WO2002060890A1 - Nouvelles substances physiologiquement actives - Google Patents

Nouvelles substances physiologiquement actives Download PDF

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Publication number
WO2002060890A1
WO2002060890A1 PCT/JP2002/000848 JP0200848W WO02060890A1 WO 2002060890 A1 WO2002060890 A1 WO 2002060890A1 JP 0200848 W JP0200848 W JP 0200848W WO 02060890 A1 WO02060890 A1 WO 02060890A1
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WO
WIPO (PCT)
Prior art keywords
active substances
physiologically active
same
novel physiologically
producing
Prior art date
Application number
PCT/JP2002/000848
Other languages
English (en)
French (fr)
Inventor
Yoshiharu Mizui
Takashi Sakai
Satoshi Yamamoto
Keisuke Komeda
Masanori Fujita
Akifumi Okuda
Kumiko Kishi
Jun Niijima
Mitsuo Nagai
Kiyoshi Okamoto
Masao Iwata
Yoshihiko Kotake
Toshimitsu Uenaka
Naoki Asai
Motoko Matsufuji
Tomohiro Sameshima
Naoto Kawamura
Kazuyuki Dobashi
Takashi Nakashima
Masashi Yoshida
Toshio Tsuchida
Susumu Takeda
Tomonari Yamada
Koji Norihisa
Takao Yamori
Original Assignee
Mercian Corporation
Eisai Co., Ltd.
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 Mercian Corporation, Eisai Co., Ltd. filed Critical Mercian Corporation
Priority to EP02711280A priority Critical patent/EP1380579A4/en
Priority to CA2436667A priority patent/CA2436667C/en
Priority to JP2002561040A priority patent/JP4439181B2/ja
Priority to KR1020037009709A priority patent/KR101115364B1/ko
Priority to US10/470,806 priority patent/US7026352B1/en
Priority to CN028041879A priority patent/CN1489583B/zh
Publication of WO2002060890A1 publication Critical patent/WO2002060890A1/ja
Priority to US11/213,962 priority patent/US7667052B2/en

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/336Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having three-membered rings, e.g. oxirane, fumagillin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/4025Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil not condensed and containing further heterocyclic rings, e.g. cromakalim
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/455Nicotinic acids, e.g. niacin; Derivatives thereof, e.g. esters, amides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/74Synthetic polymeric materials
    • AHUMAN NECESSITIES
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    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
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    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P35/00Antineoplastic agents
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/04Antineoplastic agents specific for metastasis
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D313/00Heterocyclic compounds containing rings of more than six members having one oxygen atom as the only ring hetero atom
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D407/00Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/02Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
    • C07D407/06Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D407/00Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/14Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing three or more hetero rings
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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D493/00Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
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    • C07D493/04Ortho-condensed systems
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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D493/00Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
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    • C12P17/00Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/02Oxygen as only ring hetero atoms

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  • Medicinal Chemistry (AREA)
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  • Animal Behavior & Ethology (AREA)
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  • Chemical Kinetics & Catalysis (AREA)
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  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Cardiology (AREA)
  • Biotechnology (AREA)
  • Genetics & Genomics (AREA)
  • Heart & Thoracic Surgery (AREA)
  • General Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • Rheumatology (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Microbiology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Diabetes (AREA)
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  • Pain & Pain Management (AREA)
  • Vascular Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Dermatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
PCT/JP2002/000848 2001-02-01 2002-02-01 Nouvelles substances physiologiquement actives WO2002060890A1 (fr)

Priority Applications (7)

Application Number Priority Date Filing Date Title
EP02711280A EP1380579A4 (en) 2001-02-01 2002-02-01 NEW PHYSIOLOGICALLY EFFECTIVE SUBSTANCES
CA2436667A CA2436667C (en) 2001-02-01 2002-02-01 Novel bioactive substance
JP2002561040A JP4439181B2 (ja) 2001-02-01 2002-02-01 新規生理活性物質
KR1020037009709A KR101115364B1 (ko) 2001-02-01 2002-02-01 신규한 생리 활성 물질
US10/470,806 US7026352B1 (en) 2001-02-01 2002-02-01 Physiologically active substances
CN028041879A CN1489583B (zh) 2001-02-01 2002-02-01 一种生理活性物质
US11/213,962 US7667052B2 (en) 2001-02-01 2005-08-30 Bioactive substance

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2001025458 2001-02-01
JP2001-25458 2001-02-01

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US11/213,962 Division US7667052B2 (en) 2001-02-01 2005-08-30 Bioactive substance

Publications (1)

Publication Number Publication Date
WO2002060890A1 true WO2002060890A1 (fr) 2002-08-08

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PCT/JP2002/000848 WO2002060890A1 (fr) 2001-02-01 2002-02-01 Nouvelles substances physiologiquement actives

Country Status (9)

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US (2) US7026352B1 (ja)
EP (3) EP2292610B1 (ja)
JP (1) JP4439181B2 (ja)
KR (2) KR101115364B1 (ja)
CN (1) CN1489583B (ja)
CA (1) CA2436667C (ja)
ES (1) ES2477240T3 (ja)
TW (2) TWI312681B (ja)
WO (1) WO2002060890A1 (ja)

Cited By (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003099813A1 (fr) 2002-05-29 2003-12-04 Mercian Corporation Nouvelles substances physiologiquement actives
WO2004011459A1 (ja) * 2002-07-31 2004-02-05 Mercian Corporation 新規生理活性物質
WO2004011661A1 (ja) 2002-07-31 2004-02-05 Mercian Corporation 新規生理活性物質
WO2004050890A1 (ja) * 2002-11-29 2004-06-17 Mercian Corporation マクロライド系化合物の製造方法
WO2005052152A1 (ja) * 2003-11-27 2005-06-09 Mercian Corporation マクロライド系化合物の水酸化に関与するdna
WO2005073223A1 (ja) * 2004-01-29 2005-08-11 Eisai R & D Management Co., Ltd. マクロライド系化合物の安定化方法
WO2005075681A1 (ja) * 2004-02-06 2005-08-18 Eisai R & D Management Co., Ltd. 抗癌剤に対する癌細胞の感受性を検定する方法
WO2006009276A1 (ja) * 2004-07-20 2006-01-26 Eisai R & D Management Co., Ltd. プラジエノライドの生合成に関与するポリペプチドをコードするdna
WO2006126723A1 (ja) * 2005-05-26 2006-11-30 Eisai R & D Management Co., Ltd. 遺伝子組換え微生物およびそれらの微生物を用いるマクロライド系化合物の製造方法
WO2007043621A1 (ja) 2005-10-13 2007-04-19 Eisai R & D Management Co., Ltd. プラジエノライド b及びプラジエノライド dの全合成方法
WO2008016187A1 (fr) 2006-08-02 2008-02-07 Eisai R & D Management Co., Ltd. Molécule cible de pladiénolide, composé capable de se lier à la molécule cible et procédé de criblage pour rechercher le composé
WO2008111466A1 (ja) 2007-03-05 2008-09-18 Eisai R & D Management Co., Ltd. 遺伝子の発現量減少を指標とする抗ガン剤の作用検定方法
WO2008111464A1 (ja) 2007-03-05 2008-09-18 Eisai R & D Management Co., Ltd. スプライシング異常を指標とする抗ガン剤の作用検定方法
WO2008126918A1 (ja) * 2007-04-12 2008-10-23 Eisai R & D Management Co., Ltd. 12員環マクロラクタム誘導体
WO2009008492A1 (ja) 2007-07-06 2009-01-15 Eisai R & D Management Co., Ltd. マクロライド系化合物の製造方法およびその製造中間体
US7667052B2 (en) 2001-02-01 2010-02-23 Eisai R&D Management Co., Ltd. Bioactive substance
US7790887B2 (en) 2007-01-29 2010-09-07 Eisai R&D Management Co., Ltd. Macrolide compound in solid form, process for preparation thereof, and pharmaceutical composition containing the same
CN103145740A (zh) * 2013-02-28 2013-06-12 大连理工大学 一种亚砜生物碱类化合物及其制备方法与应用
JP2015524669A (ja) * 2012-08-14 2015-08-27 コーリア リサーチ インスティテュート オブ ケミカル テクノロジー ストレプトマイセス・スコプリリディスkr−001株またはその培養液を活性成分として含む雑草防除用組成物
WO2015175594A1 (en) 2014-05-15 2015-11-19 Eisai R&D Management Co., Ltd. Pladienolide pyridine compounds and methods of use
WO2017040526A2 (en) 2015-09-01 2017-03-09 Eisai R&D Management Co., Ltd. Splice variants associated with neomorphic sf3b1 mutants
WO2017087667A1 (en) 2015-11-18 2017-05-26 Eisai R&D Management Co., Ltd. A solid state form of pladienolide pyridine compounds and methods of use
WO2018170129A1 (en) 2017-03-15 2018-09-20 Eisai Co., Ltd Spliceosome mutations and uses thereof
WO2019089641A1 (en) 2017-10-31 2019-05-09 Eisai R&D Management Co., Ltd. Combination comprising at least one spliceosome modulator and at least one inhibitor chosen from bcl2 inhibitors, bcl2/bclxl inhibitors, and bclxl inhibitors and methods of use
WO2019200100A1 (en) 2018-04-12 2019-10-17 Andrew Cook Pladienolide derivatives as spliceosome targeting agents for treating cancer
WO2019199667A2 (en) 2018-04-09 2019-10-17 Keaney Gregg F Certain pladienolide compounds and methods of use
WO2019232433A2 (en) 2018-06-01 2019-12-05 Eisai R&D Management Co., Ltd. Methods of using splicing modulators
JP2020147509A (ja) * 2019-03-12 2020-09-17 学校法人大阪医科薬科大学 抗がん剤
WO2022098712A1 (en) 2020-11-04 2022-05-12 Eisai R&D Management Co., Ltd. Biomarkers for myelodysplastic syndrome (mds) and methods of using the same
WO2023131866A1 (en) 2022-01-05 2023-07-13 Eisai R&D Management Co., Ltd. Biomarkers for myelodysplastic syndrome (mds) and methods of using the same

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CA2520377A1 (en) 2003-03-28 2004-10-14 Cornell Research Foundation, Inc. Migrastatin analog compositions and uses thereof
WO2006001967A2 (en) 2004-05-25 2006-01-05 Sloan-Kettering Institute For Cancer Research Migrastatin analogs in the treatment of cancer
CA2582766C (en) 2004-09-23 2014-07-22 Sloan-Kettering Institute For Cancer Research Isomigrastatin analogs in the treatment of cancer
WO2007110704A2 (en) * 2005-09-28 2007-10-04 Novimmune Sa Macrolide compositions as therapeutic agent
AU2007285215A1 (en) * 2006-08-14 2008-02-21 Eisai R & D Management Co., Ltd. Stable lyophilized preparation
GB0821540D0 (en) * 2008-11-25 2008-12-31 Merlion Pharmaceuticals Pte Ltd Lipopeptide compounds and their use
GB0821539D0 (en) * 2008-11-25 2008-12-31 Merlion Pharmaceuticals Pte Ltd Therapeutic compounds and their use
WO2013148324A1 (en) 2012-03-26 2013-10-03 The Regents Of The University Of California Anti-cancer polyketide compounds
WO2024119114A1 (en) * 2022-12-01 2024-06-06 Aspera Biomedicines, Inc. Chemoenzymatic synthesis of polyketides

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04352783A (ja) * 1991-05-27 1992-12-07 Taisho Pharmaceut Co Ltd 12員環マクロライド系化合物
WO2000075126A1 (en) * 1999-06-03 2000-12-14 The United States Of America, Represented By The Secretary, Department Of Health And Human Services Mycolactone and related compounds, compositions and methods of use
WO2002012533A2 (en) * 2000-08-03 2002-02-14 Kosan Biosciences, Inc. Fermentation and purification of mycolactones

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI312681B (en) 2001-02-01 2009-08-01 Novel physiologically active substance
TWI233361B (en) * 2001-04-13 2005-06-01 Gen Hospital Corp Methods of preventing UVB-induced skin damage
TWI334866B (en) 2002-05-29 2010-12-21 Mercian Corp Novel physiologically active substances
AU2003252445B2 (en) * 2002-07-31 2009-09-17 Eisai R & D Management Co., Ltd. Novel physiologically active substances
JPWO2007043621A1 (ja) * 2005-10-13 2009-04-16 エーザイ・アール・アンド・ディー・マネジメント株式会社 プラジエノライドb及びプラジエノライドdの全合成方法

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04352783A (ja) * 1991-05-27 1992-12-07 Taisho Pharmaceut Co Ltd 12員環マクロライド系化合物
WO2000075126A1 (en) * 1999-06-03 2000-12-14 The United States Of America, Represented By The Secretary, Department Of Health And Human Services Mycolactone and related compounds, compositions and methods of use
WO2002012533A2 (en) * 2000-08-03 2002-02-14 Kosan Biosciences, Inc. Fermentation and purification of mycolactones

Non-Patent Citations (9)

* Cited by examiner, † Cited by third party
Title
BESTMANN, HANS JUERGEN ET AL.: "Kumulierte ylide XX. Synthesen (E)-alpha, beta-ungesaettigter macrocyclischer lactone durch intramolekulare wittig-olefinierung via triphenylphosphoranylidenketen", SYNTHESIS, vol. 6, 1989, pages 419 - 423, XP002951018 *
BESTMANN, HANS JUERGEN ET AL.: "Neue synthese makrocyclischer lactone", ANGEW. CHEM., vol. 95, no. 10, 1983, pages 810 - 811, XP002951019 *
FUERSTNER, ALOIS ET AL.: "Efficient total syntheses of resin glycosides and analogues by ring-closing olefin metathesis", vol. 121, 1999, pages 7814 - 7821, XP002951020 *
GUNAWARDANA, GEEWANANDA ET AL.: "Characterization of novel macrolide toxins, mycolactones A and B, from a human pathogen, mycobacterium ulcerans", J. AM. CHEM. SOC., vol. 121, 1999, pages 6092 - 6093, XP002951022 *
HAMBERG, MATS: "Fatty acid allene oxides II. Formation of two macrolactones from 12,13(S)-epoxy-9(Z), 11-octadecadienoic acid", CHEM. PHYS. LIPIDS, vol. 46, no. 4, 1988, pages 235 - 243, XP002951025 *
HAMBERG, MATS: "New cyclopentenone fatty acids formed from linoleic and linolenic acids in potato", LIPIDS, vol. 35, no. 4, 2000, pages 353 - 363, XP002951024 *
KOBAYASHI, JUN'ICHI ET AL.: "Amphidinolide Q, a novel 12-membered macrolide from the cultured marine dinoflagellate amphidinium sp.", TETRAHEDRON LETTERS, vol. 37, no. 9, 1996, pages 1449 - 1450, XP004030068 *
ROHR, JUERGEN: "A new role for polyketides", ANGEW. CHEM. INT. ED., vol. 39, no. 16, 2000, pages 2847 - 2849, XP002951023 *
SEKI-ASANO, MITSUKO ET AL.: "Isolation and characterization of a new 12-membered macrolide FD-895", J. ANTIBIOT., vol. 47, no. 12, 1994, pages 1395 - 1401, XP002951021 *

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* Cited by examiner, † Cited by third party
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CN1489583B (zh) 2011-03-30
JP4439181B2 (ja) 2010-03-24
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TWI312681B (en) 2009-08-01
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