NO844573L - Fremgangsmaate til hurtig avbrytelse av narkotikamisbruksyndrom - Google Patents

Fremgangsmaate til hurtig avbrytelse av narkotikamisbruksyndrom

Info

Publication number: NO844573L
Authority: NO; Norway
Prior art keywords: ibogaine; heroin; accordance; salt; drugs
Prior art date: 1983-11-18

Application number

NO844573A

Other languages

English (en)

Norwegian (no)

Inventor

Howard S Lotsof

Original Assignee

Howard S Lotsof

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.)

1983-11-18

Filing date

1984-11-16

Publication date

1985-05-20

1984-11-16 Application filed by Howard S Lotsof filed Critical Howard S Lotsof

1985-05-20 Publication of NO844573L publication Critical patent/NO844573L/no

Links

238000000034 method Methods 0.000 title claims description 14
229940079593 drug Drugs 0.000 title description 7
239000003814 drug Substances 0.000 title description 7
HSIBGVUMFOSJPD-CFDPKNGZSA-N ibogaine Chemical compound N1([C@@H]2[C@H]3C[C@H](C1)C[C@@H]2CC)CCC1=C3NC2=CC=C(OC)C=C12 HSIBGVUMFOSJPD-CFDPKNGZSA-N 0.000 claims description 72
VOXIUXZAOFEFBL-UHFFFAOYSA-N Voacangin Natural products CCC1CC2CN3CC1C(C2)(OC(=O)C)c4[nH]c5ccc(OC)cc5c4C3 VOXIUXZAOFEFBL-UHFFFAOYSA-N 0.000 claims description 70
OLOCMRXSJQJJPL-UHFFFAOYSA-N ibogaine Natural products CCC1CC2CC3C1N(C2)C=Cc4c3[nH]c5ccc(OC)cc45 OLOCMRXSJQJJPL-UHFFFAOYSA-N 0.000 claims description 70
AREITJMUSRHSBK-UHFFFAOYSA-N ibogamine Natural products CCC1CC2C3CC1CN2CCc4c3[nH]c5ccccc45 AREITJMUSRHSBK-UHFFFAOYSA-N 0.000 claims description 70
208000003698 Heroin Dependence Diseases 0.000 claims description 9
150000003839 salts Chemical class 0.000 claims description 8
239000000463 material Substances 0.000 claims description 7
229930013930 alkaloid Natural products 0.000 claims description 6
231100000252 nontoxic Toxicity 0.000 claims description 6
230000003000 nontoxic effect Effects 0.000 claims description 6
241001246918 Tabernanthe iboga Species 0.000 claims description 4
150000003797 alkaloid derivatives Chemical class 0.000 claims description 3
CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical class Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 claims description 2
239000000203 mixture Substances 0.000 claims 3
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 1
GVGLGOZIDCSQPN-PVHGPHFFSA-N Heroin Chemical compound O([C@H]1[C@H](C=C[C@H]23)OC(C)=O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4OC(C)=O GVGLGOZIDCSQPN-PVHGPHFFSA-N 0.000 description 16
229960002069 diamorphine Drugs 0.000 description 16
238000011282 treatment Methods 0.000 description 15
230000000694 effects Effects 0.000 description 11
230000009471 action Effects 0.000 description 10
208000011580 syndromic disease Diseases 0.000 description 7
ZPUCINDJVBIVPJ-LJISPDSOSA-N cocaine Chemical compound O([C@H]1C[C@@H]2CC[C@@H](N2C)[C@H]1C(=O)OC)C(=O)C1=CC=CC=C1 ZPUCINDJVBIVPJ-LJISPDSOSA-N 0.000 description 6
206010013663 drug dependence Diseases 0.000 description 5
230000007246 mechanism Effects 0.000 description 5
230000000007 visual effect Effects 0.000 description 5
230000003400 hallucinatory effect Effects 0.000 description 4
239000000380 hallucinogen Substances 0.000 description 4
BQJCRHHNABKAKU-KBQPJGBKSA-N morphine Chemical compound O([C@H]1[C@H](C=C[C@H]23)O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O BQJCRHHNABKAKU-KBQPJGBKSA-N 0.000 description 4
239000002574 poison Substances 0.000 description 4
231100000614 poison Toxicity 0.000 description 4
QZAYGJVTTNCVMB-UHFFFAOYSA-N serotonin Chemical compound C1=C(O)C=C2C(CCN)=CNC2=C1 QZAYGJVTTNCVMB-UHFFFAOYSA-N 0.000 description 4
208000004224 Opium Dependence Diseases 0.000 description 3
241000700159 Rattus Species 0.000 description 3
UCIDWKVIQZIKEK-NXWOVTFFSA-N Tabernanthine Chemical compound N1([C@@H]2[C@H]3C[C@@H](C1)C[C@@H]2CC)CCC1=C3NC2=CC(OC)=CC=C12 UCIDWKVIQZIKEK-NXWOVTFFSA-N 0.000 description 3
239000002269 analeptic agent Substances 0.000 description 3
229960003920 cocaine Drugs 0.000 description 3
229930005303 indole alkaloid Natural products 0.000 description 3
230000001788 irregular Effects 0.000 description 3
231100000862 numbness Toxicity 0.000 description 3
230000000144 pharmacologic effect Effects 0.000 description 3
229940076279 serotonin Drugs 0.000 description 3
UCIDWKVIQZIKEK-UHFFFAOYSA-N tabernanthine Natural products CCC1CC(C2)CC3C1N2CCC1=C3NC2=CC(OC)=CC=C12 UCIDWKVIQZIKEK-UHFFFAOYSA-N 0.000 description 3
KWGRBVOPPLSCSI-WPRPVWTQSA-N (-)-ephedrine Chemical compound CN[C@@H](C)[C@H](O)C1=CC=CC=C1 KWGRBVOPPLSCSI-WPRPVWTQSA-N 0.000 description 2
102000040125 5-hydroxytryptamine receptor family Human genes 0.000 description 2
108091032151 5-hydroxytryptamine receptor family Proteins 0.000 description 2
BXNJHAXVSOCGBA-UHFFFAOYSA-N Harmine Chemical compound N1=CC=C2C3=CC=C(OC)C=C3NC2=C1C BXNJHAXVSOCGBA-UHFFFAOYSA-N 0.000 description 2
241000283973 Oryctolagus cuniculus Species 0.000 description 2
208000007271 Substance Withdrawal Syndrome Diseases 0.000 description 2
238000010521 absorption reaction Methods 0.000 description 2
230000006978 adaptation Effects 0.000 description 2
WYTGDNHDOZPMIW-RCBQFDQVSA-N alstonine Chemical compound C1=CC2=C3C=CC=CC3=NC2=C2N1C[C@H]1[C@H](C)OC=C(C(=O)OC)[C@H]1C2 WYTGDNHDOZPMIW-RCBQFDQVSA-N 0.000 description 2
230000036592 analgesia Effects 0.000 description 2
230000003542 behavioural effect Effects 0.000 description 2
244000309464 bull Species 0.000 description 2
210000003169 central nervous system Anatomy 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
230000002526 effect on cardiovascular system Effects 0.000 description 2
230000004438 eyesight Effects 0.000 description 2
DQOMBBVESFBJLX-UHFFFAOYSA-N iboluteine Natural products N1C2=CC=C(OC)C=C2C(=O)C21CCN(C1)C3C2CC1CC3CC DQOMBBVESFBJLX-UHFFFAOYSA-N 0.000 description 2
230000003993 interaction Effects 0.000 description 2
231100000566 intoxication Toxicity 0.000 description 2
230000035987 intoxication Effects 0.000 description 2
238000002372 labelling Methods 0.000 description 2
RHCSKNNOAZULRK-UHFFFAOYSA-N mescaline Chemical compound COC1=CC(CCN)=CC(OC)=C1OC RHCSKNNOAZULRK-UHFFFAOYSA-N 0.000 description 2
229960005181 morphine Drugs 0.000 description 2
230000003533 narcotic effect Effects 0.000 description 2
230000001962 neuropharmacologic effect Effects 0.000 description 2
230000002085 persistent effect Effects 0.000 description 2
230000001766 physiological effect Effects 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
QVDSEJDULKLHCG-UHFFFAOYSA-N psilocybin Chemical compound C1=CC(OP(O)(O)=O)=C2C(CCN(C)C)=CNC2=C1 QVDSEJDULKLHCG-UHFFFAOYSA-N 0.000 description 2
102000005962 receptors Human genes 0.000 description 2
108020003175 receptors Proteins 0.000 description 2
230000000862 serotonergic effect Effects 0.000 description 2
239000003762 serotonin receptor affecting agent Substances 0.000 description 2
230000004936 stimulating effect Effects 0.000 description 2
239000000126 substance Substances 0.000 description 2
210000004291 uterus Anatomy 0.000 description 2
MGBKJKDRMRAZKC-UHFFFAOYSA-N 3-aminobenzene-1,2-diol Chemical class NC1=CC=CC(O)=C1O MGBKJKDRMRAZKC-UHFFFAOYSA-N 0.000 description 1
241000208327 Apocynaceae Species 0.000 description 1
206010013654 Drug abuse Diseases 0.000 description 1
102000009025 Endorphins Human genes 0.000 description 1
108010049140 Endorphins Proteins 0.000 description 1
206010015535 Euphoric mood Diseases 0.000 description 1
RERZNCLIYCABFS-UHFFFAOYSA-N Harmaline hydrochloride Natural products C1CN=C(C)C2=C1C1=CC=C(OC)C=C1N2 RERZNCLIYCABFS-UHFFFAOYSA-N 0.000 description 1
ZAGRKAFMISFKIO-UHFFFAOYSA-N Isolysergic acid Natural products C1=CC(C2=CC(CN(C2C2)C)C(O)=O)=C3C2=CNC3=C1 ZAGRKAFMISFKIO-UHFFFAOYSA-N 0.000 description 1
VAYOSLLFUXYJDT-RDTXWAMCSA-N Lysergic acid diethylamide Chemical compound C1=CC(C=2[C@H](N(C)C[C@@H](C=2)C(=O)N(CC)CC)C2)=C3C2=CNC3=C1 VAYOSLLFUXYJDT-RDTXWAMCSA-N 0.000 description 1
241000699670 Mus sp. Species 0.000 description 1
DMULVCHRPCFFGV-UHFFFAOYSA-N N,N-dimethyltryptamine Chemical compound C1=CC=C2C(CCN(C)C)=CNC2=C1 DMULVCHRPCFFGV-UHFFFAOYSA-N 0.000 description 1
206010028813 Nausea Diseases 0.000 description 1
102000003840 Opioid Receptors Human genes 0.000 description 1
108090000137 Opioid Receptors Proteins 0.000 description 1
206010033372 Pain and discomfort Diseases 0.000 description 1
208000010340 Sleep Deprivation Diseases 0.000 description 1
206010044565 Tremor Diseases 0.000 description 1
OIPILFWXSMYKGL-UHFFFAOYSA-N acetylcholine Chemical compound CC(=O)OCC[N+](C)(C)C OIPILFWXSMYKGL-UHFFFAOYSA-N 0.000 description 1
229960004373 acetylcholine Drugs 0.000 description 1
239000013543 active substance Substances 0.000 description 1
230000001800 adrenalinergic effect Effects 0.000 description 1
230000008485 antagonism Effects 0.000 description 1
230000008901 benefit Effects 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
210000004556 brain Anatomy 0.000 description 1
244000309466 calf Species 0.000 description 1
239000002775 capsule Substances 0.000 description 1
230000002490 cerebral effect Effects 0.000 description 1
231100000313 clinical toxicology Toxicity 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
239000000470 constituent Substances 0.000 description 1
KWGRBVOPPLSCSI-UHFFFAOYSA-N d-ephedrine Natural products CNC(C)C(O)C1=CC=CC=C1 KWGRBVOPPLSCSI-UHFFFAOYSA-N 0.000 description 1
230000007423 decrease Effects 0.000 description 1
230000003292 diminished effect Effects 0.000 description 1
230000003467 diminishing effect Effects 0.000 description 1
239000002552 dosage form Substances 0.000 description 1
230000008030 elimination Effects 0.000 description 1
238000003379 elimination reaction Methods 0.000 description 1
230000002996 emotional effect Effects 0.000 description 1
230000006397 emotional response Effects 0.000 description 1
230000002708 enhancing effect Effects 0.000 description 1
229960002179 ephedrine Drugs 0.000 description 1
230000002743 euphoric effect Effects 0.000 description 1
239000000945 filler Substances 0.000 description 1
VJHLDRVYTQNASM-UHFFFAOYSA-N harmine Natural products CC1=CN=CC=2NC3=CC(=CC=C3C=21)OC VJHLDRVYTQNASM-UHFFFAOYSA-N 0.000 description 1
IKJFDJLQPHDRTD-ISYVNWANSA-N ibogaine hydrochloride Chemical compound Cl.N1([C@@H]2[C@H]3C[C@H](C1)C[C@@H]2CC)CCC1=C3NC2=CC=C(OC)C=C12 IKJFDJLQPHDRTD-ISYVNWANSA-N 0.000 description 1
DQOMBBVESFBJLX-VXLUQLENSA-N iboluteine Chemical compound N1C2=CC=C(OC)C=C2C(=O)[C@@]21CCN(C1)[C@H]3[C@@H]2C[C@@H]1C[C@H]3CC DQOMBBVESFBJLX-VXLUQLENSA-N 0.000 description 1
230000008076 immune mechanism Effects 0.000 description 1
150000002475 indoles Chemical class 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
230000000977 initiatory effect Effects 0.000 description 1
210000000936 intestine Anatomy 0.000 description 1
238000002955 isolation Methods 0.000 description 1
230000002045 lasting effect Effects 0.000 description 1
230000005923 long-lasting effect Effects 0.000 description 1
ZAGRKAFMISFKIO-QMTHXVAHSA-N lysergic acid Chemical compound C1=CC(C2=C[C@H](CN([C@@H]2C2)C)C(O)=O)=C3C2=CNC3=C1 ZAGRKAFMISFKIO-QMTHXVAHSA-N 0.000 description 1
229950002454 lysergide Drugs 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
230000002503 metabolic effect Effects 0.000 description 1
239000004081 narcotic agent Substances 0.000 description 1
230000008693 nausea Effects 0.000 description 1
230000002644 neurohormonal effect Effects 0.000 description 1
239000000712 neurohormone Substances 0.000 description 1
KJONHKAYOJNZEC-UHFFFAOYSA-N nitrazepam Chemical compound C12=CC([N+](=O)[O-])=CC=C2NC(=O)CN=C1C1=CC=CC=C1 KJONHKAYOJNZEC-UHFFFAOYSA-N 0.000 description 1
239000000825 pharmaceutical preparation Substances 0.000 description 1
239000006187 pill Substances 0.000 description 1
239000000843 powder Substances 0.000 description 1
230000009290 primary effect Effects 0.000 description 1
230000008569 process Effects 0.000 description 1
102000004169 proteins and genes Human genes 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
230000009467 reduction Effects 0.000 description 1
230000009291 secondary effect Effects 0.000 description 1
230000001953 sensory effect Effects 0.000 description 1
239000000243 solution Substances 0.000 description 1
230000000638 stimulation Effects 0.000 description 1
238000005556 structure-activity relationship Methods 0.000 description 1
208000011117 substance-related disease Diseases 0.000 description 1
208000024891 symptom Diseases 0.000 description 1
239000003826 tablet Substances 0.000 description 1
238000002560 therapeutic procedure Methods 0.000 description 1
238000006257 total synthesis reaction Methods 0.000 description 1
239000002023 wood Substances 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom

Landscapes

Health & Medical Sciences (AREA)
Chemical & Material 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)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Medicines Containing Plant Substances (AREA)

NO844573A 1983-11-18 1984-11-16 Fremgangsmaate til hurtig avbrytelse av narkotikamisbruksyndrom NO844573L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US06/553,138 US4499096A (en)	1983-11-18	1983-11-18	Rapid method for interrupting the narcotic addiction syndrome

Publications (1)

Publication Number	Publication Date
NO844573L true NO844573L (no)	1985-05-20

Family

ID=24208273

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO844573A NO844573L (no)	1983-11-18	1984-11-16	Fremgangsmaate til hurtig avbrytelse av narkotikamisbruksyndrom

Country Status (11)

Country	Link
US (1)	US4499096A (da)
EP (1)	EP0163697B1 (da)
AU (1)	AU576538B2 (da)
CA (1)	CA1237986A (da)
DE (1)	DE3482305D1 (da)
DK (1)	DK156376C (da)
IE (1)	IE58567B1 (da)
IL (1)	IL73585A (da)
IT (1)	IT1178249B (da)
NO (1)	NO844573L (da)
WO (1)	WO1985002115A1 (da)

Families Citing this family (48)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4587243A (en) *	1985-07-15	1986-05-06	Lotsof Howard S	Rapid method for interrupting the cocaine and amphetamine abuse syndrome
US4948803A (en) *	1986-11-21	1990-08-14	Glaxo Group Limited	Medicaments for treatment on prevention of withdrawal syndrome
GB8627909D0 (en) *	1986-11-21	1986-12-31	Glaxo Group Ltd	Medicaments
US4857523A (en) *	1988-07-18	1989-08-15	Nda International, Inc.	Rapid method for attenuating the alcohol dependency syndrome
US5629307A (en) *	1989-10-20	1997-05-13	Olney; John W.	Use of ibogaine in reducing excitotoxic brain damage
US5152994A (en) *	1990-05-31	1992-10-06	Lotsof Howard S	Rapid method for interrupting or attenuating poly-drug dependency syndromes
AU4613296A (en) *	1994-07-25	1996-04-19	Nda International, Inc.	A method of treating chemical dependency in mammals and a composition therefor
DE69635737D1 (de)	1995-08-08	2006-04-06	Albany Medical College Albany	Ibogamin verwandte verbindungen
US5616575A (en) *	1995-12-04	1997-04-01	Regents Of The University Of Minnesota	Bioactive tricyclic ibogaine analogs
EP2246058A1 (en)	1997-09-04	2010-11-03	Novoneuron, Inc.	Noribogaine in the treatment of pain and drug addiction
US7220737B1 (en)	1997-09-04	2007-05-22	Novoneuron, Inc	Noribogaine in the treatment of pain and drug addiction
US20030199439A1 (en) *	2002-04-22	2003-10-23	Simon David Lew	Compositions of alpha3beta4 receptor antagonists and opioid agonist analgesics
US20030199496A1 (en) *	2002-04-22	2003-10-23	Simon David Lew	Pharmaceutical compositions containing alpha3beta4 nicotinic receptor antagonists and methods of their use
US7041320B1 (en)	2002-05-31	2006-05-09	Biotek, Inc.	High drug loaded injectable microparticle compositions and methods of treating opioid drug dependence
US7157102B1 (en)	2002-05-31	2007-01-02	Biotek, Inc.	Multi-layered microcapsules and method of preparing same
US20040266659A1 (en) *	2003-06-27	2004-12-30	Stephen LaBerge	Substances that enhance recall and lucidity during dreaming
US20050251442A1 (en) *	2004-05-07	2005-11-10	Joseph Ficalora	Consumer incentive system and business method
US8267851B1 (en)	2009-06-16	2012-09-18	James M Kroll	Method and apparatus for electrically generating signal for inducing lucid dreaming
US9394294B2 (en)	2010-05-11	2016-07-19	Demerx, Inc.	Methods and compositions for preparing and purifying noribogaine
US8765737B1 (en)	2010-05-11	2014-07-01	Demerx, Inc.	Methods and compositions for preparing and purifying noribogaine
US8362007B1 (en)	2010-05-11	2013-01-29	Demerx, Inc.	Substituted noribogaine
US8741891B1 (en)	2010-06-22	2014-06-03	Demerx, Inc.	N-substituted noribogaine prodrugs
US8802832B2 (en)	2010-06-22	2014-08-12	Demerx, Inc.	Compositions comprising noribogaine and an excipient to facilitate transport across the blood brain barrier
US8637648B1 (en)	2010-06-22	2014-01-28	Demerx, Inc.	Compositions comprising noribogaine and an excipient to facilitate transport across the blood brain barrier
US9586954B2 (en)	2010-06-22	2017-03-07	Demerx, Inc.	N-substituted noribogaine prodrugs
MX2013000733A (es)	2010-07-23	2013-05-30	Demerx Inc	Composiciones de noribogaina.
EP2481740B1 (en)	2011-01-26	2015-11-04	DemeRx, Inc.	Methods and compositions for preparing noribogaine from voacangine
US9617274B1 (en)	2011-08-26	2017-04-11	Demerx, Inc.	Synthetic noribogaine
CA2855994A1 (en)	2011-12-09	2013-06-13	Demerx, Inc.	Phosphate esters of noribogaine
US20130178618A1 (en)	2012-01-10	2013-07-11	William Allen Boulanger	Novel pharmaceutical intermediates and methods for preparing the same
US9150584B2 (en)	2012-01-25	2015-10-06	Demerx, Inc.	Indole and benzofuran fused isoquinuclidene derivatives and processes for preparing them
AU2013212139A1 (en)	2012-01-25	2014-06-26	Demerx, Inc.	Synthetic voacangine
US8940728B2 (en)	2012-12-20	2015-01-27	Demerx, Inc.	Substituted noribogaine
US9045481B2 (en)	2012-12-20	2015-06-02	Demerx, Inc.	Substituted noribogaine
WO2014098877A1 (en)	2012-12-20	2014-06-26	Demerx, Inc.	Substituted noribogaine
US9561233B2 (en)	2014-03-13	2017-02-07	Demerx, Inc.	Use of ibogaine for the treatment of pain
US9550789B2 (en)	2014-06-18	2017-01-24	Demerx, Inc.	Halogenated indole and benzofuran derivatives of isoquinuclidene and processes for preparing them
US9592239B2 (en)	2014-09-12	2017-03-14	Demerx, Inc.	Methods and compositions for ibogaine treatment of impulse control disorder, anxiety-related disorders, violence and/or anger, or regulating food intake
WO2016126272A1 (en) *	2015-02-04	2016-08-11	Robert Rand	Rapid method of reducing motor and non-motor symptoms of parkinson's disease
GB2571696B (en)	2017-10-09	2020-05-27	Compass Pathways Ltd	Large scale method for the preparation of Psilocybin and formulations of Psilocybin so produced
US12459965B2 (en)	2017-10-09	2025-11-04	Compass Pathfinder Limited	Preparation of psilocybin, different polymorphic forms, intermediates, formulations and their use
US12377112B2 (en)	2019-04-17	2025-08-05	Compass Pathfinder Limited	Methods of treating neurocognitive disorders, chronic pain and reducing inflammation
US12564597B2 (en)	2020-03-05	2026-03-03	The Trustees Of Columbia University In The Of New York	Ibogaine analogs as therapeutics for neurological and psychiatric disorders
JP2023526515A (ja)	2020-05-20	2023-06-21	ザボードオブトラスティーズオブザユニヴァーシティオブイリノイ	リソソーム蓄積症をヒスタチンペプチドで処置するための方法
KR20230174211A (ko) *	2021-02-17	2023-12-27	더 트러스티이스 오브 콜롬비아 유니버시티 인 더 시티 오브 뉴욕	물질 사용 장애의 치료를 위한 옥사-이보게인 유사체
EP4577245A1 (en)	2022-08-26	2025-07-02	The Johns Hopkins University	Dendrimer compositions for targeted delivery of psychedelic therapeutics
US20240100061A1 (en)	2022-09-14	2024-03-28	The Board Of Trustees Of The Leland Stanford Junior University	Compositions of Iboga Alkaloids and Methods of Treatment
US12116372B1 (en)	2023-12-14	2024-10-15	William Allen Boulanger	Process for preparing methyl 3-bromo-2-(2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-yl)propanoate

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2877229A (en) *		1959-03-10		Process for the manufacture of indoles

1983
- 1983-11-18 US US06/553,138 patent/US4499096A/en not_active Expired - Lifetime
1984
- 1984-11-13 AU AU36744/84A patent/AU576538B2/en not_active Ceased
- 1984-11-13 EP EP84904298A patent/EP0163697B1/en not_active Expired - Lifetime
- 1984-11-13 WO PCT/US1984/001851 patent/WO1985002115A1/en not_active Ceased
- 1984-11-13 DE DE8484904298T patent/DE3482305D1/de not_active Expired - Lifetime
- 1984-11-15 IE IE293284A patent/IE58567B1/en not_active IP Right Cessation
- 1984-11-16 NO NO844573A patent/NO844573L/no unknown
- 1984-11-16 CA CA000467988A patent/CA1237986A/en not_active Expired
- 1984-11-19 IT IT49184/84A patent/IT1178249B/it active
- 1984-11-21 IL IL73585A patent/IL73585A/xx not_active IP Right Cessation
1985
- 1985-07-11 DK DK316485A patent/DK156376C/da active

Also Published As

Publication number	Publication date
IL73585A0 (en)	1985-02-28
IT1178249B (it)	1987-09-09
DK156376B (da)	1989-08-14
EP0163697B1 (en)	1990-05-23
EP0163697A4 (en)	1986-04-15
WO1985002115A1 (en)	1985-05-23
AU3674484A (en)	1985-06-03
IE842932L (en)	1985-05-18
AU576538B2 (en)	1988-09-01
DK316485A (da)	1985-07-11
DK316485D0 (da)	1985-07-11
IE58567B1 (en)	1993-10-06
DE3482305D1 (de)	1990-06-28
IT8449184A0 (it)	1984-11-19
IL73585A (en)	1990-04-29
EP0163697A1 (en)	1985-12-11
DK156376C (da)	1990-01-02
IT8449184A1 (it)	1986-05-19
CA1237986A (en)	1988-06-14
US4499096A (en)	1985-02-12

Publication	Publication Date	Title
NO844573L (no)	1985-05-20	Fremgangsmaate til hurtig avbrytelse av narkotikamisbruksyndrom
US4587243A (en)	1986-05-06	Rapid method for interrupting the cocaine and amphetamine abuse syndrome
US4857523A (en)	1989-08-15	Rapid method for attenuating the alcohol dependency syndrome
US5152994A (en)	1992-10-06	Rapid method for interrupting or attenuating poly-drug dependency syndromes
Sheppard	1994	A preliminary investigation of ibogaine: case reports and recommendations for further study
US5026697A (en)	1991-06-25	Rapid method for interrupting or attenuating the nicotine/tobacco dependency syndrome
Wikler	2013	Opioid dependence: Mechanisms and treatment
Freedman et al.	1968	Clinical studies of cyclazocine in the treatment of narcotic addiction
Smith	1986	Cocaine-alcohol abuse: epidemiological, diagnostic and treatment considerations
Gourlay et al.	1990	Antismoking products
Le Gassicke et al.	1965	The clinical state, sleep and amine metabolism of a tranylcypromine (‘Parnate’) addict
Georgotas et al.	1982	Trazodone hydrochloride: A wide spectrum antidepressant with a unique pharmacological profile: A review of its neurochemical effects, pharmacology, clinical efficacy, and toxicology
PL196334B1 (pl)	2007-12-31	Zastosowanie agonistów receptorów GABA B i ich farmaceutycznie dopuszczalnych pochodnych w terapii abstynencji nikotynowej u uzależnionych od nikotyny pacjentów
Lal et al.	1975	Apomorphine and psychopathology.
Fanchamps	1978	Some compounds with hallucinogenic activity
Eddy	1957	The history of the development of narcotics
Gold et al.	1980	Clinical utility of clonidine in opiate withdrawal
WO1999056747A1 (en)	1999-11-11	Compositions and methods for treating particular chemical addictions and mental illnesses
CN112569237B (zh)	2022-12-02	伊马替尼及其衍生物与尼古丁或其类似物联用或复方在防治尼古丁成瘾与复吸中的应用
Rein et al.	1954	Efficacy of reserpine (serpasil) in dermatological therapy
WO1997041858A1 (en)	1997-11-13	Pyridyl- and pyrimidyl-piperazines in the treatment of substance abuse disorders
CA2429801A1 (en)	2002-06-06	Behavior chemotherapy
JPH0232020A (ja)	1990-02-01	モルフィン鎮痛治療における耐性発現の抑制方法および薬剤
RU2192275C2 (ru)	2002-11-10	Способ лечения опийной наркомании
Wasacz	1981	Natural and Synthetic Narcotic Drugs: The history of narcotic drugs, which began with a crude mixture obtained from a plant, is now witnessing the isolation of substances with similar properties from the brain itself