GB1476661A - Prostaglandins - Google Patents
ProstaglandinsInfo
- Publication number
- GB1476661A GB1476661A GB2113274A GB2113274A GB1476661A GB 1476661 A GB1476661 A GB 1476661A GB 2113274 A GB2113274 A GB 2113274A GB 2113274 A GB2113274 A GB 2113274A GB 1476661 A GB1476661 A GB 1476661A
- Authority
- GB
- United Kingdom
- Prior art keywords
- formula
- alkyl
- compounds
- optionally
- substituted
- 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.)
- Expired
Links
- 229940094443 oxytocics prostaglandins Drugs 0.000 title abstract 4
- 150000003180 prostaglandins Chemical class 0.000 title abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 9
- 125000000217 alkyl group Chemical group 0.000 abstract 7
- -1 2-tetrahydropyranyloxy Chemical group 0.000 abstract 4
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 3
- BZKFMUIJRXWWQK-UHFFFAOYSA-N Cyclopentenone Chemical class O=C1CCC=C1 BZKFMUIJRXWWQK-UHFFFAOYSA-N 0.000 abstract 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 2
- 239000005977 Ethylene Substances 0.000 abstract 2
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 abstract 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 150000007513 acids Chemical class 0.000 abstract 2
- FWFSEYBSWVRWGL-UHFFFAOYSA-N cyclohex-2-enone Chemical class O=C1CCCC=C1 FWFSEYBSWVRWGL-UHFFFAOYSA-N 0.000 abstract 2
- LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical group C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 abstract 2
- 230000003301 hydrolyzing effect Effects 0.000 abstract 2
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 abstract 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 1
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 1
- 125000000081 (C5-C8) cycloalkenyl group Chemical group 0.000 abstract 1
- KYPSXNJMGRMAJH-UHFFFAOYSA-N 2-(2-hydroxyethyl)cyclopent-2-en-1-one Chemical compound OCCC1=CCCC1=O KYPSXNJMGRMAJH-UHFFFAOYSA-N 0.000 abstract 1
- MXNHBXYFTYEVDJ-UHFFFAOYSA-N 2-(2-methoxyethyl)cyclopentan-1-one Chemical compound COCCC1CCCC1=O MXNHBXYFTYEVDJ-UHFFFAOYSA-N 0.000 abstract 1
- SXFXDSORNJJSAH-UHFFFAOYSA-N 2-bromo-2-(2-methoxyethyl)cyclopentan-1-one Chemical compound BrC1(C(CCC1)=O)CCOC SXFXDSORNJJSAH-UHFFFAOYSA-N 0.000 abstract 1
- LBCASPPRURMZJK-UHFFFAOYSA-N 3,3a,6,6a-tetrahydro-2h-cyclopenta[b]furan-2-ol Chemical compound C1=CCC2OC(O)CC21 LBCASPPRURMZJK-UHFFFAOYSA-N 0.000 abstract 1
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 abstract 1
- RUECHIAQOMCGSE-UHFFFAOYSA-N [2-(2-methoxyethyl)cyclopenten-1-yl] acetate Chemical compound COCCC1=C(OC(C)=O)CCC1 RUECHIAQOMCGSE-UHFFFAOYSA-N 0.000 abstract 1
- 150000001336 alkenes Chemical class 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 235000010210 aluminium Nutrition 0.000 abstract 1
- 239000002220 antihypertensive agent Substances 0.000 abstract 1
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 abstract 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 abstract 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 1
- 239000003085 diluting agent Substances 0.000 abstract 1
- 239000003937 drug carrier Substances 0.000 abstract 1
- 125000004185 ester group Chemical group 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 238000007911 parenteral administration Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- PMOIAJVKYNVHQE-UHFFFAOYSA-N phosphanium;bromide Chemical group [PH4+].[Br-] PMOIAJVKYNVHQE-UHFFFAOYSA-N 0.000 abstract 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- 125000005346 substituted cycloalkyl group Chemical group 0.000 abstract 1
- 125000005389 trialkylsiloxy group Chemical group 0.000 abstract 1
Classifications
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- C07D303/02—Compounds containing oxirane rings
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- C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
- C07C29/136—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
- C07C29/143—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of ketones
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- C07C31/13—Monohydroxylic alcohols containing saturated rings
- C07C31/133—Monohydroxylic alcohols containing saturated rings monocyclic
- C07C31/1333—Monohydroxylic alcohols containing saturated rings monocyclic with a three-membered ring
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- C07C33/40—Halogenated unsaturated alcohols
- C07C33/44—Halogenated unsaturated alcohols containing rings other than six-membered aromatic rings
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- C07C405/0008—Analogues having the carboxyl group in the side-chains replaced by other functional groups
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- C07C405/0008—Analogues having the carboxyl group in the side-chains replaced by other functional groups
- C07C405/0025—Analogues having the carboxyl group in the side-chains replaced by other functional groups containing keto groups
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- C07C405/0008—Analogues having the carboxyl group in the side-chains replaced by other functional groups
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- C07D307/93—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems condensed with a ring other than six-membered
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- C07C2601/18—Systems containing only non-condensed rings with a ring being at least seven-membered
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/582—Recycling of unreacted starting or intermediate materials
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Materials Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2113274A GB1476661A (en) | 1974-05-13 | 1974-05-13 | Prostaglandins |
| AU69162/74A AU493932B2 (en) | 1974-05-13 | 1974-05-20 | Novel prostaglandins |
| FR7418287A FR2272641B1 (enExample) | 1974-05-13 | 1974-05-27 | |
| DE19742425573 DE2425573A1 (de) | 1974-05-13 | 1974-05-27 | Neue prostaglandine |
| BE145128A BE815979A (fr) | 1974-05-13 | 1974-06-06 | Nouveaux derives d'acides 15-hydroxyprostanoiques et leur procede de preparation. |
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2113274A GB1476661A (en) | 1974-05-13 | 1974-05-13 | Prostaglandins |
| AU69162/74A AU493932B2 (en) | 1974-05-13 | 1974-05-20 | Novel prostaglandins |
| FR7418287A FR2272641B1 (enExample) | 1974-05-13 | 1974-05-27 | |
| DE19742425573 DE2425573A1 (de) | 1974-05-13 | 1974-05-27 | Neue prostaglandine |
| BE145128A BE815979A (fr) | 1974-05-13 | 1974-06-06 | Nouveaux derives d'acides 15-hydroxyprostanoiques et leur procede de preparation. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1476661A true GB1476661A (en) | 1977-06-16 |
Family
ID=27507185
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2113274A Expired GB1476661A (en) | 1974-05-13 | 1974-05-13 | Prostaglandins |
Country Status (5)
| Country | Link |
|---|---|
| AU (1) | AU493932B2 (enExample) |
| BE (1) | BE815979A (enExample) |
| DE (1) | DE2425573A1 (enExample) |
| FR (1) | FR2272641B1 (enExample) |
| GB (1) | GB1476661A (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5185374A (en) * | 1988-05-11 | 1993-02-09 | K.K. Ueno Seiyaku Oyo Kenkyujo | Use of 15-ketoprostaglandin E or F compounds for uterine contraction |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4074063A (en) * | 1976-02-11 | 1978-02-14 | Miles Laboratories, Inc. | Bicycloalkyl derivatives of prostaglandins |
| CA1322749C (en) * | 1987-01-28 | 1993-10-05 | Ryuzo Ueno | Prostaglandins of the d series, and tranquilizers and soporifics containing the same |
| CA1323364C (en) * | 1987-01-28 | 1993-10-19 | Ryuzo Ueno | Prostaglandins e and anti ulcer agents containing same |
| CA1324129C (en) * | 1987-04-30 | 1993-11-09 | Ryuzo Ueno | Prostaglandins of the f series |
| ES2052735T3 (es) * | 1987-09-18 | 1994-07-16 | R Tech Ueno Ltd | Un metodo para producir un agente hipotensor ocular. |
-
1974
- 1974-05-13 GB GB2113274A patent/GB1476661A/en not_active Expired
- 1974-05-20 AU AU69162/74A patent/AU493932B2/en not_active Expired
- 1974-05-27 FR FR7418287A patent/FR2272641B1/fr not_active Expired
- 1974-05-27 DE DE19742425573 patent/DE2425573A1/de not_active Withdrawn
- 1974-06-06 BE BE145128A patent/BE815979A/xx unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5185374A (en) * | 1988-05-11 | 1993-02-09 | K.K. Ueno Seiyaku Oyo Kenkyujo | Use of 15-ketoprostaglandin E or F compounds for uterine contraction |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2272641B1 (enExample) | 1978-02-03 |
| AU6916274A (en) | 1975-11-20 |
| DE2425573A1 (de) | 1975-12-11 |
| BE815979A (fr) | 1974-12-06 |
| FR2272641A1 (enExample) | 1975-12-26 |
| AU493932B2 (en) | 1975-11-20 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| 48S | Specification amended (sect. 8/1949) | ||
| 49R | Reference inserted (sect. 9/1949) | ||
| SPA | Amended specification published | ||
| PCNP | Patent ceased through non-payment of renewal fee |