SK285190B6 - Kryštálová modifikácia proti plesniam a farmaceutický prostriedok s jej obsahom - Google Patents

Kryštálová modifikácia proti plesniam a farmaceutický prostriedok s jej obsahom Download PDF

Info

Publication number: SK285190B6
Authority: SK; Slovakia
Prior art keywords: vwd; crystal modification; triazol; weak; modification
Prior art date: 1997-10-07

Application number

SK512-2000A

Other languages

English (en)

Slovak (sk)

Other versions

SK5122000A3 (en

Inventor

David R. Andrews

William Leong

Anantha R. Sudhakar

Original Assignee

Schering Corporation

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.)

1997-10-07

Filing date

1998-10-05

Publication date

2006-08-03

1998-10-05 Application filed by Schering Corporation filed Critical Schering Corporation

2000-09-12 Publication of SK5122000A3 publication Critical patent/SK5122000A3/sk

2006-08-03 Publication of SK285190B6 publication Critical patent/SK285190B6/sk

Links

239000008194 pharmaceutical composition Substances 0.000 title claims abstract description 11
230000000843 anti-fungal effect Effects 0.000 title description 5
229940121375 antifungal agent Drugs 0.000 title description 5
150000001875 compounds Chemical class 0.000 claims abstract description 24
241000124008 Mammalia Species 0.000 claims abstract description 6
238000012986 modification Methods 0.000 claims description 68
230000004048 modification Effects 0.000 claims description 68
239000013078 crystal Substances 0.000 claims description 50
125000004215 2,4-difluorophenyl group Chemical group [H]C1=C([H])C(*)=C(F)C([H])=C1F 0.000 claims description 16
125000003682 3-furyl group Chemical group O1C([H])=C([*])C([H])=C1[H] 0.000 claims description 16
IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 claims description 14
239000000843 powder Substances 0.000 claims description 12
238000002329 infrared spectrum Methods 0.000 claims description 8
-1 1H-1,2,4- triazol-1-ylmethyl Chemical group 0.000 claims description 7
239000003814 drug Substances 0.000 claims description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
239000003937 drug carrier Substances 0.000 claims description 2
238000004519 manufacturing process Methods 0.000 claims description 2
MDTUWBLTRPRXBX-UHFFFAOYSA-N 1,2,4-triazol-3-one Chemical compound O=C1N=CN=N1 MDTUWBLTRPRXBX-UHFFFAOYSA-N 0.000 claims 1
241000233866 Fungi Species 0.000 claims 1
230000006806 disease prevention Effects 0.000 claims 1
206010017533 Fungal infection Diseases 0.000 abstract description 7
208000031888 Mycoses Diseases 0.000 abstract description 7
238000000034 method Methods 0.000 abstract description 7
239000000243 solution Substances 0.000 description 19
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 12
238000002360 preparation method Methods 0.000 description 12
239000007787 solid Substances 0.000 description 12
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
239000003826 tablet Substances 0.000 description 11
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
239000004480 active ingredient Substances 0.000 description 9
239000000203 mixture Substances 0.000 description 9
238000009835 boiling Methods 0.000 description 8
239000002904 solvent Substances 0.000 description 7
239000002775 capsule Substances 0.000 description 6
239000000047 product Substances 0.000 description 6
239000007858 starting material Substances 0.000 description 6
238000003756 stirring Methods 0.000 description 6
238000001757 thermogravimetry curve Methods 0.000 description 5
239000000969 carrier Substances 0.000 description 4
238000002844 melting Methods 0.000 description 4
230000008018 melting Effects 0.000 description 4
NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical compound C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
239000012458 free base Substances 0.000 description 3
239000003517 fume Substances 0.000 description 3
239000007788 liquid Substances 0.000 description 3
239000012299 nitrogen atmosphere Substances 0.000 description 3
238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 3
239000000725 suspension Substances 0.000 description 3
238000002076 thermal analysis method Methods 0.000 description 3
238000002834 transmittance Methods 0.000 description 3
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 2
239000003429 antifungal agent Substances 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
239000001768 carboxy methyl cellulose Substances 0.000 description 2
229940110456 cocoa butter Drugs 0.000 description 2
235000019868 cocoa butter Nutrition 0.000 description 2
238000002425 crystallisation Methods 0.000 description 2
230000008025 crystallization Effects 0.000 description 2
239000000796 flavoring agent Substances 0.000 description 2
235000019634 flavors Nutrition 0.000 description 2
238000011194 good manufacturing practice Methods 0.000 description 2
HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
239000000463 material Substances 0.000 description 2
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
229920000609 methyl cellulose Polymers 0.000 description 2
239000001923 methylcellulose Substances 0.000 description 2
235000010981 methylcellulose Nutrition 0.000 description 2
231100000252 nontoxic Toxicity 0.000 description 2
230000003000 nontoxic effect Effects 0.000 description 2
239000002674 ointment Substances 0.000 description 2
230000000704 physical effect Effects 0.000 description 2
230000005855 radiation Effects 0.000 description 2
235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 2
229920001027 sodium carboxymethylcellulose Polymers 0.000 description 2
239000011877 solvent mixture Substances 0.000 description 2
238000001228 spectrum Methods 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000000829 suppository Substances 0.000 description 2
239000000375 suspending agent Substances 0.000 description 2
239000012049 topical pharmaceutical composition Substances 0.000 description 2
SNTWKPAKVQFCCF-UHFFFAOYSA-N 2,3-dihydro-1h-triazole Chemical compound N1NC=CN1 SNTWKPAKVQFCCF-UHFFFAOYSA-N 0.000 description 1
241000416162 Astragalus gummifer Species 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
239000004375 Dextrin Substances 0.000 description 1
229920001353 Dextrin Polymers 0.000 description 1
238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 1
108010010803 Gelatin Proteins 0.000 description 1
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
239000004264 Petrolatum Substances 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
229920001615 Tragacanth Polymers 0.000 description 1
238000002441 X-ray diffraction Methods 0.000 description 1
239000002253 acid Substances 0.000 description 1
238000007605 air drying Methods 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
239000002585 base Substances 0.000 description 1
WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
230000037396 body weight Effects 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000003086 colorant Substances 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
239000012043 crude product Substances 0.000 description 1
235000019425 dextrin Nutrition 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
238000001938 differential scanning calorimetry curve Methods 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
229940079593 drug Drugs 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
235000003599 food sweetener Nutrition 0.000 description 1
230000002538 fungal effect Effects 0.000 description 1
229920000159 gelatin Polymers 0.000 description 1
239000008273 gelatin Substances 0.000 description 1
235000019322 gelatine Nutrition 0.000 description 1
235000011852 gelatine desserts Nutrition 0.000 description 1
239000008103 glucose Substances 0.000 description 1
239000008187 granular material Substances 0.000 description 1
239000010439 graphite Substances 0.000 description 1
229910002804 graphite Inorganic materials 0.000 description 1
239000008240 homogeneous mixture Substances 0.000 description 1
239000012535 impurity Substances 0.000 description 1
239000008101 lactose Substances 0.000 description 1
230000007774 longterm Effects 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
239000001095 magnesium carbonate Substances 0.000 description 1
229910000021 magnesium carbonate Inorganic materials 0.000 description 1
235000019359 magnesium stearate Nutrition 0.000 description 1
GBMDVOWEEQVZKZ-UHFFFAOYSA-N methanol;hydrate Chemical compound O.OC GBMDVOWEEQVZKZ-UHFFFAOYSA-N 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000001814 pectin Substances 0.000 description 1
235000010987 pectin Nutrition 0.000 description 1
229920001277 pectin Polymers 0.000 description 1
235000019271 petrolatum Nutrition 0.000 description 1
229940066842 petrolatum Drugs 0.000 description 1
239000000825 pharmaceutical preparation Substances 0.000 description 1
229940127557 pharmaceutical product Drugs 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
238000000634 powder X-ray diffraction Methods 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
239000008213 purified water Substances 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
239000007909 solid dosage form Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000008174 sterile solution Substances 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000003765 sweetening agent Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
230000000699 topical effect Effects 0.000 description 1
239000000196 tragacanth Substances 0.000 description 1
235000010487 tragacanth Nutrition 0.000 description 1
229940116362 tragacanth Drugs 0.000 description 1
238000002211 ultraviolet spectrum Methods 0.000 description 1
239000011345 viscous material Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Life Sciences & Earth Sciences (AREA)
General Chemical & Material Sciences (AREA)
Medicinal Chemistry (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Communicable Diseases (AREA)
Pharmacology & Pharmacy (AREA)
Oncology (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Plural Heterocyclic Compounds (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

SK512-2000A 1997-10-07 1998-10-05 Kryštálová modifikácia proti plesniam a farmaceutický prostriedok s jej obsahom SK285190B6 (sk)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US94618397A	1997-10-07	1997-10-07
PCT/US1998/020476 WO1999018097A1 (en)	1997-10-07	1998-10-05	Crystalline antifungal polymorph

Publications (2)

Publication Number	Publication Date
SK5122000A3 SK5122000A3 (en)	2000-09-12
SK285190B6 true SK285190B6 (sk)	2006-08-03

Family

ID=25484068

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK512-2000A SK285190B6 (sk)	1997-10-07	1998-10-05	Kryštálová modifikácia proti plesniam a farmaceutický prostriedok s jej obsahom

Country Status (30)

Country	Link
EP (1)	EP1021439B1 (2)
JP (4)	JP2001519346A (2)
KR (1)	KR100626109B1 (2)
CN (1)	CN1125067C (2)
AR (1)	AR015947A1 (2)
AT (1)	ATE263163T1 (2)
AU (1)	AU759982B2 (2)
BR (1)	BR9812866A (2)
CA (1)	CA2305803C (2)
CO (1)	CO4970829A1 (2)
CZ (1)	CZ299835B6 (2)
DE (1)	DE69822859T2 (2)
DK (1)	DK1021439T3 (2)
ES (1)	ES2217594T3 (2)
HU (1)	HU225233B1 (2)
ID (1)	ID29290A (2)
IL (1)	IL135331A (2)
IN (1)	IN1998CH02232A (2)
MX (1)	MX225999B (2)
MY (1)	MY130126A (2)
NO (1)	NO318827B1 (2)
NZ (1)	NZ503662A (2)
PE (1)	PE120499A1 (2)
PH (1)	PH11998002606B1 (2)
PL (1)	PL189317B1 (2)
PT (1)	PT1021439E (2)
SK (1)	SK285190B6 (2)
TW (1)	TW589310B (2)
WO (1)	WO1999018097A1 (2)
ZA (1)	ZA989063B (2)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP2130540A1 (en)	2008-06-02	2009-12-09	Sandoz AG	Pharmaceutical compositions containing a crystalline form of posaconazole
EP2141159A1 (en) *	2008-07-03	2010-01-06	Sandoz AG	A Crystalline form of posaconazole
EP2451805A1 (en)	2009-07-09	2012-05-16	Sandoz AG	A crystalline form of posaconazole
US9199919B2 (en)	2010-05-19	2015-12-01	Sandoz Ag	Process for the preparation of chiral hydrazides
RU2580318C2 (ru)	2010-05-19	2016-04-10	Сандоз Аг	Получение промежуточных продуктов для синтеза позаконазола
US9206146B2 (en)	2010-05-19	2015-12-08	Sandoz Ag	Purification of posaconazole and of posaconazole intermediates
EP2571871B1 (en) *	2010-05-19	2017-06-21	Sandoz AG	Process for the preparation of chiral triazolones
CN108329303A (zh)	2011-06-16	2018-07-27	桑多斯股份公司	制备手性化合物的方法
US9102664B2 (en)	2011-09-19	2015-08-11	Msn Laboratories Private Limited	Process for the preparation of triazole antifungal drug, its intermediates and polymorphs thereof
MX370849B (es) *	2013-07-25	2020-01-08	Sandoz Ag	Proceso mejorado para preparar la forma cristalina iv del posaconazol.
ITMI20132117A1 (it) *	2013-12-18	2015-06-19	Djada Pharmaceutical Sa	Una forma cristallina di posaconazolo
ITMI20132114A1 (it)	2013-12-18	2015-06-19	Djada Pharmaceutical Sa	Una forma cristallina di posaconazolo
ITMI20132118A1 (it) *	2013-12-18	2015-06-19	Djada Pharmaceutical Sa	Una forma cristallina di posaconazolo
ITMI20132115A1 (it) *	2013-12-18	2015-06-19	Djada Pharmaceutical Sa	Una forma cristallina di posaconazolo
KR102331856B1 (ko)	2014-10-21	2021-11-29	다케다 야쿠힌 고교 가부시키가이샤	결정 형태의 5-클로로-n4-[2-(디메틸포스포릴)페닐]-n2-｛2-메톡시-4-[4-(4-메틸피페라진-1-일)피페리딘-1-일]피리미딘-2,4-디아민
CN104387374A (zh) *	2014-10-21	2015-03-04	江苏恒盛药业有限公司	泊沙康唑晶型i的制备工艺
CN104370894A (zh) *	2014-10-21	2015-02-25	江苏恒盛药业有限公司	无定型泊沙康唑的制备工艺
WO2017025292A1 (en)	2015-08-08	2017-02-16	Alfred E. Tiefenbacher (Gmbh & Co. Kg)	Gastro-resistant formulation containing posaconazole
EA039213B1 (ru)	2015-12-24	2021-12-17	Такеда Фармасьютикал Компани Лимитед	Сокристалл, способ его получения и лекарственное средство, содержащее сокристалл
EP3925601B1 (en)	2016-02-26	2024-07-17	Alfred E. Tiefenbacher (GmbH & Co. KG)	Gastro-resistant formulation containing posaconazole and a polymeric precipitation inhibitor
CN105949278B (zh) *	2016-03-30	2019-12-06	南京曼杰生物科技有限公司	一种取代的四氢呋喃水溶性衍生物及其应用
WO2017032908A1 (en)	2016-07-08	2017-03-02	Synthon B.V.	Pharmaceutical composition comprising amorphous posaconazole
TR201620462A2 (tr)	2016-12-31	2018-07-23	Abdi Ibrahim Ilac Sanayi Ve Ticaret Anonim Sirketi	POSAKONAZOL İÇEREN FARMASÖTİK BİLEŞİMLER ve ÜRETİM YÖNTEMİ
TR201722493A2 (tr)	2017-12-28	2019-07-22	Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi	Posakonazol i̇çeren kati farmasöti̇k kompozi̇syon
WO2022034232A1 (en)	2020-08-13	2022-02-17	Alfred E. Tiefenbacher (Gmbh & Co. Kg)	Gastro-resistant high-strength formulation containing posaconazole
AU2022324717A1 (en)	2021-11-25	2024-06-13	Alfred E. Tiefenbacher (Gmbh Und Co. Kg)	Granules containing posaconazole
EP4091604B1 (en)	2021-11-25	2024-04-03	Alfred E. Tiefenbacher (GmbH & Co. KG)	Granules containing posaconazole

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
IL103558A0 (en) *	1991-10-30	1993-03-15	Schering Corp	Tri-substituted tetrahydrofuran antifungals
PL181193B1 (pl) *	1993-12-21	2001-06-29	Schering Corp	Nowe pochodne tetrahydrofuranowe o działaniu przeciwgrzybicznym, kompozycja farmaceutyczna do leczenia infekcji grzybiczych oraz sposób wytwarzania tych związków
NZ278882A (en) *	1994-01-24	1997-06-24	Janssen Pharmaceutica Nv	Piperazine-containing azole antifungal compounds
US5625064A (en) *	1995-04-19	1997-04-29	Schering Corporation	Process for the preparation of triazolones
SK27097A3 (en) *	1995-06-02	1997-09-10	Schering Corp	Tetrahydrofuran antifungals

1998
- 1998-10-05 JP JP2000514908A patent/JP2001519346A/ja not_active Withdrawn
- 1998-10-05 WO PCT/US1998/020476 patent/WO1999018097A1/en not_active Ceased
- 1998-10-05 BR BR9812866-3A patent/BR9812866A/pt not_active Application Discontinuation
- 1998-10-05 CN CN98811886A patent/CN1125067C/zh not_active Expired - Lifetime
- 1998-10-05 ZA ZA989063A patent/ZA989063B/xx unknown
- 1998-10-05 PL PL98339659A patent/PL189317B1/pl unknown
- 1998-10-05 PT PT98951994T patent/PT1021439E/pt unknown
- 1998-10-05 CO CO98057733A patent/CO4970829A1/es unknown
- 1998-10-05 ID IDW20000632A patent/ID29290A/id unknown
- 1998-10-05 NZ NZ503662A patent/NZ503662A/xx not_active IP Right Cessation
- 1998-10-05 CA CA002305803A patent/CA2305803C/en not_active Expired - Lifetime
- 1998-10-05 EP EP98951994A patent/EP1021439B1/en not_active Expired - Lifetime
- 1998-10-05 ES ES98951994T patent/ES2217594T3/es not_active Expired - Lifetime
- 1998-10-05 KR KR20007003709A patent/KR100626109B1/ko not_active Expired - Lifetime
- 1998-10-05 CZ CZ20001264A patent/CZ299835B6/cs not_active IP Right Cessation
- 1998-10-05 IL IL13533198A patent/IL135331A/xx not_active IP Right Cessation
- 1998-10-05 AT AT98951994T patent/ATE263163T1/de active
- 1998-10-05 DE DE69822859T patent/DE69822859T2/de not_active Expired - Lifetime
- 1998-10-05 SK SK512-2000A patent/SK285190B6/sk not_active IP Right Cessation
- 1998-10-05 AU AU97803/98A patent/AU759982B2/en not_active Expired
- 1998-10-05 DK DK98951994T patent/DK1021439T3/da active
- 1998-10-05 AR ARP980104957A patent/AR015947A1/es not_active Application Discontinuation
- 1998-10-05 HU HU0004899A patent/HU225233B1/hu unknown
- 1998-10-05 PE PE1998000942A patent/PE120499A1/es not_active IP Right Cessation
- 1998-10-06 TW TW087116562A patent/TW589310B/zh not_active IP Right Cessation
- 1998-10-06 MY MYPI98004576A patent/MY130126A/en unknown
- 1998-10-06 IN IN2232CH1998 patent/IN1998CH02232A/en unknown
- 1998-10-06 PH PH11998002606A patent/PH11998002606B1/en unknown
2000
- 2000-04-06 NO NO20001779A patent/NO318827B1/no not_active IP Right Cessation
- 2000-04-06 MX MXPA00003404 patent/MX225999B/es active IP Right Grant
2008
- 2008-01-04 JP JP2008000110A patent/JP2008106075A/ja not_active Withdrawn
2012
- 2012-05-18 JP JP2012114724A patent/JP2012153729A/ja active Pending
- 2012-05-18 JP JP2012114725A patent/JP2012153730A/ja active Pending

Also Published As

Publication number	Publication date
ES2217594T3 (es)	2004-11-01
HU225233B1 (en)	2006-08-28
ATE263163T1 (de)	2004-04-15
KR100626109B1 (ko)	2006-09-20
NZ503662A (en)	2002-10-25
ZA989063B (en)	1999-04-06
HUP0004899A2 (hu)	2002-02-28
NO318827B1 (no)	2005-05-09
CZ20001264A3 (cs)	2000-08-16
PL339659A1 (en)	2001-01-02
IL135331A0 (en)	2001-05-20
CN1281449A (zh)	2001-01-24
CA2305803C (en)	2009-12-22
PH11998002606B1 (en)	2006-08-10
PL189317B1 (pl)	2005-07-29
CN1125067C (zh)	2003-10-22
DE69822859T2 (de)	2005-01-27
KR20010030959A (ko)	2001-04-16
WO1999018097A1 (en)	1999-04-15
TW589310B (en)	2004-06-01
PE120499A1 (es)	1999-12-04
AR015947A1 (es)	2001-05-30
NO20001779L (no)	2000-06-06
HK1029588A1 (en)	2001-04-06
CA2305803A1 (en)	1999-04-15
SK5122000A3 (en)	2000-09-12
AU9780398A (en)	1999-04-27
MX225999B (es)	2005-02-02
HUP0004899A3 (en)	2002-03-28
DK1021439T3 (da)	2004-05-10
BR9812866A (pt)	2000-08-08
CZ299835B6 (cs)	2008-12-10
IN1998CH02232A (2)	2005-03-04
JP2001519346A (ja)	2001-10-23
EP1021439A1 (en)	2000-07-26
MY130126A (en)	2007-06-29
PT1021439E (pt)	2004-07-30
JP2008106075A (ja)	2008-05-08
JP2012153730A (ja)	2012-08-16
AU759982B2 (en)	2003-05-01
NO20001779D0 (no)	2000-04-06
EP1021439B1 (en)	2004-03-31
DE69822859D1 (de)	2004-05-06
MXPA00003404A (es)	2000-11-01
CO4970829A1 (es)	2000-11-07
JP2012153729A (ja)	2012-08-16
ID29290A (id)	2001-08-16
IL135331A (en)	2005-08-31

Legal Events

Date

Code

Title

Description

2013-01-02

TC4A

Change of owner's name

Owner name: MERCK SHARP & DOHME CORP., RAHWAY, NJ, US

Effective date: 20121108

2018-12-03

MK4A

Expiry of patent

Expiry date: 20181005

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