SK143694A3 - Phosphonocarboxylate compounds for treating abnormal calcium and phosphate metabolism - Google Patents
Phosphonocarboxylate compounds for treating abnormal calcium and phosphate metabolism Download PDFInfo
- Publication number
- SK143694A3 SK143694A3 SK1436-94A SK143694A SK143694A3 SK 143694 A3 SK143694 A3 SK 143694A3 SK 143694 A SK143694 A SK 143694A SK 143694 A3 SK143694 A3 SK 143694A3
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- Slovakia
- Prior art keywords
- substituted
- unsubstituted
- group
- alkyl
- chain
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- ZJAOAACCNHFJAH-UHFFFAOYSA-N phosphonoformic acid Chemical class OC(=O)P(O)(O)=O ZJAOAACCNHFJAH-UHFFFAOYSA-N 0.000 title claims abstract description 29
- 239000011575 calcium Substances 0.000 title claims abstract description 27
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 title claims abstract description 26
- 229910052791 calcium Inorganic materials 0.000 title claims abstract description 26
- 229910019142 PO4 Inorganic materials 0.000 title claims abstract description 23
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 title claims abstract description 23
- 239000010452 phosphate Substances 0.000 title claims abstract description 23
- 230000002159 abnormal effect Effects 0.000 title claims abstract description 14
- 230000004060 metabolic process Effects 0.000 title claims abstract description 12
- 239000000203 mixture Substances 0.000 claims abstract description 74
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 67
- 239000001257 hydrogen Substances 0.000 claims abstract description 65
- 125000002950 monocyclic group Chemical group 0.000 claims abstract description 52
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 43
- 238000011282 treatment Methods 0.000 claims abstract description 29
- 150000003839 salts Chemical class 0.000 claims abstract description 26
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 21
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 19
- 150000002367 halogens Chemical class 0.000 claims abstract description 19
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract description 13
- 239000003937 drug carrier Substances 0.000 claims abstract description 9
- 125000002619 bicyclic group Chemical group 0.000 claims abstract description 8
- -1 okahydroquinoline Chemical compound 0.000 claims description 93
- 125000000217 alkyl group Chemical group 0.000 claims description 57
- 229920006395 saturated elastomer Polymers 0.000 claims description 56
- 125000000623 heterocyclic group Chemical group 0.000 claims description 48
- 229910052757 nitrogen Inorganic materials 0.000 claims description 48
- 125000004429 atom Chemical group 0.000 claims description 45
- 125000001424 substituent group Chemical group 0.000 claims description 45
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 41
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 38
- 125000004404 heteroalkyl group Chemical group 0.000 claims description 34
- 125000003367 polycyclic group Chemical group 0.000 claims description 31
- 229910052717 sulfur Inorganic materials 0.000 claims description 30
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 27
- 239000008194 pharmaceutical composition Substances 0.000 claims description 25
- 229910052760 oxygen Inorganic materials 0.000 claims description 21
- 229910052799 carbon Inorganic materials 0.000 claims description 19
- 150000002431 hydrogen Chemical class 0.000 claims description 18
- 125000003118 aryl group Chemical group 0.000 claims description 16
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 15
- 125000006413 ring segment Chemical group 0.000 claims description 15
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 14
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 13
- 229910052720 vanadium Inorganic materials 0.000 claims description 13
- 125000002837 carbocyclic group Chemical group 0.000 claims description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 11
- 125000005843 halogen group Chemical group 0.000 claims description 11
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 11
- 229910018828 PO3H2 Inorganic materials 0.000 claims description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 9
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 9
- 125000005842 heteroatom Chemical group 0.000 claims description 9
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 9
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 9
- 125000004585 polycyclic heterocycle group Chemical group 0.000 claims description 9
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 7
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 7
- 239000011593 sulfur Substances 0.000 claims description 7
- 125000006732 (C1-C15) alkyl group Chemical group 0.000 claims description 6
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims description 6
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 6
- 125000003277 amino group Chemical group 0.000 claims description 5
- 125000003107 substituted aryl group Chemical group 0.000 claims description 5
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims description 4
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 4
- 239000003814 drug Substances 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 3
- 125000004076 pyridyl group Chemical group 0.000 claims description 3
- VNHBYKHXBCYPBJ-UHFFFAOYSA-N 5-ethynylimidazo[1,2-a]pyridine Chemical compound C#CC1=CC=CC2=NC=CN12 VNHBYKHXBCYPBJ-UHFFFAOYSA-N 0.000 claims description 2
- 125000001620 monocyclic carbocycle group Chemical group 0.000 claims description 2
- LBUJPTNKIBCYBY-UHFFFAOYSA-N 1,2,3,4-tetrahydroquinoline Chemical compound C1=CC=C2CCCNC2=C1 LBUJPTNKIBCYBY-UHFFFAOYSA-N 0.000 claims 4
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 claims 4
- AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical compound C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 claims 4
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims 2
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 claims 2
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 claims 2
- CEKSPMMCISUSTR-UHFFFAOYSA-N 1,2,3,4,4a,5,6,7-octahydroquinoline Chemical compound C1CCC2CCCNC2=C1 CEKSPMMCISUSTR-UHFFFAOYSA-N 0.000 claims 1
- 241000282994 Cervidae Species 0.000 claims 1
- RAXXELZNTBOGNW-UHFFFAOYSA-O Imidazolium Chemical compound C1=C[NH+]=CN1 RAXXELZNTBOGNW-UHFFFAOYSA-O 0.000 claims 1
- 125000002618 bicyclic heterocycle group Chemical group 0.000 claims 1
- 239000004927 clay Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 125000003386 piperidinyl group Chemical group 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 abstract description 74
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- 230000001575 pathological effect Effects 0.000 abstract description 7
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- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 161
- 230000015572 biosynthetic process Effects 0.000 description 119
- 238000003786 synthesis reaction Methods 0.000 description 116
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 90
- 239000000243 solution Substances 0.000 description 82
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 60
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 42
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 39
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 39
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 37
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 33
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 27
- 239000000047 product Substances 0.000 description 27
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 26
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- 239000012043 crude product Substances 0.000 description 24
- 235000002639 sodium chloride Nutrition 0.000 description 24
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- 239000000460 chlorine Substances 0.000 description 17
- LXCYSACZTOKNNS-UHFFFAOYSA-N diethoxy(oxo)phosphanium Chemical compound CCO[P+](=O)OCC LXCYSACZTOKNNS-UHFFFAOYSA-N 0.000 description 17
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- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
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- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 8
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- BAVFNIOVBGSPTG-UHFFFAOYSA-N ethyl 2-oxobut-3-enoate Chemical compound CCOC(=O)C(=O)C=C BAVFNIOVBGSPTG-UHFFFAOYSA-N 0.000 description 8
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- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 8
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- 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 5
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- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical group OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 5
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Classifications
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
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- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6561—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings
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- C07F9/3873—Polyphosphonic acids containing nitrogen substituent, e.g. N.....H or N-hydrocarbon group which can be substituted by halogen or nitro(so), N.....O, N.....S, N.....C(=X)- (X =O, S), N.....N, N...C(=X)...N (X =O, S)
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- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
- C07F9/6503—Five-membered rings
- C07F9/6506—Five-membered rings having the nitrogen atoms in positions 1 and 3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
- C07F9/6509—Six-membered rings
- C07F9/6512—Six-membered rings having the nitrogen atoms in positions 1 and 3
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Rheumatology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Physical Education & Sports Medicine (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Diabetes (AREA)
- Endocrinology (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Materials For Medical Uses (AREA)
Applications Claiming Priority (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US89148792A | 1992-05-29 | 1992-05-29 | |
US89149092A | 1992-05-29 | 1992-05-29 | |
US89088592A | 1992-05-29 | 1992-05-29 | |
US89135592A | 1992-05-29 | 1992-05-29 | |
US89088692A | 1992-05-29 | 1992-05-29 | |
US89130992A | 1992-05-29 | 1992-05-29 | |
PCT/US1993/004993 WO1993024131A1 (en) | 1992-05-29 | 1993-05-27 | Phosponocarboxylate compounds for treating abnormal calcium and phosphate metabolism |
Publications (1)
Publication Number | Publication Date |
---|---|
SK143694A3 true SK143694A3 (en) | 1997-01-08 |
Family
ID=27560336
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SK1436-94A SK143694A3 (en) | 1992-05-29 | 1993-05-27 | Phosphonocarboxylate compounds for treating abnormal calcium and phosphate metabolism |
Country Status (17)
Country | Link |
---|---|
US (1) | US5731299A (ja) |
EP (1) | EP0788362B1 (ja) |
JP (1) | JP3781770B2 (ja) |
KR (2) | KR950701930A (ja) |
AT (1) | ATE203409T1 (ja) |
AU (1) | AU663966B2 (ja) |
CA (1) | CA2136824C (ja) |
CZ (1) | CZ296894A3 (ja) |
DE (1) | DE69330498T2 (ja) |
DK (1) | DK0788362T3 (ja) |
FI (1) | FI945599A (ja) |
HU (1) | HUT71906A (ja) |
NO (1) | NO310463B1 (ja) |
NZ (1) | NZ253852A (ja) |
PL (1) | PL174726B1 (ja) |
SK (1) | SK143694A3 (ja) |
WO (1) | WO1993024131A1 (ja) |
Families Citing this family (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5763611A (en) * | 1992-05-29 | 1998-06-09 | The Procter & Gamble Company | Thio-substituted cyclic phosphonate compounds, pharmaceutical compositions, and methods for treating abnormal calcium and phosphate metabolism |
ES2123057T3 (es) * | 1992-05-29 | 1999-01-01 | Procter & Gamble Pharma | Compuestos de fosfonosulfonato para tratar un metabolismo anormal del calcio y los fosfatos. |
US5312814A (en) * | 1992-12-09 | 1994-05-17 | Bristol-Myers Squibb Co. | α-phosphonocarboxylate squalene synthetase inhibitors |
DE4320223A1 (de) * | 1993-06-18 | 1994-12-22 | Boehringer Mannheim Gmbh | Neue Phosphonobernsteinsäurederivate, Verfahren zu deren Herstellung und diese Verbindungen enthaltende Arzneimittel |
DE4336099A1 (de) * | 1993-10-22 | 1995-04-27 | Boehringer Mannheim Gmbh | Neue 2.4-Diphosphonoglutarsäurederivate, Verfahren zu deren Herstellung und diese Verbindungen enthaltende Arzneimittel |
DE4410601A1 (de) * | 1994-03-26 | 1995-09-28 | Boehringer Mannheim Gmbh | Neue 2.4-Diphosphonoglutarsäurederivate, Verfahren zu deren Herstellung und diese Verbindungen enthaltende Arzneimittel |
DE19502209A1 (de) * | 1995-01-25 | 1996-08-01 | Hoechst Ag | Phosphonoessigsäure-Derivate und deren Verwendung zur Behandlung von degenerativen Gelenkserkrankungen |
ATE246197T1 (de) * | 1998-09-09 | 2003-08-15 | Metabasis Therapeutics Inc | Neue heteroaromatische fructose 1,6- bisphosphatase inhibitoren |
CZ301401B6 (cs) * | 1999-12-22 | 2010-02-17 | Metabasis Therapeutics, Inc. | Bisamidátfosfonátová predléciva a farmaceutické prostredky s jejich obsahem |
US7563774B2 (en) | 2000-06-29 | 2009-07-21 | Metabasis Therapeutics, Inc. | Combination of FBPase inhibitors and antidiabetic agents useful for the treatment of diabetes |
ES2331561T3 (es) * | 2001-04-04 | 2010-01-08 | Ortho-Mcneil-Janssen Pharmaceuticals, Inc. | Terapia combinada que comprende inhibidores de la reabsorcion de glucosa y moduladores de receptores de retinoides x. |
CA2442917C (en) * | 2001-04-04 | 2011-02-01 | Ortho-Mcneil Pharmaceutical, Inc. | Combination therapy comprising glucose reabsorption inhibitors and ppar modulators |
MXPA04005361A (es) * | 2001-12-13 | 2004-09-27 | Vital Health Sciences Pyt Ltd | Transporte transdermico de compuestos. |
AU2002950713A0 (en) | 2002-08-09 | 2002-09-12 | Vital Health Sciences Pty Ltd | Carrier |
BRPI0514372A (pt) * | 2004-08-18 | 2008-06-10 | Metabasis Therapeutics Inc | inibidores de tiazol de frutose 1, 6-bisfosfatase |
MX2007015949A (es) | 2005-06-17 | 2008-03-07 | Vital Health Sciences Pty Ltd | Un vehiculo que comprende uno o mas derivados de fosfato de di- y/o mono-(agentes de transferencia de electrones) o complejos de los mismos. |
EP2531047B1 (en) | 2010-02-05 | 2024-11-13 | Phosphagenics Limited | Carrier comprising non-neutralised tocopheryl phosphate |
EP2552486B1 (en) | 2010-03-30 | 2020-08-12 | Phosphagenics Limited | Transdermal delivery patch |
EP2685992A4 (en) | 2011-03-15 | 2014-09-10 | Phosphagenics Ltd | AMINO-QUINOLINES AS KINASE INHIBITORS |
RU2466732C1 (ru) * | 2011-05-31 | 2012-11-20 | Общество С Ограниченной Ответственностью "Парафарм" | Способ заполнения полостных образований в метафизарных (трабекулярных) участках костей кальцием и предотвращения выведения из них кальция |
WO2017096427A1 (en) | 2015-12-09 | 2017-06-15 | Phosphagenics Limited | Pharmaceutical formulation |
FR3046791B1 (fr) * | 2016-01-18 | 2020-01-10 | Adisseo France S.A.S. | Procede de preparation d'analogues de la methionine |
MX2019006845A (es) | 2016-12-21 | 2019-10-15 | Avecho Biotechnology Ltd | Proceso. |
Family Cites Families (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2336230A (en) * | 1941-08-15 | 1943-12-07 | Eastman Kodak Co | Surface-active agent |
GB756099A (en) * | 1953-06-10 | 1956-08-29 | Boehme Fettchemie Gmbh | A process for the manufacture of esters containing phosphorus, oxygen and sulphur |
US3819676A (en) * | 1969-04-25 | 1974-06-25 | Merck & Co Inc | Alkyl-or arylsulfonyloxy,alkanoyloxy substituted propylphosphoric acid lower alkyl esters |
US4032521A (en) * | 1972-12-29 | 1977-06-28 | Merck & Co., Inc. | Cephalosporin phosphonic acid, sulfonic acid and sulfonamide compounds |
DE2310450A1 (de) * | 1973-03-02 | 1974-09-05 | Henkel & Cie Gmbh | Komplexbildner fuer mehrwertige metallionen |
DE2360797C2 (de) * | 1973-12-06 | 1985-05-23 | Henkel KGaA, 4000 Düsseldorf | Pharmazeutische Präparate |
GB1509068A (en) * | 1974-05-27 | 1978-04-26 | Mitsubishi Petrochemical Co | Phosphonic and thiophosphonic acid derivatives and their use as plant growth regulants |
SU585172A1 (ru) * | 1976-08-06 | 1977-12-25 | Предприятие П/Я В-2343 | Способ получени -/3-алкилсульфонилпропил/-0,0-диалкилтиофосфатов |
IL77243A (en) * | 1984-12-21 | 1996-11-14 | Procter & Gamble | Pharmaceutical compositions containing geminal diphosphonic acid compounds and certain such novel compounds |
US4781865A (en) * | 1986-09-29 | 1988-11-01 | Ecolab, Inc. | Phosphinated and phosphonated sulfonic acids |
IL86951A (en) * | 1987-07-06 | 1996-07-23 | Procter & Gamble Pharma | Methylene phosphonoalkylphosphinates and pharmaceutical preparations containing them |
US4937367A (en) * | 1987-07-15 | 1990-06-26 | Zambon Group S.P.A. | Process for the preparation of intermediates for the synthesis of fosfomycin |
US4959360A (en) * | 1988-06-01 | 1990-09-25 | Smithkline Beecham Corporation | α-adrenergic receptor antagonists |
KR900011782A (ko) * | 1989-01-03 | 1990-08-02 | 추후보정 | 불화 포스포노술폰산 및 그의 유도체 |
WO1990007480A1 (en) * | 1989-01-03 | 1990-07-12 | Catalytica, Inc. | Acid catalyzed process |
US5011938A (en) * | 1989-10-02 | 1991-04-30 | Eli Lilly And Company | 7-substituted bicyclic pyrazolidinones |
EP0517765A1 (de) * | 1990-03-02 | 1992-12-16 | Byk Gulden Lomberg Chemische Fabrik Gmbh | Zubereitungen für die mr-diagnostik |
EP0477454A1 (en) * | 1990-09-28 | 1992-04-01 | Merrell Dow Pharmaceuticals Inc. | Novel phosphonate derivatives of certain nucleosides |
GB2248832A (en) * | 1990-10-04 | 1992-04-22 | Britoil Plc | Method for inhibiting scale formation |
GB2248831A (en) * | 1990-10-04 | 1992-04-22 | Britoil Plc | Method for inhibiting scale formation |
ATE127808T1 (de) * | 1991-04-06 | 1995-09-15 | Fisons Plc | Atp-analogen. |
US5272128A (en) * | 1992-04-01 | 1993-12-21 | Rohm And Haas Company | Phosphosulfonate herbicides |
ES2123057T3 (es) * | 1992-05-29 | 1999-01-01 | Procter & Gamble Pharma | Compuestos de fosfonosulfonato para tratar un metabolismo anormal del calcio y los fosfatos. |
-
1993
- 1993-05-07 US US08/055,809 patent/US5731299A/en not_active Expired - Fee Related
- 1993-05-26 KR KR1019940704308A patent/KR950701930A/ko not_active Application Discontinuation
- 1993-05-27 PL PL93306383A patent/PL174726B1/pl unknown
- 1993-05-27 AT AT93915131T patent/ATE203409T1/de not_active IP Right Cessation
- 1993-05-27 NZ NZ253852A patent/NZ253852A/en not_active IP Right Cessation
- 1993-05-27 DE DE69330498T patent/DE69330498T2/de not_active Expired - Fee Related
- 1993-05-27 CA CA002136824A patent/CA2136824C/en not_active Expired - Fee Related
- 1993-05-27 WO PCT/US1993/004993 patent/WO1993024131A1/en active IP Right Grant
- 1993-05-27 JP JP50073794A patent/JP3781770B2/ja not_active Expired - Fee Related
- 1993-05-27 AU AU45231/93A patent/AU663966B2/en not_active Ceased
- 1993-05-27 SK SK1436-94A patent/SK143694A3/sk unknown
- 1993-05-27 CZ CZ942968A patent/CZ296894A3/cs unknown
- 1993-05-27 DK DK93915131T patent/DK0788362T3/da active
- 1993-05-27 EP EP93915131A patent/EP0788362B1/en not_active Expired - Lifetime
- 1993-05-27 HU HU9403405A patent/HUT71906A/hu unknown
-
1994
- 1994-11-25 NO NO19944515A patent/NO310463B1/no not_active Application Discontinuation
- 1994-11-28 KR KR1019940704301A patent/KR100272286B1/ko not_active IP Right Cessation
- 1994-11-28 FI FI945599A patent/FI945599A/fi unknown
Also Published As
Publication number | Publication date |
---|---|
DK0788362T3 (da) | 2001-11-12 |
FI945599A (fi) | 1995-01-25 |
KR950701930A (ko) | 1995-05-17 |
US5731299A (en) | 1998-03-24 |
KR100272286B1 (en) | 2000-11-15 |
WO1993024131A1 (en) | 1993-12-09 |
JP3781770B2 (ja) | 2006-05-31 |
HUT71906A (en) | 1996-02-28 |
AU4523193A (en) | 1993-12-30 |
DE69330498T2 (de) | 2002-05-23 |
ATE203409T1 (de) | 2001-08-15 |
FI945599A0 (fi) | 1994-11-28 |
CA2136824C (en) | 1999-08-17 |
NZ253852A (en) | 1997-02-24 |
NO944515L (no) | 1995-01-30 |
EP0788362A1 (en) | 1997-08-13 |
CA2136824A1 (en) | 1993-12-09 |
JPH07507318A (ja) | 1995-08-10 |
AU663966B2 (en) | 1995-10-26 |
NO944515D0 (no) | 1994-11-25 |
NO310463B1 (no) | 2001-07-09 |
PL174726B1 (pl) | 1998-09-30 |
HU9403405D0 (en) | 1995-02-28 |
DE69330498D1 (de) | 2001-08-30 |
EP0788362B1 (en) | 2001-07-25 |
CZ296894A3 (en) | 1996-01-17 |
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