eprosartan

{{Short description|Angiotensin II receptor antagonist}}

{{Drugbox

| Watchedfields = changed

| verifiedrevid = 461094389

| image = Eprosartan.svg

| tradename = Teveten

| Drugs.com = {{drugs.com|monograph|teveten}}

| MedlinePlus = a601237

| DailyMedID = Eprosartan

| pregnancy_AU = D

| pregnancy_AU_comment =

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| routes_of_administration = By mouth

| ATC_prefix = C09

| ATC_suffix = CA02

| legal_AU = S4

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| legal_US = Rx-only

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| bioavailability = 15% (Eprosartan mesylate)

| metabolism = not metabolized

| elimination_half-life = 5 to 9 hours

| excretion = Kidney 10%, bile duct 90%

| index2_label = as mesylate

| IUPHAR_ligand = 588

| CAS_number_Ref = {{cascite|correct|??}}

| CAS_number = 133040-01-4

| PubChem = 5281037

| DrugBank_Ref = {{drugbankcite|correct|drugbank}}

| DrugBank = DB00876

| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}

| ChemSpiderID = 4444504

| UNII_Ref = {{fdacite|correct|FDA}}

| UNII = 2KH13Z0S0Y

| KEGG_Ref = {{keggcite|correct|kegg}}

| KEGG = D04040

| KEGG2_Ref = {{keggcite|correct|kegg}}

| KEGG2 = D02082

| ChEBI_Ref = {{ebicite|correct|EBI}}

| ChEBI = 4814

| ChEMBL_Ref = {{ebicite|correct|EBI}}

| ChEMBL = 813

| IUPAC_name = 4-({2-Butyl-5-[2-carboxy-2-(thiophen-2-ylmethyl)eth-1-en-1-yl]-1H-imidazol-1-yl}methyl)benzoic acid

| C=23 | H=24 | N=2 | O=4 | S=1

| SMILES = O=C(O)\C(=C\c1cnc(n1Cc2ccc(C(=O)O)cc2)CCCC)Cc3sccc3

| StdInChI_Ref = {{stdinchicite|correct|chemspider}}

| StdInChI = 1S/C23H24N2O4S/c1-2-3-6-21-24-14-19(12-18(23(28)29)13-20-5-4-11-30-20)25(21)15-16-7-9-17(10-8-16)22(26)27/h4-5,7-12,14H,2-3,6,13,15H2,1H3,(H,26,27)(H,28,29)/b18-12+

| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}

| StdInChIKey = OROAFUQRIXKEMV-LDADJPATSA-N

}}

Eprosartan, sold under the brand name Teveten among others, is an angiotensin II receptor antagonist used for the treatment of high blood pressure.{{Cite web |title=Eprosartan mesylate- eprosartan mesylate tablet, film coated |url=https://dailymed.nlm.nih.gov/dailymed/archives/fdaDrugInfo.cfm?archiveid=475394 |access-date=7 June 2023 |website=DailyMed}}

Eprosartan is sometimes paired with hydrochlorothiazide.{{Cite web |date=3 January 2012 |title=Teveten HCT- eprosartan mesylate and hydrochlorothiazide tablet |url=https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=b1dfcac3-ef66-4d3e-9d58-37d3f516eb31 |access-date=7 June 2023 |website=DailyMed}}

As with other angiotensin II receptor antagonists, eprosartan is generally better tolerated than enalapril (an ACE inhibitor), especially among the elderly.{{Cite journal |vauthors=Ruilope L, Jäger B, Prichard B |year=2001 |title=Eprosartan versus enalapril in elderly patients with hypertension: a double-blind, randomized trial |journal=Blood Press. |volume=10 |issue=4 |pages=223–9 |doi=10.1080/08037050152669747 |pmid=11800061 |s2cid=13063704 |doi-access=free}}

History

The compound came into the Abbott Laboratories cardiovascular pipeline with its acquisition of Kos Pharmaceuticals in 2006, which had licensed it, along with "a range of hypertensive treatments", from the Biovail Corporation.Anon., 2006, Abbott Laboratories: Kos Pharmaceuticals a wise buy, Datamonitor ResearchStore (online), November 8, 2006, see [http://www.datamonitor.com/store/News/abbott_laboratories_kos_pharmaceuticals_a_wise_buy?productid=0BE8B1AB-14F9-4B92-99D2-80E8DC7ECA16], accessed 29 January 2015.

References

{{reflist}}

{{Angiotensin II receptor antagonists}}

{{Angiotensin receptor modulators}}

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Category:Angiotensin II receptor antagonists

Category:Imidazoles

Category:Thiophenes

Category:Drugs developed by AbbVie

Category:Benzoic acids