Inhibitor
| Cat.No. | Name | Information |
|---|---|---|
| M59317 | CNDAC hydrochloride | CNDAC hydrochloride is a metabolite of Sapacitabine, and it is a nucleoside analog. CNDAC hydrochloride induces DNA damage and apoptosis. |
| M59316 | Troxacitabine | Troxacitabine is a nucleoside analog with potent anticancer activity. |
| M58525 | 5-Bromouridine | 5-Bromouridine is a purine nucleoside analog, with broad antitumor activity rely on inhibition of DNA synthesis, induction of apoptosis, etc. |
| M41564 | 5-Cyanouridine | 5-Cyanouridine is a thymidine analog. |
| M38937 | N6-(2-Hydroxyethyl)adenosine | N6-(2-Hydroxyethyl)adenosine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc. |
| M59409 | 2′-Deoxy-2′-fluoroadenosine | 2′-Deoxy-2′-fluoroadenosine is a fluorinated deoxyadenosine with antitumor and antiviral activity, able to interfere with viral or cancer cell replication by being incorporated into DNA. |
| M59408 | 1-Methylinosine | 1-Methylinosine is a modified nucleotide found at position 37 in tRNA 3' to the anticodon of eukaryotic tRNA. |
| M59407 | 5-Iodo-cytidine | 5-Iodo-cytidine (5-Iodo-D-cytidine) is a purine nucleoside analogue. |
| M56005 | 6-Azathymine | 6-Azathymine, a 6-nitrogen analog of thymine, is a potent D-3-aminoisobutyrate-pyruvate aminotransferase inhibitor. |
| M56004 | N1-Methylpseudouridine | N1-methyl-pseudouridine (1-Methylpseudouridine), a methylpseudouridine, outperforms 5 mC and 5 mC/N1-methyl-pseudouridine in translation. |
| M56003 | Diguanosine 5′-triphosphate | Diguanosine 5′-triphosphate (Gp3G) is a dinucleoside triphosphates. |
| M56002 | Gemcitabine elaidate hydrochloride | Gemcitabine elaidate (CP-4126) hydrochloride is lipophilic pro-agent of Gemcitabine. |
| M49835 | 8-Chloroguanosine | 8-Chloroguanosine is a purine nucleoside analogue. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc. |
| M41568 | FMAU | FMAU is a thymidine analogue. |
| M41567 | Xylocytidine | Xylocytidine is a cytidine analog. |
| M41566 | N3-Allyluridine | N3-Allyluridine is a uridine analog. |
| M41565 | Homouridine | Homouridine, is an uridine analogue. |
| M41563 | 5-Ethyl cytidine | 5-Ethyl cytidine is a cytidine analog. |
| M41562 | TLR7 agonist 13 | TLR7 agonist 13 is a guanosine analog. |
| M41561 | 2-Iodoadenosine | 2-Iodoadenosine is an adenosine analog. |
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