WO1996036612A1 - Utilisation de trisbenzimidazols en tant qu'inhibiteurs de la topoisomerase i - Google Patents
Utilisation de trisbenzimidazols en tant qu'inhibiteurs de la topoisomerase i Download PDFInfo
- Publication number
- WO1996036612A1 WO1996036612A1 PCT/US1996/006853 US9606853W WO9636612A1 WO 1996036612 A1 WO1996036612 A1 WO 1996036612A1 US 9606853 W US9606853 W US 9606853W WO 9636612 A1 WO9636612 A1 WO 9636612A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- compound
- alkyl
- mmol
- topoisomerase
- pyridyl
- Prior art date
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- 239000000365 Topoisomerase I Inhibitor Substances 0.000 title abstract description 13
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- BJEPYKJPYRNKOW-UHFFFAOYSA-N malic acid Chemical compound OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000004949 mass spectrometry Methods 0.000 description 1
- 238000001819 mass spectrum Methods 0.000 description 1
- 201000001441 melanoma Diseases 0.000 description 1
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
- OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- KKZJGLLVHKMTCM-UHFFFAOYSA-N mitoxantrone Chemical compound O=C1C2=C(O)C=CC(O)=C2C(=O)C2=C1C(NCCNCCO)=CC=C2NCCNCCO KKZJGLLVHKMTCM-UHFFFAOYSA-N 0.000 description 1
- 229960001156 mitoxantrone Drugs 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 238000010369 molecular cloning Methods 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 238000004264 monolayer culture Methods 0.000 description 1
- 230000036457 multidrug resistance Effects 0.000 description 1
- GPHJWIXICBRURA-UHFFFAOYSA-N n-bromo-n-phenylnitramide Chemical class [O-][N+](=O)N(Br)C1=CC=CC=C1 GPHJWIXICBRURA-UHFFFAOYSA-N 0.000 description 1
- VBEGHXKAFSLLGE-UHFFFAOYSA-N n-phenylnitramide Chemical class [O-][N+](=O)NC1=CC=CC=C1 VBEGHXKAFSLLGE-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen(.) Chemical compound [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 239000007968 orange flavor Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229940049954 penicillin Drugs 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 229960003742 phenol Drugs 0.000 description 1
- 229950000688 phenothiazine Drugs 0.000 description 1
- GJSGGHOYGKMUPT-UHFFFAOYSA-N phenoxathiine Chemical compound C1=CC=C2OC3=CC=CC=C3SC2=C1 GJSGGHOYGKMUPT-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 150000008298 phosphoramidates Chemical class 0.000 description 1
- LFSXCDWNBUNEEM-UHFFFAOYSA-N phthalazine Chemical compound C1=NN=CC2=CC=CC=C21 LFSXCDWNBUNEEM-UHFFFAOYSA-N 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001592 potato starch Polymers 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
- CPNGPNLZQNNVQM-UHFFFAOYSA-N pteridine Chemical compound N1=CN=CC2=NC=CN=C21 CPNGPNLZQNNVQM-UHFFFAOYSA-N 0.000 description 1
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 125000006413 ring segment Chemical group 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
- 239000004208 shellac Substances 0.000 description 1
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
- 229940113147 shellac Drugs 0.000 description 1
- 235000013874 shellac Nutrition 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000007892 solid unit dosage form Substances 0.000 description 1
- 210000001082 somatic cell Anatomy 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 206010041823 squamous cell carcinoma Diseases 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229960005322 streptomycin Drugs 0.000 description 1
- 238000005556 structure-activity relationship Methods 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 238000000967 suction filtration Methods 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 229960001278 teniposide Drugs 0.000 description 1
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
- OSBSFAARYOCBHB-UHFFFAOYSA-N tetrapropylammonium Chemical compound CCC[N+](CCC)(CCC)CCC OSBSFAARYOCBHB-UHFFFAOYSA-N 0.000 description 1
- 150000003536 tetrazoles Chemical class 0.000 description 1
- RTKIYNMVFMVABJ-UHFFFAOYSA-L thimerosal Chemical compound [Na+].CC[Hg]SC1=CC=CC=C1C([O-])=O RTKIYNMVFMVABJ-UHFFFAOYSA-L 0.000 description 1
- 229940033663 thimerosal Drugs 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 229940044693 topoisomerase inhibitor Drugs 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 229960002622 triacetin Drugs 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- GYUURHMITDQTRU-UHFFFAOYSA-N tributyl(pyridin-2-yl)stannane Chemical compound CCCC[Sn](CCCC)(CCCC)C1=CC=CC=N1 GYUURHMITDQTRU-UHFFFAOYSA-N 0.000 description 1
- CFQJBWKKHCMCGJ-UHFFFAOYSA-N tributyl(pyridin-3-yl)stannane Chemical compound CCCC[Sn](CCCC)(CCCC)C1=CC=CN=C1 CFQJBWKKHCMCGJ-UHFFFAOYSA-N 0.000 description 1
- UNEPXPMBVGDXGH-UHFFFAOYSA-N tributyl(pyridin-4-yl)stannane Chemical compound CCCC[Sn](CCCC)(CCCC)C1=CC=NC=C1 UNEPXPMBVGDXGH-UHFFFAOYSA-N 0.000 description 1
- GZJNLVYEAQGOSJ-UHFFFAOYSA-N tributyl-(4-chlorophenyl)stannane Chemical compound CCCC[Sn](CCCC)(CCCC)C1=CC=C(Cl)C=C1 GZJNLVYEAQGOSJ-UHFFFAOYSA-N 0.000 description 1
- PIILXFBHQILWPS-UHFFFAOYSA-N tributyltin Chemical class CCCC[Sn](CCCC)CCCC PIILXFBHQILWPS-UHFFFAOYSA-N 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 230000004565 tumor cell growth Effects 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 229960003048 vinblastine Drugs 0.000 description 1
- JXLYSJRDGCGARV-XQKSVPLYSA-N vincaleukoblastine Chemical compound C([C@@H](C[C@]1(C(=O)OC)C=2C(=CC3=C([C@]45[C@H]([C@@]([C@H](OC(C)=O)[C@]6(CC)C=CCN([C@H]56)CC4)(O)C(=O)OC)N3C)C=2)OC)C[C@@](C2)(O)CC)N2CCC2=C1NC1=CC=CC=C21 JXLYSJRDGCGARV-XQKSVPLYSA-N 0.000 description 1
- 235000012431 wafers Nutrition 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000009637 wintergreen oil Substances 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/18—Benzimidazoles; Hydrogenated benzimidazoles with aryl radicals directly attached in position 2
Definitions
- Y' is preferably H or CH 3 .
- the present phosphoramidate compounds may be orally administered, for example, in combination with a pharmaceutically acceptable vehicle such as an inert diluent or an assimilable edible carrier. They may be enclosed in hard or soft shell gelatin capsules, may be compressed into tablets, or may be incorporated directly with the food of the patient's diet.
- a pharmaceutically acceptable vehicle such as an inert diluent or an assimilable edible carrier.
- the active compound may be combined with one or more excipients and used in the form of ingestible tablets, buccal tablets, troches, capsules, elixirs, suspensions, syrups, wafers, and the like.
- Such compositions and preparations should contain at least 0.1% of active compound.
- isotonic agents for example, sugars, buffers or sodium chloride.
- Prolonged absorption of the injectable compositions can be brought about by the use in the compositions of agents delaying absorption, for example, aluminum monostearate and gelatin.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (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)
- Plural Heterocyclic Compounds (AREA)
Abstract
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8534375A JPH11508229A (ja) | 1995-05-17 | 1996-05-14 | トポイソメラーゼインヒビターとして有用なトリスベンズイミダゾール類 |
NZ307959A NZ307959A (en) | 1995-05-17 | 1996-05-14 | Substituted tribenzimidazole derivatives where the substituent can be aryl or heteroaryl and medicaments |
PL96324034A PL324034A1 (en) | 1995-05-17 | 1996-05-14 | Tribenzimidazoles useful as inhibitors of topoisomerase i |
HU9900071A HUP9900071A3 (en) | 1995-05-17 | 1996-05-14 | Tribenzimidazoles useful as topoisomerase i inhibitors, pharmaceutical compositions containing them and their use |
AU57466/96A AU713317B2 (en) | 1995-05-17 | 1996-05-14 | Trisbenzimidazoles useful as topoisomerase I inhibitors |
BR9608476A BR9608476A (pt) | 1995-05-17 | 1996-05-14 | Composto processo para inibir o crescimento de uma célula tumoral de mam¡fero e composicão terapéutica |
EP96915784A EP0839140A1 (fr) | 1995-05-17 | 1996-05-14 | Utilisation de trisbenzimidazols en tant qu'inhibiteurs de la topoisomerase i |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/442,657 | 1995-05-17 | ||
US08/442,657 US5807874A (en) | 1995-05-17 | 1995-05-17 | Trisbenzimidazoles useful as topoisomerase I inhibitors |
US08/618,988 US5767142A (en) | 1996-03-20 | 1996-03-20 | Trisbenzimidazoles useful as topoisomerase I inhibitors |
US08/618,988 | 1996-03-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1996036612A1 true WO1996036612A1 (fr) | 1996-11-21 |
Family
ID=27033238
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1996/006853 WO1996036612A1 (fr) | 1995-05-17 | 1996-05-14 | Utilisation de trisbenzimidazols en tant qu'inhibiteurs de la topoisomerase i |
Country Status (10)
Country | Link |
---|---|
EP (1) | EP0839140A1 (fr) |
JP (1) | JPH11508229A (fr) |
AU (1) | AU713317B2 (fr) |
BR (1) | BR9608476A (fr) |
CA (1) | CA2221248A1 (fr) |
CZ (1) | CZ363197A3 (fr) |
HU (1) | HUP9900071A3 (fr) |
NZ (1) | NZ307959A (fr) |
PL (1) | PL324034A1 (fr) |
WO (1) | WO1996036612A1 (fr) |
Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998031673A1 (fr) * | 1997-01-21 | 1998-07-23 | Rutgers, The State University Of New Jersey | Terbenzimidazoles s'utilisant dans un traitement medical (inhibiteurs de topoisomerase) |
WO1999033824A1 (fr) * | 1997-12-31 | 1999-07-08 | Rutgers, The State University Of New Jersey | Poisons topo-isomerase heterocycliques |
WO1999041241A1 (fr) * | 1998-02-12 | 1999-08-19 | Rutgers, The State University Of New Jersey | Poisons topoisomerase heterocycliques |
US6740650B2 (en) | 1999-10-29 | 2004-05-25 | Rutgers, The State University Of New Jersey | Heterocyclic cytotoxic agents |
US6833373B1 (en) | 1998-12-23 | 2004-12-21 | G.D. Searle & Co. | Method of using an integrin antagonist and one or more antineoplastic agents as a combination therapy in the treatment of neoplasia |
US6858598B1 (en) | 1998-12-23 | 2005-02-22 | G. D. Searle & Co. | Method of using a matrix metalloproteinase inhibitor and one or more antineoplastic agents as a combination therapy in the treatment of neoplasia |
US6964964B2 (en) | 2001-11-14 | 2005-11-15 | Rutgers The State University Of New Jersey | Topoisomerase poison agents |
US6987109B2 (en) | 2001-11-14 | 2006-01-17 | Rutgers, The State University Of New Jersey | Solubilized topoisomerase poison agents |
US6989387B2 (en) | 2002-08-09 | 2006-01-24 | Rutgers, The State University Of New Jersey | Nitro and amino substituted topoisomerase agents |
US6992089B2 (en) | 2002-08-09 | 2006-01-31 | Rutgers, The University Of New Jersey | Nitro and amino substituted topoisomerase agents |
US6992088B2 (en) | 2002-08-09 | 2006-01-31 | Rutgers, The State University Of New Jersey | Nitro and amino substituted heterocycles as topoisomerase I targeting agents |
US7049315B2 (en) | 2001-11-14 | 2006-05-23 | Rutgers, The State University Of New Jersey | Solubilized topoisomerase poisons |
US7208492B2 (en) | 2002-11-12 | 2007-04-24 | Rutgers, The State University Of New Jersey | Topoisomerase-targeting agents |
US7319105B2 (en) | 2001-11-14 | 2008-01-15 | Rutgers, The State University Of New Jersey | Cytotoxic agents |
US9321781B2 (en) | 2009-05-01 | 2016-04-26 | Rutgers, The State University Of New Jersey | Topoisomerase inhibitors |
US9562051B2 (en) | 2009-03-06 | 2017-02-07 | Rutgers, The State University Of New Jersey | Methylenedioxybenzo [I] phenanthridine derivatives used to treat cancer |
US11091498B2 (en) | 2016-04-04 | 2021-08-17 | Rutgers, The State University Of New Jersey | Topoisomerase poisons |
-
1996
- 1996-05-14 EP EP96915784A patent/EP0839140A1/fr not_active Withdrawn
- 1996-05-14 BR BR9608476A patent/BR9608476A/pt not_active Application Discontinuation
- 1996-05-14 CZ CZ973631A patent/CZ363197A3/cs unknown
- 1996-05-14 HU HU9900071A patent/HUP9900071A3/hu unknown
- 1996-05-14 JP JP8534375A patent/JPH11508229A/ja not_active Ceased
- 1996-05-14 WO PCT/US1996/006853 patent/WO1996036612A1/fr not_active Application Discontinuation
- 1996-05-14 CA CA002221248A patent/CA2221248A1/fr not_active Abandoned
- 1996-05-14 PL PL96324034A patent/PL324034A1/xx unknown
- 1996-05-14 AU AU57466/96A patent/AU713317B2/en not_active Ceased
- 1996-05-14 NZ NZ307959A patent/NZ307959A/en unknown
Non-Patent Citations (2)
Title |
---|
A.Y. CHEN ET AL.: "A New Mammalian DNA Topoisomerase I Poison Hoechst 33342: Cytotoxicity and Drug Resistance in Human Cell Cultures", CANCER RESEARCH, vol. 53, no. 6, 15 March 1993 (1993-03-15), MD US, pages 1332 - 1337, XP002010634 * |
Q. SUN ET AL.: "Synthesis and Evaluation of Terbenzimidazoles as Topoisomerase I Inhibitors", JOURNAL OF MEDICINAL CHEMISTRY, vol. 38, no. 18, 1 September 1995 (1995-09-01), WASHINGTON US, pages 3638 - 3644, XP002010635 * |
Cited By (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998031673A1 (fr) * | 1997-01-21 | 1998-07-23 | Rutgers, The State University Of New Jersey | Terbenzimidazoles s'utilisant dans un traitement medical (inhibiteurs de topoisomerase) |
US6995154B2 (en) | 1997-12-31 | 2006-02-07 | Rutgers, The State University Of New Jersey | Heterocyclic topoisomerase poisons |
WO1999033824A1 (fr) * | 1997-12-31 | 1999-07-08 | Rutgers, The State University Of New Jersey | Poisons topo-isomerase heterocycliques |
AU753268B2 (en) * | 1997-12-31 | 2002-10-10 | Jun Sung Kim | Heterocyclic topoisomerase poisons |
US6667302B2 (en) | 1997-12-31 | 2003-12-23 | Rutgers, The State University Of New Jersey | Heterocyclic topoisomerase poisons |
WO1999041241A1 (fr) * | 1998-02-12 | 1999-08-19 | Rutgers, The State University Of New Jersey | Poisons topoisomerase heterocycliques |
US6063801A (en) * | 1998-02-12 | 2000-05-16 | Rutgers, The State University Of New Jersey | Heterocyclic topoisomerase poisons |
US6221892B1 (en) | 1998-02-12 | 2001-04-24 | The State Of University Of New Jersey, Rutgers | Heterocyclic topoisomerase poisons |
US6399642B2 (en) | 1998-02-12 | 2002-06-04 | Rutgers, The State University Of New Jersey | Benzimidazole topoisomerase poisons |
US6833373B1 (en) | 1998-12-23 | 2004-12-21 | G.D. Searle & Co. | Method of using an integrin antagonist and one or more antineoplastic agents as a combination therapy in the treatment of neoplasia |
US6858598B1 (en) | 1998-12-23 | 2005-02-22 | G. D. Searle & Co. | Method of using a matrix metalloproteinase inhibitor and one or more antineoplastic agents as a combination therapy in the treatment of neoplasia |
US6740650B2 (en) | 1999-10-29 | 2004-05-25 | Rutgers, The State University Of New Jersey | Heterocyclic cytotoxic agents |
US7517883B2 (en) | 2001-11-14 | 2009-04-14 | Rutgers, The State University Of New Jersey | Solubilized topoisomerase poisons |
US6964964B2 (en) | 2001-11-14 | 2005-11-15 | Rutgers The State University Of New Jersey | Topoisomerase poison agents |
US8389721B2 (en) | 2001-11-14 | 2013-03-05 | Rutgers, The State University Of New Jersey | Solubilized topoisomerase poisons |
US7781587B2 (en) | 2001-11-14 | 2010-08-24 | Rutgers, The State University Of New Jersey | Solubilized topoisomerase poisons |
US6987109B2 (en) | 2001-11-14 | 2006-01-17 | Rutgers, The State University Of New Jersey | Solubilized topoisomerase poison agents |
US7049315B2 (en) | 2001-11-14 | 2006-05-23 | Rutgers, The State University Of New Jersey | Solubilized topoisomerase poisons |
US7468366B2 (en) | 2001-11-14 | 2008-12-23 | Rutgers, The State University Of New Jersey | Cytotoxic agents |
US7319105B2 (en) | 2001-11-14 | 2008-01-15 | Rutgers, The State University Of New Jersey | Cytotoxic agents |
US6989387B2 (en) | 2002-08-09 | 2006-01-24 | Rutgers, The State University Of New Jersey | Nitro and amino substituted topoisomerase agents |
US6992088B2 (en) | 2002-08-09 | 2006-01-31 | Rutgers, The State University Of New Jersey | Nitro and amino substituted heterocycles as topoisomerase I targeting agents |
US6992089B2 (en) | 2002-08-09 | 2006-01-31 | Rutgers, The University Of New Jersey | Nitro and amino substituted topoisomerase agents |
US7208492B2 (en) | 2002-11-12 | 2007-04-24 | Rutgers, The State University Of New Jersey | Topoisomerase-targeting agents |
US7858627B2 (en) | 2002-11-12 | 2010-12-28 | Rutgers, The State University Of New Jersey | Topoisomerase-targeting agents |
US9562051B2 (en) | 2009-03-06 | 2017-02-07 | Rutgers, The State University Of New Jersey | Methylenedioxybenzo [I] phenanthridine derivatives used to treat cancer |
US10179789B2 (en) | 2009-03-06 | 2019-01-15 | Rutgers, The State University Of New Jersey | Methylenedioxybenzo [I] phenanthridine derivatives used to treat cancer |
US9321781B2 (en) | 2009-05-01 | 2016-04-26 | Rutgers, The State University Of New Jersey | Topoisomerase inhibitors |
US11091498B2 (en) | 2016-04-04 | 2021-08-17 | Rutgers, The State University Of New Jersey | Topoisomerase poisons |
Also Published As
Publication number | Publication date |
---|---|
NZ307959A (en) | 1998-08-26 |
JPH11508229A (ja) | 1999-07-21 |
BR9608476A (pt) | 1999-08-17 |
CA2221248A1 (fr) | 1996-11-21 |
MX9708822A (es) | 1998-06-30 |
PL324034A1 (en) | 1998-05-11 |
CZ363197A3 (cs) | 1998-05-13 |
AU713317B2 (en) | 1999-11-25 |
HUP9900071A2 (hu) | 2000-03-28 |
HUP9900071A3 (en) | 2002-01-28 |
EP0839140A1 (fr) | 1998-05-06 |
AU5746696A (en) | 1996-11-29 |
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