IL96666A - Pharmaceutical preparations containing polytocyclic compounds - Google Patents

Pharmaceutical preparations containing polytocyclic compounds

Info

Publication number: IL96666A
Authority: IL; Israel
Prior art keywords: composition; bis; compounds; hiv; tetraazacyclotetradecane
Prior art date: 1989-12-21

Application number

IL9666690A

Other languages

English (en)

Hebrew (he)

Other versions

IL96666A0 (en

Original Assignee

Johnson Matthey Plc

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.)

1989-12-21

Filing date

1990-12-14

Publication date

1996-01-31

1990-12-14 Application filed by Johnson Matthey Plc filed Critical Johnson Matthey Plc

1991-09-16 Publication of IL96666A0 publication Critical patent/IL96666A0/xx

1996-01-31 Publication of IL96666A publication Critical patent/IL96666A/en

Links

239000008194 pharmaceutical composition Substances 0.000 title claims abstract description 12
125000002950 monocyclic group Chemical group 0.000 title claims description 6
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 6
150000001923 cyclic compounds Chemical class 0.000 claims abstract description 3
229910052757 nitrogen Inorganic materials 0.000 claims abstract description 3
150000001875 compounds Chemical class 0.000 claims description 46
239000000203 mixture Substances 0.000 claims description 14
125000002947 alkylene group Chemical group 0.000 claims description 8
125000003118 aryl group Chemical group 0.000 claims description 8
-1 polyoxoethylene Polymers 0.000 claims description 8
239000003085 diluting agent Substances 0.000 claims description 6
239000000546 pharmaceutical excipient Substances 0.000 claims description 5
231100000252 nontoxic Toxicity 0.000 claims description 4
230000003000 nontoxic effect Effects 0.000 claims description 4
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
150000007942 carboxylates Chemical class 0.000 claims description 3
150000002148 esters Chemical class 0.000 claims description 3
229940002612 prodrug Drugs 0.000 claims description 3
239000000651 prodrug Substances 0.000 claims description 3
239000002253 acid Substances 0.000 claims description 2
125000003368 amide group Chemical group 0.000 claims description 2
150000004696 coordination complex Chemical group 0.000 claims description 2
125000004122 cyclic group Chemical group 0.000 claims description 2
150000003839 salts Chemical class 0.000 claims description 2
239000002552 dosage form Substances 0.000 claims 1
125000005647 linker group Chemical group 0.000 claims 1
238000011282 treatment Methods 0.000 abstract description 15
208000036142 Viral infection Diseases 0.000 abstract description 3
125000004429 atom Chemical group 0.000 abstract description 3
230000009385 viral infection Effects 0.000 abstract description 3
206010038997 Retroviral infections Diseases 0.000 abstract description 2
239000004480 active ingredient Substances 0.000 abstract description 2
125000003277 amino group Chemical group 0.000 abstract 1
101001110286 Homo sapiens Ras-related C3 botulinum toxin substrate 1 Proteins 0.000 description 15
102100022122 Ras-related C3 botulinum toxin substrate 1 Human genes 0.000 description 15
208000031886 HIV Infections Diseases 0.000 description 11
241000713772 Human immunodeficiency virus 1 Species 0.000 description 11
241000713340 Human immunodeficiency virus 2 Species 0.000 description 11
238000000034 method Methods 0.000 description 10
210000004027 cell Anatomy 0.000 description 5
238000012360 testing method Methods 0.000 description 5
241000725303 Human immunodeficiency virus Species 0.000 description 4
241000700605 Viruses Species 0.000 description 4
201000010099 disease Diseases 0.000 description 4
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 4
230000000694 effects Effects 0.000 description 4
208000030507 AIDS Diseases 0.000 description 3
125000002619 bicyclic group Chemical group 0.000 description 3
238000000338 in vitro Methods 0.000 description 3
125000004433 nitrogen atom Chemical group N* 0.000 description 3
UEUPDYPUTTUXLJ-UHFFFAOYSA-N 1-[[4-(1,4,8,11-tetrazacyclotetradec-1-ylmethyl)phenyl]methyl]-1,4,8,11-tetrazacyclotetradecane;octahydrochloride Chemical compound Cl.Cl.Cl.Cl.Cl.Cl.Cl.Cl.C=1C=C(CN2CCNCCCNCCNCCC2)C=CC=1CN1CCCNCCNCCCNCC1 UEUPDYPUTTUXLJ-UHFFFAOYSA-N 0.000 description 2
241000282414 Homo sapiens Species 0.000 description 2
230000004071 biological effect Effects 0.000 description 2
210000001124 body fluid Anatomy 0.000 description 2
239000010839 body fluid Substances 0.000 description 2
230000037396 body weight Effects 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
239000003814 drug Substances 0.000 description 2
208000015181 infectious disease Diseases 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
230000001681 protective effect Effects 0.000 description 2
239000000243 solution Substances 0.000 description 2
239000000725 suspension Substances 0.000 description 2
BGHCVCJVXZWKCC-UHFFFAOYSA-N tetradecane Chemical compound CCCCCCCCCCCCCC BGHCVCJVXZWKCC-UHFFFAOYSA-N 0.000 description 2
230000001225 therapeutic effect Effects 0.000 description 2
MDAXKAUIABOHTD-UHFFFAOYSA-N 1,4,8,11-tetraazacyclotetradecane Chemical compound C1CNCCNCCCNCCNC1 MDAXKAUIABOHTD-UHFFFAOYSA-N 0.000 description 1
SCMFKRCYKTYWIW-UHFFFAOYSA-N 1-[3-(1,4,8,11-tetrazacyclotetradec-1-yl)propyl]-1,4,8,11-tetrazacyclotetradecane Chemical compound C1CCNCCNCCCNCCN1CCCN1CCCNCCNCCCNCC1 SCMFKRCYKTYWIW-UHFFFAOYSA-N 0.000 description 1
QWTAISGGJUDPMS-UHFFFAOYSA-N 1-[5-(1,4,8,11-tetrazacyclotetradec-2-yl)pentyl]-1,4,8,11-tetrazacyclotetradecane Chemical compound C1CCNCCNCCCNCCN1CCCCCC1CNCCCNCCNCCCN1 QWTAISGGJUDPMS-UHFFFAOYSA-N 0.000 description 1
KQMSYFWGOQIZPD-UHFFFAOYSA-N 6-(1,4,8,11-tetrazacyclotetradec-6-yl)-1,4,8,11-tetrazacyclotetradecane Chemical compound C1NCCNCCCNCCNCC1C1CNCCNCCCNCCNC1 KQMSYFWGOQIZPD-UHFFFAOYSA-N 0.000 description 1
HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 1
206010001513 AIDS related complex Diseases 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
241000736839 Chara Species 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
241000282412 Homo Species 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
206010061598 Immunodeficiency Diseases 0.000 description 1
208000029462 Immunodeficiency disease Diseases 0.000 description 1
241000124008 Mammalia Species 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
208000005074 Retroviridae Infections Diseases 0.000 description 1
239000005864 Sulphur Substances 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
239000013543 active substance Substances 0.000 description 1
230000036436 anti-hiv Effects 0.000 description 1
230000000840 anti-viral effect Effects 0.000 description 1
230000005540 biological transmission Effects 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000002775 capsule Substances 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000000969 carrier Substances 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
229910017052 cobalt Inorganic materials 0.000 description 1
239000010941 cobalt Substances 0.000 description 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
229940124558 contraceptive agent Drugs 0.000 description 1
239000003433 contraceptive agent Substances 0.000 description 1
239000006071 cream Substances 0.000 description 1
KATXJJSCAPBIOB-UHFFFAOYSA-N cyclotetradecane Chemical compound C1CCCCCCCCCCCCC1 KATXJJSCAPBIOB-UHFFFAOYSA-N 0.000 description 1
231100000135 cytotoxicity Toxicity 0.000 description 1
230000003013 cytotoxicity Effects 0.000 description 1
238000011161 development Methods 0.000 description 1
239000000539 dimer Substances 0.000 description 1
239000008298 dragée Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
238000009510 drug design Methods 0.000 description 1
125000004185 ester group Chemical group 0.000 description 1
230000001747 exhibiting effect Effects 0.000 description 1
210000002950 fibroblast Anatomy 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
231100000086 high toxicity Toxicity 0.000 description 1
150000003840 hydrochlorides Chemical class 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
230000007813 immunodeficiency Effects 0.000 description 1
238000002513 implantation Methods 0.000 description 1
238000002347 injection Methods 0.000 description 1
239000007924 injection Substances 0.000 description 1
230000002262 irrigation Effects 0.000 description 1
238000003973 irrigation Methods 0.000 description 1
231100001231 less toxic Toxicity 0.000 description 1
150000002678 macrocyclic compounds Chemical class 0.000 description 1
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
230000000813 microbial effect Effects 0.000 description 1
150000002815 nickel Chemical class 0.000 description 1
239000002674 ointment Substances 0.000 description 1
230000000144 pharmacologic effect Effects 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
238000004393 prognosis Methods 0.000 description 1
238000011321 prophylaxis Methods 0.000 description 1
125000006239 protecting group Chemical group 0.000 description 1
230000001105 regulatory effect Effects 0.000 description 1
238000011160 research Methods 0.000 description 1
229910052703 rhodium Inorganic materials 0.000 description 1
239000010948 rhodium Substances 0.000 description 1
MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000008247 solid mixture Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
230000000153 supplemental effect Effects 0.000 description 1
239000000829 suppository Substances 0.000 description 1
239000012730 sustained-release form Substances 0.000 description 1
208000011580 syndromic disease Diseases 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
239000003826 tablet Substances 0.000 description 1
125000003831 tetrazolyl group Chemical group 0.000 description 1
238000002560 therapeutic procedure Methods 0.000 description 1
238000011200 topical administration Methods 0.000 description 1
241000712461 unidentified influenza virus Species 0.000 description 1
241001430294 unidentified retrovirus Species 0.000 description 1
230000003612 virological effect Effects 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc 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
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV

Landscapes

Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Medicinal Chemistry (AREA)
Veterinary Medicine (AREA)
Public Health (AREA)
General Health & Medical Sciences (AREA)
Chemical & Material Sciences (AREA)
Animal Behavior & Ethology (AREA)
Pharmacology & Pharmacy (AREA)
Epidemiology (AREA)
Virology (AREA)
Communicable Diseases (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Organic Chemistry (AREA)
General Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Oncology (AREA)
Tropical Medicine & Parasitology (AREA)
Molecular Biology (AREA)
AIDS & HIV (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Medicinal Preparation (AREA)
Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

IL9666690A 1989-12-21 1990-12-14 Pharmaceutical preparations containing polytocyclic compounds IL96666A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US07/454,418 US5021409A (en)	1989-12-21	1989-12-21	Antiviral cyclic polyamines

Publications (2)

Publication Number	Publication Date
IL96666A0 IL96666A0 (en)	1991-09-16
IL96666A true IL96666A (en)	1996-01-31

Family

ID=23804523

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL9666690A IL96666A (en)	1989-12-21	1990-12-14	Pharmaceutical preparations containing polytocyclic compounds

Country Status (17)

Country	Link
US (1)	US5021409A (da)
EP (1)	EP0434385B1 (da)
JP (1)	JP3133345B2 (da)
KR (1)	KR0180019B1 (da)
AT (1)	ATE130514T1 (da)
AU (1)	AU639514B2 (da)
CA (1)	CA2032261C (da)
DE (1)	DE69023748T2 (da)
DK (1)	DK0434385T3 (da)
ES (1)	ES2079453T3 (da)
GR (1)	GR3018206T3 (da)
HU (2)	HUT67031A (da)
IE (1)	IE71640B1 (da)
IL (1)	IL96666A (da)
NZ (1)	NZ236463A (da)
PT (1)	PT96289B (da)
ZA (1)	ZA9010184B (da)

Families Citing this family (76)

* Cited by examiner, † Cited by third party
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1989
- 1989-12-21 US US07/454,418 patent/US5021409A/en not_active Expired - Lifetime
1990
- 1990-12-14 NZ NZ236463A patent/NZ236463A/en unknown
- 1990-12-14 AU AU68090/90A patent/AU639514B2/en not_active Ceased
- 1990-12-14 CA CA002032261A patent/CA2032261C/en not_active Expired - Lifetime
- 1990-12-14 IL IL9666690A patent/IL96666A/en not_active IP Right Cessation
- 1990-12-18 ZA ZA9010184A patent/ZA9010184B/xx unknown
- 1990-12-19 DK DK90313899.8T patent/DK0434385T3/da active
- 1990-12-19 AT AT90313899T patent/ATE130514T1/de not_active IP Right Cessation
- 1990-12-19 DE DE69023748T patent/DE69023748T2/de not_active Expired - Lifetime
- 1990-12-19 ES ES90313899T patent/ES2079453T3/es not_active Expired - Lifetime
- 1990-12-19 KR KR1019900021096A patent/KR0180019B1/ko not_active Expired - Fee Related
- 1990-12-19 EP EP90313899A patent/EP0434385B1/en not_active Expired - Lifetime
- 1990-12-20 IE IE461990A patent/IE71640B1/en not_active IP Right Cessation
- 1990-12-20 HU HU908367A patent/HUT67031A/hu unknown
- 1990-12-20 PT PT96289A patent/PT96289B/pt not_active IP Right Cessation
- 1990-12-21 JP JP02404955A patent/JP3133345B2/ja not_active Expired - Lifetime
1994
- 1994-07-11 HU HU94P/P00011P patent/HU210534A9/hu unknown
1995
- 1995-11-23 GR GR950403260T patent/GR3018206T3/el unknown

Also Published As

Publication number	Publication date
ZA9010184B (en)	1991-11-27
EP0434385A3 (en)	1992-03-04
KR910011267A (ko)	1991-08-07
JP3133345B2 (ja)	2001-02-05
IE904619A1 (en)	1991-07-17
HUT67031A (en)	1995-01-30
AU639514B2 (en)	1993-07-29
CA2032261C (en)	2002-04-23
IL96666A0 (en)	1991-09-16
DE69023748D1 (de)	1996-01-04
JPH06219945A (ja)	1994-08-09
EP0434385A2 (en)	1991-06-26
DK0434385T3 (da)	1995-12-18
CA2032261A1 (en)	1991-06-22
KR0180019B1 (ko)	1999-03-20
ATE130514T1 (de)	1995-12-15
HU210534A9 (en)	1995-04-28
US5021409A (en)	1991-06-04
DE69023748T2 (de)	1996-05-02
PT96289B (pt)	1998-06-30
HU908367D0 (en)	1991-07-29
PT96289A (pt)	1991-10-15
ES2079453T3 (es)	1996-01-16
GR3018206T3 (en)	1996-02-29
IE71640B1 (en)	1997-02-26
EP0434385B1 (en)	1995-11-22
NZ236463A (en)	1992-04-28
AU6809090A (en)	1991-06-27

Legal Events

Date	Code	Title
1996-07-23	FF	Patent granted
1997-03-18	KB	Patent renewed
2001-04-30	KB	Patent renewed
2004-02-08	HP	Change in proprietorship
2004-02-19	HP	Change in proprietorship
2005-02-20	KB	Patent renewed
2009-06-15	KB	Patent renewed
2011-07-31	EXP	Patent expired

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Hammer et al.	1987	Synergistic activity of granulocyte-macrophage colony-stimulating factor and 3'-azido-3'-deoxythymidine against human immunodeficiency virus in vitro
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JPH11500130A (ja)	1999-01-06	抗ウイルス性トリアザ化合物
ES2148234T3 (es)	2000-10-16	Composicion farmaceutica a base de flavopereirina y su utilizacion en el tratamiento del virus vih.
EA015132B1 (ru)	2011-06-30	Лекарственное средство для лечения вирусных инфекций
EP0392666B1 (en)	1994-07-20	Anti-HIV compositions
WO2006104292A1 (en)	2006-10-05	Pharmaceutical composition comprising arsenic acid, meta-arsenite, and pharmaceutically acceptable salts
KR100532542B1 (ko)	2005-12-01	아르세닉산, 메타아르세나이트 또는 이들의 약제학적허용가능한 염을 함유한 에이즈 예방 및 치료용 약제 조성물
WO1992009292A1 (en)	1992-06-11	Improvements in chemical compounds
PT97609A (pt)	1992-02-28	Processo para a preparacao de uma composicao farmaceutica para o tratamento de celulas infectadas com o virus da imunodeficiencia humana e dispositivo ou artigo tratado com essa composicao
JPH05117143A (ja)	1993-05-14	抗ウイルス剤
JPH01168616A (ja)	1989-07-04	糖ラクタムを含有する抗ウイルス剤
JPH01172321A (ja)	1989-07-07	６−０−置換−Ｄ−グルコ−δ−ラクタムを含有する抗ウイルス剤
JPH05105626A (ja)	1993-04-27	抗ウイルス剤
JPWO1995020388A1 (ja)	1996-06-25	抗ｈｉｖ剤
KR19990072051A (ko)	1999-09-27	티아민디술피드류및이를유효성분으로하는의약