Benidipine: Difference between revisions
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{{Short description|Antihypertensive drug of the calcium channel blocker class}} |
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{{drugbox |
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{{Drugbox |
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| Verifiedfields = changed |
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| Watchedfields = changed |
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| verifiedrevid = 444524924 |
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| IUPAC_name = O5-methyl O3-[(3''R'')-1-(phenylmethyl)piperidin-3-yl] 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate |
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| image = Benidipine structure.svg |
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| alt = Skeletal formula of benidipine |
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| width = 250px |
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| image2 = Benidipine-3D-balls.png |
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| alt2 = Ball-and-stick model of the benidipine molecule |
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<!--Clinical data--> |
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| tradename = |
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| Drugs.com = {{drugs.com|international|benidipine}} |
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| pregnancy_AU = <!-- A / B1 / B2 / B3 / C / D / X --> |
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| pregnancy_US = <!-- A / B / C / D / X --> |
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| pregnancy_category = |
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| legal_AU = <!-- Unscheduled / S2 / S3 / S4 / S5 / S6 / S7 / S8 / S9 --> |
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| legal_CA = <!-- / Schedule I, II, III, IV, V, VI, VII, VIII --> |
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| legal_UK = <!-- GSL / P / POM / CD / Class A, B, C --> |
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| legal_US = <!-- OTC / Rx-only / Schedule I, II, III, IV, V --> |
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| legal_status = |
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| routes_of_administration = By mouth |
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<!--Pharmacokinetic data--> |
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| bioavailability = |
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| protein_bound = |
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| metabolism = |
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| elimination_half-life = |
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| excretion = |
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<!--Identifiers--> |
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| PubChem = 656668 |
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| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}} |
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| ChemSpiderID = 571013 |
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| smiles = [O-][N+](=O)c1cccc(c1)[C@@H]4C(/C(=O)OC)=C(\N\C(=C4\C(=O)O[C@@H]3CCCN(Cc2ccccc2)C3)C)C |
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| StdInChI_Ref = {{stdinchicite|changed|chemspider}} |
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| StdInChI = 1S/C28H31N3O6/c1-18-24(27(32)36-3)26(21-11-7-12-22(15-21)31(34)35)25(19(2)29-18)28(33)37-23-13-8-14-30(17-23)16-20-9-5-4-6-10-20/h4-7,9-12,15,23,26,29H,8,13-14,16-17H2,1-3H3/t23-,26-/m1/s1 |
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| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}} |
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| StdInChIKey = QZVNQOLPLYWLHQ-ZEQKJWHPSA-N |
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| CAS_number_Ref = {{cascite|correct|??}} |
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| CAS_number = 105979-17-7 |
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| ChEMBL_Ref = {{ebicite|changed|EBI}} |
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| ChEMBL = 2218858 |
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| ATC_prefix = C08 |
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| ATC_suffix = CA15 |
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| ATC_supplemental = |
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| DrugBank_Ref = {{drugbankcite|correct|drugbank}} |
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| DrugBank = |
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| UNII_Ref = {{fdacite|correct|FDA}} |
| UNII_Ref = {{fdacite|correct|FDA}} |
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| UNII = 4G9T91JS7E |
| UNII = 4G9T91JS7E |
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| verifiedrevid = 437143972 |
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<!--Chemical data--> |
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| IUPAC_name = O5-methyl O3-[(3''R'')-1-(phenylmethyl)piperidin-3-yl] 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate |
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| image = Benidipine.svg |
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| CAS_number = 105979-17-7 |
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| ATC_prefix = C08 |
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| ATC_suffix = CA15 |
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| ATC_supplemental = |
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| PubChem = 60065 |
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| DrugBank_Ref = {{drugbankcite|correct|drugbank}} |
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| DrugBank = |
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| C=28 | H=31 | N=3 | O=6 |
| C=28 | H=31 | N=3 | O=6 |
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| molecular_weight = |
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| bioavailability = |
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| protein_bound = |
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| metabolism = |
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| elimination_half-life = |
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| excretion = |
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| pregnancy_AU = <!-- A / B1 / B2 / B3 / C / D / X --> |
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| pregnancy_US = <!-- A / B / C / D / X --> |
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| pregnancy_category= |
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| legal_AU = <!-- Unscheduled / S2 / S3 / S4 / S5 / S6 / S7 / S8 / S9 --> |
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| legal_CA = <!-- / Schedule I, II, III, IV, V, VI, VII, VIII --> |
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| legal_UK = <!-- GSL / P / POM / CD / Class A, B, C --> |
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| legal_US = <!-- OTC / Rx-only / Schedule I, II, III, IV, V --> |
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| legal_status = |
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| routes_of_administration = Oral |
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}} |
}} |
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<!-- Definition and medical uses --> |
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'''Benidipine''' ([[International Nonproprietary Name|INN]]), also known as Benidipinum or benidipine hydrochloride, is a dihydropyridine calcium channel blocker for the treatment of [[Hypertension|high blood pressure (hypertension)]]. |
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'''Benidipine''' is a dihydropyridine calcium channel blocker for the treatment of [[Hypertension|high blood pressure (hypertension)]]. It is a triple <small>L</small>-, <small>T</small>-, and <small>N</small>-type [[calcium channel blocker]]. It is reno- and cardioprotective. |
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<!-- Society and culture --> |
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It was patented in 1981 and approved for medical use in 1991.<ref>{{cite book | vauthors = Fischer J, Ganellin CR |title=Analogue-based Drug Discovery |date=2006 |publisher=John Wiley & Sons |isbn=9783527607495 |page=465 |url=https://books.google.com/books?id=FjKfqkaKkAAC&pg=PA465 |language=en}}</ref> |
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== Dosing == |
== Dosing == |
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Benidipine is dosed as |
Benidipine is dosed as mg once daily.<ref>{{cite web | url = http://www.mims-online.com/Page.aspx?menuid=mng&name=Coniel%20film-coated%20tab | title = Coniel (benidipine) package insert (Philippines) | author = Hi-Eisai Pharmaceutical, Inc. | = 2008-03-31 | publisher = CMPMedica | work = MIMS Philippines}}</ref> |
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== |
==== |
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Benidipine is |
Benidipine is . |
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Benidipine has additionally been found to act as an [[receptor antagonist|antagonist]] of the [[mineralocorticoid receptor]], or as an [[antimineralocorticoid]].<ref name="Luther2014">{{cite journal | vauthors = Luther JM | title = Is there a new dawn for selective mineralocorticoid receptor antagonism? | journal = Current Opinion in Nephrology and Hypertension | volume = 23 | issue = 5 | pages = 456–61 | date = September 2014 | pmid = 24992570 | pmc = 4248353 | doi = 10.1097/MNH.0000000000000051 }}</ref> |
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Benidipine is only licensed for use in Japan and selected [[South East Asia|Southeast Asian]] countries, where it is sold as 4 mg tablets. |
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== |
==== |
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Other names include Benidipinum or benidipine hydrochloride. |
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{{reflist}} |
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Benidipine is sold as Coniel by Kyowa Hakko Kogyo. |
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Benidipine is initially licensed for use in Japan and selected [[South East Asia|Southeast Asian]] countries and later in Turkey, where it is sold as 4 mg tablets. |
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{{Calcium channel blockers}} |
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== References == |
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{{Reflist}} |
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{{Channelergics}} |
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{{Mineralocorticoidics}} |
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[[Category:Antimineralocorticoids]] |
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[[Category:Calcium channel blockers]] |
[[Category:Calcium channel blockers]] |
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[[Category:Dihydropyridines]] |
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[[Category:Piperidines]] |
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[[Category:Carboxylate esters]] |
[[Category:Carboxylate esters]] |
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[[Category: |
[[Category:]] |
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[[Category:Methyl esters]] |
[[Category:Methyl esters]] |
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[[Category:Nitrobenzene derivatives]] |
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[[Category:Piperidines]] |
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[[ja:ベニジピン]] |