CA1075604A - Compose antispasmodique - Google Patents

Compose antispasmodique

Info

Publication number: CA1075604A
Authority: CA; Canada
Prior art keywords: composition; allyl; compound; acid; radical
Prior art date: 1976-05-18
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

Application number

CA278,449A

Other languages

English (en)

Inventor

Rolf Deininger

Erich Wolf

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Chimicasa GmbH

Original Assignee

Chimicasa GmbH

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.)

1976-05-18

Filing date

1977-05-16

Publication date

1980-04-15

1977-05-16 Application filed by Chimicasa GmbH filed Critical Chimicasa GmbH

1980-04-15 Application granted granted Critical

1980-04-15 Publication of CA1075604A publication Critical patent/CA1075604A/fr

Status Expired legal-status Critical Current

Links

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239000002775 capsule Substances 0.000 claims description 7
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239000000725 suspension Substances 0.000 claims description 4
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YJVWPNSZWZRJBB-UHFFFAOYSA-N 2,3-dimethylcyclohexene-1-carboxylic acid Chemical compound CC1CCCC(C(O)=O)=C1C YJVWPNSZWZRJBB-UHFFFAOYSA-N 0.000 description 1
PSHADDQTSCEAHY-UHFFFAOYSA-N 2-(2-methylpropyl)benzoic acid Chemical compound CC(C)CC1=CC=CC=C1C(O)=O PSHADDQTSCEAHY-UHFFFAOYSA-N 0.000 description 1
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QXKNDUSXGFIHHU-UHFFFAOYSA-N 2-methylcyclopentene-1-carboxylic acid Chemical compound CC1=C(C(O)=O)CCC1 QXKNDUSXGFIHHU-UHFFFAOYSA-N 0.000 description 1
125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
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125000001624 naphthyl group Chemical group 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
125000001196 nonadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000005187 nonenyl group Chemical group C(=CCCCCCCC)* 0.000 description 1
125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
ZWLPBLYKEWSWPD-UHFFFAOYSA-N o-toluic acid Chemical compound CC1=CC=CC=C1C(O)=O ZWLPBLYKEWSWPD-UHFFFAOYSA-N 0.000 description 1
125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 1
125000005064 octadecenyl group Chemical group C(=CCCCCCCCCCCCCCCCC)* 0.000 description 1
125000004365 octenyl group Chemical group C(=CCCCCCC)* 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000003921 oil Substances 0.000 description 1
235000019198 oils Nutrition 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000002958 pentadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000002255 pentenyl group Chemical group C(=CCCC)* 0.000 description 1
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
235000019271 petrolatum Nutrition 0.000 description 1
229940066842 petrolatum Drugs 0.000 description 1
230000000144 pharmacologic effect Effects 0.000 description 1
125000005592 polycycloalkyl group Polymers 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
210000000664 rectum Anatomy 0.000 description 1
CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
229940081974 saccharin Drugs 0.000 description 1
235000019204 saccharin Nutrition 0.000 description 1
239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
230000037321 sleepiness Effects 0.000 description 1
239000002002 slurry Substances 0.000 description 1
241000894007 species Species 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229910052682 stishovite Inorganic materials 0.000 description 1
210000002784 stomach Anatomy 0.000 description 1
208000011117 substance-related disease Diseases 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
235000012222 talc Nutrition 0.000 description 1
125000005063 tetradecenyl group Chemical group C(=CCCCCCCCCCCCC)* 0.000 description 1
238000002560 therapeutic procedure Methods 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
125000005040 tridecenyl group Chemical group C(=CCCCCCCCCCCC)* 0.000 description 1
125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229910052905 tridymite Inorganic materials 0.000 description 1
UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
125000005065 undecenyl group Chemical group C(=CCCCCCCCCC)* 0.000 description 1
125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
ABDKAPXRBAPSQN-UHFFFAOYSA-N veratrole Chemical compound COC1=CC=CC=C1OC ABDKAPXRBAPSQN-UHFFFAOYSA-N 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
238000010792 warming Methods 0.000 description 1
125000005023 xylyl group Chemical group 0.000 description 1

Classifications

- 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
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/22—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
- 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
- A61K31/075—Ethers or acetals
- A61K31/085—Ethers or acetals having an ether linkage to aromatic ring nuclear carbon
- A61K31/09—Ethers or acetals having an ether linkage to aromatic ring nuclear carbon having two or more such linkages
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
- C07C43/23—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing hydroxy or O-metal groups
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/007—Esters of unsaturated alcohols having the esterified hydroxy group bound to an acyclic carbon atom
- C07C69/01—Vinyl esters
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/02—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
- C07C69/12—Acetic acid esters
- C07C69/16—Acetic acid esters of dihydroxylic compounds

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Pharmacology & Pharmacy (AREA)
Epidemiology (AREA)
Life Sciences & Earth Sciences (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Emergency Medicine (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Medicinal Preparation (AREA)

CA278,449A 1976-05-18 1977-05-16 Compose antispasmodique Expired CA1075604A (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
LU74973A LU74973A1 (fr)	1976-05-18	1976-05-18

Publications (1)

Publication Number	Publication Date
CA1075604A true CA1075604A (fr)	1980-04-15

Family

ID=19728242

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA278,449A Expired CA1075604A (fr)	1976-05-18	1977-05-16	Compose antispasmodique

Country Status (9)

Country	Link
JP (1)	JPS52142030A (fr)
BE (1)	BE854716A (fr)
CA (1)	CA1075604A (fr)
DE (1)	DE2719623A1 (fr)
ES (1)	ES458893A1 (fr)
FR (1)	FR2362625A1 (fr)
GB (1)	GB1572119A (fr)
LU (1)	LU74973A1 (fr)
NL (1)	NL7705436A (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2466458A1 (fr) *	1979-09-27	1981-04-10	Mathieu Andre	Nouveaux medicaments derives de l'eugenol
US4533746A (en) *	1983-06-16	1985-08-06	International Flavors & Fragrances Inc.	2-Methoxy-4-(2-methylpropenyl) phenyl ester of isobutyric acid, flavor use thereof and process for preparing same

1976
- 1976-05-18 LU LU74973A patent/LU74973A1/xx unknown
1977
- 1977-05-03 DE DE19772719623 patent/DE2719623A1/de not_active Ceased
- 1977-05-16 CA CA278,449A patent/CA1075604A/fr not_active Expired
- 1977-05-16 FR FR7714850A patent/FR2362625A1/fr active Granted
- 1977-05-16 BE BE177645A patent/BE854716A/fr not_active IP Right Cessation
- 1977-05-16 GB GB2043377A patent/GB1572119A/en not_active Expired
- 1977-05-17 JP JP5605377A patent/JPS52142030A/ja active Pending
- 1977-05-17 NL NL7705436A patent/NL7705436A/xx not_active Application Discontinuation
- 1977-05-18 ES ES458893A patent/ES458893A1/es not_active Expired

Also Published As

Publication number	Publication date
FR2362625A1 (fr)	1978-03-24
ES458893A1 (es)	1978-03-16
FR2362625B1 (fr)	1980-01-18
JPS52142030A (en)	1977-11-26
BE854716A (fr)	1977-09-16
LU74973A1 (fr)	1977-12-22
NL7705436A (nl)	1977-11-22
GB1572119A (en)	1980-07-23
DE2719623A1 (de)	1977-12-08

Legal Events

Date	Code	Title	Description
1997-04-15	MKEX	Expiry

Publication	Publication Date	Title
CA1239587A (fr)	1988-07-26	Compose d'acides gras pour abaisser les taux de cholesterol et de triglycerides sanguins
KR850000072B1 (ko)	1985-02-18	5-(2-포르밀-3-히드록시페녹시)펜타노익산류
CA1246544A (fr)	1988-12-13	Tigogenine-cellobioside pour le traitement de l'hypercholesterolemie et de l'arteriosclerose
DE69909633T2 (de)	2004-05-13	Gut wasserlösliche triptolid-prodrugs
JPS63225340A (ja)	1988-09-20	リポキシゲナーゼ抑制化合物
IE44639B1 (en)	1982-02-10	Oxadiazoloyl-substituted compounds having pharmacological activity
CA1075604A (fr)	1980-04-15	Compose antispasmodique
DE1593901B2 (de)	1976-12-23	Basisch substituierte benzofurane oder indole und verfahren zu deren herstellung sowie diese verbindungen enthaltende arzneimittel
US4119730A (en)	1978-10-10	Treating muscle spasms
AU2003209616B2 (en)	2008-07-10	Bicyclic CB2 cannabinoid receptor ligands
EP0623138A1 (fr)	1994-11-09	Nouveaux derives de l'adenosine, leurs procedes de preparation, compositions pharmaceutiques les contenant.
US3906030A (en)	1975-09-16	New amino ether derivatives of orthothymotic esters
US3504028A (en)	1970-03-31	Primary amides
US4540709A (en)	1985-09-10	Method for treatment of diseases mediated by PAF using 5-allyl-2-(3,4-Dimethoxyphenyl)-3a,α-methoxy-3-methyl-2,3,3a,6-tetrahydro-6-oxobenzofuran
US4053624A (en)	1977-10-11	Indole-2-carbaldehyde compounds and blood sugar reducing compositions
US3143469A (en)	1964-08-04	Anti-cholesterol nicotinic acid nu-oxide
Cordier et al.	1982	The Influence of Chromium, Manganese and Copper on the Tensile Properties and Stress Corrosion Cracking of the Weldable AlZn 5 Mg 1. 7 Alloy
DE2726435A1 (de)	1978-01-12	P-isobutylhydratropsaeureguajacolester
CA1252108A (fr)	1989-04-04	Derives de ( )-cyanidan-3-01, procede de production, preparations pharmaceutiques contenant lesdits derives et applications
DD202024A5 (de)	1983-08-24	Verfahren zur herstellung von 1-(1,3-benzodioxol-5-yl)-2-pyrrolidinon
US4647412A (en)	1987-03-03	Anti-tumor derivatives of butanediol and process of preparation
US4423073A (en)	1983-12-27	Fluorinated diaminopentene derivatives
DE69705238T2 (de)	2002-04-18	Derivate der asiatica-saeure mit einem modifizierten a-ring
US3646067A (en)	1972-02-29	Adamantylaminophenoxypropanols and ester derivatives
Gualtieri et al.	1974	Cyclopentane analog of muscarone