Skip to main content

Batanopride









Batanopride


From Wikipedia, the free encyclopedia

Jump to navigation
Jump to search



























































Batanopride
Batanopride.png
Clinical data
Routes of
administration
Oral
ATC code
  • none
Legal status
Legal status

  • In general: uncontrolled


Identifiers
CAS Number

  • 102670-46-2 ☒N

PubChem CID
  • 59692
ChemSpider

  • 53849 ☑Y
UNII
  • 1AT99K728N
ChEMBL

  • ChEMBL38594 ☑Y
Chemical and physical data
Formula
C17H26ClN3O3
Molar mass 355.860 g/mol
3D model (JSmol)
  • Interactive image

.mw-parser-output .nobold{font-weight:normal}
 ☒N☑Y (what is this?)
  (verify)

Batanopride (BMY-25,801) is an antiemetic drug of the benzamide class which acts as a selective 5-HT3 receptor antagonist.[1] It was trialled to reduce nausea during cancer chemotherapy, but was never approved for medical use due to dose-limiting side effects including hypotension and long QT syndrome.[2]



References[edit]





  1. ^ Gylys JA, Wright RN, Nicolosi WD, Buyniski JP, Crenshaw RR. BMY-25801, an antiemetic agent free of D2-dopamine receptor antagonist properties. Journal of Pharmacology and Experimental Therapeutics. 1988 Mar;244(3):830-7. .mw-parser-output cite.citation{font-style:inherit}.mw-parser-output q{quotes:"""""""'""'"}.mw-parser-output code.cs1-code{color:inherit;background:inherit;border:inherit;padding:inherit}.mw-parser-output .cs1-lock-free a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/6/65/Lock-green.svg/9px-Lock-green.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-lock-limited a,.mw-parser-output .cs1-lock-registration a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/d/d6/Lock-gray-alt-2.svg/9px-Lock-gray-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-lock-subscription a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/a/aa/Lock-red-alt-2.svg/9px-Lock-red-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration{color:#555}.mw-parser-output .cs1-subscription span,.mw-parser-output .cs1-registration span{border-bottom:1px dotted;cursor:help}.mw-parser-output .cs1-hidden-error{display:none;font-size:100%}.mw-parser-output .cs1-visible-error{font-size:100%}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration,.mw-parser-output .cs1-format{font-size:95%}.mw-parser-output .cs1-kern-left,.mw-parser-output .cs1-kern-wl-left{padding-left:0.2em}.mw-parser-output .cs1-kern-right,.mw-parser-output .cs1-kern-wl-right{padding-right:0.2em}
    PMID 2978041



  2. ^ Fleming GF, Vokes EE, McEvilly JM, Janisch L, Francher D, Smaldone L. Double-blind, randomized crossover study of metoclopramide and batanopride for prevention of cisplatin-induced emesis. Cancer Chemotherapy and Pharmacology. 1991;28(3):226-7.
    PMID 1855280
















Retrieved from "https://en.wikipedia.org/w/index.php?title=Batanopride&oldid=781659408"





Navigation menu

























(window.RLQ=window.RLQ||).push(function(){mw.config.set({"wgPageParseReport":{"limitreport":{"cputime":"0.688","walltime":"0.850","ppvisitednodes":{"value":4763,"limit":1000000},"ppgeneratednodes":{"value":0,"limit":1500000},"postexpandincludesize":{"value":294440,"limit":2097152},"templateargumentsize":{"value":4124,"limit":2097152},"expansiondepth":{"value":16,"limit":40},"expensivefunctioncount":{"value":1,"limit":500},"unstrip-depth":{"value":1,"limit":20},"unstrip-size":{"value":4729,"limit":5000000},"entityaccesscount":{"value":1,"limit":400},"timingprofile":["100.00% 524.427 1 -total"," 74.86% 392.575 1 Template:Drugbox"," 54.89% 287.834 1 Template:Infobox"," 20.26% 106.251 18 Template:Navbox"," 18.63% 97.693 16 Template:Unbulleted_list"," 9.35% 49.012 1 Template:Serotonergics"," 8.92% 46.768 1 Template:Reflist"," 8.40% 44.034 1 Template:Infobox_drug/chemical_formula"," 7.12% 37.337 2 Template:PMID"," 6.51% 34.142 2 Template:Catalog_lookup_link"]},"scribunto":{"limitreport-timeusage":{"value":"0.145","limit":"10.000"},"limitreport-memusage":{"value":3098811,"limit":52428800}},"cachereport":{"origin":"mw1249","timestamp":"20181215042344","ttl":1900800,"transientcontent":false}}});});{"@context":"https://schema.org","@type":"Article","name":"Batanopride","url":"https://en.wikipedia.org/wiki/Batanopride","sameAs":"http://www.wikidata.org/entity/Q4868616","mainEntity":"http://www.wikidata.org/entity/Q4868616","author":{"@type":"Organization","name":"Contributors to Wikimedia projects"},"publisher":{"@type":"Organization","name":"Wikimedia Foundation, Inc.","logo":{"@type":"ImageObject","url":"https://www.wikimedia.org/static/images/wmf-hor-googpub.png"}},"datePublished":"2010-03-12T04:44:02Z","dateModified":"2017-05-22T14:32:31Z","image":"https://upload.wikimedia.org/wikipedia/commons/7/72/Batanopride.png","headline":"chemical compound"}(window.RLQ=window.RLQ||).push(function(){mw.config.set({"wgBackendResponseTime":104,"wgHostname":"mw1241"});});

Popular posts from this blog

Full-time equivalent

さくらももこ

13 indicted, 8 arrested in Calif. drug cartel investigation