SE7703786L - Triazolo-pyrimidiner och farmaceutiska kompositioner innehallande sadana foreningar - Google Patents
Triazolo-pyrimidiner och farmaceutiska kompositioner innehallande sadana foreningarInfo
- Publication number
- SE7703786L SE7703786L SE7703786A SE7703786A SE7703786L SE 7703786 L SE7703786 L SE 7703786L SE 7703786 A SE7703786 A SE 7703786A SE 7703786 A SE7703786 A SE 7703786A SE 7703786 L SE7703786 L SE 7703786L
- Authority
- SE
- Sweden
- Prior art keywords
- triazolo
- pyrimidines
- associations
- pharmaceutical compositions
- compositions containing
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US67378576A | 1976-04-05 | 1976-04-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
SE7703786L true SE7703786L (sv) | 1977-10-06 |
Family
ID=24704115
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SE7703787A SE7703787L (sv) | 1976-04-05 | 1977-03-31 | Trizzolo-pyrimidiner |
SE7703786A SE7703786L (sv) | 1976-04-05 | 1977-03-31 | Triazolo-pyrimidiner och farmaceutiska kompositioner innehallande sadana foreningar |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SE7703787A SE7703787L (sv) | 1976-04-05 | 1977-03-31 | Trizzolo-pyrimidiner |
Country Status (10)
Country | Link |
---|---|
US (1) | US4076711A (sv) |
JP (2) | JPS52122632A (sv) |
AU (2) | AU2384177A (sv) |
BE (2) | BE853086A (sv) |
DE (2) | DE2714263A1 (sv) |
DK (2) | DK146677A (sv) |
FR (2) | FR2347044A1 (sv) |
NL (2) | NL7703515A (sv) |
SE (2) | SE7703787L (sv) |
ZA (2) | ZA771997B (sv) |
Families Citing this family (47)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4172829A (en) * | 1978-05-09 | 1979-10-30 | Bristol-Myers Company | 2,9-Disubstituted adenine derivatives and their use as non-adrenergic bronchodilators |
US4742064A (en) * | 1985-09-10 | 1988-05-03 | Regents Of The University Of Minnesota | Antiviral carbocyclic analogs of xylofuranosylpurines |
LU86547A1 (fr) * | 1986-08-07 | 1988-03-02 | Oreal | Suspension pour induire et stimuler la croissance des cheveux et diminuer leur chute a base de derives de la pyrimidine |
EP0288431B1 (de) * | 1987-04-07 | 1992-08-19 | Ciba-Geigy Ag | 3H-1,2,3-Triazolo[4,5-d]pyrimidine |
US5204353A (en) * | 1987-04-07 | 1993-04-20 | Ciba-Geigy Corporation | 3-benzyl-3H-1,2,3-triazolo[4,5-d]pyrimidines, compositions thereof, and method of treating epilepsy therewith |
US5175292A (en) * | 1988-01-20 | 1992-12-29 | Regents Of The University Of Minnesota | Intermediates for the preparation of dideoxycarbocyclic nucleosides |
US5631370A (en) * | 1988-01-20 | 1997-05-20 | Regents Of The University Of Minnesota | Optically-active isomers of dideoxycarbocyclic nucleosides |
US4950758A (en) * | 1988-01-20 | 1990-08-21 | Regents Of The University Of Minnesota | Optically-active isomers of dideoxycarbocyclic nucleosides |
US4931559A (en) * | 1988-01-20 | 1990-06-05 | Regents Of The University Of Minnesota | Optically-active isomers of dideoxycarbocyclic nucleosides |
US4916224A (en) * | 1988-01-20 | 1990-04-10 | Regents Of The University Of Minnesota | Dideoxycarbocyclic nucleosides |
US4996116A (en) * | 1989-12-21 | 1991-02-26 | General Electric Company | Enhanced direct bond structure |
AU647822B2 (en) * | 1990-09-14 | 1994-03-31 | Marion Merrell Dow Inc. | Novel carbocyclic adenosine analogs useful as immunosuppressants |
US5244896A (en) * | 1990-09-14 | 1993-09-14 | Marion Merrell Dow Inc. | Carbocyclic adenosine analogs useful as immunosuppressants |
US5514688A (en) * | 1990-09-14 | 1996-05-07 | Merrell Dow Pharmaceuticals Inc. | Carbocyclic adenosine analogs useful as immunosuppressants |
US5817661A (en) * | 1991-12-06 | 1998-10-06 | Hoechst Marion Roussel, Inc. | Trans cyclopentanyl purine analogs useful as immunosuppressants |
US5817660A (en) * | 1991-12-06 | 1998-10-06 | Hoechst Marion Roussel, Inc. | Trans cyclopentanyl purine analogs useful as immunosuppressants |
US5723466A (en) * | 1991-12-06 | 1998-03-03 | Hoechst Marion Roussel, Inc. | Trans cyclopentanyl purine analogs useful as immunosuppressants |
US5817672A (en) * | 1991-12-06 | 1998-10-06 | Hoechst Marion Roussel, Inc. | Trans cyclopentanyl purine analogs useful as immunosuppressants |
AU658698B2 (en) * | 1991-12-06 | 1995-04-27 | Aventis Pharmaceuticals Inc. | Novel trans cyclopentanyl purine analogs useful as immunosuppressants |
AU725254B2 (en) * | 1996-03-26 | 2000-10-12 | Du Pont Pharmaceuticals Company | Aryloxy- and arylthio- fused pyridines and pyrimidines and derivatives |
ZA971896B (en) * | 1996-03-26 | 1998-09-07 | Du Pont Merck Pharma | Aryloxy-and arythio-fused pyridines and pyrimidines and derivatives |
US6107300A (en) * | 1996-03-27 | 2000-08-22 | Dupont Pharmaceuticals | Arylamino fused pyrimidines |
ZA972497B (en) | 1996-03-27 | 1998-09-25 | Du Pont Merck Pharma | Arylamino fused pyridines and pyrimidines |
CA2238283C (en) * | 1997-05-30 | 2002-08-20 | Cell Pathways, Inc. | Method for identifying compounds for inhibition of neoplastic lesions, pharmaceutical compositions from such compounds and uses of such compounds and compositions for treating neoplastic lesions |
US5858694A (en) * | 1997-05-30 | 1999-01-12 | Cell Pathways, Inc. | Method for identifying compounds for inhibition of cancerous lesions |
US6410584B1 (en) * | 1998-01-14 | 2002-06-25 | Cell Pathways, Inc. | Method for inhibiting neoplastic cells with indole derivatives |
DE19838705A1 (de) * | 1998-08-26 | 2000-03-02 | Bayer Ag | Neue Dihydro-(1,2,3)-triazolo-[4,5-d]pyrimidin-7-one |
US6200771B1 (en) | 1998-10-15 | 2001-03-13 | Cell Pathways, Inc. | Method of using a novel phosphodiesterase in pharmaceutical screeing to identify compounds for treatment of neoplasia |
US6130053A (en) * | 1999-08-03 | 2000-10-10 | Cell Pathways, Inc. | Method for selecting compounds for inhibition of neoplastic lesions |
US6133271A (en) * | 1998-11-19 | 2000-10-17 | Cell Pathways, Inc. | Method for inhibiting neoplastic cells and related conditions by exposure thienopyrimidine derivatives |
US6187779B1 (en) | 1998-11-20 | 2001-02-13 | Cell Pathways, Inc. | Method for inhibiting neoplastic cells and related conditions by exposure to 2,8-disubstituted quinazoline derivatives |
US6369092B1 (en) | 1998-11-23 | 2002-04-09 | Cell Pathways, Inc. | Method for treating neoplasia by exposure to substituted benzimidazole derivatives |
US6034099A (en) * | 1998-11-24 | 2000-03-07 | Cell Pathways, Inc. | Method for inhibiting neoplastic lesions by administering 4-(arylmethylene)- 2, 3- dihydro-pyrazol-3-ones |
US6486155B1 (en) | 1998-11-24 | 2002-11-26 | Cell Pathways Inc | Method of inhibiting neoplastic cells with isoquinoline derivatives |
US6077842A (en) * | 1998-11-24 | 2000-06-20 | Cell Pathways, Inc. | Method of inhibiting neoplastic cells with pyrazolopyridylpyridazinone derivatives |
US6025394A (en) | 1999-01-29 | 2000-02-15 | Cell Pathways, Inc. | Method for treating patients with acne by administering substituted sulfonyl indenyl acetic acids, amides and alcohols |
US6020379A (en) * | 1999-02-19 | 2000-02-01 | Cell Pathways, Inc. | Position 7 substituted indenyl-3-acetic acid derivatives and amides thereof for the treatment of neoplasia |
US6555547B1 (en) | 2000-02-28 | 2003-04-29 | Cell Pathways, Inc. | Method for treating a patient with neoplasia by treatment with a vinca alkaloid derivative |
US6569638B1 (en) | 2000-03-03 | 2003-05-27 | Cell Pathways, Inc | Method for screening compounds for the treatment of neoplasia |
EP1703668A1 (en) * | 2005-03-18 | 2006-09-20 | Nederlandse Organisatie voor toegepast-natuurwetenschappelijk Onderzoek TNO | System for processing quality-of-service parameters in a communication network |
EP2008210A1 (en) * | 2006-03-15 | 2008-12-31 | Csir | Modulation of phosphoryl transferase activity of glutamine synthetase |
GB2451594A (en) * | 2006-03-15 | 2009-02-04 | Csir | Modulation of phosphoryl transferase activity of glutamine synthetase |
CA2668180A1 (en) * | 2006-10-31 | 2008-05-08 | Janssen Pharmaceutica N.V. | Triazolopyrimidine derivatives as adp p2y12 receptor antagonists |
CA2668182A1 (en) | 2006-10-31 | 2008-05-08 | Janssen Pharmaceutica N.V. | Triazolopyrimidine derivatives as adp p2y12 receptor antagonists |
JP4927502B2 (ja) * | 2006-11-08 | 2012-05-09 | 東京電力株式会社 | ケーブル拘束装置 |
UA111640C2 (uk) * | 2011-11-08 | 2016-05-25 | Ф. Хоффманн-Ля Рош Аг | ПОХІДНІ [1,2,3]ТРИАЗОЛО[4,5-d]ПІРИМІДИНУ ЯК АГОНІСТИ КАНАБІНОЇДНОГО РЕЦЕПТОРА 2 |
CN109937038A (zh) | 2016-08-26 | 2019-06-25 | 田边三菱制药株式会社 | 双环式含氮杂环化合物 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2407204A (en) * | 1944-07-22 | 1946-09-03 | American Cyanamid Co | Triazolo (d) pyrimidines and methods of preparing the same |
-
1976
- 1976-12-22 US US05/753,205 patent/US4076711A/en not_active Expired - Lifetime
-
1977
- 1977-03-31 AU AU23841/77A patent/AU2384177A/en not_active Expired
- 1977-03-31 NL NL7703515A patent/NL7703515A/xx not_active Application Discontinuation
- 1977-03-31 NL NL7703514A patent/NL7703514A/xx not_active Application Discontinuation
- 1977-03-31 AU AU23842/77A patent/AU2384277A/en not_active Expired
- 1977-03-31 SE SE7703787A patent/SE7703787L/sv unknown
- 1977-03-31 BE BE176289A patent/BE853086A/xx unknown
- 1977-03-31 FR FR7709750A patent/FR2347044A1/fr not_active Withdrawn
- 1977-03-31 DE DE19772714263 patent/DE2714263A1/de active Pending
- 1977-03-31 DE DE19772714254 patent/DE2714254A1/de active Pending
- 1977-03-31 FR FR7709749A patent/FR2347367A1/fr not_active Withdrawn
- 1977-03-31 BE BE176288A patent/BE853085A/xx unknown
- 1977-03-31 SE SE7703786A patent/SE7703786L/sv unknown
- 1977-04-01 DK DK146677A patent/DK146677A/da not_active IP Right Cessation
- 1977-04-01 ZA ZA00771997A patent/ZA771997B/xx unknown
- 1977-04-01 DK DK146077A patent/DK146077A/da not_active IP Right Cessation
- 1977-04-01 JP JP3748077A patent/JPS52122632A/ja active Pending
- 1977-04-01 ZA ZA00771998A patent/ZA771998B/xx unknown
- 1977-04-01 JP JP3747977A patent/JPS52122395A/ja active Pending
Also Published As
Publication number | Publication date |
---|---|
NL7703514A (nl) | 1977-10-07 |
ZA771997B (en) | 1978-03-29 |
FR2347367A1 (fr) | 1977-11-04 |
US4076711A (en) | 1978-02-28 |
JPS52122632A (en) | 1977-10-15 |
JPS52122395A (en) | 1977-10-14 |
DK146677A (da) | 1977-10-06 |
ZA771998B (en) | 1978-03-29 |
SE7703787L (sv) | 1977-10-06 |
DE2714263A1 (de) | 1977-10-13 |
AU2384277A (en) | 1978-10-05 |
DK146077A (da) | 1977-10-06 |
DE2714254A1 (de) | 1977-10-06 |
AU2384177A (en) | 1978-10-12 |
NL7703515A (nl) | 1977-10-07 |
BE853085A (fr) | 1977-09-30 |
BE853086A (fr) | 1977-09-30 |
FR2347044A1 (fr) | 1977-11-04 |
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