75507-68-5 Flupirtine maleate CAS NO.75507-68-5

Min.Order Quantity:: 1 Metric Ton

Purity:: 98%

Port:: Shanghai

Payment Terms:: L/C,T/T,MoneyGram,Other

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Keywords

75507-68-5
Flupirtine maleate
98%

Quick Details

ProName: 75507-68-5 Flupirtine maleate
CasNo: 75507-68-5
Molecular Formula: C19H21FN4O6
Appearance: Solid
Application: General reagent/ pharmaceutical inte...
DeliveryTime: Prompt
PackAge: As required
Port: Shanghai
ProductionCapacity: 20 Metric Ton/Month
Purity: 98%
Storage: 2-8°C
Transportation: By Sea/ By Air/ By Courier
LimitNum: 1 Metric Ton
Heavy metal: ppm
Grade: Industrial Grade,Food Grade,Pharma Gra...
Assay: 99%

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Details

flupirtine maleate basic information

description painkiller references

product name:	flupirtine maleate
synonyms:	2-amino-6-[[(4-fluorophenyl)methyl]amino]-3-pyridinyl]-carbamic acid, ethyl ester maleate;flupirtinemaleatelupirtine;ethyl-2-amino-6-[(4-fluorbenzyl)amino]pyridin-3-carbamat, verbindung mit maleinsure (1:1);keiton;ketadolon;n-[2-amino-6-[[4-fluorophenyl)methyl]amino]-3-pyridinyl]carbamicacidethylestermaleate;flupirtine maleate salt;2-amino-6-[(p-fluorobenzyl)amino]-3-pyridinecarbamic acid ethyl ester maleate
cas:	75507-68-5
mf:	c19h21fn4o6
mw:	420.3916432
einecs:	278-225-0
product categories:	other potassium channel modulators;apis;amines;heterocycles;intermediates & fine chemicals;pharmaceuticals;other apis;inhibitors;api
mol file:	75507-68-5.mol

flupirtine maleate chemical properties

melting point	186-188°c
storage temp.	2-8°c
solubility	dmso: soluble >20mg/ml
color	white
λmax	343nm(ch3cn)(lit.)
merck	14,4190

safety information

safety statements	22-24/25-35-20
rtecs	ey8555800

msds information

flupirtine maleate usage and synthesis

description	flupirtine is a selective neuronal potassium channel opener (snepco) that also has n-methyl-d-aspartate (nmda) receptor antagonist property which has been shown to be effective in the management of body pain. flupirtine is used as an analgesic for acute pain, in moderate-to-severe cases. its muscle relaxant properties make it popular for back pain and other orthopedic uses, but it is also used for migraines, in oncology, postoperative care, and gynecology. it is also effective in other painful conditions in which the primary requirement for analgesia is without sedation or anti-inflammatory effects. it first became available in europe in 1984 under the brand name katadolon. flupirtine is a derivative of triaminopyridine with a chemical formula of ethyl-n-{2-amino-6-(4-fluorophenylmethylamino) pyridine-3 yl} cabamate. it is available as the maleate salt because flupirtine is itself poorly water soluble. flupirtine is a base and is weakly lipophilic.
painkiller	at present, the pain medications, used in the clinical in china, are divided into two categories: a class is to morphine on behalf of narcotic analgesics, and the other is aspirin antipyretic analgesics as representative. while the former high pain intensity, but addiction is its achilles heel, which greatly limits its application; but the latter, although with no addictive analgesic strength, but it is weak, and has serious gastrointestinal effects. flupirtine maleate, developed by pliva,is subsidiary company german awd, a new non-opioid analgesics central, listed in germany in 1986 for the treatment of postoperative pain, dental pain, painful wounds and burns. then in 1990, it was applied in the treatment of degenerative joint disease, neuropathic and cancer pain, migraine, headache and dysmenorrhea indications. after that, the flupirtine maleate list in brazil and portugal. china approved the company's german awd flupirtine maleate capsules imports in september in 2006, trade name: kodak dolong (katadolon (r)). flupirtine maleate is a selective neuronal potassium channel opener, oral easily absorbed, which has three efficacy about analgesic, muscle relaxant and neuroprotective. it showed analgesic effects to pain caused by a variety of reasons. flupirtine maleate has no affinity to ah receptor, which do not inhibit prostaglandin synthesis. it is not antagonistic naloxone. pain intensity (ed50) was weaker than methadone, buprenorphine and morphine, about 50% of morphine. comparable to that of pentazocine, flupirtine maleate is better than pethidine, codeine, phenacetin and paracetamol. such as in the hot plate test, the effect of the strength of flupirtine (ed50 of 32mg/kg, oral administration) is about half of morphine, codeine is 2 times, 10 times stronger than paracetamol and phenacetin. in the wake of dog dental pulp stimulation experiment, the analgesic intensity (ed50 of 3.5mg/ kg, oral administration) is same with pentazocine. oral absorption of this product is about 90%, and rectal administration of this product is about 70%. after oral administration of 20~30min. it showed the pharmacological effects, and the duration of action is 3~5h. plasma half-life is 8~11h. the drug is in the body tissues, mainly in the liver metabolism, and about 70% of the drug is eliminated by the kidneys. flupirtine maleate is inhibited to pain caused by various diseases. the analgesic effect is between methadone and paracetamol. centrally acting, but it did not inhibit the respiratory cardiovascular systems, and has no pharmacological activity impact for cough center, nor constipation and urinary retention. long-term use does not produce tolerance and dependence. it has no painkillers side effects like other medicines on the market, such as addiction, gastrointestinal symptoms. long term use after a few years the efficacy is not reduced, but can reduce the amount of taking. in short, flupirtine maleate has good clinical application prospect.
references	# #
chemical properties	off-white solid
uses	analgesic. substituted pyridine with central analgesic properties.
biological activity	non-opioid analgesic with muscle relaxant properties. activates k + channels and indirectly antagonizes nmda receptors. exhibits neuroprotective actions in a model of cerebral ischemia in mice and reduces apoptosis and necrosis induced by noxious stimuli.