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| Other names | Selandopam; (–)-(S)-7,8-Dihydroxy-4-(3,4-dihydroxyphenyl)-1,2,3,4-tetrahydroisoquinoline; 7,8-DDPTI; YM-435; YM435; MYD-37; MYD37 |
| Routes of administration | Intravenous administration |
| Drug class | Dopamine D1-like receptor agonists |
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| Formula | C15H15NO4 |
| Molar mass | 273.288 g·mol−1 |
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Zelandopam (INN Tooltip International Nonproprietary Name; developmental code names YM-435, MYD-37) is a selective dopamine D1-like receptor agonist related to fenoldopam which was under development in Japan for the treatment of hypertension and heart failure but was never marketed. [1] [2] [3] The drug was being developed for use by intravenous administration. [1] The development of zelandopam appears to have been discontinued by the early 2000s. [1] It was first described in the scientific literature by 1991. [4]
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