PH27557A - Hexa-cyclic compound - Google Patents

Hexa-cyclic compound

Info

Publication number
PH27557A
PH27557A PH37104A PH37104A PH27557A PH 27557 A PH27557 A PH 27557A PH 37104 A PH37104 A PH 37104A PH 37104 A PH37104 A PH 37104A PH 27557 A PH27557 A PH 27557A
Authority
PH
Philippines
Prior art keywords
compound
hexa
cyclic compound
antitumour
camptothecin
Prior art date
Application number
PH37104A
Other languages
English (en)
Inventor
Hiroaki Tagawa
Masamichi Sugimori
Hirofumi Terasawa
Akio Ejima
Satoru Ohsuki
Original Assignee
Daiichi Seiyaku Co
Yakult Honsha Kk
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 Daiichi Seiyaku Co, Yakult Honsha Kk filed Critical Daiichi Seiyaku Co
Publication of PH27557A publication Critical patent/PH27557A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/22Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains four or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/22Heterocyclic 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 systems contains four or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/22Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains four or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D515/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D515/22Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains four or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Luminescent Compositions (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Lubricants (AREA)
  • Fats And Perfumes (AREA)
  • Liquid Crystal Substances (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
PH37104A 1987-06-24 1988-07-22 Hexa-cyclic compound PH27557A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP15699087 1987-06-24
JP550388 1988-01-13

Publications (1)

Publication Number Publication Date
PH27557A true PH27557A (en) 1993-08-18

Family

ID=26339454

Family Applications (1)

Application Number Title Priority Date Filing Date
PH37104A PH27557A (en) 1987-06-24 1988-07-22 Hexa-cyclic compound

Country Status (13)

Country Link
US (2) US4939255A (fr)
EP (1) EP0296597B1 (fr)
KR (1) KR960002853B1 (fr)
AT (1) ATE111913T1 (fr)
AU (1) AU610189B2 (fr)
CA (1) CA1304370C (fr)
DE (1) DE3851577T2 (fr)
DK (1) DK344488A (fr)
ES (1) ES2064329T3 (fr)
FI (1) FI91872C (fr)
IE (1) IE61281B1 (fr)
NO (1) NO167738C (fr)
PH (1) PH27557A (fr)

Families Citing this family (36)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4939255A (en) * 1987-06-24 1990-07-03 Daiichi Pharmaceutical Co., Ltd. Hexa-cyclic camptothecin derivatives
US5552154A (en) * 1989-11-06 1996-09-03 The Stehlin Foundation For Cancer Research Method for treating cancer with water-insoluble s-camptothecin of the closed lactone ring form and derivatives thereof
US5658920A (en) * 1991-01-16 1997-08-19 Daiichi Pharmaceutical Co., Ltd. Substituted 1H,12H-benz-[DE]pyrano[3',4':6,7] indolizino[1,2-B]quinoline-10,13(9H,15H)-dione compound
JP3008226B2 (ja) * 1991-01-16 2000-02-14 第一製薬株式会社 六環性化合物
US6407115B1 (en) * 1991-01-16 2002-06-18 Daiichi Pharmaceutical Co., Ltd. Hexa-cyclic compound
US6080751A (en) * 1992-01-14 2000-06-27 The Stehlin Foundation For Cancer Research Method for treating pancreatic cancer in humans with water-insoluble S-camptothecin of the closed lactone ring form and derivatives thereof
US5391745A (en) * 1992-07-23 1995-02-21 Sloan-Kettering Institute For Cancer Research Methods of preparation of camptothecin analogs
US5446047A (en) * 1992-07-23 1995-08-29 Sloan-Kettering Institute For Cancer Research Camptothecin analogues
US6504029B1 (en) 1995-04-10 2003-01-07 Daiichi Pharmaceutical Co., Ltd. Condensed-hexacyclic compounds and a process therefor
US5663177A (en) * 1995-05-31 1997-09-02 Smithkline Beecham Corporation Water soluble camptothecin analogs
US5670500A (en) * 1995-05-31 1997-09-23 Smithkline Beecham Corporation Water soluble camptothecin analogs
US5942386A (en) * 1995-06-07 1999-08-24 Thomas Jefferson University Anti-fungal agents and methods of identifying and using the same
SG50747A1 (en) * 1995-08-02 1998-07-20 Tanabe Seiyaku Co Comptothecin derivatives
SG88737A1 (en) * 1996-10-30 2002-05-21 Tanabe Seiyaku Co S type 2-substituted hydroxy-2-indolidinylbutyric ester compounds and process for preparation thereof
KR19980076076A (ko) * 1997-04-04 1998-11-16 유현식 전선용 발포성 수지조성물
US6046209A (en) * 1997-05-27 2000-04-04 Smithkline Beecham Corporation Water soluble camptothecin analogs
IN189180B (fr) * 1997-07-09 2003-01-04 Chong Kun Dang Corp
JP4094710B2 (ja) 1997-11-06 2008-06-04 株式会社ヤクルト本社 新規なカンプトテシン誘導体
CA2385528C (fr) 1999-10-01 2013-12-10 Immunogen, Inc. Compositions et methodes de traitement du cancer utilisant des immunoconjugues et des agents chimiotherapeutiques
FR2801309B1 (fr) * 1999-11-18 2002-01-04 Adir Nouveaux composes analogues de la camptothecine, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
MXPA04005185A (es) * 2001-11-30 2004-08-11 Chugai Pharmaceutical Co Ltd Compuestos hexaciclicos.
US7563810B2 (en) 2002-11-06 2009-07-21 Celgene Corporation Methods of using 3-(4-amino-1-oxo-1,3-dihydroisoindol-2-yl)-piperidine-2,6-dione for the treatment and management of myeloproliferative diseases
US8034831B2 (en) 2002-11-06 2011-10-11 Celgene Corporation Methods for the treatment and management of myeloproliferative diseases using 4-(amino)-2-(2,6-Dioxo(3-piperidyl)-isoindoline-1,3-dione in combination with other therapies
WO2004073601A2 (fr) * 2003-02-21 2004-09-02 Chugai Seiyaku Kabushiki Kaisha Nouveau procede de preparation de composes hexacycliques
MXPA06011679A (es) 2004-04-09 2007-01-23 Chugai Pharmaceutical Co Ltd Novedosos profarmacos solubles en agua.
TW200744603A (en) 2005-08-22 2007-12-16 Chugai Pharmaceutical Co Ltd Novel anticancer concomitant drug
CN102060713A (zh) * 2010-12-09 2011-05-18 中华人民共和国嘉兴出入境检验检疫局 用于检测偶氮类染料的芳香胺半抗原及其制备方法
US20220211863A1 (en) 2019-03-29 2022-07-07 Medimmune Limited Compounds and conjugates thereof
CN114980934A (zh) 2020-01-22 2022-08-30 免疫医疗有限公司 化合物及其缀合物
TW202140076A (zh) * 2020-01-22 2021-11-01 英商梅迪繆思有限公司 化合物及其軛合物
US11806405B1 (en) 2021-07-19 2023-11-07 Zeno Management, Inc. Immunoconjugates and methods
WO2023180484A1 (fr) 2022-03-23 2023-09-28 Synaffix B.V. Conjugués d'anticorps pour le ciblage de tumeurs exprimant ptk7
WO2023180485A1 (fr) 2022-03-23 2023-09-28 Synaffix B.V. Anticorps-conjugués pour le ciblage de tumeurs exprimant trop-2
WO2023180490A1 (fr) 2022-03-23 2023-09-28 Synaffix B.V. Conjugués d'anticorps pour le ciblage de tumeurs exprimant nectine-4
WO2023180489A1 (fr) 2022-03-23 2023-09-28 Synaffix B.V. Anticorps-conjugués pour le ciblage de tumeurs exprimant un antigène carcinoembryonnaire
WO2024140933A1 (fr) * 2022-12-30 2024-07-04 长春金赛药业有限责任公司 Dérivé de camptothécine, composition pharmaceutique et procédé de préparation et utilisation associés

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US32518A (en) * 1861-06-11 Improvement in city railroads
JPS51288A (ja) * 1974-06-18 1976-01-05 Tamura Seisakusho Kk Hanshakyoshinhoshasochi
US4399282A (en) 1979-07-10 1983-08-16 Kabushiki Kaisha Yakult Honsha Camptothecin derivatives
US4399276A (en) * 1981-01-09 1983-08-16 Kabushiki Kaisha Yakult Honsha 7-Substituted camptothecin derivatives
US4473692A (en) * 1981-09-04 1984-09-25 Kabushiki Kaisha Yakult Honsha Camptothecin derivatives and process for preparing same
JPS5839685A (ja) * 1981-09-04 1983-03-08 Yakult Honsha Co Ltd 新規なカンプトテシン誘導体及びその製造法
JPS58154582A (ja) * 1982-03-10 1983-09-14 Yakult Honsha Co Ltd 新規なカンプトテシン誘導体およびその製造法
JPS6019790A (ja) * 1983-07-14 1985-01-31 Yakult Honsha Co Ltd 新規なカンプトテシン誘導体
EP0220601B1 (fr) * 1985-10-21 1991-12-11 Daiichi Seiyaku Co., Ltd. Dérivés de la pyranoindolizine et procédé de préparation
US4939255A (en) * 1987-06-24 1990-07-03 Daiichi Pharmaceutical Co., Ltd. Hexa-cyclic camptothecin derivatives
US5004758A (en) * 1987-12-01 1991-04-02 Smithkline Beecham Corporation Water soluble camptothecin analogs useful for inhibiting the growth of animal tumor cells
JPH0615547B2 (ja) * 1988-01-20 1994-03-02 株式会社ヤクルト本社 新規なカンプトテシン誘導体

Also Published As

Publication number Publication date
NO882785L (no) 1988-12-27
DK344488D0 (da) 1988-06-23
CA1304370C (fr) 1992-06-30
KR890000489A (ko) 1989-03-15
DE3851577T2 (de) 1995-04-27
FI883050A (fi) 1988-12-25
DE3851577D1 (de) 1994-10-27
NO167738C (no) 1991-12-04
DK344488A (da) 1989-02-24
NO167738B (no) 1991-08-26
FI91872C (fi) 1994-08-25
FI883050A0 (fi) 1988-06-23
US4939255A (en) 1990-07-03
EP0296597B1 (fr) 1994-09-21
IE61281B1 (en) 1994-10-19
FI91872B (fi) 1994-05-13
ATE111913T1 (de) 1994-10-15
US5061795A (en) 1991-10-29
AU1834988A (en) 1989-01-05
ES2064329T3 (es) 1995-02-01
EP0296597A3 (fr) 1991-07-31
NO882785D0 (no) 1988-06-23
EP0296597A2 (fr) 1988-12-28
AU610189B2 (en) 1991-05-16
IE881860L (en) 1988-12-24
KR960002853B1 (ko) 1996-02-27

Similar Documents

Publication Publication Date Title
PH27557A (en) Hexa-cyclic compound
GR3020395T3 (en) Hexa-cyclic compound
YU69289A (en) Substituted flavonoidic compounds, their salts and process for producing thereof
AU577928B2 (en) Labd-14-en-11-one derivatives
CA2030346A1 (fr) Traitement de troubles cardiaques a l'aide de composes de 15-ceto-prostaglandines
HUT46214A (en) Process for producing medical preparation suitable for treatment of peptic ulcer
IE883116L (en) Preparation of antiviral and antitumour pharmaceutical and¹veterinary composition
GR890300022T1 (en) Process for the preparation of 5-hydroxydipraphenone and its salts with acids
PT75881A (en) Process for preparing 3-methyl-3-(4-acetylaminophenoxy)-2,4-dioxa-benzocyclohexen-1-one having analgesic antiinflammatory and antipiretic activity and of pharmaceutical compositions containing the same
EP0307226B1 (en) Process for the preparation of a macrolide compound