Therapeutic Class Overview Anticonvulsants
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
United States July 2016 2 Table of Contents
Deuterium Labelled Compounds United States July 2016 2 Table of Contents International Distributors 3 Corporate Overview 4 General Information 5 Pricing and Payment 5 Quotations 5 Custom Synthesis 5 Shipping 5 Quality Control 6 Quotations 6 Custom Synthesis 6 Shipping 6 Quality Control 6 Chemical Abstract Service Numbers 6 Handling Hazardous Compounds 6 Our Products are Not Intended for Use in Humans 7 Limited Warranty 7 Packaging Information 7 Alphabetical Listings 8 Stock Clearance 236 Products by Category 242 n-Alkanes 243 α-Amino Acids, N-Acyl α-Amino Acids, N-t-BOC Protected α-Amino Acid 243 and N-FMOC Protected α-Amino Acids Buffers and Reagents for NMR Studies 245 Detergents 245 Environmental Standards 246 Fatty Acids and Fatty Acid Esters 249 Flavours and Fragrances 250 Gases 253 Medical Research Products 254 Nucleic Acid Bases and Nucleosides 255 Pesticides and Pesticide Metabolites 256 Pharmaceutical Standards 257 Polyaromatic Hydrocarbons (PAHs), Alkyl-PAHs, Amino-PAHs, 260 Hydroxy-PAHs and Nitro-PAHs Polychlorinated Biphenyls (PCBs) 260 Spin Labels 261 Steroids 261 3 International Distributors C Beijng Zhenxiang H EQ Laboratories GmbH Australia K Technology Company Graf-von-Seyssel-Str. 10 Rm. 15A01, Changyin Bld. 86199 Augsburg Austria H No. 88, YongDingLu Rd. Germany Beijing 100039 Tel.: (49) 821 71058246 Belgium J China Fax: (49) 821 71058247 Tel.: (86) 10-58896805 [email protected] China C Fax: (86) 10-58896158 www.eqlabs.de Czech Republic H [email protected] Germany, Austria, China Czech Republic, Greece, Denmark I Hungary, -
(12) Patent Application Publication (10) Pub. No.: US 2011/0244057 A1 Ehrenberg (43) Pub
US 2011024.4057A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2011/0244057 A1 Ehrenberg (43) Pub. Date: Oct. 6, 2011 (54) COMBINATION THERAPIES WITH Related U.S. Application Data TOPIRAMATE FOR SEIZURES, RESTLESS LEGS SYNDROME, AND OTHER (60) Provisional application No. 61/100,232, filed on Sep. NEUROLOGICAL CONDITIONS 25, 2008. Publication Classification (51) Int. Cl. (76) Inventor: Bruce L. Ehrenberg, New York, A633/26 (2006.01) NY (US) A63L/35 (2006.01) A633/06 (2006.01) A6IP 25/00 (2006.01) (21) Appl. No.: 13/120,933 A6IP 25/28 (2006.01) A6IP 25/08 (2006.01) (22) PCT Filed: Sep. 25, 2009 (52) U.S. Cl. .......... 424/648: 514/454; 424/682; 424/646 (57) ABSTRACT (86). PCT No.: PCT/US2009/058495 The invention provides compositions and methods of treating various conditions, including neurological conditions, with S371 (c)(1), pharmaceutical compositions including a sulfamate (e.g., (2), (4) Date: Jun. 9, 2011 topiramate) and magnesium. US 2011/024.4057 A1 Oct. 6, 2011 COMBINATION THERAPES WITH TOPIRAMATE FOR SEIZURES, RESTLESS LEGS SYNDROME, AND OTHER II NEUROLOGICAL CONDITIONS CROSS-REFERENCE TO RELATED APPLICATIONS 0001. This application claims the benefit of the priority date of U.S. Application No. 61/100,232, filed Sep. 25, 2008. For the purpose of any U.S. patent that may issue from the 0005 wherein RandR, are the same or different and are U.S. national phase correlate of the present application, the hydrogen, lower alkyl or are alkyl and are joined to form a content of the priority document is hereby incorporated by cyclopentyl or cyclohexyl ring, and (b) magnesium. -
Campro Catalog Stable Isotope
Introduction & Welcome Dear Valued Customer, We are pleased to present to you our Stable Isotopes Catalog which contains more than three thousand (3000) high quality labeled compounds. You will find new additions that are beneficial for your research. Campro Scientific is proud to work together with Isotec, Inc. for the distribution and marketing of their stable isotopes. We have been working with Isotec for more than twenty years and know that their products meet the highest standard. Campro Scientific was founded in 1981 and we provide services to some of the most prestigious universities, research institutes and laboratories throughout Europe. We are a research-oriented company specialized in supporting the requirements of the scientific community. We are the exclusive distributor of some of the world’s leading producers of research chemicals, radioisotopes, stable isotopes and environmental standards. We understand the requirements of our customers, and work every day to fulfill them. In working with us you are guaranteed to receive: - Excellent customer service - High quality products - Dependable service - Efficient distribution The highly educated staff at Campro’s headquarters and sales office is ready to assist you with your questions and product requirements. Feel free to call us at any time. Sincerely, Dr. Ahmad Rajabi General Manager 180/280 = unlabeled 185/285 = 15N labeled 181/281 = double labeled (13C+15N, 13C+D, 15N+18O etc.) 186/286 = 12C labeled 182/282 = d labeled 187/287 = 17O labeled 183/283 = 13C labeleld 188/288 = 18O labeled 184/284 = 16O labeled, 14N labeled 189/289 = Noble Gases Table of Contents Ordering Information.................................................................................................. page 4 - 5 Packaging Information .............................................................................................. -
Hydantoin and Succinimide-Substituted
(1 9) J Eur°Pean Patent Office <*S Office europeen des brevets (11) EP 0 533 243 B1 (12) EUROPEAN PATENT SPECIFICATION (45) Date of publication and mention (51) int. CI.6: C07D 401/1 2, C07D 471/10, of the grant of the patent: A61 K 31/445 Q07D 401 /1 4 17,2,997 Buiietin 1997/51 // (C07D471/1 0, 235:00, (21) Application number: 92202723.0 221:00) (22) Date of filing: 08.09.1992 (54) Hydantoin and succinimide-substituted spiroindanylcamphorsulfonyl derivatives Hydantoin und Succinimid-substituierte Spiroindanylcamphorsulfonyl als Oxytocin-Antagonisten Derives de spiroindanylcamphorsulfonyl substitues par un radical hydantoine ou succinimide comme antagonists d'oxytocine (84) Designated Contracting States: (74) Representative: CH DE FR GB IT LI NL Thompson, John Dr. et al Merck & Co., Inc. (30) Priority: 16.09.1991 US 760416 European Patent Department Terlings Park (43) Date of publication of application: Eastwick Road 24.03.1993 Bulletin 1993/12 Harlow, Essex CM20 2QR (GB) (73) Proprietor: Merck & Co., Inc. (56) References cited: Rahway New Jersey 07065-0900 (US) EP-A- 0 444 945 EP-A- 0 445 974 EP-A- 0 450 761 EP-A- 0 486 280 (72) Inventors: US-A- 3 654 287 • Gilbert, Kevin Bally, PA 19503 (US) • EP-A- 0 444 945 • Williams, Peter D. • EP-A- 0 445 974 Harleysville, PA 19438 (US) • EP-A- 0 450 761 • Hobbs, Doug W. • EP-A- 0 486 280 Lansdale, PA 19446 (US) • US-A- 3 654 287 • Evans, Ben E. Lansdale, PA 19446 (US) Remarks: • Veber, Daniel F. The file contains technical information submitted Ambler, PA 19002 (US) after the application was filed and not included in this specification CO CO CM CO CO Note: Within nine months from the publication of the mention of the grant of the European patent, give IO any person may notice to the European Patent Office of opposition to the European patent granted. -
Calcium Channel Blocker As a Drug Candidate for the Treatment of Generalised Epilepsies
UNIVERSITAT DE BARCELONA Faculty of Pharmacy and Food Sciences Calcium channel blocker as a drug candidate for the treatment of generalised epilepsies Final degree project Author: Janire Sanz Sevilla Bachelor's degree in Pharmacy Primary field: Organic Chemistry, Pharmacology and Therapeutics Secondary field: Physiology, Pathophysiology and Molecular Biology March 2019 This work is licensed under a Creative Commons license ABBREVIATIONS AED antiepileptic drug AMPA α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid ANNA-1 antineuronal nuclear antibody 1 BBB blood-brain barrier Bn benzyl BnBr benzyl bromide BnNCO benzyl isocyanate Boc tert-butoxycarbonyl Bu4NBr tetrabutylammonium bromide Ca+2 calcium ion CACNA1 calcium channel voltage-dependent gene cAMP cyclic adenosine monophosphate CCB calcium channel blocker cGMP cyclic guanosine monophosphate CH3CN acetonitrile Cl- chlorine ion Cmax maximum concentration CMV cytomegalovirus CTScan computed axial tomography DCM dichloromethane DIPEA N,N-diisopropylethylamine DMF dimethylformamide DMPK drug metabolism and pharmacokinetics DNET dysembryoplastic neuroepithelial tumours EEG electroencephalogram EPSP excitatory post-synaptic potential FDA food and drug administration Fe iron FLIPR fluorescence imaging plate reader fMRI functional magnetic resonance imaging GABA γ-amino-α-hydroxybutyric acid GAD65 glutamic acid decarboxylase 65 GAERS generalised absence epilepsy rat of Strasbourg GluR5 kainate receptor GTC generalised tonic-clonic H+ hydrogen ion H2 hydrogen H2O dihydrogen dioxide (water) -
Hypothalamic Principles Necessary for the Release of Ovulating Hormone from the Adenohypophysis
EFFECT OF AMINOGLUTETHIMIDE ON REPRODUCTIVE PROCESSES IN FEMALE RATS W. J. EVERSOLE and D. J. THOMPSON Department of Life Sciences, Indiana State University, Terre Haute, Indiana 47809, U.S.A. (Received "òlst January 1974) Summary. Adult female rats injected subcutaneously with 100 mg aminoglutethimide phosphate (AGP)/kg/day for 4 weeks failed to become pregnant when placed in cohabitation with males during the last 2 weeks of the injection period. Lower doses depressed the fertility rate and reduced the litter size: the average litter size of three of eleven rats given 50 mg/kg/day was 4\m=.\7 young and of four of eleven rats given 25 mg was 7\m=.\0 young. Twenty-nine controls averaged 10\m=.\1/litter. Doses of 100 mg AGP/kg/day stopped vaginal cycling, prevented ovulation in adults, and delayed dissolution of the vaginal membrane in pubertal rats. Histological studies of the ovaries from rats with initial ages of 17 or 21 days which were injected with 25 to 100 mg AGP/kg/day for 2 weeks showed an increase in the number and size of vesicular follicles. Treatment of 27-day-old rats with 25 mg/kg/day for 2 weeks reduced the number of CL and three of four rats given 50 mg had ovaries lacking such bodies; all control ovaries in this group contained CL. These findings are taken as evidence that AGP inhibits ovulation but does not prevent follicular maturation. INTRODUCTION Many pharmacological compounds originally developed as anaesthetics, tranquillizers and anticonvulsants modify endocrine structures and functions (see Gaunt, Chart & Renzi, 1965). -
Mechanisms of Action of Antiepileptic Drugs
Review Mechanisms of action of antiepileptic drugs Epilepsy affects up to 1% of the general population and causes substantial disability. The management of seizures in patients with epilepsy relies heavily on antiepileptic drugs (AEDs). Phenobarbital, phenytoin, carbamazepine and valproic acid have been the primary medications used to treat epilepsy for several decades. Since 1993 several AEDs have been approved by the US FDA for use in epilepsy. The choice of the AED is based primarily on the seizure type, spectrum of clinical activity, side effect profile and patient characteristics such as age, comorbidities and concurrent medical treatments. Those AEDs with broad- spectrum activity are often found to exert an action at more than one molecular target. This article will review the proposed mechanisms of action of marketed AEDs in the US and discuss the future of AEDs in development. 1 KEYWORDS: AEDs anticonvulsant drugs antiepileptic drugs epilepsy Aaron M Cook mechanism of action seizures & Meriem K Bensalem-Owen† The therapeutic armamentarium for the treat- patients with refractory seizures. The aim of this 1UK HealthCare, 800 Rose St. H-109, ment of seizures has broadened significantly article is to discuss the past, present and future of Lexington, KY 40536-0293, USA †Author for correspondence: over the past decade [1]. Many of the newer AED pharmacology and mechanisms of action. College of Medicine, Department of anti epileptic drugs (AEDs) have clinical advan- Neurology, University of Kentucky, 800 Rose Street, Room L-455, tages over older, so-called ‘first-generation’ First-generation AEDs Lexington, KY 40536, USA AEDs in that they are more predictable in their Broadly, the mechanisms of action of AEDs can Tel.: +1 859 323 0229 Fax: +1 859 323 5943 dose–response profile and typically are associ- be categorized by their effects on the neuronal [email protected] ated with less drug–drug interactions. -
A Coniparative Evaluation of Operating Conditions for the Electrochemical Bromination and Chlorination of Succinimide
Bulletin of Electrochemistry 16 (12) December 2000, pp 544-550 0256-1654/2000/$ 3-50 © 2000 CECRI • A CONIPARATIVE EVALUATION OF OPERATING CONDITIONS FOR THE ELECTROCHEMICAL BROMINATION AND CHLORINATION OF SUCCINIMIDE S KRISHNAMOORTHY, R KANAKAM SRINIVASAN AND M NOEL Central Electrochemical Research Institute, Karaikudi 630 006. INDIA [Received: 20 September 1998 Accepted: 19 September 2000] Platinum was found to be the electrode of choice for both electrochlorination and bromination of succinimide leading to the formation of N chloro succinimide (NCS) and N bromo succinimide (NBS) respectively. Because of the competitive processes 150% and 285% of theoretical charge has to be passed for bromination and chlorination respectively. 12% (w!v) of succinimide could be used for bromination while only 2% (w!v) of this reactant is optimum for chlorination. Optimum conditions have been evaluated for the process. A maximum yield of 55% and 88% could be achieved for bromination and chlorination of succinimide respectively. Keywords: •Chlorination, bromination succinimide INTRODUCTION A thermostated closed glass vessel with provIsions for working electrode (platinum, graphite, TSIA and GSLD) Probably because of the facile bromination [1-4] and [14-15], counter electrode, platinum (4 x 3 ems) chlorination [5-9] of succinimide (SI) by chemical means, thermometer and a glass stirrer was used as the the corresponding electrohalogenation process have not preparative cell. received considerable attention. A brief report on the After completion of electrolysis, NCS and NBS are preparation of N- bromosuccinimide (NBS) in aqueous separated by filtration and washed with a cold (275 K) sodium bromide solution on platinum electrode is saturated solution of the corresponding N-halosuccinimide. -
Stems for Nonproprietary Drug Names
USAN STEM LIST STEM DEFINITION EXAMPLES -abine (see -arabine, -citabine) -ac anti-inflammatory agents (acetic acid derivatives) bromfenac dexpemedolac -acetam (see -racetam) -adol or analgesics (mixed opiate receptor agonists/ tazadolene -adol- antagonists) spiradolene levonantradol -adox antibacterials (quinoline dioxide derivatives) carbadox -afenone antiarrhythmics (propafenone derivatives) alprafenone diprafenonex -afil PDE5 inhibitors tadalafil -aj- antiarrhythmics (ajmaline derivatives) lorajmine -aldrate antacid aluminum salts magaldrate -algron alpha1 - and alpha2 - adrenoreceptor agonists dabuzalgron -alol combined alpha and beta blockers labetalol medroxalol -amidis antimyloidotics tafamidis -amivir (see -vir) -ampa ionotropic non-NMDA glutamate receptors (AMPA and/or KA receptors) subgroup: -ampanel antagonists becampanel -ampator modulators forampator -anib angiogenesis inhibitors pegaptanib cediranib 1 subgroup: -siranib siRNA bevasiranib -andr- androgens nandrolone -anserin serotonin 5-HT2 receptor antagonists altanserin tropanserin adatanserin -antel anthelmintics (undefined group) carbantel subgroup: -quantel 2-deoxoparaherquamide A derivatives derquantel -antrone antineoplastics; anthraquinone derivatives pixantrone -apsel P-selectin antagonists torapsel -arabine antineoplastics (arabinofuranosyl derivatives) fazarabine fludarabine aril-, -aril, -aril- antiviral (arildone derivatives) pleconaril arildone fosarilate -arit antirheumatics (lobenzarit type) lobenzarit clobuzarit -arol anticoagulants (dicumarol type) dicumarol -
Membrane Stabilizer Medications in the Treatment of Chronic Neuropathic Pain: a Comprehensive Review
Current Pain and Headache Reports (2019) 23: 37 https://doi.org/10.1007/s11916-019-0774-0 OTHER PAIN (A KAYE AND N VADIVELU, SECTION EDITORS) Membrane Stabilizer Medications in the Treatment of Chronic Neuropathic Pain: a Comprehensive Review Omar Viswanath1,2,3 & Ivan Urits4 & Mark R. Jones4 & Jacqueline M. Peck5 & Justin Kochanski6 & Morgan Hasegawa6 & Best Anyama7 & Alan D. Kaye7 Published online: 1 May 2019 # Springer Science+Business Media, LLC, part of Springer Nature 2019 Abstract Purpose of Review Neuropathic pain is often debilitating, severely limiting the daily lives of patients who are affected. Typically, neuropathic pain is difficult to manage and, as a result, leads to progression into a chronic condition that is, in many instances, refractory to medical management. Recent Findings Gabapentinoids, belonging to the calcium channel blocking class of drugs, have shown good efficacy in the management of chronic pain and are thus commonly utilized as first-line therapy. Various sodium channel blocking drugs, belonging to the categories of anticonvulsants and local anesthetics, have demonstrated varying degrees of efficacy in the in the treatment of neurogenic pain. Summary Though there is limited medical literature as to efficacy of any one drug, individualized multimodal therapy can provide significant analgesia to patients with chronic neuropathic pain. Keywords Neuropathic pain . Chronic pain . Ion Channel blockers . Anticonvulsants . Membrane stabilizers Introduction Neuropathic pain, which is a result of nervous system injury or lives of patients who are affected. Frequently, it is difficult to dysfunction, is often debilitating, severely limiting the daily manage and as a result leads to the progression of a chronic condition that is, in many instances, refractory to medical This article is part of the Topical Collection on Other Pain management. -
Staged Anticonvulsant Screening for Chronic Epilepsy
Staged anticonvulsant screening for chronic epilepsy The Harvard community has made this article openly available. Please share how this access benefits you. Your story matters Citation Berdichevsky, Yevgeny, Yero Saponjian, Kyung#Il Park, Bonnie Roach, Wendy Pouliot, Kimberly Lu, Waldemar Swiercz, F. Edward Dudek, and Kevin J. Staley. 2016. “Staged anticonvulsant screening for chronic epilepsy.” Annals of Clinical and Translational Neurology 3 (12): 908-923. doi:10.1002/acn3.364. http://dx.doi.org/10.1002/ acn3.364. Published Version doi:10.1002/acn3.364 Citable link http://nrs.harvard.edu/urn-3:HUL.InstRepos:30371039 Terms of Use This article was downloaded from Harvard University’s DASH repository, and is made available under the terms and conditions applicable to Other Posted Material, as set forth at http:// nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of- use#LAA RESEARCH ARTICLE Staged anticonvulsant screening for chronic epilepsy Yevgeny Berdichevsky1,a, Yero Saponjian2,3,a, Kyung-Il Park4,a, Bonnie Roach5, Wendy Pouliot5, Kimberly Lu6, Waldemar Swiercz2,3, F. Edward Dudek5 & Kevin J. Staley2,3 1Department of Electrical and Computer Engineering and Bioengineering Program, Lehigh University, Bethlehem, Pennsylvania 18015 2Department of Neurology, Massachusetts General Hospital, Boston, Massachusetts 02129 3Harvard Medical School, Boston, Massachusetts 02129 4Department of Neurology, Seoul National University Hospital Healthcare System Gangnam Center, Seoul, South Korea 06236 5Department of Neurosurgery, University of Utah School of Medicine, Salt Lake City, Utah 84108 6Boston University School of Medicine, Boston, Massachusetts 02119 Correspondence Abstract Kevin J. Staley, Department of Neurology, Massachusetts General Hospital, Boston, MA Objective: Current anticonvulsant screening programs are based on seizures 02129. -
Treatment of Myoclonus with Pheneturide
J Neurol Neurosurg Psychiatry: first published as 10.1136/jnnp.41.7.598 on 1 July 1978. Downloaded from Journal ofNeurology, Neurosurgery, andPsychiatry, 1978, 41, 598-602 Treatment of myoclonus with pheneturide C. D. WARD From the Royal Hospital, Sheffield S U M M A R Y Twenty-one patients with various forms of myoclonus are presented. Phena- cemide was given to five patients with considerable benefit to three, but with serious toxic effects in two. Another acetylurea derivative, pheneturide, was given to 19 patients and was well tolerated. Myoclonus was completely or substantially controlled in 12 patients. The term "myoclonus" may be applied to very between 1965 and 1976. They had displayed myo- abrupt involuntary movements which are neur- clonic jerks and had been treated with phena- onally determined, asynergic, and arrhythmic. An cemide or pheneturide. Of these patients, 16 were assortment of involuntary movements share these seen personally for review and three responded to characteristics but differ in their relationship to a questionnaire. Records of outpatient follow-up movement, relaxation, posture, or sensory stimuli, were available for one patient who had died and Protected by copyright. and in their anatomical disposition (Gasaut, 1968); for one who could not be traced. All had given a they may involve parts of muscles, whole muscles, history of repeated, instantaneous involuntary or, more usually, muscle groups. Such movements, movements and had reported at least one of the collectively termed myoclonus, are seen in a wide following: sudden jerks of the arms causing ob- variety of pathological conditions (Halliday, 1967) jects to fly out of the hands; sudden interruption and may often be associated with epilepsy.