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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T21195 | AICAR monophosphate | Aica ribonucleotide,AICA riboside,Acadesine 5'-monophosphate,Z-nucleotide | Others |
AICAR monophosphate (Aica ribonucleotide) is a purine precursor with antineoplastic activity and can be used in studies about type 2 diabetes. | |||
T9210 | CD73-IN-4 | CD73 | |
CD73-IN-4 is a potent and selective methylenephosphonic acid CD73 inhibitor | |||
T14864 | Caracemide | NSC-253272 | Others , DNA/RNA Synthesis , Antibacterial |
Caracemide (NSC-253272) inhibits the enzyme ribonucleotide reductase of Escherichia coli. Caracemide can be used in anticancer studies. | |||
T0297 | Clofarabine | Clofarex,Evoltra,Clolar | Apoptosis , Nucleoside Antimetabolite/Analog , DNA/RNA Synthesis , Autophagy |
Clofarabine (Clofarex)m, a second generation purine nucleoside analog with antineoplastic activity, inhibits the enzymatic activities of ribonucleotide reductase (IC50 = 65 nM) and DNA polymerase. | |||
T3157 | COH29 | RNR Inhibitor COH29 | DNA/RNA Synthesis |
COH29 (RNR Inhibitor COH29) is an orally available, aromatically substituted thiazole and inhibitor of the human ribonucleotide reductase (RNR), with potential antineoplastic activity. Upon oral administration, the RNR i... | |||
T8855 | Polydeoxyribonucleotide(Sodium salt) | Polydeoxyribonucleotide from salmon | Others |
Polydeoxyribonucleotide can improve secretion of various growth factors, promote collagen synthesis, and restore tensile strength of the Achilles tendon in a rat model with Achilles tendon injury. | |||
T0353 | Osalmid | Oxaphenamide,4'-Hydroxysalicylanilide | HBV , DNA/RNA Synthesis |
Osalmid (Oxaphenamide) is a choleretic drug, inhibits ribonucleotide reductase activity by targeting ribonucleotide reductase small subunit M2 (RRM2). | |||
T31163 | Cytidine 5'-diphosphate disodium | CDP sodium salt,Cytidine 5'-diphosphate disodium salt,Cytidine diphosphate sodium salt | Others |
Cytidine 5'-diphosphate disodium (CDP sodium salt) produces CTP to support DNA and RNA biosynthesis and ribonucleotide reductase to produce dCMP. | |||
T1982 | 3-AP | NSC663249,Triapine,PAN-811,OCX191 | DNA/RNA Synthesis |
3-AP (Triapine) is a novel inhibitor of the M2 subunit of ribonucleotide reductase (RR). | |||
T1705 | 5-Amino-3H-imidazole-4-Carboxamide | 4-Amino-5-imidazolecarboxamide,AICA,5-Aminoimidazole-4-carboxamide | Endogenous Metabolite |
5-Amino-3H-imidazole-4-Carboxamide (AICA) is an imidazole derivative which is a metabolite of the antineoplastic agents BIC and DIC. By itself, or as the ribonucleotide, it is used as a condensation agent in the preparat... | |||
T5073 | Inosine 5'-monophosphate disodium salt hydrate | Inosine 5'-monophosphate disodium salt,5'-IMP-Na2,Disodium 5'-inosinate monohydrate | Others , Endogenous Metabolite |
Inosine 5'-monophosphate disodium salt hydrate (Inosine 5'-monophosphate disodium salt), or inosinic acid, is the ribonucleotide of hypoxanthine and the first nucleotide formed during purine synthesis. | |||
T7525 | Didox | NSC-324360 | DNA/RNA Synthesis |
Didox (NSC-324360) is a synthetic ribonucleotide reductase (RR) inhibitor that has been found to reduce the levels of oxidative injury markers in the brains of HIV patients with dementia. | |||
T8800 | NSAH | 2-hydroxy-N'-[(E)-(2-hydroxynaphthalen-1-yl)methylidene]benzohydrazide | DNA/RNA Synthesis |
NSAH (2-hydroxy-N'-[(E)-(2-hydroxynaphthalen-1-yl)methylidene]benzohydrazide) is a nonnucleoside inhibitor of human ribonucleotide reductase (hRR).with cell-free IC50 of 32 μM and cell-based IC50 of ~250 nM, respectively... | |||
T4685 | INOSINIC ACID | Inosine 5′-monophosphate,IMP,I-5'-P | Endogenous Metabolite |
Inosinic acid (IMP) is a purine nucleotide which has hypoxanthine as the base and one phosphate group esterified to the sugar moiety. Inosinic acid is a nucleotide present in muscle and other tissues. It is formed by the... | |||
T15826 | Lometrexol | LY 264618,DDATHF | DHFR |
Lometrexol (LY 264618), an antipurine Antifolate, can inhibit the activity of glycinamide ribonucleotide formyltransferase (GARFT) but do not induce detectable levels of DNA strand breaks. Lometrexol can further inhibit ... | |||
T4809 | Pyrimidine | Metadiazine | Others , Endogenous Metabolite |
Pyrimidine (Metadiazine)s are heterocyclic, six-membered, nitrogen-containing carbon ring structures, with uracil, cytosine and thymine being the basal structures of ribose-containing nucleosides (uridine, cytidine, and ... | |||
T6501 | Fludarabine Phosphate | NSC 312887 Phosphate,fludara Phosphate,F-ara-A (NSC 312887) Phosphate,F-ara-AMP | Apoptosis , Nucleoside Antimetabolite/Analog , DNA/RNA Synthesis |
Fludarabine Phosphate (NSC 312887 Phosphate) is the phosphate salt of a fluorinated nucleotide antimetabolite analog of the antiviral agent vidarabine (ara-A) with antineoplastic activity. Fludarabine phosphate is rapidl... | |||
T4826 | L-Histidine monohydrochloride monohydrat | Others , Endogenous Metabolite | |
Histidine (abbreviated as His or H) is an alpha-amino acid. The L-isomer is one of the 22 proteinogenic amino acids, i.e., the building blocks of proteins. It is classified as a charged, polar because of the hydrophilic ... | |||
T29197 | YZ51 | ||
YZ51, a novel potent inhibitor of ribonucleotide reductase (RR), inhibits hepatitis B virus replication by targeting ribonucleotide reductase M2 protein. | |||
T14147 | Pelitrexol | AG 2037 | DHFR |
Pelitrexol (AG 2037) is a glycinamide ribonucleotide formyltransferase (GARFT) inhibitor. |