Inhibitor
| Cat.No. | Name | Information |
|---|---|---|
| M9888 | ABT-702 dihydrochloride | ABT-702 dihydrochloride is a potent non-nucleoside adenosine kinase inhibitor, selective over other sites of adenosine interaction like A1, A2A and A3 receptors, adenosine transporter and adenosine deaminase. |
| M6703 | EHNA hydrochloride | EHNA hydrochloride is a potent and selective dual inhibitor of cyclic nucleotide phosphodiesterase 2 (PDE2)(IC50=4 μM) and adenosine deaminase (ADA). EHNA hydrochloride exerts a concentration inhibition of the cGMP-stimulated PDE II (cGs-PDE)(IC50:0.8 μM (human), 2 μM (porcine myocardium)). |
| M6322 | 1-Deazaadenosine | 1-Deazaadenosine is a adenosine deaminase inhibitor. |
| M5524 | Cladribine | Cladribine is an adenosine deaminase inhibitor for U266, RPMI8226, and MM1.S cells with IC50 of approximately 2.43 μM, 0.75 μM, and 0.18 μM, respectively. |
| M3749 | Pentostatin | Pentostatin (Deoxycoformycin) is an irreversible inhibitor of adenosine deaminase (Ki = 2.5 pM). |
| M56587 | AMPD2 inhibitor 1 | AMPD2 inhibitor 1 is an adenosine monophosphate deaminase 2 (AMPD2) inhibitor, used in the research of sugar craving, salt craving, umami craving, and addictions including agent, tobacco, nicotine and alcohol addictions. |
| M50172 | Rebecsinib | Rebecsinib, an RNA adenosine deaminase (ADAR) inhibitor, reverses malignant over-editing by inhibiting ADAR1 p150-driven self-renewal of leukemic stem cells. |
| M42280 | FR221647 | FR221647 is an orally active non-nucleoside inhibitor of adenosine deaminase. |
| M19328 | Hibifolin | Hibifolin, a flavonol glycoside, is a potential inhibitor of adenosine deaminase (ADA), with a Ki of 49.92 μM. Hibifolin protects neurons against beta-amyloid-induced neurotoxicity. |
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