US3755584A - Tranquilizers - Google Patents
Tranquilizers Download PDFInfo
- Publication number
- US3755584A US3755584A US00240770A US3755584DA US3755584A US 3755584 A US3755584 A US 3755584A US 00240770 A US00240770 A US 00240770A US 3755584D A US3755584D A US 3755584DA US 3755584 A US3755584 A US 3755584A
- Authority
- US
- United States
- Prior art keywords
- test
- doses
- animals
- dose
- activity
- 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 - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Definitions
- the new series is represented by the formula wherein R is fluorine at the 6- or 8-position, R is hydrogen or hydroxy, R" is fluorine, amino or acetylamino and n is 1 or 3.
- Example 1 The antogonism of methamphetamine-induced hyperactivity in mice was evaluated in motor activity chambers equipped with photocells connected to a counting device. Groups of mice were subcutaneously injected with 3 mg./ kg. of methamphetamine 2 hours after they had received an oral dose of the compound of Formula I wherein R is fluorine in the 8-position, R is hydrogen, R" is fluorine and 11:3. Three mice were placed in each chamber and a total of 9 mice were used per test dose. Changes in motor activity recorded are shown in the Table I.
- mice show a motor-activity reduction of 18% at 5 mg./kg., 60% at 10 mg./kg. and 66% at 20 mg./kg. Overt sedative effects (atoxia) were seen only at very high doses (1000 mg./kg.).
- Example 2 By following the same procedure as shown in Example 1 but using rats weighing between 200 and 300 g. as the test animals, the above identified compound showed the activity reduction listed in Table II.
- Table II shows similarly to Table I that the test compound identified above significantly reduces hyperactivity induced by methamphetamine.
- Example 3 8 fluoro-2-(4-p-fiuorophenylbutyl)-1,2,3,4-tetrahydro- 'y-carboline was administered orally to dogs at doses of 025-20 mg./ kg. followed in 2 hours with an oral dose of 5 mg./kg. of methamphetamine.
- the motor activity of the test dogs was measured on an activity scale of 0-3 with 3 being used for pronounced effects.
- doses of 5 mg./kg. of methamphetamine prodnced ratings of 3 in activity increase, mydriasis and sterotypy. When the methamphetamine was followed by 0.25 and 0.5 rug/kg.
- Example 4 The same compound as used in the preceding examples was tested orally in monkeys made hyperactive with methamphetamine doses of 5 mg./kg. At an oral treatment dose of 1-5 mg./kg. a significant reduction of stereotypy (head weaving and bobbing) and hyperactivity was observed. At higher doses (-20 mg./kg.) stereotypy and hyperactivity were not only antagonized but spontaneous motor activity was also reduced significantly. Similar antagonism was observed with chlorpromazine at doses of 2.5-5 mg./kg.
- Example 5 The methamphetamine test described above was carried out for other compounds encompassed by structure I.
- a group of mice were intraperitoneally treated with the test compound and the activity decrease measured in percent reduction from a control group.
- the animals received 3 mg./kg. of methamphethamine by the subcutaneous route and 2 hour activity comparisons were recorded in Table IV.
- Table IV Also shown in Table IV are the values observed in the modified DOPA test described by Everett in Proc. 1st Intl. Symp. Anti-depressant Drugs (Excerpta Med. Int. Congr. Sec.
- tranquilizing as used in this disclosure is meant to indicate primarily the reduction of hyperactivity and stereotypy as induced in test animals by methamphethamine.
- test results shown clearly indicate the advantageous use of the new compounds in treatment of schizophrenia, psychosis and depressions, whether these symptoms are clinical or brought on by hallucinogens.
- the oral route of administration intramuscular, intravenous and other routes are similarly useful.
- intravenous administration a dosage range of 0.1-5 mg./kg. is preferred while the intramuscular dose range is similar to the oral dose.
- parenteral administration the above drugs are preferably dissolved in physiological saline while oral dosage forms may be prepared in tablet, capsule, wafer or pill form according to well-known principles.
- the above compounds may be processed and administered in their base form or suitable pharmacologically acceptable salts may first be prepared. Particularly suitable are the acid addition salts formed with hydrochloric, sulfuric, phosphoric, acetic, succinic, tartaric or citric acid. Injectable solutions are preferably adjusted to a pH of 7 or slightly above by the use of a suitable buffer.
- the compounds used in the present invention are prepared by the method set forth in U.S. Pat. 3,654,289.
- H F 3 20 91 1 1 OH F 3 95 1 1 H NH: 1 50 98 2 3 H NHAo l 50 93 2 2 H NH: 3 50 92 2 2 H F 3 50 79 2 2
- the oral dosage range is therefore preferably chosen within the range of 1-5 mg./kg.
- the therapeutic index is as high as 1000 since the oral LD values of the above compounds are mostly between 250 and above 1000 mg./kg.
Abstract
Y-CARBOLINES CARRYING FLUORINE IN THE 6-OR 8-POSITION AND A SPECIFIC P-SUBSTITUTED PHENYLALKYL MOIETY AT THE 2POSITION WERE FOUND TO BE MAJOR TRANQUILIZERS AT LOW DOSES IN WARM-BLOODED ANIMALS.
Description
3,755,584 TRANQUILIZERS Nicholas Peter Plotnikolf, Lake Bluff, Ill., assignor to Abbott Laboratories, North Chicago, Ill. No Drawing. Filed Apr. 3, 1972, Ser. No. 240,770 Int. Cl. A61k 27/00 U.S. Cl. 424-263 4 Claims ABSTRACT OF THE DISCLOSURE 'y-Carbolines carrying fluorine in the 6- or 8-position and a specific p-substituted phenylalkyl moiety at the 2- position were found to be major tranquilizers at low doses in warm-blooded animals.
DETAILED DESCRIPTION OF THE INVENTION Many of the known antipsychotics (major tranquilizers) are very active in reducing hyperactivity and stereotypy induced by methamphetamine but, unfortunately, that desirable activity is often accompanied by sedative effects and tremors (Psychopharmacolog A Review of Progress 1957-1967, Public Health Service, Publication No. 1836 of 1968, Session XI). A new series of compounds has now been found which in its desirable antipsychotic potency is similar to chlorpromazine but produces no or almost no arkinson-like side effects or sedation.
The new series is represented by the formula wherein R is fluorine at the 6- or 8-position, R is hydrogen or hydroxy, R" is fluorine, amino or acetylamino and n is 1 or 3. When'these compounds are administered orally at doses of 0.52() mg./kg. to warm-blooded animals, strong tranquilization is achieved with no parkinson-like side effects and with minor sedative effects only in the upper range of the given dose limit. Acute toxicity studies in mice, rats, dogs and monkeys indicate a wide margin of safety or, expressed differently, the compounds of Formula I have a very high therapeutic index.
In order to show the efficacy of the new compounds, standard test methods were used in animals and comparative tests were carried out with commercial tranquilizers.
Example 1 The antogonism of methamphetamine-induced hyperactivity in mice was evaluated in motor activity chambers equipped with photocells connected to a counting device. Groups of mice were subcutaneously injected with 3 mg./ kg. of methamphetamine 2 hours after they had received an oral dose of the compound of Formula I wherein R is fluorine in the 8-position, R is hydrogen, R" is fluorine and 11:3. Three mice were placed in each chamber and a total of 9 mice were used per test dose. Changes in motor activity recorded are shown in the Table I.
United States Patent O In the above table, the last column represents the difference in activity chamber counts over the methamphetamine control when chlorpromazine is administered as the test drug in the same dose as listed for the test drug. The table clearly points out that for reducing hyperactivity, the above test drug, 8-fiuoro-2-(4-x-fluorophenylbutyl)-1,2,3,4-tetrahydro- -carboline, is comparable with chlorpromazine, although at the lower dose range, the new compound appears to be more efficient. No sedative action was noted with the test animals upon gross observation during and following the above 2 hour test.
Using the same procedure and setting but without inducing hyperactivity with methamphetamine, the above test in mice shows a motor-activity reduction of 18% at 5 mg./kg., 60% at 10 mg./kg. and 66% at 20 mg./kg. Overt sedative effects (atoxia) were seen only at very high doses (1000 mg./kg.).
Example 2 By following the same procedure as shown in Example 1 but using rats weighing between 200 and 300 g. as the test animals, the above identified compound showed the activity reduction listed in Table II.
Table II shows similarly to Table I that the test compound identified above significantly reduces hyperactivity induced by methamphetamine.
Example 3 8 fluoro-2-(4-p-fiuorophenylbutyl)-1,2,3,4-tetrahydro- 'y-carboline was administered orally to dogs at doses of 025-20 mg./ kg. followed in 2 hours with an oral dose of 5 mg./kg. of methamphetamine. The motor activity of the test dogs was measured on an activity scale of 0-3 with 3 being used for pronounced effects. In control animals, doses of 5 mg./kg. of methamphetamine prodnced ratings of 3 in activity increase, mydriasis and sterotypy. When the methamphetamine was followed by 0.25 and 0.5 rug/kg. of the test drug, one of two dogs of each dose level showed a 2 rating in stereotypy while all other symptoms for all 4 animals involved were the same as in the control animals. At a dose of 1 mg./kg. mydriasis was reduced to 2 in one dog, sterotypy was reduced to 2 in two animals and to 1 in the other two dogs. The higher doses produced the results shown in Table III.
1 Average of 6 dogs.
The values shown in parentheses above are those observed when the test drug is chlorpromazine. The above results, alone or in comparison with the commercial material, clearly show the pronounced effect of the tested drug.
Three other dogs were treated with the same drug at an oral dose of 10 mg./kg./ day for days. No behavorial or neurological eifects were seen. At higher doses (20 mg./kg.) this subacute test showed tremors on the 3rd and 5th day. When this test was carried out with chlorpromazine, tremors and decreased activity were observed already at lower doses.
Example 4 The same compound as used in the preceding examples was tested orally in monkeys made hyperactive with methamphetamine doses of 5 mg./kg. At an oral treatment dose of 1-5 mg./kg. a significant reduction of stereotypy (head weaving and bobbing) and hyperactivity was observed. At higher doses (-20 mg./kg.) stereotypy and hyperactivity were not only antagonized but spontaneous motor activity was also reduced significantly. Similar antagonism was observed with chlorpromazine at doses of 2.5-5 mg./kg.
Chronic toxicity studies revealed that tremors were seen only at doses of -40 mg./kg. establishing a wide margin of safety. Oral doses of 100-1000 mg./kg. administered as a 5-25% tragacanth suspension produced moderate to marked sedative efiects lasting up to 4 days. All 14 animals used in this test recovered fully by the fifth day.
Example 5 The methamphetamine test described above was carried out for other compounds encompassed by structure I. In this test, a group of mice were intraperitoneally treated with the test compound and the activity decrease measured in percent reduction from a control group. In all instances, the animals received 3 mg./kg. of methamphethamine by the subcutaneous route and 2 hour activity comparisons were recorded in Table IV. Also shown in Table IV are the values observed in the modified DOPA test described by Everett in Proc. 1st Intl. Symp. Anti-depressant Drugs (Excerpta Med. Int. Congr. Sec.
The term tranquilizing as used in this disclosure is meant to indicate primarily the reduction of hyperactivity and stereotypy as induced in test animals by methamphethamine. For higher animals and humans, the test results shown clearly indicate the advantageous use of the new compounds in treatment of schizophrenia, psychosis and depressions, whether these symptoms are clinical or brought on by hallucinogens.
While the above examples show, for the main part, the oral route of administration, intramuscular, intravenous and other routes are similarly useful. For intravenous administration, a dosage range of 0.1-5 mg./kg. is preferred while the intramuscular dose range is similar to the oral dose. For parenteral administration, the above drugs are preferably dissolved in physiological saline while oral dosage forms may be prepared in tablet, capsule, wafer or pill form according to well-known principles. For all routes, the above compounds may be processed and administered in their base form or suitable pharmacologically acceptable salts may first be prepared. Particularly suitable are the acid addition salts formed with hydrochloric, sulfuric, phosphoric, acetic, succinic, tartaric or citric acid. Injectable solutions are preferably adjusted to a pH of 7 or slightly above by the use of a suitable buffer.
The compounds used in the present invention are prepared by the method set forth in U.S. Pat. 3,654,289.
I claim:
1. The process of tranquilizing a warm-blooded animal comprising administering to said animal a small but tranquilizing amount of a compound of the formula N-CHm-GH-Q-R" Du i wherein R is fluorine attached to the 6- or S-position, R' is hydrogen or hydroxy, R" is fluorine, amino or acetylamino and n is 1 or 3 or a non-toxic acid addition salt thereof.
No. 122 of 1966) using a scale of 0-3. 2. The process of claim 1 wherein said compound or TABLE IV Antidepressant Compound of structure I fleet DGCI'GnSB Dose, in activity, 25 100 R R n mgJkg. percent mgJkg. mg.lkg.
H F 3 20 91 1 1 OH F 3 95 1 1 H NH: 1 50 98 2 3 H NHAo l 50 93 2 2 H NH: 3 50 92 2 2 H F 3 50 79 2 2 As demonstrated above, warm-blooded animals exhibit strong tranquilization when treated with a compound of structure I in doses similar or below amounts of commercial tranquilizers, In addition, the new treatment shows significant advantages over other drugs used for this type of therapy: tremors and sedation are totally absent when a dose within the lower effective amount is administered. The oral dosage range is therefore preferably chosen within the range of 1-5 mg./kg. In many instances, the therapeutic index is as high as 1000 since the oral LD values of the above compounds are mostly between 250 and above 1000 mg./kg.
UNITED STATES PATENTS 3,448,114 6/ 1969 Johnson et a1 260-296 STANLEY J. FRIEDMAN, Primary Examiner UNITED STATES PATENT OFFICE Certificate Patent No. 3,755,584 Patented August 28, 1973 Nicholas Peter Plotnikofi Application having been made by Nicholas Peter Plotnikofi, the inventor named in the patent above identified, and Abbott Laboratories, North Chicago, Illinois, a corporation of Illinois, the assignee, for the issuance of a certificate under the provisions of Title 35, Section 256, of the United States Code, adding the name of Robert P. J obnson as a joint inventor, and a showing and proof of facts satisfying the requirements of the said section having been submitted, it is this 2nd day of July 1974, certified that the name of the said Robert P. Johnson is hereby added to the said patent as a joint inventor with the said Nicholas Peter Plotnikofi'.
FRED W. SHERLING,
Associate Solicitor.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US24077072A | 1972-04-03 | 1972-04-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3755584A true US3755584A (en) | 1973-08-28 |
Family
ID=22907879
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US00240770A Expired - Lifetime US3755584A (en) | 1972-04-03 | 1972-04-03 | Tranquilizers |
Country Status (1)
Country | Link |
---|---|
US (1) | US3755584A (en) |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5512566A (en) * | 1993-10-25 | 1996-04-30 | Ortho Pharmaceutical Corporation | Tricyclic compounds having affinity for the 5-HT1A receptor |
US20030153555A1 (en) * | 2000-06-20 | 2003-08-14 | Tomas Eriksson | Novel compounds |
US20030158225A1 (en) * | 2000-02-25 | 2003-08-21 | Peter Hansen | Novel compounds |
US20030162772A1 (en) * | 2000-06-20 | 2003-08-28 | Tomas Eriksson | Novel compounds |
US20040006081A1 (en) * | 2000-05-17 | 2004-01-08 | Jeremy Burrows | Pharmaceutically active piperidine derivatives, in particular as modulators of chemokine receptor activity |
US20040102483A1 (en) * | 2001-02-19 | 2004-05-27 | Stephen Brough | Chemical compounds |
US20040110794A1 (en) * | 2001-03-22 | 2004-06-10 | Jeremy Burrows | Novel piperidine derivatives as modulators of chemokine receptors |
US20040267016A1 (en) * | 2001-11-15 | 2004-12-30 | Howard Tucker | Piperidine derivatives and their use as modulators of chemokine receptor activity (especially ccr5) |
US6903085B1 (en) | 1999-08-24 | 2005-06-07 | Astrazeneca, Ab | Substituted piperidine compounds useful as modulators of chemokine receptor activity |
US20070015788A1 (en) * | 2003-05-09 | 2007-01-18 | John Cumming | Chemical compounds |
US7345063B2 (en) | 2001-03-23 | 2008-03-18 | Astrazeneca Ab | Amides, preparation and therapeutic use as modulators of CCR-receptor activity |
US7388020B2 (en) | 2001-03-19 | 2008-06-17 | Astrazeneca Ab | Benzimidazol derivatives modulate chemokine receptors |
US20080227817A1 (en) * | 2005-08-02 | 2008-09-18 | Astrazeneca Ab | New Salt I |
-
1972
- 1972-04-03 US US00240770A patent/US3755584A/en not_active Expired - Lifetime
Cited By (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5512566A (en) * | 1993-10-25 | 1996-04-30 | Ortho Pharmaceutical Corporation | Tricyclic compounds having affinity for the 5-HT1A receptor |
US20050250792A1 (en) * | 1999-08-24 | 2005-11-10 | Stephen Thom | Substituted piperidine compounds useful as modulators of chemokine receptor activity |
US6903085B1 (en) | 1999-08-24 | 2005-06-07 | Astrazeneca, Ab | Substituted piperidine compounds useful as modulators of chemokine receptor activity |
US20030158225A1 (en) * | 2000-02-25 | 2003-08-21 | Peter Hansen | Novel compounds |
US6951874B2 (en) | 2000-02-25 | 2005-10-04 | Astrazeneca Ab | Compounds |
US6927222B2 (en) * | 2000-02-25 | 2005-08-09 | Astrazeneca Ab | Compounds |
US20040006081A1 (en) * | 2000-05-17 | 2004-01-08 | Jeremy Burrows | Pharmaceutically active piperidine derivatives, in particular as modulators of chemokine receptor activity |
US20090306141A1 (en) * | 2000-06-20 | 2009-12-10 | Tomas Eriksson | Novel Compounds |
US6911458B2 (en) | 2000-06-20 | 2005-06-28 | Astra Zeneca | Compounds |
US20030162772A1 (en) * | 2000-06-20 | 2003-08-28 | Tomas Eriksson | Novel compounds |
US20050239801A1 (en) * | 2000-06-20 | 2005-10-27 | Tomas Eriksson | Novel compounds |
US7528156B2 (en) | 2000-06-20 | 2009-05-05 | Astrazeneca Ab | Compounds |
US20030153555A1 (en) * | 2000-06-20 | 2003-08-14 | Tomas Eriksson | Novel compounds |
US7005439B2 (en) | 2000-06-20 | 2006-02-28 | Astrazeneca Ab | Compounds |
US20040102483A1 (en) * | 2001-02-19 | 2004-05-27 | Stephen Brough | Chemical compounds |
US6958350B2 (en) | 2001-02-19 | 2005-10-25 | Astrazeneca Ab | Chemical compounds |
US7388020B2 (en) | 2001-03-19 | 2008-06-17 | Astrazeneca Ab | Benzimidazol derivatives modulate chemokine receptors |
US20040110794A1 (en) * | 2001-03-22 | 2004-06-10 | Jeremy Burrows | Novel piperidine derivatives as modulators of chemokine receptors |
US6960602B2 (en) | 2001-03-22 | 2005-11-01 | Astrazeneca Ab | Piperidine derivatives as modulators of chemokine receptors |
US7345063B2 (en) | 2001-03-23 | 2008-03-18 | Astrazeneca Ab | Amides, preparation and therapeutic use as modulators of CCR-receptor activity |
US7192973B2 (en) | 2001-11-15 | 2007-03-20 | Astrazeneca Ab | Piperidine derivatives and their use as modulators of chemokine receptor activity (especially CCR5) |
US20070161646A1 (en) * | 2001-11-15 | 2007-07-12 | Astrazeneca Ab | Piperidine Derivatives and Their Use as Modulators of Chemokine Receptor Activity (Especially CCR5) |
US20040267016A1 (en) * | 2001-11-15 | 2004-12-30 | Howard Tucker | Piperidine derivatives and their use as modulators of chemokine receptor activity (especially ccr5) |
US7294636B2 (en) | 2003-05-09 | 2007-11-13 | Astrazeneca Ab | Chemical compounds |
US20070015788A1 (en) * | 2003-05-09 | 2007-01-18 | John Cumming | Chemical compounds |
US20080227817A1 (en) * | 2005-08-02 | 2008-09-18 | Astrazeneca Ab | New Salt I |
US8148405B2 (en) | 2005-08-02 | 2012-04-03 | Astrazeneca Ab | Salt I |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3755584A (en) | Tranquilizers | |
US4593034A (en) | 2-alkoxy-N-(1-azabicyclo[2.2.2]oct-3-yl)benzamides and thiobenzamides | |
CH616677A5 (en) | ||
DE4341403A1 (en) | N-substituted 3-azabicycloalkane derivatives, their preparation and use | |
DE2431178C2 (en) | Piperazine derivatives, processes for their preparation and medicinal preparations containing these compounds | |
Corne et al. | Pharmacological properties of pempidine (1: 2: 2: 6: 6‐pentamethylpiperidine), a new ganglion‐blocking compound | |
EP0282547B1 (en) | Method for controlling emesis caused by chemotherapeutic agents and antiemetic agents useful therein | |
US4717563A (en) | 2-alkoxy-N-(1-azabicyclo(2.2.2)oct-3-yl) benzamides and thiobenzamides in a method for alleviating emesis caused by non-platinum anticancer drugs | |
US20020147195A1 (en) | Piperidine derivatives and anti-platelet agents containing the same | |
US2890985A (en) | Composition and method for relieving spasticity | |
US4877794A (en) | 2-Alkoxy-n-(1-azabicyclo(2.2.2)oct-3-yl) benzamide and thiobenzamide compositions and the use thereof to treat schizophrenia | |
EP0391971A1 (en) | Improving toxicity profiles in chemotherapy. | |
DE1913199B2 (en) | Mannich bases from alpha-tetralone or its derivatives and arylalkylamines and their salts | |
US3328249A (en) | Process for counteracting depressive states | |
US3472874A (en) | 2-substituted 1,4-benzodioxanes | |
US3726979A (en) | Method of producing serotonin antagonism | |
US3485873A (en) | N-benzyl-n-methyl-omega-phenyl-omega-cycloalkyl-lower-alkylamines | |
US3860719A (en) | Antagonism of ethanol intoxication with 2-{8 (3,4-dichlorophenoxy)methyl{9 -2-imidazoline | |
EP0418327B1 (en) | Antiemesis ergoline derivatives | |
JPS6323880A (en) | Substituted hexahydroarylquinolidine | |
DE3231088C2 (en) | ||
US3088869A (en) | Antiemetic compositions and methods of treating nausea and vomiting | |
WO1982002891A1 (en) | Amino-2,1,3-benzothiadiazol and benzoxadiazol derivatives,preparation thereof and drugs containing them | |
US3150139A (en) | Nu-methylpiperazinocyclohexanol derivatives | |
AT336605B (en) | PROCESS FOR THE PREPARATION OF NEW TRIAZOLOPYRIDAZINES AND THEIR SALT |