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Ranolazine dihydrochloride
CAS No. : 95635-56-6
Biological Activity：Ranolazine dihydrochloride (CVT 303 dihydrochloride) is an anti-angina drug that achieves its effects by inhibiting the late phase of inward sodium current (INa and IKr with IC50 values of 6 μM and 12 μM, respectively) without affecting heart rate or blood pressure (BP)[2]. Ranolazine dihydrochloride is also a partial fatty acid oxidation inhibitor[3].
Research Area：Cardiovascular Disease|Cancer
Targets：Autophagy|Calcium Channel|Sodium Channel
Related Screening Libraries:Drug Repurposing Compound Library Plus;FDA-Approved Drug Library Plus;FDA-Approved Drug Library Mini;Bioactive Compound Library Plus;Membrane Transporter/Ion Channel Compound Library;Neuronal Signaling Compound Library;FDA-Approved Drug Library;Anti-Cancer Compound Library;Autophagy Compound Library;Drug Repurposing Compound Library;Anti-Cardiovascular Disease Compound Library;Orally Active Compound Library;FDA Approved & Pharmacopeial Drug Library;Neuroprotective Compound Library;Drug-Induced Liver Injury (DILI) Compound Library;Rare Diseases Drug Library;EMA-Approved Drug Library;Calcium Channel Blocker Library;Sodium Channel Blocker Library;FDA-Approved Anticancer Drug Library;Human Metabolite Library;Anti-Prostate Cancer Compound Library;Non-steroidal Anti-Inflammatory Compound Library;
Related Small Molecules:Benidipine hydrochloride;Lu AE98134;CaV1.3 antagonist-1;14-Deoxyandrographolide;Zandatrigine;(Rac)-MEM 1003;Glaucine;Veratridine;Efonidipine hydrochloride monoethanolate;L-Ascorbic acid sodium salt;Brompheniramine-d6 maleate;MRS 1523;GX-674;Nilvadipine;Dibucaine;Lercanidipine;CP-060;Sodium Channel inhibitor 2;3-Deoxyaconitine;Anipamil-d25 hydrochloride;ISX-9;ω-Conotoxin MVIIC;Catharanthine;Thapsigargin
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