JPWO2021091585A5 - - Google Patents

Download PDF

Info

Publication number
JPWO2021091585A5
JPWO2021091585A5 JP2022526009A JP2022526009A JPWO2021091585A5 JP WO2021091585 A5 JPWO2021091585 A5 JP WO2021091585A5 JP 2022526009 A JP2022526009 A JP 2022526009A JP 2022526009 A JP2022526009 A JP 2022526009A JP WO2021091585 A5 JPWO2021091585 A5 JP WO2021091585A5
Authority
JP
Japan
Prior art keywords
pain
cough
chronic
pharmaceutical composition
syndrome
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2022526009A
Other languages
Japanese (ja)
Other versions
JP2023500891A (en
Publication date
Application filed filed Critical
Priority claimed from PCT/US2020/021978 external-priority patent/WO2021091585A1/en
Publication of JP2023500891A publication Critical patent/JP2023500891A/en
Publication of JPWO2021091585A5 publication Critical patent/JPWO2021091585A5/ja
Pending legal-status Critical Current

Links

Claims (6)

患者に、請求項1記載の化合物の有効量を投与する工程を含む、患者において疼痛、咳、かゆみまたは神経性炎症性障害を治療する方に使用するための、請求項17または18記載の医薬組成物 19. A compound according to claim 17 or 18 for use in a method of treating pain, cough, itch or neuroinflammatory disorders in a patient comprising administering to the patient an effective amount of a compound according to claim 1. pharmaceutical composition of 該疼痛が、背頸部疼痛、腰部疼痛、癌の疼痛、婦人科学および分娩の疼痛、線維筋痛症、関節炎、関節リウマチ、変形性関節症、リウマチ学的疼痛、整形外科的疼痛、急性のヘルペス後神経痛および他のニューロパシー疼痛(末梢ニューロパシーなど)、鎌状赤血球発症、外陰痛、肛門周囲の疼痛、過敏性腸疾患、過敏性腸症候群、炎症性腸疾患、口腔粘膜炎、食道炎、間質性膀胱炎、尿道炎および他の泌尿器科学的疼痛、歯痛、頭痛、三叉神経栄養障害症候群、先端紅痛症、腹部壁の疼痛、慢性の腹部壁の疼痛、アレルギー性鼻炎、筋肉痛、直腸の疼痛、肛門挙筋症候群、一過性直腸痛、痔痛、胃痛、皮膚潰瘍、胃潰瘍、熱傷痛、眼の過敏、結膜炎(例えばアレルギー性結膜炎)、眼の赤み、ドライアイ、眼乾燥症候群(慢性の眼の疼痛)、複合局所疼痛症候群、外科手術後の眼の疼痛、術後の疼痛、急性の術後の疼痛、および処置による疼痛(すなわち注射、膿瘍の排液、外科的手術、歯科的処置、眼の処置、眼の過敏、結膜炎(例えばアレルギー性結膜炎)、眼の赤み、ドライアイ、関節鏡検査および他の医療機器の使用、美容外科的処置、皮膚科学的処置、骨折の硬化、生検等に関連する疼痛)のための疼痛からなる群より選択される、請求項19記載の医薬組成物The pain is back and neck pain, lower back pain, cancer pain, gynecological and labor pain, fibromyalgia, arthritis, rheumatoid arthritis, osteoarthritis, rheumatic pain, orthopedic pain, acute Postherpetic neuralgia and other neuropathic pain (including peripheral neuropathy), sickle cell disease, vulvar pain, perianal pain, irritable bowel disease, irritable bowel syndrome, inflammatory bowel disease, oral mucositis, esophagitis, interstitial Qualitative cystitis, urethritis and other urological pain, toothache, headache, trigeminal neurotrophic syndrome, erythromelalgia, abdominal wall pain, chronic abdominal wall pain, allergic rhinitis, myalgia, rectum pain, levator ani syndrome, transient rectal pain, hemorrhoidal pain, stomach pain, skin ulcer, gastric ulcer, burn pain, eye sensitivity, conjunctivitis (e.g. allergic conjunctivitis), eye redness, dry eye, dry eye syndrome (chronic ocular pain), complex regional pain syndrome, post-surgical ocular pain, post-operative pain, acute post-operative pain, and procedural pain (i.e. injections, abscess drainage, surgery, dental procedures, eye procedures, eye sensitivity, conjunctivitis (e.g. allergic conjunctivitis), eye redness, dry eyes, arthroscopy and other medical device use, cosmetic surgery, dermatological procedures, bone fractures 20. The pharmaceutical composition according to claim 19, selected from the group consisting of pain for induration, pain associated with biopsies, etc.). 該咳が、喘息、COPD、喘息-COPDオーバーラップ症候群(ACOS)、間質性肺線維症(IPF)、特発性肺線維症、ウイルス後の咳、感染後の咳、慢性特発性の咳および肺癌を有する患者における咳からなる群より選択される、請求項19記載の医薬組成物the cough is asthma, COPD, asthma-COPD overlap syndrome (ACOS), interstitial pulmonary fibrosis (IPF), idiopathic pulmonary fibrosis, postviral cough, postinfectious cough, chronic idiopathic cough and 20. The pharmaceutical composition according to claim 19, selected from the group consisting of cough in patients with lung cancer. 該かゆみが、そう痒、腕橈骨筋そう痒、慢性特発性のそう痒、生殖器/肛門のそう痒、背部感覚異常、頭皮そう痒、アレルギー性皮膚炎、接触皮膚炎、アトピー性皮膚炎、手湿疹、ツタウルシ、感染、寄生虫、昆虫の噛み傷、妊娠、代謝性障害、肝臓または腎臓の不全、薬物反応、アレルギー反応、湿疹、生殖器および肛門のかゆみ、痔のかゆみ、および癌のためのかゆみからなる群より選択される、請求項19記載の医薬組成物The itch is pruritus, brachioradialis pruritus, chronic idiopathic pruritus, genital/anal pruritus, back paresthesia, scalp pruritus, allergic dermatitis, contact dermatitis, atopic dermatitis, hands Itching due to eczema, poison ivy, infections, parasites, insect bites, pregnancy, metabolic disorders, liver or kidney failure, drug reactions, allergic reactions, eczema, genital and anal itching, hemorrhoids, and cancer 20. The pharmaceutical composition of claim 19, selected from the group consisting of 該神経性炎症性障害が、アレルギー性炎症、喘息、慢性の咳、結膜炎、鼻炎、乾癬、炎症性腸疾患、間質性膀胱炎、関節炎、大腸炎、接触皮膚炎、糖尿病、湿疹、膀胱炎、胃炎、片頭痛、しゅさ、日焼け、膵炎、慢性の鼻副鼻腔炎(rhinosinusistis)、外傷性脳損傷、複数細菌性敗血症、腱障害、慢性じんま疹、リウマチ性疾患、急性肺損傷、刺激物への暴露、刺激物、汚染物質、化学兵器剤の吸入、およびアトピー皮膚炎からなる群より選択される、請求項19記載の医薬組成物The neuroinflammatory disorder is allergic inflammation, asthma, chronic cough, conjunctivitis, rhinitis, psoriasis, inflammatory bowel disease, interstitial cystitis, arthritis, colitis, contact dermatitis, diabetes, eczema, cystitis , gastritis, migraine, rosacea, sunburn, pancreatitis, chronic rhinosinusitis, traumatic brain injury, polybacterial sepsis, tendon disorders, chronic urticaria, rheumatic disease, acute lung injury, irritation 20. The pharmaceutical composition of claim 19, selected from the group consisting of exposure to substances, irritants, pollutants, inhalation of chemical warfare agents, and atopic dermatitis. 式(I)で表される化合物が、1つ以上の外因性大孔型受容体アゴニストと組み合わせて使用される、請求項19記載の医薬組成物20. A pharmaceutical composition according to claim 19, wherein the compound of formula (I) is used in combination with one or more exogenous large pore receptor agonists.
JP2022526009A 2019-11-06 2020-03-11 Charged ion channel blockers and methods of use Pending JP2023500891A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201962931444P 2019-11-06 2019-11-06
US62/931,444 2019-11-06
PCT/US2020/021978 WO2021091585A1 (en) 2019-11-06 2020-03-11 Charged ion channel blockers and methods for use

Publications (2)

Publication Number Publication Date
JP2023500891A JP2023500891A (en) 2023-01-11
JPWO2021091585A5 true JPWO2021091585A5 (en) 2023-03-03

Family

ID=73462106

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2022526009A Pending JP2023500891A (en) 2019-11-06 2020-03-11 Charged ion channel blockers and methods of use

Country Status (11)

Country Link
US (2) US10842798B1 (en)
EP (1) EP4054559A4 (en)
JP (1) JP2023500891A (en)
KR (1) KR20220123381A (en)
CN (1) CN114828845A (en)
AU (1) AU2020380118A1 (en)
BR (1) BR112022008575A2 (en)
CA (1) CA3155586A1 (en)
IL (1) IL292505A (en)
MX (1) MX2022005335A (en)
WO (1) WO2021091585A1 (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2022527690A (en) 2019-03-11 2022-06-03 ノシオン セラピューティクス,インコーポレイテッド Charged ion channel blockers and usage
MA55320A (en) 2019-03-11 2022-01-19 Nocion Therapeutics Inc ESTER SUBSTITUTED ION CHANNEL BLOCKERS AND METHODS OF USE
EP3937945A4 (en) 2019-03-11 2023-01-04 Nocion Therapeutics, Inc. Charged ion channel blockers and methods for use
US10933055B1 (en) 2019-11-06 2021-03-02 Nocion Therapeutics, Inc. Charged ion channel blockers and methods for use
CN114828845A (en) * 2019-11-06 2022-07-29 诺西恩医疗公司 Charged ion channel blockers and methods of use thereof
JP2023517604A (en) 2020-03-11 2023-04-26 ノシオン セラピューティクス,インコーポレイテッド Charged ion channel blockers and methods of use
CN117586223A (en) * 2022-08-16 2024-02-23 四川大学 Phenylthiazine compound and application thereof

Family Cites Families (183)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE151036C (en)
DE150423C (en)
US1889645A (en) 1930-12-22 1932-11-29 Winthrop Chem Co Inc Beta-dimethylaminoethyl ester of para-butylamino-benzoic acid
US2441498A (en) 1943-07-15 1948-05-11 Astra Apotekarnes Kem Fab Alkyl glycinanilides
US2689248A (en) 1950-06-17 1954-09-14 Sterling Drug Inc Tertiary-aminoalkyl 4-amino-2-alkoxybenzoates and their synth esis
GB692332A (en) 1950-07-18 1953-06-03 Geigy Ag J R Improvements relating to quaternary ammonium compounds, and their uses
US2774770A (en) 1951-09-20 1956-12-18 Smith Kline French Lab Sulfur-containing amines
CH311610A (en) 1952-02-25 1955-11-30 Cilag Ag Process for the production of a new basic substituted fatty acid (2-halogen-6-methyl-anilide).
CH311608A (en) 1952-02-25 1955-11-30 Cilag Ag Process for the production of a new basic substituted fatty acid (2-halogen-6-methyl-anilide).
CH311612A (en) 1952-02-25 1955-11-30 Cilag Ag Process for the production of a new basic substituted fatty acid (2-halogen-6-methyl-anilide).
CH311606A (en) 1952-02-25 1955-11-30 Cilag Ag Process for the production of a new basic substituted fatty acid (2-halogen-6-methyl-anilide).
CH311609A (en) 1952-02-25 1955-11-30 Cilag Ag Process for the production of a new basic substituted fatty acid (2-halogen-6-methyl-anilide).
CH311613A (en) 1952-02-25 1955-11-30 Cilag Ag Process for the production of a new basic substituted fatty acid (2-halogen-6-methyl-anilide).
CH311611A (en) 1952-02-25 1955-11-30 Cilag Ag Process for the production of a new basic substituted fatty acid (2-halogen-6-methyl-anilide).
CH311614A (en) 1952-02-25 1955-11-30 Cilag Ag Process for the production of a new basic substituted fatty acid (2-halogen-6-methyl-anilide).
CH311615A (en) 1952-02-25 1955-11-30 Cilag Ag Process for the production of a new basic substituted fatty acid (2-halogen-6-methyl-anilide).
CH311607A (en) 1952-02-25 1955-11-30 Cilag Ag Process for the production of a new basic substituted fatty acid (2-halogen-6-methyl-anilide).
US2759975A (en) 1952-05-28 1956-08-21 Gen Aniline & Film Corp Mixed alkyl-benzyl-alkylol quaternary ammonium salts
US2783230A (en) 1953-03-16 1957-02-26 Hoffmann La Roche Derivatives of meta hydroxy aniline
GB751522A (en) 1953-03-16 1956-06-27 Roche Products Ltd Novel derivatives of úÝ-hydroxy-aniline and the manufacture thereof
GB756538A (en) 1953-12-24 1956-09-05 Bayer Ag Alkylation of aromatic amines
US2799679A (en) 1955-04-28 1957-07-16 Bofors Ab Process of preparing amides of heterocyclic carboxylic acids
US2955111A (en) 1957-01-28 1960-10-04 Bofors Ab Synthesis of n-alkyl-piperidine and n-alkyl-pyrrolidine-alpha-carboxylic acid amides
US3160662A (en) 1957-06-26 1964-12-08 Astra Apotekarnes Kem Fab Lower alkylaminoacyl amide anesthetics
GB895601A (en) 1957-11-20 1962-05-02 Sterling Drug Inc N[n-(monocarbocyclic aryl) carbamyl-lower-alkyl] amines and their preparation
DE1146872B (en) 1959-01-29 1963-04-11 Bayer Ag Process for the production of organic isocyanates
US3049546A (en) 1959-03-05 1962-08-14 Geigy Chem Corp Process for the decarbalkoxylation of alkyl esters of unsaturated, nitrogencontaining carboxylic acids
US3264309A (en) 1959-08-24 1966-08-02 Sterling Drug Inc N' [nu-(monocarbocyclic aryl) carbamyllower-alkyl]-1, 5-iminocycloalkanes, -iminocycloalkenes and related compounds
US3080327A (en) 1959-11-20 1963-03-05 T & H Smith Ltd Quaternary salts as denaturants for organic substances
NL281394A (en) 1961-07-25
DE1251764B (en) 1965-08-18 1967-10-12 C H Boehnnger Sohn Ingelheim/ Rhein Process for the production of antimicrobially active 12 3,4-Tetra hydro 9 -ammo acridmiumverbmdungen
GB1221061A (en) 1967-01-18 1971-02-03 May & Baker Ltd Quaternary ammonium derivatives, their use as anthelmintics and methods for their preparation
US3574216A (en) 1968-04-12 1971-04-06 American Home Prod Quaternary 3-pyridinium-2-quinolones
US3812147A (en) 1970-12-22 1974-05-21 Astra Pharma Prod Acylxylidide local anaesthetics
US3931195A (en) 1971-03-03 1976-01-06 Mead Johnson & Company Substituted piperidines
BE786875A (en) 1971-07-28 1973-01-29 Astra Pharma Prod AMIDE, METHOD FOR ITS PREPARATION AND ITS THERAPEUTIC COMPOSITIONS
US3773939A (en) 1971-11-24 1973-11-20 Janssen Pharmaceutica Nv N-arallyl-n'-aralkyl piperazine pharmaceutical compositions
US4069309A (en) 1972-09-19 1978-01-17 Avon Products, Inc. Cationic skin substantive sunscreen composition and method
US3900481A (en) 1974-04-01 1975-08-19 Riker Laboratories Inc Derivatives of pyrrolidine and piperidine
US4005038A (en) 1974-04-15 1977-01-25 Peerless Paint And Varnish Corporation Paint composition containing denatonium benzoate or lignocaine benzyl octanoate with a latex resin binder for application over old paint films to prevent ingestion of poisons therefrom
ZA767606B (en) 1975-12-23 1977-11-30 Ciba Geigy Ag Compositions for influencing plant growth
CS195321B2 (en) 1975-12-23 1980-01-31 Ciba Geigy Ag Plant growth suppressing agents
US4070347A (en) 1976-08-16 1978-01-24 Alza Corporation Poly(orthoester) co- and homopolymers and poly(orthocarbonate) co- and homopolymers having carbonyloxy functionality
US4147792A (en) 1977-02-04 1979-04-03 Ciba-Geigy Corporation Fungicidal compositions
DE2915250A1 (en) 1979-04-14 1980-10-30 Basf Ag SALTS OF ALPHA -AMINOACETANILIDES
US4293539A (en) 1979-09-12 1981-10-06 Eli Lilly And Company Controlled release formulations and method of treatment
US4877805A (en) 1985-07-26 1989-10-31 Kligman Albert M Methods for treatment of sundamaged human skin with retinoids
US4757128A (en) 1986-08-01 1988-07-12 Massachusetts Institute Of Technology High molecular weight polyanhydride and preparation thereof
US5169637A (en) 1983-03-24 1992-12-08 The Liposome Company, Inc. Stable plurilamellar vesicles
ATE40994T1 (en) 1983-08-01 1989-03-15 Astra Laekemedel Ab L-N-N-PROPYLPIPECOLIC-2,6-XYLIDIDE AND ITS PRODUCTION.
CA1237671A (en) 1983-08-01 1988-06-07 Michael W. Fountain Enhancement of pharmaceutical activity
US4975282A (en) 1985-06-26 1990-12-04 The Liposome Company, Inc. Multilamellar liposomes having improved trapping efficiencies
US5409704A (en) 1985-06-26 1995-04-25 The Liposome Company, Inc. Liposomes comprising aminoglycoside phosphates and methods of production and use
US5023087A (en) 1986-02-10 1991-06-11 Liposome Technology, Inc. Efficient method for preparation of prolonged release liposome-based drug delivery system
IE60901B1 (en) 1986-08-21 1994-08-24 Vestar Inc Improved treatment of systemic fungal infections with phospholipid particles encapsulating polyene antifungal antibiotics
US5049388A (en) 1986-11-06 1991-09-17 Research Development Foundation Small particle aerosol liposome and liposome-drug combinations for medical use
US5032582A (en) 1987-02-27 1991-07-16 Liposome Technology, Inc. Method for treating fungal infections with amphotericin B/cholesterol sulfate composition
GB8727504D0 (en) 1987-11-24 1987-12-23 Glaxo Group Ltd Chemical compositions
US4994213A (en) 1988-05-17 1991-02-19 Liposome Technology, Inc. Method of preparing lipid structures
US4980378A (en) 1988-06-01 1990-12-25 Odontex, Inc. Biodegradable absorption enhancers
US5082866A (en) 1988-06-01 1992-01-21 Odontex, Inc. Biodegradable absorption enhancers
US5194581A (en) 1989-03-09 1993-03-16 Leong Kam W Biodegradable poly(phosphoesters)
US5194266A (en) 1989-08-08 1993-03-16 Liposome Technology, Inc. Amphotericin B/cholesterol sulfate composition and method
US5356633A (en) 1989-10-20 1994-10-18 Liposome Technology, Inc. Method of treatment of inflamed tissues
DK0580817T3 (en) 1991-04-19 1996-08-05 Nexstar Pharmaceuticals Inc Pharmaceutical composition and method of preparation thereof
US5176907A (en) 1991-08-13 1993-01-05 The Johns Hopkins University School Of Medicine Biocompatible and biodegradable poly (phosphoester-urethanes)
GR1002207B (en) 1992-08-06 1996-03-27 Johnson & Johnson Consumer Skin care compositions containing imidazoles.
US5552155A (en) 1992-12-04 1996-09-03 The Liposome Company, Inc. Fusogenic lipsomes and methods for making and using same
US5480971A (en) 1993-06-17 1996-01-02 Houghten Pharmaceuticals, Inc. Peralkylated oligopeptide mixtures
US5409805A (en) 1993-07-29 1995-04-25 Konica Corporation Solid processing agent for silver halide photographic light-sensitive materials
US6051576A (en) 1994-01-28 2000-04-18 University Of Kentucky Research Foundation Means to achieve sustained release of synergistic drugs by conjugation
US5591317A (en) 1994-02-16 1997-01-07 Pitts, Jr.; M. Michael Electrostatic device for water treatment
US5716622A (en) 1995-01-06 1998-02-10 The Rockefeller University Functionally active regions of signal transducer and activators of transcription
US5783683A (en) 1995-01-10 1998-07-21 Genta Inc. Antisense oligonucleotides which reduce expression of the FGFRI gene
US5747470A (en) 1995-06-07 1998-05-05 Gen-Probe Incorporated Method for inhibiting cellular proliferation using antisense oligonucleotides to gp130 mRNA
AU5938996A (en) 1995-06-07 1996-12-30 Nexstar Pharmaceuticals, Inc. Method for encapsulating pharmaceutical materials
US6413961B1 (en) 1995-12-12 2002-07-02 Omeros Medical Systems, Inc. Irrigation solution and method for inhibition of pain and inflammation
SE508357C2 (en) 1996-01-02 1998-09-28 Kay Laserow Measuring instruments for measuring pain and a method for measuring pain with a measuring instrument
WO1998024428A1 (en) 1996-12-02 1998-06-11 Brigham & Women's Hospital, Inc. Long-acting local anesthetics
SE9604751D0 (en) 1996-12-20 1996-12-20 Astra Ab New therapy
US5837713A (en) 1997-02-26 1998-11-17 Mayo Foundation For Medical Education And Research Treatment of eosinophil-associated pathologies by administration of topical anesthetics and glucocorticoids
DE69805071T2 (en) 1997-06-18 2002-11-14 Guilford Pharm Inc TWO-STAGE SOLUTION POLYMERIZATION OF HIGH MOLECULAR POLY (PHOSPHORESTERS)
RU2105554C1 (en) 1997-06-24 1998-02-27 Всероссийский научный центр по безопасности биологически активных веществ N-(2,4,6-trimethylphenylcarbamoylmethyl)-n-allylmorpholinium bromide showing antiischemic and antiarrhythmic effects at ischemic heart disease and a method of its synthesis
US6028163A (en) 1997-06-27 2000-02-22 Guilford Pharmaceuticals Inc. Solution polymerization of high molecular weight poly(phosphoesters) in toluene
EP0997147B1 (en) 1997-07-08 2006-03-15 Ono Pharmaceutical Co., Ltd. Amino acid derivatives
TW536401B (en) 1997-09-03 2003-06-11 Cardiome Pharma Corp A pharmaceutical composition of N,N-bis(phenylcarbamoylmethyl)dimethylammomum chloride and derivatives for the treatment of pain
US6623040B1 (en) 1997-09-03 2003-09-23 Recot, Inc. Method for determining forced choice consumer preferences by hedonic testing
US5891919A (en) 1997-09-19 1999-04-06 Burlington Bio-Medical & Scientific Corp. Denatonium capsaicinate and methods of producing the same
US6083996A (en) 1997-11-05 2000-07-04 Nexmed Holdings, Inc. Topical compositions for NSAI drug delivery
US6140351A (en) 1997-12-19 2000-10-31 Berlex Laboratories, Inc. Ortho-anthranilamide derivatives as anti-coagulants
US6207290B1 (en) 1998-04-07 2001-03-27 Burlington Bio-Medical & Scientific Corp. Antifoulant compositions and methods of treating wood
AU762127B2 (en) * 1998-06-09 2003-06-19 Nortran Pharmaceuticals Inc. Compositions and methods for treatment of cough
JP2000143635A (en) 1998-06-10 2000-05-26 Takeda Chem Ind Ltd Arterialization inhibitor
US6153212A (en) 1998-10-02 2000-11-28 Guilford Pharmaceuticals Inc. Biodegradable terephthalate polyester-poly (phosphonate) compositions, articles, and methods of using the same
US7507545B2 (en) 1999-03-31 2009-03-24 Cardiome Pharma Corp. Ion channel modulating activity method
US6103255A (en) 1999-04-16 2000-08-15 Rutgers, The State University Porous polymer scaffolds for tissue engineering
US6118020A (en) 1999-05-19 2000-09-12 Nexmed Holdings, Inc. Crystalline salts of dodecyl 2-(N,N-dimethylamino)-propionate
EP1216243A1 (en) 1999-10-01 2002-06-26 Advanced Medicine, Inc. Quinazolinones and analogues and their use as local anesthetics
EE200200314A (en) 1999-12-15 2003-08-15 Ucb Farchim S.A. Cyclic quaternary ammonium compounds
CN1423641A (en) 1999-12-15 2003-06-11 Ucb法奇姆股份有限公司 Quaternary salts of N-substituted cyclic or acyclic amines as pharmaceuticals
AU3162001A (en) 1999-12-21 2001-07-03 Id-Pharma Gmbh Medicament, a method for its production and the use thereof
WO2001083828A1 (en) 2000-05-04 2001-11-08 Dzgenes, Llc TGFβ-RII PROMOTER POLYMORPHISMS
AU7138601A (en) 2000-06-23 2002-01-08 Mayo Foundation Methods of treating neutrophil-related diseases with topical anesthetics
DE10039449A1 (en) 2000-08-11 2003-07-24 Id Pharma Gmbh I Ins Pharmaceutical composition, useful for the treatment or prevention of hyperalgesia, comprises an infusion solution of local anesthetic adjusted to alkaline pH
WO2002026712A2 (en) 2000-09-29 2002-04-04 Millennium Pharmaceuticals, Inc. Quaternary amines and related inhibitors of factor xa
US6766319B1 (en) 2000-10-31 2004-07-20 Robert J. Might Method and apparatus for gathering and evaluating information
US6884782B2 (en) 2000-11-08 2005-04-26 Amgen Inc. STAT modulators
WO2002058670A1 (en) 2001-01-25 2002-08-01 Euroceltique S.A. Local anesthetic, and method of use
US20040146590A1 (en) 2001-03-22 2004-07-29 Iadarola Michael J Molecular neurochirurgie for pain control administering locally capsaicin or resinferatoxin
CA2446060A1 (en) 2001-05-07 2002-11-14 Corium International Compositions and delivery systems for administration of a local anesthetic agent
US6825190B2 (en) 2001-06-15 2004-11-30 Vertex Pharmaceuticals Incorporated Protein kinase inhibitors and uses thereof
US7157103B2 (en) 2001-08-06 2007-01-02 Euro-Celtique S.A. Pharmaceutical formulation containing irritant
US20030068276A1 (en) 2001-09-17 2003-04-10 Lyn Hughes Dosage forms
ITMI20012025A1 (en) 2001-09-28 2003-03-28 Dompe Spa QUATERNARY AMMONIUM SALTS OF OMEGA-AMINO ALKYLAMIDS OF R 2-ARY-PROPIONIC ACIDS AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
US7585511B2 (en) 2002-08-02 2009-09-08 Universite Libre De Bruxelles Apolipoprotein L-I and/or derivated polypeptide for the treatment of and/or the prevention of diseases induced by trypanosoma
AU2003286757B2 (en) 2002-11-01 2009-06-04 Merck Sharp & Dohme Corp. Carbonylamino-benzimidazole derivatives as androgen receptor modulators
US7943166B2 (en) 2003-04-10 2011-05-17 Neurogesx, Inc. Methods and compositions for administration of TRPV1 agonists
US20040220187A1 (en) 2003-04-22 2004-11-04 Pharmacia Corporation Compositions of a cyclooxygenase-2 selective inhibitor and a sodium ion channel blocker for the treatment of pain, inflammation or inflammation mediated disorders
ES2223277B1 (en) 2003-06-19 2006-03-01 Fernando Bouffard Fita ANESTHETIC COMPOSITION FOR TOPICAL ADMINISTRATION.
WO2005014849A2 (en) 2003-07-03 2005-02-17 Euro-Celtique, S.A. Genes associated with responses to neuropathic pain
US8361467B2 (en) 2003-07-30 2013-01-29 Depuy Spine, Inc. Trans-capsular administration of high specificity cytokine inhibitors into orthopedic joints
NO20034069L (en) 2003-09-12 2005-03-14 Aximed As Preparation and use of capsaicin derivatives
US20070149469A1 (en) 2003-10-02 2007-06-28 Christian Korherr Medical use of tbk-1 or of inhibitors thereof
US20050142596A1 (en) 2003-11-14 2005-06-30 Krolewski Andrzej S. Methods of diagnosing renal and cardiovascular disease
JP4751336B2 (en) 2003-12-11 2011-08-17 ボード・オブ・リージエンツ,ザ・ユニバーシテイ・オブ・テキサス・システム Compound for treating cell proliferative disorders
US20070196866A1 (en) 2004-03-13 2007-08-23 Irm Llc Modulators of ion channel trpa1
US7161034B2 (en) 2004-04-20 2007-01-09 Dade Behring Inc. Lidocaine analogs and methods of making and using same
US20060106020A1 (en) 2004-04-28 2006-05-18 Rodgers James D Tetracyclic inhibitors of Janus kinases
ES2542847T3 (en) 2004-06-02 2015-08-12 Neurogesx Inc. Formulations comprising capsaicin, a local anesthetic and / or an antipruritic agent for the treatment of pain
RU2258700C1 (en) 2004-06-28 2005-08-20 Государственное образовательное учреждение высшего профессионального образования "Мордовский государственный университет им. Н.П. Огарева" Quaternary ammonium derivative of lidocaine eliciting anti-arrhythmic activity and method for its preparing
MX2007000793A (en) 2004-07-24 2007-03-21 Esteve Labor Dr Use of compounds active on the sigma receptor for the treatment of mechanical allodynia.
ITMI20041566A1 (en) 2004-07-30 2004-10-30 Indena Spa "TRPV1 AGONISTS, FORMULATIONS THAT CONTAIN THEM AND THEIR USES"
JP2008513444A (en) 2004-09-20 2008-05-01 コラス ファーマ インコーポレイテッド Methods for targeted delivery of lidocaine and other local anesthetics and treatment of cough and cough attacks
US7947682B2 (en) 2004-12-29 2011-05-24 University Of Southern California Substituted N′-pyrrolo[1,2-a]quinoxalin-4-yl-hydrazides as anti-cancer agents
US20090306429A1 (en) 2004-12-06 2009-12-10 Henk Pluim Preparation of a quaternary ammonium hydroxide and use thereof for the preparation of a quaternary ammonium salt
EP1824466A4 (en) 2004-12-16 2008-03-05 Advanced Inhalation Res Inc Compositions and methods for pulmonary conditions
AR054416A1 (en) 2004-12-22 2007-06-27 Incyte Corp PIRROLO [2,3-B] PIRIDIN-4-IL-AMINAS AND PIRROLO [2,3-B] PIRIMIDIN-4-IL-AMINAS AS INHIBITORS OF THE JANUS KINASES. PHARMACEUTICAL COMPOSITIONS.
WO2006133588A1 (en) 2005-06-13 2006-12-21 Oncalis Ag ARYL UREA COMPOUNDS AS β-SECRETASE INHIBITORS
GB0517966D0 (en) 2005-09-02 2005-10-12 Novartis Ag Organic compounds
US20070149506A1 (en) 2005-09-22 2007-06-28 Arvanitis Argyrios G Azepine inhibitors of Janus kinases
CN104278037B (en) 2005-10-12 2020-09-15 艾德拉药物股份有限公司 Immunomodulatory oligonucleotide (IRO) compounds for modulating Toll-like receptors based on variant response
TWI468162B (en) 2005-12-13 2015-01-11 英塞特公司 Heteroaryl substituted pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidines as janus kinase inhibitors
CA2634491A1 (en) 2005-12-21 2007-06-28 Painceptor Pharma Corporation Compositions and methods for modulating gated ion channels
GB0526244D0 (en) 2005-12-22 2006-02-01 Novartis Ag Organic compounds
EP1867338A1 (en) 2006-05-30 2007-12-19 Université Libre De Bruxelles Pharmaceutical composition comprising apolipoproteins for the treatment of human diseases
JP2010510227A (en) 2006-11-20 2010-04-02 プレジデント アンド フェロウズ オブ ハーバード カレッジ Pain and itching treatment methods, compositions and kits
US8513270B2 (en) 2006-12-22 2013-08-20 Incyte Corporation Substituted heterocycles as Janus kinase inhibitors
GB0702382D0 (en) 2007-02-07 2007-03-21 Argenta Discovery Ltd New salt
DE602008000809D1 (en) 2007-03-23 2010-04-29 Icagen Inc Ion channel inhibitors
EP3184527B1 (en) 2007-06-22 2020-01-29 Eli Lilly and Company 2,6-dioxo,-2,3-dihydro-1h-purine compounds useful for treating disorders related to the activity of the trpa1 channel
WO2009026107A1 (en) 2007-08-17 2009-02-26 Portola Pharmaceuticals, Inc. Protein kinase inhibitors
CN101156851A (en) 2007-09-27 2008-04-09 刘全胜 Nicardipine hydrochloride dispersion piece and method for making same
WO2009114139A2 (en) 2008-03-11 2009-09-17 President And Fellows Of Harvard College Methods, compositions, and kits for treating pain and pruritis
US8138339B2 (en) 2008-04-16 2012-03-20 Portola Pharmaceuticals, Inc. Inhibitors of protein kinases
US8258144B2 (en) 2008-04-22 2012-09-04 Portola Pharmaceuticals, Inc. Inhibitors of protein kinases
WO2009140519A1 (en) 2008-05-14 2009-11-19 Hydra Biosciences, Inc. Compounds and compositions for treating chemical warfare agent-induced injuries
EP2307367B1 (en) 2008-07-08 2014-09-24 Board of Regents, The University of Texas System Novel inhibitors of proliferation and activation of signal transducer and activator of transcription (stats)
DE102008037682A1 (en) 2008-08-14 2010-04-08 Strackharn, Klaus, Dr.med. Use of equipotent doses of local anesthetics or derivatives thereof for the treatment of chronic pain
CN101347427A (en) 2008-09-22 2009-01-21 北京理工大学 Compound of losartan compound or its medical salt and calcium channel blocker or its medical salt
CL2009001884A1 (en) 2008-10-02 2010-05-14 Incyte Holdings Corp Use of 3-cyclopentyl-3- [4- (7h-pyrrolo [2,3-d] pyrimidin-4-yl) -1h-pyrazol-1-yl) propanonitrile, janus kinase inhibitor, and use of a composition that understands it for the treatment of dry eye.
CA2738816A1 (en) 2008-10-06 2010-04-15 Idera Pharmaceuticals, Inc. Use of inhibitors of toll-like receptors in the prevention and treatment of hypercholesterolemia and hyperlipidemia and diseases related thereto
EP2411019A2 (en) 2009-03-27 2012-02-01 Merck Sharp&Dohme Corp. RNA INTERFERENCE MEDIATED INHIBITION OF SIGNAL TRANSDUCER AND ACTIVATOR OF TRANSCRIPTION 1 (STAT1) GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACID (siNA)
WO2011006073A1 (en) 2009-07-10 2011-01-13 President And Fellows Of Harvard College Permanently charged sodium and calcium channel blockers as anti-inflammatory agents
US9023355B2 (en) 2010-04-13 2015-05-05 Beth Israel Deaconess Medical Center, Inc. Compositions and methods for treating renal disease
US9828637B2 (en) 2010-04-18 2017-11-28 Wake Forest University Health Sciences Methods of predicting predisposition to or risk of kidney disease
US20130225578A1 (en) 2010-09-01 2013-08-29 Ambit Biosciences Corporation 7-cyclylquinazoline derivatives and methods of use thereof
US8916565B2 (en) 2011-02-02 2014-12-23 Vertex Pharmaceuticals Incorporated Pyrrolopyrazine-spirocyclic piperidine amides as modulators of ion channels
DK2771320T3 (en) * 2011-10-24 2016-10-03 Endo Pharmaceuticals Inc Cyclohexylamines
WO2013064884A1 (en) 2011-10-31 2013-05-10 Purdue Pharma L.P. Quaternized amines as sodium channel blockers
WO2013130808A1 (en) 2012-02-29 2013-09-06 D.E. Shaw Research, Llc Methods for screening voltage gated proteins
EP2882429B1 (en) 2012-08-07 2024-04-10 The General Hospital Corporation Potassium-channel openers for use in treating amyotrophic lateral sclerosis (ALS)
WO2014044849A1 (en) 2012-09-24 2014-03-27 Boehringer Ingelheim International Gmbh Heterocyclic compounds, medicaments containing said compounds, use thereof and processes for the preparation thereof
US8822537B2 (en) 2012-09-27 2014-09-02 Achelios Therapeutics, Inc. Topical ketoprofen composition
LV15002B (en) 2013-10-29 2015-07-20 Latvijas Organiskās Sintēzes Institūts Substituted heterocycle [(2-carboxy or -methoxycarbonyl)phenylcarbamoyl-methyl (or trimethylen)]-pyridinium or isoquinolinium bromides as hydroxycarboxylic acid receptor (hca2) family novel class of ligands
CN105566148B (en) 2014-10-14 2017-10-03 沈阳中化农药化工研发有限公司 A kind of quaternary ammonium compound and its application
CA2977387C (en) 2015-03-04 2020-04-28 The Procter & Gamble Company Fibrous elements, fibrous structures, and products comprising a deterrent agent and methods for making same
CN106310289B (en) 2015-06-24 2020-10-13 天津键凯科技有限公司 Conjugate of polyethylene glycol and anesthetic and preparation method thereof
AU2016301282B2 (en) * 2015-08-03 2022-03-17 Children's Medical Center Corporation Charged ion channel blockers and methods for use
DE102016009766A1 (en) 2016-08-11 2018-02-15 Julius-Maximilians-Universität Würzburg Production of bitter substance derivatives
JOP20190245A1 (en) 2017-04-20 2019-10-15 Novartis Ag Sustained release delivery systems comprising traceless linkers
CN108929263B (en) 2017-05-26 2022-07-22 中国医学科学院药物研究所 Arylamide Kv2.1 inhibitor and preparation method, pharmaceutical composition and application thereof
US10835505B2 (en) 2018-06-11 2020-11-17 Aardvark Therapeutics, Inc. Oral pharmaceutical formulation for weight loss, diabetes and related disorders
CN114828845A (en) * 2019-11-06 2022-07-29 诺西恩医疗公司 Charged ion channel blockers and methods of use thereof

Similar Documents

Publication Publication Date Title
ES2374994T3 (en) N-ARIL-HYDROXIALQUILIDEN-CARBOXAMIDE COMPOUNDS AND THEIR USE.
JPWO2021091585A5 (en)
JP2018530518A (en) Charged ion channel blocker and method of use
JPWO2020185830A5 (en)
JPWO2020185881A5 (en)
JPWO2020185928A5 (en)
JPWO2021091586A5 (en)
JP2023500891A (en) Charged ion channel blockers and methods of use
JP2023500890A (en) Charged ion channel blockers and methods of use
JPWO2020185915A5 (en)
US10485826B2 (en) Pharmaceutical formula for the treatment and/or prevention of arthritis and its manufacture
JP2022554359A (en) Phosphonium ion channel blockers and methods of use
Liu et al. Transdermal delivery of colchicine using dissolvable microneedle arrays for the treatment of acute gout in a rat model
JP2021503002A (en) Emulsion for topical treatment of skin and mucosal infections
WO2024041596A1 (en) Use of phenytoin sodium as mitophagy inducer
Villa et al. Animal models of endotoxic shock
AU2019336248A1 (en) New use of R-enantiomer of adrenergic β2 receptor agonists for treatment of inflammatory bowel disease and its extra intestinal manifestations
Speca et al. GED-0507 is a novel potential antifibrotic treatment option for pulmonary fibrosis
Dowers et al. Effect of short-term sequential administration of nonsteroidal anti-inflammatory drugs on the stomach and proximal portion of the duodenum in healthy dogs
RU2390341C2 (en) Method of conservative treatment of bladder leukoplakia (squamous metaplasia)
JP2007277222A (en) Antiinflammatory pharmaceutical composition
Wang et al. Natural compound fraxinellone ameliorates intestinal fibrosis in mice via direct intervention of HSP47-collagen interaction in the epithelium
RU2773949C1 (en) Drug for symptomatic treatment of colds, acute respiratory and / or other infectious and inflammatory diseases of the throat
RU2021127310A (en) ESTER-SUBSTITUTED ION CHANNEL BLOCKERS AND METHODS OF APPLICATION
RU2021127314A (en) CHARGED ION CHANNEL BLOCKERS AND METHODS OF APPLICATION