2Y11 receptor with EC50 values of 1.2 and 19.3 µM, respectively. At a concentration of 10 µM, ATPγS mitigates Junin virus-induced mRNA boosts pertaining to bone morphogenetic protein 6 (BMP6) and diminishes particle forming units (PFUs) in infected primary rat osteoblasts. Furthermore, when applied at 25 µM, it triggers insulin secretion in MIN6 pancreatic β-cells.
    • $398
    35 days
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    Adenosine 5'-diphosphoribose sodium
    T1024768414-18-6
    Adenosine 5'-diphosphoribose sodium (ADP ribose sodium) is a metabolite of nicotinamide adenine nucleotide (NAD+), which is widely present in organisms.Adenosine 5'-diphosphoribose sodium (ADP ribose sodium) is a potent intracellular Ca2+-permeable cation TRPM2 channel activator. Adenosine 5'-diphosphoribose sodium (ADP ribose sodium) is a potent intracellular Ca2+ permeable cation TRPM2 channel activator that also induces autophagy.)
    • $61
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    N6-Benzyl-5'-ethylcarboxamido adenosine
    T39011152918-32-6
    N6-Benzyl-5'-ethylcarboxamido adenosine is a selective A3 adenosine receptor agonist.
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    5'-O-DMTr-2'-O-methyl-N6-methyl adenosine 3'-CED phosphoramidite
    TNU16182348385-04-4
    5'-O-DMTr-2'-O-methyl-N6-methyl adenosine 3'-CED phosphoramidite is a Nucleoside Phosphoramidite.
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    7-10 days
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    N4-Benzoyl-5'-O-DMT-2'-O-propargyl adenosine
    TNU0936171486-51-4
    N4-Benzoyl-5'-O-DMT-2'-O-propargyl adenosine is a Nucleoside Derivative - 2'-Modified nucleoside; Protected nucleoside with NH2/OH group.
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    7-10 days
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    5’-O-(4,4’-Dimethoxytrityl)-2’-O-(2-methoxyethyl) adenosine
    TNU13421384253-67-1
    Nucleoside Derivatives - Protected nucleosides w/ NH2/OH open
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    7-10 days
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    5’-O-(4,4’-Dimethoxytrityl)-2’-O-t-butyldimethylsilyl adenosine
    TNU060081794-13-0
    Nucleoside; Used for RNA synthesis and special nucleoside modification
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    7-10 days
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    5’-O-(4,4’-Dimethoxytrityl)-N6-Phenoxyacetyl adenosine
    TNU0707121076-16-2
    5'-O-(4,4'-Dimethoxytrityl)-N6-Phenoxyacetyl adenosine is a 2/6/8-modified purine nucleoside.
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    7-10 days
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    Rp-Adenosine-5'-O-(1-thiodiphosphate) sodium
    T838052005478-89-5
    Rp-Adenosine-5'-O-(1-thiodiphosphate) (Rp-ADP-α-S), a sulfur-containing isomer of the nucleotide derivative ADP-α-S, acts as an inhibitor of phosphorylase kinase with an inhibition constant (Ki) of 0.53 µM. This compound also induces aggregation in isolated human platelets with an effective concentration (EC50) of 20 µM and promotes relaxation in guinea pig taenia coli that has been precontracted with carbamoylcholine, with an EC50 of 58.9 µM.
    • $830
    35 days
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    Sp-Adenosine-5'-O-(1-thiodiphosphate) sodium
    T838062005478-90-8
    Sp-Adenosine-5’-O-(1-thiodiphosphate) (Sp-ADP-α-S), an isomer of the sulfur-containing nucleotide derivative ADP-α-S, functions as an inhibitor of phosphorylase kinase with an inhibition constant (Ki) of 0.53 µM. This compound also promotes aggregation of isolated human platelets with an effective concentration (EC50) of 20 µM and induces relaxation in carbamoylcholine-precontracted guinea pig taenia coli with an EC50 of 58.9 µM.
    • $830
    35 days
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    N6-Benzoyl-5’-O-(4,4-dimethoxytrityl)-3’-deoxy  adenosine
    TNU111884138-86-3
    Nucleoside Derivatives - 3’-Deoxy nucleosides; Protected nucleosides with NH2/OH open; Ready for phosporylation
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    7-10 days
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    5'-O-DMT-2'-O-TBDMS-N-Bz-Adenosine
    T3714681265-93-2
    5'-O-DMT-2'-O-TBDMS-N-Bz-Adenosine, an adenosine derivative, serves as an intermediate in the synthesis of oligonucleotides.
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    7-10 days
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    5’-O-(4,4’-Dimethoxytrityl)-3’-O-t-butyldimethylsilyl adenosine
    TNU060181794-12-9
    Nucleoside; Used for special nucleoside or RNA modification
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    7-10 days
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    N6-Bz-5’-O-DMTr-2’-O-hexadecanyl adenosine
    TNU16512382942-34-7
    N6-Bz-5’-O-DMTr-2’-O-hexadecanyl adenosine is a useful organic compound for research related to life sciences. The catalog number is TNU1651 and the CAS number is 2382942-34-7.
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    7-10 days
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    N-Benzoyl-5'-O-dmtr-2'-O-(2-methoxyethyl)-adenosine
    TNU0957251647-48-0
    N-Benzoyl-5'-O-dmtr-2'-O-(2-methoxyethyl)-adenosine is a Nucleoside Derivative - 2'-Modified nucleoside; Protected nucleoside with NH2/OH group.
    • $41
    5 days
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    Adenosine 5'-phosphosulfate (sodium salt)
    T35574102029-95-8
    Adenosine 5'-phosphosulfate is an ATP and sulfate competitive inhibitor of ATP sulfurylase in humans, S. cerevisiae, and P. chrysogenum (Ki = 18, 2500, and 1500 nM, respectively). Adenosine 5'-phosphosulfate also inhibits human adenosine 5'-phosphosulfate kinase (Ki = 47.5 μM) to prevent sulfation.
    • $110
    35 days
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    5’-O-(4-Cyanobenzyl)-2’,3’-O-isopropylidene adenosine
    TNU07951134156-51-6
    5’-Modified nucleoside
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    7-10 days
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