Therapeutic Targets Database
BIDD Pharmainformatics Databases


TTD Drug ID: DAP000264

Drug Information
SynonymsUNII-P10582JYYK; D08473; 1-Piperidinepropanoic acid, 4-(methoxy-carbonyl)-4-((1-oxopropyl)phenylamino)-, methyl ester; CHEMBL1005; GI87084B; Ultiva (TN); 3-(4-methoxycarbonyl-4-((1-oxopropyl)phenylamino)-1-piperidine)propanoic acid methyl ester; REMIFENTANIL; DEA No. 9739; AC1Q5ZGR; CID60815; Remifentanil [INN:BAN]; AC1L1TZ8; MolPort-004-286-006; GI 87084B; BIDD:GT0029; Remifentanil (INN); GI 87084X; CHEBI:8802; 4-carboxy-4-(n-phenylpropionamido)-1-piperidinepropionic acid dimethyl ester; LS-115982; DB00899; 132539-07-2 (mono-hydrochloride); L001266; Ultiva; methyl 1-(3-methoxy-3-oxopropyl)-4-(N-propanoylanilino)piperidine-4-carboxylate; Remifentanyl; C08021; 132875-61-7    
Trade NameUltiva    
CompanyAbbott Laboratories    
IndicationGeneral anesthesiaApproved    [1]

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Therapeutic ClassHypnotics and Sedatives    
CAS NumberCAS 132875-61-7
PubChem Compound IDCID 60815.    
PubChem Substance IDSID 10221.    
SuperDrug ATC IDN01AH06;    
SuperDrug CAS ID132875617;    
TargetMu-type opioid receptorAgonist[2]
Ref 1FDA Approved Drug Products from FDA Official Website. 2009. Application Number: (NDA) 020630 To Reference
Ref 2The pro-nociceptive effects of remifentanil or surgical injury in mice are associated with a decrease in delta-opioid receptor mRNA levels: Prevention of the nociceptive response by on-site delivery of enkephalins. Pain. 2009 Jan;141(1-2):88-96. Epub 2008 Dec 5. To Reference


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