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Results for "

purines

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    15
    TargetMol | Inhibitors_Agonists
  • Natural Products
    3
    TargetMol | Natural_Products
  • Recombinant Protein
    6
    TargetMol | Recombinant_Protein
Olomoucine
T21588101622-51-9In house
Olomoucine is an ATP-competitive inhibitor of Cdk2 cyclin A, Cdc2 CyclinB, CDK2 CyclinE, CDK5 p35, and ERK1 p44 MAP kinase with IC50s of 7, 7, 7, 3, and 25 µM, respectively. It regulates the cell cycle and exhibits anti-melanin tumor activities.
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Zeatin
TMS217913114-27-7
Zeatin is a cytokinin derived from adenine. Zeatin was discovered in immature corn kernels from the genus Zea. It promotes growth of lateral buds and when sprayed on meristems stimulates cell division to produce bushier plants.
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trans-Zeatin
(E)-Zeatin
TMS21811637-39-4
trans-Zeatin ((E)-Zeatin) is the member of the plant growth hormone family known as cytokinins, which regulate cell division, development, and nutrient processing.
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Proguanil
Chloroguanide, Chlorguanide
T22409500-92-5
Proguanil (Chloroguanide) is a prophylactic antimalarial drug that acts primarily through its active metabolite, Cycloguanil, which inhibits the dihydrofolate reductase (DHFR) enzyme of Plasmodium falciparum, preventing the synthesis of purines and pyrimidines and inhibiting the growth and reproduction of the parasite.
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1-2 weeks
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Purine
7H-Imidazo(4,5-d)pyrimidine
T4746120-73-0
Purine (7H-Imidazo(4,5-d)pyrimidine) is a heterocyclic aromatic organic compound, consisting of a pyrimidine ring fused to an imidazole ring. Two of the bases in nucleic acids, adenine and guanine, are purines. Purines from food (or from tissue turnover) are metabolised by several enzymes, including xanthine oxidase, into uric acid. High levels of uric acid can predispose to gout when the acid crystalises in joints; this phenomenon only happens in humans and some animal species (e.g. dogs) that lack an intrinsic uricase enzyme that can further degrade uric acid.
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Lometrexol disodium
T63240120408-07-3
Lometrexol (DDATHF) disodium is a potent inhibitor of human serine hydroxymethyltransferase 1 2 (hSHMT1 2) and antifolate, which reduces the activity of glycinamide ribonucleotide formyltransferase (GARFT) without causing detectable levels of DNA strand breaks. Lometrexol disodium exhibits anticancer effects by inhibiting the de novo synthesis of purines, causing abnormal cell proliferation, apoptosis and cell cycle arrest.
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10-14 weeks
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4-amino-3-iodo-1H-pyrazolo[3,4-d]pyrimidine
TNU0611151266-23-8
Heterocyclic compound –purines, intermediate and building block; Used for modified nucleosides and nucleic acids
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7-10 days
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2-Amino-6-ethoxypurine
TNU090051866-19-4
Heterocyclic Compounds –Purines; Intermediates and Building Blocks - Nucleoside bases
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7-10 days
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6-Chloro-9-methyl-9H-purine
TNU09072346-74-9
Heterocyclic Compounds - Purines; Intermediates and Building Blocks - Electrophiles
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7-10 days
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9-Methyladenine
TNU0908700-00-5
Heterocyclic Compounds - Purines; Intermediates and Building Blocks - Nucleophiles
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7-10 days
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1,9-Dihydro-9-methyl-6H-purin-6-one
TNU0909875-31-0
1,9-Dihydro-9-methyl-6H-purin-6-one belongs to Heterocyclic Compounds - Purines.
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7-10 days
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6-Chloro-2-(trifluoromethyl)-9H-purine
TNU11041998-63-6
Heterocyclic Compounds - Purines; Intermediates and Building Blocks - Nucleoside bases; Multi-functional; Scaffolds and Templates
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7-10 days
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1,7-Dibenzyl-3-methylxanthine
TNU113316154-03-3
1,7-Dibenzyl-3-methylxanthine belongs to Heterocyclic Compounds - Purines.
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7-10 days
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7-benzyl-3-methylxanthine
TNU113456025-86-6
7-benzyl-3-methylxanthine belongs to Heterocyclic Compounds - Purines.
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7-10 days
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1H-Imidazo[4,5-d]pyridazin-7-amine
TNU126210310-25-5
1H-Imidazo[4,5-d]pyridazin-7-amine belongs to Heterocyclic Compounds - Purines; Intermediates and Building Blocks - Nucleoside bases.
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7-10 days
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