Enalaprilat dihydrate, >=98% (HPLC)

Code: E9658-5MG D2-231

Not available outside of the UK & Ireland.

Biochem/physiol Actions

Enalapril, the ethyl ester ofenalaprilat exhibits slight pharmacological activity until it is hydrolyzed in the liver toenalaprilat. Enalaprilat, a IV...


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$156.16 5MG
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Not available outside of the UK & Ireland.

Biochem/physiol Actions

Enalapril, the ethyl ester ofenalaprilat exhibits slight pharmacological activity until it is hydrolyzed in the liver toenalaprilat. Enalaprilat, a IV form of an angiotensin-converting-enzyme inhibitor (ACE) prevents the transformation of angiotensin I to angiotensin II, a potent vasoconstrictor.

Enalaprilat is an inhibitor of angiotensin converting enzyme (ACE), antihypertensive, and a Bradykinin B1 receptor activator. Enalaprilat has nM potency versus ACE and also activates B1 receptors to release NO.

Features and Benefits

This compound was developed by Merck & Co., Inc., Kenilworth, NJ, U.S.. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

This compound is featured on the Angiotensin Receptors and Bradykinin Receptors pages of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Packaging

5, 25 mg in glass bottle

assay≥98% (HPLC)
Gene Informationhuman ... ACE(1636)
InChI keyMZYVOFLIPYDBGD-MLZQUWKJSA-N
InChI1S/C18H24N2O5.2H2O/c1-12(16(21)20-11-5-8-15(20)18(24)25)19-14(17(22)23)10-9-13-6-3-2-4-7-13;;/h2-4,6-7,12,14-15,19H,5,8-11H2,1H3,(H,22,23)(H,24,25);2*1H2/t12-,14-,15-;;/m0../s1
originatorMerck & Co., Inc., Kenilworth, NJ, U.S.
Quality Level100
SMILES stringO.O.C[C@H](N[C@@H](CCc1ccccc1)C(O)=O)C(=O)N2CCC[C@H]2C(O)=O
solubilityH2O: 14 mg/mL at 60 °C (warming for 5 minutes), DMSO: 64 mg/mL
storage temp.room temp
Cas Number84680-54-6
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