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Cisapride - ≥99%, high purity , CAS No.81098-60-4, Agonist of 5-HT 4 receptor;Agonist of 5-HT 7 receptor;Channel blocker of K v11.1

  • Moligand™
  • ≥99%
Item Number
C275070
Grouped product items
SKUSizeAvailabilityPrice Qty
C275070-10mg
10mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$77.90
C275070-50mg
50mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$122.90
C275070-100mg
100mg
In stock
$195.90
C275070-250mg
250mg
In stock
$441.90

5-HT 4 receptor agonist. hERG blocker.

Basic Description

Synonymscisapride|81098-60-4|Cisaprida|Cisapridum|Prepulsid|Kaudalit|Pridesia|(+-)-Cisapride|CHEBI:3720|R 51619|Propulsid|Acenalin|Risamol|UVL329170W|86718-70-9|Kinestase|cis-4-Amino-5-chloro-N-(1-(3-(p-fluorophenoxy)propyl)-3-methoxy-4-piperidyl)-o-anisamide|CHE
Specifications & Purity≥99%
Storage TempStore at -20°C
Shipped InDry ice
GradeMoligand™
Action TypeAGONIST, CHANNEL BLOCKER
Mechanism of actionAgonist of 5-HT 4 receptor;Agonist of 5-HT 7 receptor;Channel blocker of K v11.1
Product Description

Product Description:
Cisapride (R 51619, Kaudalit, Kinestase, Prepulsid, Presid, Pridesia, Propulsid) is a nonselective 5-HT4 receptor agonist with gastroprokinetic effects.

Associated Targets

HTR4 Tclin 5-hydroxytryptamine receptor 4 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HTR7 Tclin 5-hydroxytryptamine receptor 7 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

KCNH2 Tclin Potassium voltage-gated channel subfamily H member 2 2 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name 4-amino-5-chloro-N-[(3S,4R)-1-[3-(4-fluorophenoxy)propyl]-3-methoxypiperidin-4-yl]-2-methoxybenzamide
INCHI InChI=1S/C23H29ClFN3O4/c1-30-21-13-19(26)18(24)12-17(21)23(29)27-20-8-10-28(14-22(20)31-2)9-3-11-32-16-6-4-15(25)5-7-16/h4-7,12-13,20,22H,3,8-11,14,26H2,1-2H3,(H,27,29)/t20-,22+/m1/s1
InChi Key DCSUBABJRXZOMT-IRLDBZIGSA-N
Canonical SMILES COC1CN(CCC1NC(=O)C2=CC(=C(C=C2OC)N)Cl)CCCOC3=CC=C(C=C3)F
Isomeric SMILES CO[C@H]1CN(CC[C@H]1NC(=O)C2=CC(=C(C=C2OC)N)Cl)CCCOC3=CC=C(C=C3)F
PubChem CID 6917698
Molecular Weight 465.95

Certificates

Certificate of Analysis(COA)

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4 results found

Lot NumberCertificate TypeDateItem
K2103559Certificate of AnalysisJun 14, 2023 C275070
K2103561Certificate of AnalysisJun 14, 2023 C275070
K2103790Certificate of AnalysisJun 14, 2023 C275070
K2103791Certificate of AnalysisJun 14, 2023 C275070

Chemical and Physical Properties

SolubilitySoluble in DMSO to 100 mM and in ethanol to 25 mM (with warming)

Safety and Hazards(GHS)

Pictogram(s) GHS05
Signal Danger
Hazard Statements

H318:Causes serious eye damage

Precautionary Statements

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes.

P305+P354+P338:IF IN EYES: Immediately rinse with water for several minutes. Remove contact lenses if present and easy to do. Continue rinsing.

P317:Get emergency medical help.

Related Documents

Solution Calculators