DK0920422T3 - Krystallinsk form af 4-[5-methyl-3-phenylisoxazol-4-yl]benzensulfonamid - Google Patents

Krystallinsk form af 4-[5-methyl-3-phenylisoxazol-4-yl]benzensulfonamid

Info

Publication number
DK0920422T3
DK0920422T3 DK97938656T DK97938656T DK0920422T3 DK 0920422 T3 DK0920422 T3 DK 0920422T3 DK 97938656 T DK97938656 T DK 97938656T DK 97938656 T DK97938656 T DK 97938656T DK 0920422 T3 DK0920422 T3 DK 0920422T3
Authority
DK
Denmark
Prior art keywords
phenylisoxazol
benzenesulfonamide
methyl
crystalline form
crystalline
Prior art date
Application number
DK97938656T
Other languages
Danish (da)
English (en)
Inventor
J Talley John
R Medich John
T Mclaughlin Kathleen
T Gaud Henry
E Yonan Edward
Original Assignee
Searle & Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Searle & Co filed Critical Searle & Co
Application granted granted Critical
Publication of DK0920422T3 publication Critical patent/DK0920422T3/da

Links

Classifications

    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L23/00—Details of semiconductor or other solid state devices
    • H01L23/34—Arrangements for cooling, heating, ventilating or temperature compensation ; Temperature sensing arrangements
    • H01L23/40—Mountings or securing means for detachable cooling or heating arrangements ; fixed by friction, plugs or springs
    • H01L23/4006—Mountings or securing means for detachable cooling or heating arrangements ; fixed by friction, plugs or springs with bolts or screws
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/42—Oxazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
    • C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
    • C07D261/08—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L23/00—Details of semiconductor or other solid state devices
    • H01L23/34—Arrangements for cooling, heating, ventilating or temperature compensation ; Temperature sensing arrangements
    • H01L23/42—Fillings or auxiliary members in containers or encapsulations selected or arranged to facilitate heating or cooling
    • H01L23/427—Cooling by change of state, e.g. use of heat pipes
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2924/00—Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
    • H01L2924/0001—Technical content checked by a classifier
    • H01L2924/0002—Not covered by any one of groups H01L24/00, H01L24/00 and H01L2224/00
DK97938656T 1996-08-14 1997-08-12 Krystallinsk form af 4-[5-methyl-3-phenylisoxazol-4-yl]benzensulfonamid DK0920422T3 (da)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US2437896P 1996-08-14 1996-08-14
PCT/US1997/015126 WO1998006708A1 (en) 1996-08-14 1997-08-12 Crystalline form of 4-[5-methyl-3-phenylisoxazol-4-yl]benzenesulfonamide

Publications (1)

Publication Number Publication Date
DK0920422T3 true DK0920422T3 (da) 2003-03-17

Family

ID=21820280

Family Applications (1)

Application Number Title Priority Date Filing Date
DK97938656T DK0920422T3 (da) 1996-08-14 1997-08-12 Krystallinsk form af 4-[5-methyl-3-phenylisoxazol-4-yl]benzensulfonamid

Country Status (39)

Country Link
US (2) US6441014B2 (hu)
EP (2) EP0920422B1 (hu)
JP (2) JP3631763B2 (hu)
KR (1) KR100383148B1 (hu)
CN (1) CN1205193C (hu)
AP (1) AP1055A (hu)
AR (1) AR009244A1 (hu)
AT (1) ATE228117T1 (hu)
AU (1) AU722072B2 (hu)
BG (1) BG64259B1 (hu)
BR (1) BR9711151A (hu)
CA (1) CA2264104A1 (hu)
CZ (1) CZ297679B6 (hu)
DE (1) DE69717281T2 (hu)
DK (1) DK0920422T3 (hu)
EA (2) EA001472B1 (hu)
EE (1) EE04237B1 (hu)
ES (1) ES2188971T3 (hu)
GE (1) GEP20022636B (hu)
HK (1) HK1023125A1 (hu)
HU (1) HUP0400923A3 (hu)
IL (2) IL128255A (hu)
IS (1) IS1989B (hu)
LT (1) LT4551B (hu)
LV (1) LV12274B (hu)
NO (1) NO312461B1 (hu)
NZ (1) NZ334132A (hu)
OA (1) OA11298A (hu)
PL (1) PL191313B1 (hu)
PT (1) PT920422E (hu)
RO (1) RO120771B1 (hu)
RS (1) RS49671B (hu)
SI (1) SI9720059B (hu)
SK (1) SK283558B6 (hu)
TR (1) TR199900298T2 (hu)
TW (1) TW527350B (hu)
UA (1) UA52684C2 (hu)
WO (1) WO1998006708A1 (hu)
ZA (1) ZA977314B (hu)

Families Citing this family (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EE04237B1 (et) * 1996-08-14 2004-02-16 G.D. Searle & Co. 4-(5-metüül-3-fenüülisoksasool-4-üül)benseensulfoonamiidi kristalliline vorm, selle kasutamine ja valmistamise meetod
NZ333399A (en) 1997-12-24 2000-05-26 Sankyo Co Cyclooxygenase-2 inhibitors (COX-2) for the prevention and treatment of tumors, cachexia and tumor-metastasis
GB9810920D0 (en) * 1998-05-21 1998-07-22 Merck Sharp & Dohme Therapeutic use
WO2000008001A1 (en) * 1998-08-07 2000-02-17 Chiron Corporation Substituted isoxazole as estrogen receptor modulators
AU1398899A (en) * 1998-11-12 2000-06-05 Algos Pharmaceutical Corporation Cox-2 inhibitors in combination with centrally acting analgesics
AU3384200A (en) * 1999-03-01 2000-09-21 Ortho-Mcneil Pharmaceutical, Inc. Composition comprising a tramadol material and a selective cox-2 inhibitor drug
EA006598B1 (ru) * 1999-08-20 2006-02-24 Орто-Макнейл Фармасьютикал, Инк. Композиция, содержащая трамадол и противосудорожное лекарственное средство
EP1212051A4 (en) * 1999-08-27 2004-03-31 Merck & Co Inc METHOD FOR TREATING OR PREVENTING CHEMICAL PROSTATITIS OR CHRONIC POOL PAIN
DE10032132A1 (de) * 2000-07-01 2002-01-17 Lohmann Therapie Syst Lts Dermales Therapeutisches System enthaltend nichtsteroidale Antiphlogistika mit selektiver COX-2-Hemmung
DK3168218T3 (en) 2001-08-15 2019-01-14 Pharmacia & Upjohn Co Llc Crystalline comprising an L-malic acid salt of N- [2- (DIETHYLAMINO) ETHYL] -5 - [(5-FLUOR-1,2-DIHYDRO-2-OXO-3H-INDOL-3-YLIDE) METHYL] -2,4 -DIMETHYL-1H-PYRROL-3-CARBOXAMIDE FOR USE AS A MEDICINE
US20070072921A1 (en) * 2002-07-26 2007-03-29 Talley John J Crystalline form of 4-[5-methyl-3-phenylisoxazol-4-yl] benzenesulfonamide
WO2004087683A1 (en) 2003-04-04 2004-10-14 Hetero Drugs Limited Novel crystalline forms of valdecoxib
EP2266585B1 (en) 2003-05-07 2013-06-26 Osteologix A/S Water-soluble strontium salts for use in treatment of cartilage and/or bone conditions
US20050182113A1 (en) * 2003-12-30 2005-08-18 Venkataraman Sundaram Method for preparing diaryl-substituted isoxazole compounds
US20050272787A1 (en) * 2004-05-19 2005-12-08 Eswaraiah Sajja Process for preparing crystalline form A of valdecoxib
WO2005120499A1 (en) * 2004-06-10 2005-12-22 Chandiran Thakashinamoorthy Form a of valdecoxib suitable for pharmaceutical formulations
MY147767A (en) 2004-06-16 2013-01-31 Janssen Pharmaceutica Nv Novel sulfamate and sulfamide derivatives useful for the treatment of epilepsy and related disorders
EP1612203B1 (en) * 2004-06-28 2007-08-01 Grünenthal GmbH Crystalline forms of (-)-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochloride
KR100591786B1 (ko) 2004-10-19 2006-06-26 휴먼팜 주식회사 프란루카스트를 함유하는 약학적 조성물 및 이의 제조 방법
US8283478B2 (en) 2005-05-20 2012-10-09 Janssen Pharmaceutica Nv Process for preparation of sulfamide derivatives
US8492431B2 (en) 2005-12-19 2013-07-23 Janssen Pharmaceutica, N.V. Use of benzo-fused heterocycle sulfamide derivatives for the treatment of obesity
US8497298B2 (en) 2005-12-19 2013-07-30 Janssen Pharmaceutica Nv Use of benzo-fused heterocycle sulfamide derivatives for lowering lipids and lowering blood glucose levels
US8691867B2 (en) 2005-12-19 2014-04-08 Janssen Pharmaceutica Nv Use of benzo-fused heterocycle sulfamide derivatives for the treatment of substance abuse and addiction
US8716231B2 (en) 2005-12-19 2014-05-06 Janssen Pharmaceutica Nv Use of benzo-fused heterocycle sulfamide derivatives for the treatment of pain
US8937096B2 (en) 2005-12-19 2015-01-20 Janssen Pharmaceutica Nv Use of benzo-fused heterocyle sulfamide derivatives for the treatment of mania and bipolar disorder
JP2009537635A (ja) 2006-05-19 2009-10-29 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ 癲癇の処置のための共同−療法
US8809385B2 (en) 2008-06-23 2014-08-19 Janssen Pharmaceutica Nv Crystalline form of (2S)-(-)-N-(6-chloro-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl)-sulfamide
US8815939B2 (en) 2008-07-22 2014-08-26 Janssen Pharmaceutica Nv Substituted sulfamide derivatives
CN103172583A (zh) * 2013-03-07 2013-06-26 深圳市资福药业有限公司 一种制备帕瑞昔布的方法
US10028904B2 (en) 2014-12-04 2018-07-24 Wisconsin Alumni Research Foundation Transdermal cannabinoid formulations
US9375417B2 (en) 2014-12-04 2016-06-28 Mary's Medicinals LLC Transdermal cannabinoid formulations
CN114441666B (zh) * 2020-11-05 2024-02-27 成都百裕制药股份有限公司 一种4-(5-甲基-3-苯基-4-异恶唑)苯磺酰氯中杂质的检测方法
IL305573A (en) 2021-03-15 2023-10-01 Saul Yedgar Hyaluronic acid conjugated with dipalmitoyl phosphatidyl ethanolamine in combination with non-steroidal anti-inflammatory drugs (NSAIDs) for the treatment or suppression of inflammatory diseases

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5474995A (en) * 1993-06-24 1995-12-12 Merck Frosst Canada, Inc. Phenyl heterocycles as cox-2 inhibitors
US5633272A (en) 1995-02-13 1997-05-27 Talley; John J. Substituted isoxazoles for the treatment of inflammation
PL185544B1 (pl) * 1995-02-13 2003-05-30 Nowa pochodna podstawionego izoksazolu i środek farmaceutyczny
US5643933A (en) * 1995-06-02 1997-07-01 G. D. Searle & Co. Substituted sulfonylphenylheterocycles as cyclooxygenase-2 and 5-lipoxygenase inhibitors
EE04237B1 (et) * 1996-08-14 2004-02-16 G.D. Searle & Co. 4-(5-metüül-3-fenüülisoksasool-4-üül)benseensulfoonamiidi kristalliline vorm, selle kasutamine ja valmistamise meetod
WO2004087683A1 (en) * 2003-04-04 2004-10-14 Hetero Drugs Limited Novel crystalline forms of valdecoxib
US20050272787A1 (en) * 2004-05-19 2005-12-08 Eswaraiah Sajja Process for preparing crystalline form A of valdecoxib

Also Published As

Publication number Publication date
EA199900200A1 (ru) 1999-06-24
LT99024A (en) 1999-07-26
AU722072B2 (en) 2000-07-20
OA11298A (en) 2003-10-22
EA003754B1 (ru) 2003-08-28
TR199900298T2 (xx) 1999-05-21
EP1283203A1 (en) 2003-02-12
JP2005015497A (ja) 2005-01-20
EA001472B1 (ru) 2001-04-23
PL331607A1 (en) 1999-08-02
LV12274A (lv) 1999-05-20
HK1023125A1 (en) 2000-09-01
RO120771B1 (ro) 2006-07-28
CN1205193C (zh) 2005-06-08
CZ33499A3 (cs) 1999-06-16
IL161224A0 (en) 2004-09-27
NO990541L (no) 1999-02-05
YU7499A (sh) 2000-03-21
US7135489B2 (en) 2006-11-14
WO1998006708A1 (en) 1998-02-19
EP0920422A1 (en) 1999-06-09
AP9901458A0 (en) 1999-03-31
NZ334132A (en) 2000-06-23
IS4961A (is) 1999-01-29
GEP20022636B (en) 2002-02-25
JP2000506542A (ja) 2000-05-30
SK13699A3 (en) 1999-07-12
HUP0400923A2 (hu) 2004-08-30
BG64259B1 (bg) 2004-07-30
RS49671B (sr) 2007-11-15
IS1989B (is) 2005-02-15
KR100383148B1 (ko) 2003-05-09
PL191313B1 (pl) 2006-04-28
CN1233243A (zh) 1999-10-27
SI9720059A (sl) 1999-12-31
AU4093697A (en) 1998-03-06
IL128255A (en) 2004-06-20
CA2264104A1 (en) 1998-02-19
EP0920422B1 (en) 2002-11-20
EA200000891A1 (ru) 2001-02-26
IL128255A0 (en) 1999-11-30
PT920422E (pt) 2003-03-31
SK283558B6 (sk) 2003-09-11
AR009244A1 (es) 2000-04-12
US20030004200A1 (en) 2003-01-02
US20010003752A1 (en) 2001-06-14
BR9711151A (pt) 1999-08-17
NO990541D0 (no) 1999-02-05
SI9720059B (sl) 2011-11-30
LT4551B (lt) 1999-10-25
ATE228117T1 (de) 2002-12-15
DE69717281T2 (de) 2003-09-04
JP3631763B2 (ja) 2005-03-23
HUP0400923A3 (en) 2007-11-28
TW527350B (en) 2003-04-11
EE9900053A (et) 1999-08-16
ES2188971T3 (es) 2003-07-01
ZA977314B (en) 1998-08-14
UA52684C2 (uk) 2003-01-15
NO312461B1 (no) 2002-05-13
US6441014B2 (en) 2002-08-27
LV12274B (en) 1999-09-20
CZ297679B6 (cs) 2007-03-07
DE69717281D1 (de) 2003-01-02
AP1055A (en) 2002-04-04
EE04237B1 (et) 2004-02-16
KR20000029994A (ko) 2000-05-25
BG103155A (en) 1999-11-30

Similar Documents

Publication Publication Date Title
DK0920422T3 (da) Krystallinsk form af 4-[5-methyl-3-phenylisoxazol-4-yl]benzensulfonamid
DK0984957T3 (da) Hidtil ukendt form af S-omeprazol
DK1288206T3 (da) Substituerede benzensulfonamidderivater som prolægemidler af COX-2-inhibitorer
DK0975778T3 (da) Anvendelse af glyphostat-resistende majslinier
DK0991641T3 (da) Krystallinsk form af omeprazol-natriumsalt
DK1107980T3 (da) Krystallinske former af EtO2C-CH2-(R)Cgl-Aze-Pab-OH
ID24481A (id) Gastrokinetik monosiklik benzamida dari derivat-3-atau-tersubstitusi 4-(aminometil)-piperidin
DE69604510T2 (de) Monolithische keramische Kondensatoren
NO984290D0 (no) Farmas°ytisk nyttige forbindelser
DE60107074D1 (de) Kristallin form ii von cabergolin
IS5821A (is) Kristalluð form af ósanetant
IS6620A (is) Nýr fjölgervingur V af tórasemíði
DK0941081T3 (da) Ny anvendelse af creatin
IS5155A (is) Fjölgervingur af zópólrestat mónóhýdrati
DK1088010T3 (da) Fremstilling af polyolefiner
DK0882722T3 (da) Fremstilling af alpha-tocopherol
DK0859001T3 (da) Fremstilling af oxazolderivater
DK0810216T3 (da) Derivater af 10,11-dihydro-10-oxo-5H-dibenz/b/,f/azepin-5-carboxamid
DK0950051T3 (da) Mikropartikulær form af en tetrahydropyridinforbindelse
NO20004583D0 (no) Krystallinsk form av paroxetine
EE200400073A (et) 4-(5-metüül-3-fenüülisoksasool-4-üül)benseensulfoonamiidi kristalliline vorm ja selle kasutamine
DE29723078U1 (de) Ziegel-Mauerwerk
DE29719010U1 (de) Dübelschraubverbindung
DK108697A (da) Disruption of iapp fibrils
DK1362591T3 (da) Anvendelse af en sammensætning indeholdende 5-androsten-3beta, 17alfa-diol