ethyl 2-amino-6-[[p-fluorobenzyl]amino]pyridine-3-carbamate monohydrochloride

Product Name
ethyl 2-amino-6-[[p-fluorobenzyl]amino]pyridine-3-carbamate monohydrochloride
CAS No.
33400-45-2
Chemical Name
ethyl 2-amino-6-[[p-fluorobenzyl]amino]pyridine-3-carbamate monohydrochloride
Synonyms
Flupirtine HCl;Flupirtine Hydrochloride;ethyl 2-amino-6-[[p-fluorobenzyl]amino]pyridine-3-carbamate monohydrochloride;ethyl N-[2-amino-6-[(4-fluorophenyl)methylamino]pyridin-3-yl]carbamate,hydrochloride
CBNumber
CB8937085
Molecular Formula
C15H18ClFN4O2
Formula Weight
340.78
MOL File
33400-45-2.mol
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
HCH0260627
Product name
ETHYL 2-AMINO-6-[[P-FLUOROBENZYL]AMINO]PYRIDINE-3-CARBAMATE MONOHYDROCHLORIDE
Purity
95.00%
Packaging
5MG
Price
$495.99
Updated
2021/12/16
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ethyl 2-amino-6-[[p-fluorobenzyl]amino]pyridine-3-carbamate monohydrochloride Chemical Properties,Usage,Production

Uses

Flupirtine hydrochloride (D 9998 hydrochloride) is a selective neuropotassium channel opener with analgesic activity. Flupirtine hydrochloride is used to inhibit a variety of pain conditions, including chronic musculoskeletal pain, migraines, and neuralgia. Flupirtine hydrochloride has antidepressant and antioxidant properties and may increase the analgesic effect in combination therapy with morphine. Flupirtine hydrochloride relieves abnormally increased muscle tension and has a muscle relaxant effect. Flupirtine hydrochloride is clinically superior to other drugs, such as tramadol and pantoxan, plus its side effects are better tolerated. Flupirtine hydrochloride has a significant effect on inhibiting neural hyperexcitability and therefore exhibits inhibitory potential in various pain states[1].

References

[1] Kornhuber J, et al. Flupirtine shows functional NMDA receptor antagonism by enhancing Mg2+ block via activation of voltageindependent potassium channels. Rapid communication. J Neural Transm. 1999;106(9-10):857-67. DOI:10.1007/s007020050206
[2] Flupirtine in pain management: pharmacological properties and clinical use DOI:10.2165/11536230-000000000-00000
[3] Klinger F, et al. Concomitant facilitation of GABAA receptors and KV7 channels by the non-opioid analgesic flupirtine. Br J Pharmacol. 2012 Jul;166(5):1631-42. DOI:10.1111/j.1476-5381.2011.01821.x
[4] Swedberg MD, et al. Pharmacological mechanisms of action of flupirtine: a novel, centrally acting, nonopioid analgesic evaluated by its discriminative effects in the rat. J Pharmacol Exp Ther. 1988 Sep;246(3):1067-74. PMID:2901483
[5] Wu SN, et al. Evidence for inhibitory effects of flupirtine, a centrally acting analgesic, on delayed rectifier k(+) currents in motor neuron-like cells. Evid Based Complement Alternat Med. 2012;2012:148403. DOI:10.1155/2012/148403
[6] Kolosov A, et al. Flupirtine enhances the anti-hyperalgesic effects of morphine in a rat model of prostate bone metastasis. Pain Med. 2012 Nov;13(11):1444-56. DOI:10.1111/j.1526-4637.2012.01502.x
[7] Michel MC, et al. Unexpected frequent hepatotoxicity of a prescription drug, flupirtine, marketed for about 30 years. Br J Clin Pharmacol. 2012 May;73(5):821-5. DOI:10.1111/j.1365-2125.2011.04138.x

ethyl 2-amino-6-[[p-fluorobenzyl]amino]pyridine-3-carbamate monohydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

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ethyl 2-amino-6-[[p-fluorobenzyl]amino]pyridine-3-carbamate monohydrochloride Suppliers

TCI (Shanghai) Chemical Trading Co., Ltd.
Tel
021-61109150
Fax
021-61105897
Email
sales@tcisct.com
Country
China
ProdList
29668
Advantage
58
TargetMol Chemicals Inc.
Tel
4008200310
Email
marketing@tsbiochem.com
Country
China
ProdList
24961
Advantage
58

33400-45-2, ethyl 2-amino-6-[[p-fluorobenzyl]amino]pyridine-3-carbamate monohydrochlorideRelated Search:


  • ethyl 2-amino-6-[[p-fluorobenzyl]amino]pyridine-3-carbamate monohydrochloride
  • Flupirtine Hydrochloride
  • ethyl N-[2-amino-6-[(4-fluorophenyl)methylamino]pyridin-3-yl]carbamate,hydrochloride
  • Flupirtine HCl
  • 33400-45-2