SU1496632A3 - Cпocoб пoлучehия зameщehhыx бehзamидob - Google Patents

Cпocoб пoлучehия зameщehhыx бehзamидob Download PDF

Info

Publication number
SU1496632A3
SU1496632A3 SU864028722A SU4028722A SU1496632A3 SU 1496632 A3 SU1496632 A3 SU 1496632A3 SU 864028722 A SU864028722 A SU 864028722A SU 4028722 A SU4028722 A SU 4028722A SU 1496632 A3 SU1496632 A3 SU 1496632A3
Authority
SU
USSR - Soviet Union
Prior art keywords
day
substituted benzamides
producing substituted
nmol
diphenin
Prior art date
Application number
SU864028722A
Other languages
English (en)
Inventor
Zhak Asher
Zhan-Klod Mone
Zhan-Pol Shmitt
Rene Gardeks-Lyutro
Brenda Kostal
Rober Nejlor
Original Assignee
Ile De France
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.)
Filing date
Publication date
Application filed by Ile De France filed Critical Ile De France
Application granted granted Critical
Publication of SU1496632A3 publication Critical patent/SU1496632A3/ru

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/04Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D233/28Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/44Nitrogen atoms not forming part of a nitro radical
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/08Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/26Psychostimulants, e.g. nicotine, cocaine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/04Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D233/28Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/44Nitrogen atoms not forming part of a nitro radical
    • C07D233/50Nitrogen atoms not forming part of a nitro radical with carbocyclic radicals directly attached to said nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D263/00Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/08Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D263/16Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D263/28Nitrogen atoms not forming part of a nitro radical
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/08Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D277/12Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D277/18Nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links

Description

Изобретение относится к медицине, а именно к гинекологии.
Целью изобретения является предупреждение побочного действия от введения лекарственных средств.
Пример. Больная Н., 43 лет, обратилась с жалобами на боли в нижних отделах живота, больна в течение 6 лет. Диагноз при поступлении: миома матки. При обследовании размер образования соответствует 8-недельному сроку беременности, количество лимфоцитов 1782, Т-лимфоцитов 56%, содержание дофамина в суточной моче 1453 нмоль/сут; норадреналина 163,2 нмоль/сут, адреналина 74,2 нмоль/сут, серотонина 1,82 мкмоль/л, адаптационная реакция тренировки. Назначено: дифенин по 2 таблетки в день, настойка элеутерококка по 20 капель 2 раза в день, с 10-го дня очередного менструального цикла дигидроэрготамин по 15 капель 2 раза в день до 19 дня цикла включительно; лечение дифенином и настойкой элеутерококка продолжалось непрерывно в течение 2 мес., дигидроэрготамин повторно добавлен с 10-го дня второго менструального цикла на 10 дней.
После проведения курса лечения при обследовании размеры матки соответствуют 6-7-недельному сроку беременности, боли отсутствуют, количество лимфоцитов 1830, Т-лимфоцитов 62%, уровень экскретируемого дофамина 1605,1 нмоль/сут; норадреналина 136,1 нмоль/сут, адреналина 48,3 нмоль/сут, серотонина 1,1 мкмоль/л.
Способ лечения апробирован на 72 больных с различным клиническим течением миомы матки. После лечения у всех больных установлена нормализация психоэмоционального состояния и ликвидация болей; снижение менструальной кровопотери у 94,4%, стабилизация и уменьшение размеров матки у 95,8% больных.

Claims (1)

  1. Формула изобретения
    511 „149В7НУ
    Способ лечения миомы матки путем введения лекарственных средств, отличающийся тем, что, с целью предупреждения побочного действия, вводят дифенин, настойку элеутерококка и дигидроэрготамин в течение двух месяцев, при этом дифенин и настойку элеутерококка вводят ежедневно, а дигидроэрготамин в середине менструального цикла в течение 10 дней.
    1496799
    Соетавнтс.тк ,Ί. : [урышева
SU864028722A 1985-12-19 1986-12-18 Cпocoб пoлучehия зameщehhыx бehзamидob SU1496632A3 (ru)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR8518829A FR2592042B1 (fr) 1985-12-19 1985-12-19 Nouveaux ortho-anisamides, leur procede d'obtention, et leurs applications therapeutiques

Publications (1)

Publication Number Publication Date
SU1496632A3 true SU1496632A3 (ru) 1989-07-23

Family

ID=9325965

Family Applications (1)

Application Number Title Priority Date Filing Date
SU864028722A SU1496632A3 (ru) 1985-12-19 1986-12-18 Cпocoб пoлучehия зameщehhыx бehзamидob

Country Status (37)

Country Link
US (2) US4835172A (ru)
EP (1) EP0236646B1 (ru)
JP (1) JPS62246553A (ru)
KR (1) KR930004653B1 (ru)
CN (1) CN1018454B (ru)
AR (1) AR242193A1 (ru)
AT (1) ATE57376T1 (ru)
AU (1) AU586057B2 (ru)
CA (2) CA1298301C (ru)
CH (1) CH671396A5 (ru)
CS (1) CS274285B2 (ru)
DD (1) DD260495A5 (ru)
DE (2) DE3674916D1 (ru)
DK (1) DK612886A (ru)
ES (1) ES2036178T3 (ru)
FI (1) FI865190A (ru)
FR (1) FR2592042B1 (ru)
GB (1) GB2184723B (ru)
GR (1) GR3002524T3 (ru)
HU (1) HU196794B (ru)
IE (1) IE59212B1 (ru)
IL (1) IL81010A (ru)
IN (1) IN163130B (ru)
IS (1) IS1448B6 (ru)
MA (1) MA20835A1 (ru)
NO (1) NO168176C (ru)
NZ (1) NZ218675A (ru)
OA (1) OA08564A (ru)
PH (2) PH24365A (ru)
PL (1) PL148408B1 (ru)
PT (1) PT83982B (ru)
SU (1) SU1496632A3 (ru)
TN (1) TNSN86165A1 (ru)
YU (1) YU44796B (ru)
ZA (1) ZA869560B (ru)
ZM (1) ZM10686A1 (ru)
ZW (1) ZW24886A1 (ru)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3782651T2 (de) * 1987-06-17 1993-03-25 Delagrange Lab Anwendung von n-(2-(diaethylamino)aethyl)-2-methoxy-4((1-h-4,5-dihydro-2-imidazolyl)amino)-5-chlorobenzamid als anxiolytisches und antipsychotisches mittel.
FR2640139A1 (fr) * 1988-12-14 1990-06-15 Delagrange Laboratoires Application de benzamides substitues comme gastromoteurs
FR2640507A1 (fr) * 1988-12-20 1990-06-22 Delagrange Laboratoires Application de benzamides substitues comme anxiolytiques et anti-psychotiques
FR2645742A1 (fr) * 1989-04-12 1990-10-19 Delagrange Laboratoires Application de derives de 2-methoxy 4-(4,5-dihydro 2-imidazolyl (ou 2-oxazolyl) amino) 5-chloro benzamide dans le traitement des troubles de la fonction cognitive
US5401851A (en) * 1992-06-03 1995-03-28 Eli Lilly And Company Angiotensin II antagonists
US20050140688A1 (en) * 2003-12-29 2005-06-30 Kim Pallister Method and mechanism for programmable filtering of texture map data in 3D graphics subsystems

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3342826A (en) * 1964-01-13 1967-09-19 Ile De France Heterocyclic aminoalkyl benzamides
FR1539104A (fr) * 1967-07-31 1968-09-13 Ile De France Nouveaux benzamides et leur procédé de préparation
US3682968A (en) * 1969-06-25 1972-08-08 Merck & Co Inc Anti-inflammatory salicylic acid derivatives
DE1963193A1 (de) * 1969-12-17 1971-06-24 Bayer Ag N-substituierte 2-Arylimino-oxazolidine,Verfahren zu ihrer Herstellung und ihre Verwendung als Ektoparasiticide
FR2432513A1 (fr) * 1977-10-24 1980-02-29 Merieux Inst Nouveaux derives de la thiazoline et leur application comme medicaments
DE2905883A1 (de) * 1979-02-16 1980-08-28 Boehringer Sohn Ingelheim Radioimmuntest fuer clonidin
US4461904A (en) * 1981-11-20 1984-07-24 Alcon Laboratories, Inc. 2-(Trisubstituted phenylimino)-imidazolines
CA1201066A (en) * 1981-11-20 1986-02-25 Alcon Laboratories, Inc. N-¬3,5-dichloro-4-(2-imidazolidinylideneamino)- phenyl|-acetamide solutions for lowering intraocular pressure
DE3514351A1 (de) * 1985-04-20 1986-11-06 Boehringer Ingelheim KG, 6507 Ingelheim Neue substituierte 2-(n-alkinyl-n-phenyl)amino)-imidazolinderivate, deren saeureadditionssalze, diese enthaltende arzneimittel und verfahren zu deren herstellung
JPS6341471A (ja) * 1986-08-08 1988-02-22 Nippon Soda Co Ltd オキサ(チア)ゾリジン誘導体、その製造法及び殺ダニ剤
US4826990A (en) * 1987-09-30 1989-05-02 American Home Products Corporation 2-aryl substituted heterocyclic compounds as antiallergic and antiinflammatory agents

Also Published As

Publication number Publication date
CA1298301C (fr) 1992-03-31
GB2184723B (en) 1989-12-28
GB8630143D0 (en) 1987-01-28
DK612886A (da) 1987-06-20
IE59212B1 (en) 1994-01-26
YU44796B (en) 1991-02-28
OA08564A (fr) 1988-09-30
CH671396A5 (ru) 1989-08-31
GB2184723A (en) 1987-07-01
FI865190A (fi) 1987-06-20
DE3674916D1 (de) 1990-11-15
IL81010A (en) 1991-06-30
ATE57376T1 (de) 1990-10-15
NO168176B (no) 1991-10-14
IS1448B6 (is) 1991-01-16
AU6668786A (en) 1987-06-25
HUT43844A (en) 1987-12-28
IS3178A7 (is) 1987-06-20
US4914117A (en) 1990-04-03
PH24365A (en) 1990-06-13
TNSN86165A1 (fr) 1990-01-01
IE863270L (en) 1987-06-19
CN86108972A (zh) 1987-11-18
MA20835A1 (fr) 1987-07-01
FR2592042B1 (fr) 1988-03-25
EP0236646B1 (fr) 1990-10-10
DD260495A5 (de) 1988-09-28
KR870006008A (ko) 1987-07-08
YU217986A (en) 1987-12-31
NO865148L (no) 1987-06-22
AR242193A1 (es) 1993-03-31
ZA869560B (en) 1987-11-25
DE3643103A1 (de) 1987-06-25
US4835172A (en) 1989-05-30
GR3002524T3 (en) 1993-01-25
ZW24886A1 (en) 1987-05-13
CS274285B2 (en) 1991-04-11
PT83982A (en) 1987-01-01
EP0236646A1 (fr) 1987-09-16
NO168176C (no) 1992-01-22
NO865148D0 (no) 1986-12-18
PL263078A1 (en) 1988-04-14
HU196794B (en) 1989-01-30
NZ218675A (en) 1990-06-26
DK612886D0 (da) 1986-12-18
ES2036178T3 (es) 1993-05-16
ZM10686A1 (en) 1987-11-27
IL81010A0 (en) 1987-03-31
KR930004653B1 (ko) 1993-06-02
JPS62246553A (ja) 1987-10-27
FI865190A0 (fi) 1986-12-18
AU586057B2 (en) 1989-06-29
PL148408B1 (en) 1989-10-31
CS960386A2 (en) 1990-09-12
IN163130B (ru) 1988-08-13
FR2592042A1 (fr) 1987-06-26
CN1018454B (zh) 1992-09-30
PH24469A (en) 1990-07-18
PT83982B (pt) 1989-01-17
CA1299579C (fr) 1992-04-28

Similar Documents

Publication Publication Date Title
West Curare in man
Oppel et al. The effect of pituitary adrenocorticotropin (ACTH) in dermatomyositis
Martin Imipramine pamoate in the treatment of childhood enuresis: A double-blind study
SU1496632A3 (ru) Cпocoб пoлучehия зameщehhыx бehзamидob
Daley et al. Another hypotensive agent—methyldopa
TWI760194B (zh) 一種改善睡眠品質的飲用水
Valle et al. Auricular Hematoma in a Dog Treated by Homeopathic Therapy-Case Report
LENNOX et al. Studies in epilepsy: VIII. The clinical effect of fasting
SU1496799A1 (ru) Способ лечени миомы матки
Kamman The psychosomatic aspects of sterility
MARTIN et al. Disseminated actinomycosis treated with tetracycline
Mulinos Studies on cholin as a motor hormone for the alimentary tract
Godlowski Stimulation of the Suprarenal Glands in the Treatment of Rheumatoid Arthritis: Preliminary Report
Bauer et al. Studies of Calcium and Phosphorus Metabolism: X a. The Use of Calcium Chloride to Relieve Peristaltic Pain
Elman The oral use of the amino-acids of hydrolyzed casein (Amigen) in surgical patients
CN115475162B (zh) 4-异丁基-2-吡咯烷酮在制备镇痛药物中的应用、一种镇痛药物
Duffy et al. The HELLP syndrome mimics cholecystitis
COMROE SULPHUR THERAPY IN ARTHRITIS: With a Review of the Literature
RU2132187C1 (ru) Способ лечения заболеваний кожи и слизистых оболочек и магнитоактивное органическое соединение железа, используемое в нем
SU1210847A1 (ru) Способ лечени больных псориатическим артритом
SU1487907A1 (ru) Способ лечения овуляторных болей
RU1804851C (ru) Способ лечени хронических воспалительных заболеваний внутренних женских половых органов
SCHNEIDERMAN Recklinghausen's disease
Wheeldon The use of calcium ortho-iodoxybenzoate in the treatment of arthritis, with a discussion of its possible value in some other orthopedic conditions
Mullen et al. Dreaming, fenfluramine, and vitamin C.