METHYSERGIDE MALEATE

METHYSERGIDE MALEATE Suppliers list
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Products Intro: Product Name:Methysergide maleate;Deseril, Sansert;UML 491;UML-491;UML491;Methysergide
CAS:129-49-7
Package:100 mg;500 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
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Products Intro: Product Name:METHYSERGIDE MALEATE
CAS:129-49-7
Purity:98% Package:1KG;1.8USD
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Products Intro: Product Name:Methysergide maleate
CAS:129-49-7
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Products Intro: Product Name:Methysergide maleate
CAS:129-49-7
Purity:>=99% Package:$215.9/10mg;$904.9/50mg;Bulk package Remarks:99%
Company Name: 3B Pharmachem (Wuhan) International Co.,Ltd.  
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Products Intro: Product Name:Methysergide Maleate;[8β(S)]-9,10-Didehydro-N-[1-(hydroxyMethyl)propyl]-1,6-diMethylergoline-8-carboxaMideMaleate
CAS:129-49-7
Purity:99% HPLC Package:1Mg ; 5Mg;10Mg ;100Mg;250Mg ;500Mg ;1g;2.5g ;5g ;10g
METHYSERGIDE MALEATE Basic information
Product Name:METHYSERGIDE MALEATE
Synonyms:1-(hydroxymethyl)propylamideof1-methyl-(+)-lysergicacidhydrogenmaleate;deseril-retard;ergoline-8-beta-carboxamide,9,10-didehydro-n-(1-(hydroxymethyl)propyl)-1,6-dim;maleate(1:1)(salt);Methysergide Maleate, USP;Methysergide Maleate (350 mg);methysergidebimaleate;methysergidedimaleate
CAS:129-49-7
MF:C25H31N3O6
MW:469.54
EINECS:204-950-9
Product Categories:Antagonists;Neurotransmitters;Serotonergics;Serotonin receptor;ATRAVET
Mol File:129-49-7.mol
METHYSERGIDE MALEATE Structure
METHYSERGIDE MALEATE Chemical Properties
storage temp. Store at RT
solubility DMSO: >10 mg/mL
form solid
color white to off-white
Water Solubility Soluble to 10 mM in water with gentle warming
Stability:Hygroscopic
Safety Information
Hazard Codes T
Risk Statements 25
Safety Statements 45
RIDADR UN 2811 6.1/PG 3
WGK Germany 3
RTECS KE5410000
HazardClass 6.1(b)
PackingGroup III
HS Code 2939690000
Toxicitymouse,LD50,intravenous,185mg/kg (185mg/kg),"Psychotropic Drugs and Related Compounds," 2nd ed., Usdin, E., and D.H. Efron, Washington, DC, 1972Vol. -, Pg. 101, 1972.
MSDS Information
ProviderLanguage
SigmaAldrich English
METHYSERGIDE MALEATE Usage And Synthesis
DescriptionMethysergide is an agonist of the serotonin (5-HT) receptor subtype 5-HT1 and an antagonist of 5-HT2 receptors. It binds to recombinant human 5-HT1A (KD = 23.44 nM), 5-HT1E (Ki = 229.09 nM), 5-HT1F (Ki = 33.88 nM), and rodent 5-HT1B receptors (KD = 1,513.56 nM). It also binds to recombinant human 5-HT2A (Ki = 2.69 nM) and 5-HT2C receptors (KD = 1.26 nM) and is an insurmountable antagonist at 5-HT2B receptors. It inhibits vasoconstriction induced by 5-HT in isolated postmortem human basilar arterial spiral strips (pA2 = 8.07). Methysergide decreases external carotid blood flow in a dose-dependent manner in vagosympathectomized dogs, an effect that is inhibited by the 5-HT1B/1D receptor antagonist GR127935 . It has antinociceptive activity in mouse models of pain induced by intrathecal injection of substance P , glutamate, NMDA , AMPA , or kainic acid. Methysergide reduces zymosan-induced paw edema in rats when administered at a dose of 10 mg/kg. Formulations containing methysergide were previously used in the prevention and treatment of vascular headaches.
OriginatorSansert ,Sandoz,US,1962
UsesMethysergide maleate salt has been used as a serotonin (5HT) receptor antagonist to evaluate the potential systemic effects of methysergide (METH) and 5-HT infusions on production and milk composition in multiparous Holstein cows. It may also be used as a serotonin receptor blocker to identify the serotonergic receptor type involved in the direct excitation of mitral cells in the main olfactory bulb.
Usessedative
DefinitionChEBI: Methysergide maleate is an ergoline alkaloid.
Manufacturing ProcessAs described in US Patent 3,218,324, 0.9 part of potassium are dissolved in 500 parts by volume of liquid ammonia, then oxidized with ferric nitrate to potassium amide, after which 4.85 parts of lysergic acid-1'-hydroxybutylamide-2' are dissolved in the obtained mixture. After 15 minutes there are added to the obtained yellow solution 4.1 parts of methyl iodide in 5 parts by volume of ether, the mixture being allowed to stand for 30 more minutes at -60°C. The liquid ammonia is thereupon evaporated and the dry residue is shaken out between water and chloroform. The mixture of bases which remains after the evaporation of the chloroform is chromatographed on a column of 250 parts of aluminum oxide, the desired 1-methyl-lysergic acid-1'- hydroxy-butylamide-2' being washed into the filtrate with chloroform and chloroform-0.2% ethanol. The 1-methyl-lysergic acid-1'hydroxy-butylamide-2' crystallizes from chloroform in the form of plates which melt at 194° to 196°C. Reaction with maleic acid gives the dimaleate, melting at 187° to 188°C.
Brand nameSansert (Novartis).
Therapeutic FunctionMigraine therapy
Biological ActivityMixed 5-HT 1 /5-HT 2 receptor antagonist.
Biochem/physiol ActionsMethysergide maleate, also known as sansert, is a semisynthetic ergot alkaloid ergometrine derivative. Methysergide is a serotonin 1(5-HT1) receptor agonist and a nonselective 5-HT2 and 5-HT7 serotonin receptor antagonist. Methysergide maleate is used as a pharmacological agent to treat migraines and other vascular headaches. But, prolonged and uncontrolled use of this drug may cause Leriche′s syndrome, angina pectoris, acute ischemia of the limbs. In addition, gastrointestinal side effects, such as abdominal cramps, nausea, and diarrhea have also been observed in few patients.
Safety ProfilePoison by ingestion and intravenous routes. Experimental reproductive effects. Human mutation effects reported. When heated to decomposition it emits toxic fumes of NOx.
storageStore at RT
METHYSERGIDE MALEATE Preparation Products And Raw materials
Raw materialsAmmonia-->Iodomethane-->Potassium-->Maleic acid
Tag:METHYSERGIDE MALEATE(129-49-7) Related Product Information
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