ChemicalBook > Product Catalog >API >Digestive system drugs >Emetics and antiemetics >dolasetron

dolasetron

dolasetron Suppliers list
Company Name: career henan chemical co
Tel: +86-0371-86658258 +8613203830695
Email: sales@coreychem.com
Products Intro: Product Name:(2alpha,6alpha,8alpha,9abeta)-Octahydro-3-oxo-2,6-methano-2H-quinolizin-8-yl-1H-indole-3-carboxylate
CAS:115956-12-2
Purity:98% Package:1KG;1USD
Company Name: CONIER CHEM AND PHARMA LIMITED
Tel: +8618523575427
Email: sales@conier.com
Products Intro: Product Name:dolasteron
CAS:115956-12-2
Purity:0.99 Package:1kg
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354; +17819995354
Email: marketing@targetmol.com
Products Intro: Product Name:Dolasetron
CAS:115956-12-2
Purity:99.86% Package:5mg;40USD|10mg;60USD|25mg;123USD Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: HANGZHOU CLAP TECHNOLOGY CO.,LTD
Tel: 86-571-88216897,88216896 13588875226
Email: sales@hzclap.com
Products Intro: Product Name:Dolasetron
CAS:115956-12-2
Purity:99% Package:10kg 25kg 200 kilograms per barrel Remarks:good
Company Name: Shaanxi Dideu Medichem Co. Ltd
Tel: +86-029-89586680 +86-18192503167
Email: 1026@dideu.com
Products Intro: Product Name:dolasetron USP/EP/BP
CAS:115956-12-2
Purity:99.9% Package:25kgs/Drum;200kgs/Drum Remarks:FDA GMP CEP Approved Manufacturer

dolasetron manufacturers

  • Dolasetron
  • Dolasetron pictures
  • 2026-06-22
  • CAS:115956-12-2
  • Min. Order: 1g
  • Purity: 98%min
  • Supply Ability: 1000g
  • Dolasetron
  • Dolasetron pictures
  • $40.00
  • 2026-05-11
  • CAS:115956-12-2
  • Purity: 99.84%
  • Supply Ability: 10g
  • Dolasetron
  • Dolasetron pictures
  • $15.00
  • 2021-07-13
  • CAS:115956-12-2
  • Min. Order: 1KG
  • Purity: 99%+ HPLC
dolasetron Basic information
Product Name:dolasetron
Synonyms:(2alpha,6alpha,8alpha,9abeta)-Octahydro-3-oxo-2,6-methano-2H-quinolizin-8-yl-1H-indole-3-carboxylate;Dolasteron;Octahydro-3-oxo-2,6-Methano-2H-quinolizin-8-yl Ester;1H-Indole-3-carboxylic acid, octahydro-3-oxo-2,6-methano-2H-quinolizin-8-yl ester, (2alpha,6alpha,8alpha,9abeta)-;Dolasetronum;Dolasetronum [inn-latin];Hsdb 7565;Unii-82wi2L7Q6e
CAS:115956-12-2
MF:C19H20N2O3
MW:324.37
EINECS:
Product Categories:API;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File:115956-12-2.mol
dolasetron Structure
dolasetron Chemical Properties
Melting point 278 ºC
Boiling point 535.1±50.0 °C(Predicted)
density 1.37±0.1 g/cm3(Predicted)
storage temp. Sealed in dry,2-8°C
solubility Chloroform (Slightly), DMSO (Slightly), Methanol (Sparingly)
pka15.36±0.30(Predicted)
form Solid
color White
Water Solubility Soluble
CAS DataBase Reference115956-12-2
Safety Information
Hazardous Substances Data115956-12-2(Hazardous Substances Data)
MSDS Information
dolasetron Usage And Synthesis
DescriptionDolasetron is an antagonist of the serotonin (5-HT) receptor subtype 5-HT3 (Ki = 20 nM). It is selective for 5-HT3 receptors over 5-HT1A, 5-HT1B, 5-HT2, dopamine D2, α1-, α2-, β-adrenergic, M1-5 muscarinic acetylcholine, and neurokinin-1 (NK1) receptors (IC50s = >10 μM for all). Dolasetron inhibits 5-HT-induced membrane currents in NG 108-15 cells (IC50 = 3.8 nM). It increases the latency to emesis and reduces the number of vomiting and retching episodes induced by cisplatin in ferrets when administered at doses of 0.5 or 2 mg/kg. Formulations containing dolasetron have been used in the prevention of postoperative or chemotherapy-induced nausea.
Chemical PropertiesWhite Solid
Usesprevention and treatment of postoperative nausea and vomiting
UsesDolasetron is a bridged pseudopelletierine derivative; specific serotonin (5HT3) receptor antagonist.It is used as antiemetic.
UsesBridged pseudopelletierine derivative; specific serotonin (5HT3) receptor antagonist. Antiemetic.
DefinitionChEBI: LSM-5418 is an indolyl carboxylic acid.
Brand nameAnzemet (Sanofi Aventis.
SynthesisEthyl cyclopentenecarboxylate (I), in the presence of a catalytic amount of osmium tetroxide, was oxidized to diol (II) with N-methylmorpholine-N-oxide. It was then split to dialdehyde (III) in the presence of sodium periodate and its aqueous solution was converted to bicyclization (IV) at pH 4 by Robinson-Schoepf reaction. (IV) was then reduced to alcohol (V) with sodium borohydride and reacted with dihydropyran to form tetrahydrofuran ether (VI) to protect the hydroxyl group formed. This is then converted to the tricyclic compound (VII), which is then acylated to give dolasetron by reacting with an acyl chloride (VIII) in the presence of silver tetrafluoroborate.
References[1] PETER H. BOEIJINGA . Characterization of the novel 5-HT3 antagonists MDL 73147EF (dolasetron mesilate) and MDL 74156 in NG108-15 neuroblastoma × glioma cells[J]. European journal of pharmacology, 1992, 219 1: Pages 9-13. DOI: 10.1016/0014-2999(92)90573-m
[2] ROBERT C. MILLER. Pharmacological properties of dolasetron, a potent and selective antagonist at 5-HT3 receptors[J]. Drug Development Research, 1993, 28 1: 87-93. DOI: 10.1002/ddr.430280111
dolasetron Preparation Products And Raw materials
Preparation ProductsSuprofen
Tag:dolasetron(115956-12-2) Related Product Information
Olanzapine DROPERIDOL PENTAZOCINE Dexmedetomidine Omeprazole Ramosetron hydrochloride 4-Amino-5-chloro-N-(2-(diethylamino)ethyl)-2-methoxybenzamide Azasetron hydrochloride Dolasetron mesylate 1-ISOPROPYL-3-PIPERIDINONE (2a,6a,8a,9ab)-Hexahydro-8-hydroxy-2,6-methano-2H-quinolizin-3(4H)-one 3-QUINUCLIDINONE CHEMBRDG-BB 4015185 1-(2-methylpiperidin-1-yl)acetone 2-CYCLOOCTYL-ETHYLAMINE 1-piperidinoacetone dolasetron Hexahydro-8-Hydroxy-2, 6-Methano-2h-Quinolizin-3(4h)-One