IT1362675B - N-idrossiammidi -sostituiti con gruppi triciclici come inibitori dell'istone deacelitasi,loro preparazione ed impiego in formulazioni farmaceutiche - Google Patents

N-idrossiammidi -sostituiti con gruppi triciclici come inibitori dell'istone deacelitasi,loro preparazione ed impiego in formulazioni farmaceutiche

Info

Publication number: IT1362675B
Authority: IT; Italy
Prior art keywords: deacelitasis; hydroxyamides; islands; inhibitors; substituted
Prior art date: 2005-03-15

Application number

Other languages

English (en)

Inventor

Tula Dimoulas

Danilo Giannotti

Antonio Guidi

Nicholas Harmat

Original Assignee

Menarini Internat Operations Luxembourg Sa

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.)

2005-03-15

Filing date

2005-03-15

Publication date

2009-06-25

2005-03-15 Application filed by Menarini Internat Operations Luxembourg Sa filed Critical Menarini Internat Operations Luxembourg Sa

2005-03-15 Priority to IT000042 priority Critical patent/IT1362675B/it

2006-03-07 Priority to TW095107553A priority patent/TW200719900A/zh

2006-03-13 Priority to AU2006222883A priority patent/AU2006222883A1/en

2006-03-13 Priority to JP2008501283A priority patent/JP2008533088A/ja

2006-03-13 Priority to AP2007004170A priority patent/AP2007004170A0/xx

2006-03-13 Priority to CA002600521A priority patent/CA2600521A1/en

2006-03-13 Priority to PCT/EP2006/060661 priority patent/WO2006097449A1/en

2006-03-13 Priority to EP06708743A priority patent/EP1863776A1/en

2006-03-13 Priority to BRPI0608549-0A priority patent/BRPI0608549A2/pt

2006-03-13 Priority to CNA2006800082490A priority patent/CN101142197A/zh

2006-03-13 Priority to EA200701969A priority patent/EA013015B1/ru

2006-03-13 Priority to MX2007011071A priority patent/MX2007011071A/es

2006-03-13 Priority to KR1020077023278A priority patent/KR20080003336A/ko

2006-03-13 Priority to US11/886,168 priority patent/US20080275023A1/en

2006-03-14 Priority to ARP060100976A priority patent/AR053171A1/es

2006-05-08 Priority to SA06270133A priority patent/SA06270133B1/ar

2006-09-16 Publication of ITFI20050042A1 publication Critical patent/ITFI20050042A1/it

2007-08-23 Priority to NI200700222A priority patent/NI200700222A/es

2007-09-10 Priority to IL185879A priority patent/IL185879A0/en

2007-10-11 Priority to MA30292A priority patent/MA29673B1/fr

2007-10-12 Priority to ZA200708754A priority patent/ZA200708754B/xx

2007-10-12 Priority to NO20075229A priority patent/NO20075229L/no

2007-10-12 Priority to CO07107398A priority patent/CO6321131A2/es

2009-06-25 Application granted granted Critical

2009-06-25 Publication of IT1362675B publication Critical patent/IT1362675B/it

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D243/00—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
- C07D243/06—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4
- C07D243/10—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
- C07D243/38—[b, e]- or [b, f]-condensed with six-membered rings
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D267/00—Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D267/02—Seven-membered rings
- C07D267/08—Seven-membered rings having the hetero atoms in positions 1 and 4
- C07D267/12—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
- C07D267/16—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems condensed with two six-membered rings
- C07D267/20—[b, f]-condensed
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D281/00—Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one sulfur atom as the only ring hetero atoms
- C07D281/02—Seven-membered rings
- C07D281/04—Seven-membered rings having the hetero atoms in positions 1 and 4
- C07D281/08—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
- C07D281/12—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems condensed with two six-membered rings
- C07D281/16—[b, f]-condensed
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/36—Seven-membered rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D291/00—Heterocyclic compounds containing rings having nitrogen, oxygen and sulfur atoms as the only ring hetero atoms
- C07D291/08—Heterocyclic compounds containing rings having nitrogen, oxygen and sulfur atoms as the only ring hetero atoms condensed with carbocyclic rings or ring systems
- 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
- C07D401/02—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 two hetero rings
- C07D401/06—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 two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic 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
- C07D471/02—Heterocyclic 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 system contains two hetero rings
- C07D471/04—Ortho-condensed systems
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
- C07D473/16—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two nitrogen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic 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 two hetero rings
- C07D495/04—Ortho-condensed systems

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Veterinary Medicine (AREA)
General Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Pharmacology & Pharmacy (AREA)
Life Sciences & Earth Sciences (AREA)
Animal Behavior & Ethology (AREA)
Public Health (AREA)
General Chemical & Material Sciences (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Chemical Kinetics & Catalysis (AREA)
Engineering & Computer Science (AREA)
Bioinformatics & Cheminformatics (AREA)
Diabetes (AREA)
Hematology (AREA)
Immunology (AREA)
Gastroenterology & Hepatology (AREA)
Epidemiology (AREA)
Rheumatology (AREA)
Tropical Medicine & Parasitology (AREA)
Emergency Medicine (AREA)
Endocrinology (AREA)
Obesity (AREA)
Oncology (AREA)
Pain & Pain Management (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
Plural Heterocyclic Compounds (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

IT000042 2005-03-15 2005-03-15 N-idrossiammidi -sostituiti con gruppi triciclici come inibitori dell'istone deacelitasi,loro preparazione ed impiego in formulazioni farmaceutiche IT1362675B (it)

Priority Applications (22)

Application Number	Priority Date	Filing Date	Title
IT000042 IT1362675B (it)	2005-03-15	2005-03-15	N-idrossiammidi -sostituiti con gruppi triciclici come inibitori dell'istone deacelitasi,loro preparazione ed impiego in formulazioni farmaceutiche
TW095107553A TW200719900A (en)	2005-03-15	2006-03-07	N-hydroxyamides ω-substituted with tricyclic groups as histone deacetylase inhibitors, their preparation and use in pharmaceutical formulations
US11/886,168 US20080275023A1 (en)	2005-03-15	2006-03-13	N-Hydroxyamides Omege-Substituted with Tricyclic Groups as Histone Deacetylase Inhibitors, Their Preparation and Use in Pharmaceutical Formulations
AP2007004170A AP2007004170A0 (en)	2005-03-15	2006-03-13	N-hydroxyamides omega-substituted with tricyclic groups as histone deacetylase inhibitors, their preparation and use in pharmaceutical formulations
CA002600521A CA2600521A1 (en)	2005-03-15	2006-03-13	N-hydroxyamides omega-substituted with tricyclic groups as histone deacetylase inhibitors, their preparation and use in pharmaceutical formulations
PCT/EP2006/060661 WO2006097449A1 (en)	2005-03-15	2006-03-13	N-hydroxyamides omega-substituted with tricyclic groups as histone deacetylase inhibitors, their preparation and use in pharmaceutical formulations
EP06708743A EP1863776A1 (en)	2005-03-15	2006-03-13	N-hydroxyamides omega-substituted with tricyclic groups as histone deacetylase inhibitors, their preparation and use in pharmaceutical formulations
BRPI0608549-0A BRPI0608549A2 (pt)	2005-03-15	2006-03-13	inibidores da enzima histona deacetilase à base de n-hidroxiamidas (omega)-substituìdas por grupos tricìclicos
CNA2006800082490A CN101142197A (zh)	2005-03-15	2006-03-13	作为组蛋白去乙酰基酶抑制剂的3环基团ω-取代的N-羟酰胺及其制备方法以及在药物配方中的用途
EA200701969A EA013015B1 (ru)	2005-03-15	2006-03-13	N-ГИДРОКСИАМИДЫ, ω-ЗАМЕЩЕННЫЕ ТРИЦИКЛИЧЕСКИМИ ГРУППАМИ, КАК ИНГИБИТОРЫ ГИСТОНДЕАЦЕТИЛАЗЫ, ИХ ПОЛУЧЕНИЕ И ПРИМЕНЕНИЕ В ФАРМАЦЕВТИЧЕСКИХ ФОРМАХ
AU2006222883A AU2006222883A1 (en)	2005-03-15	2006-03-13	N-hydroxyamides omega-substituted with tricyclic groups as histone deacetylase inhibitors, their preparation and use in pharmaceutical formulations
KR1020077023278A KR20080003336A (ko)	2005-03-15	2006-03-13	히스톤 탈아세틸화제 저해제로서 삼중환기로 오메가-치환된엔-히드록시아미드, 그 제조 방법 및 약학적 제제로서의용도
JP2008501283A JP2008533088A (ja)	2005-03-15	2006-03-13	ヒストンデアセチラーゼ阻害剤としての、三員環基でω位置換したＮ−ヒドロキシアミド、その調製方法、及び医薬組成物への使用
MX2007011071A MX2007011071A (es)	2005-03-15	2006-03-13	N-hidroxiamidas omega-sustituidas con grupos triciclicos como inhibidores de histona desacetilasa, su preparacion y uso en formulaciones farmaceuticas.
ARP060100976A AR053171A1 (es)	2005-03-15	2006-03-14	N-hidroxiamidas omega-sustituidos con grupos triciclicos como inhibidores de la histona deacetilasa sus preparaciones y empleo en formulaciones farmaceuticas
SA06270133A SA06270133B1 (ar)	2005-03-15	2006-05-08	تحضير مركبات n- هيدروكسي أميد تحمل بدائل عند الموقع أوميغا من مجموعات ثلاثسة الحلقه بصفتها مثبطات لهستون دياستيلاز واستخدامها في التراكيب الصيدلانية
NI200700222A NI200700222A (es)	2005-03-15	2007-08-23	N-hydroxiamidas omega-sustituidas con grupos triciclicos como inhibidores de histona de desacetilasa, su preparación y su uso en formulaciones farmacéuticas.
IL185879A IL185879A0 (en)	2005-03-15	2007-09-10	N-hydroxyamides omega-substituted with tricyclic groups as histone deacetylase inhibitors, their preparation and use in pharmaceutical formulations
MA30292A MA29673B1 (fr)	2005-03-15	2007-10-11	N-hydroxyamides omega-substitues par des groupes tricycliques, servant d'inhibiteurs d'histone desacetylase, leur preparation et leur utilisation dans des formulations pharmaceutiques
ZA200708754A ZA200708754B (en)	2005-03-15	2007-10-12	N-hydroxyamides omega-substituted with tricyclic groups as histone deacetylase inhibitors, their preparation and use in pharmaceutical formulations
NO20075229A NO20075229L (no)	2005-03-15	2007-10-12	N-hydroksyamider omega-substituert med trisykliske grupper som histondeacetylasehemmere, deres fremstilling og anvendelse i farmasoytiske formuleringer
CO07107398A CO6321131A2 (es)	2005-03-15	2007-10-12	N-hidroxiamidas omega- sustituidas con grupos triciclicos como inhibidores de histona desacetilasa su preparacion y uso en formulaciones farmaceuticas

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
IT000042 IT1362675B (it)	2005-03-15	2005-03-15	N-idrossiammidi -sostituiti con gruppi triciclici come inibitori dell'istone deacelitasi,loro preparazione ed impiego in formulazioni farmaceutiche

Publications (2)

Publication Number	Publication Date
ITFI20050042A1 ITFI20050042A1 (it)	2006-09-16
IT1362675B true IT1362675B (it)	2009-06-25

Family

ID=36676439

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IT000042 IT1362675B (it)	2005-03-15	2005-03-15	N-idrossiammidi -sostituiti con gruppi triciclici come inibitori dell'istone deacelitasi,loro preparazione ed impiego in formulazioni farmaceutiche

Country Status (22)

Country	Link
US (1)	US20080275023A1 (it)
EP (1)	EP1863776A1 (it)
JP (1)	JP2008533088A (it)
KR (1)	KR20080003336A (it)
CN (1)	CN101142197A (it)
AP (1)	AP2007004170A0 (it)
AR (1)	AR053171A1 (it)
AU (1)	AU2006222883A1 (it)
BR (1)	BRPI0608549A2 (it)
CA (1)	CA2600521A1 (it)
CO (1)	CO6321131A2 (it)
EA (1)	EA013015B1 (it)
IL (1)	IL185879A0 (it)
IT (1)	IT1362675B (it)
MA (1)	MA29673B1 (it)
MX (1)	MX2007011071A (it)
NI (1)	NI200700222A (it)
NO (1)	NO20075229L (it)
SA (1)	SA06270133B1 (it)
TW (1)	TW200719900A (it)
WO (1)	WO2006097449A1 (it)
ZA (1)	ZA200708754B (it)

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GB0523040D0 (en) *	2005-11-11	2005-12-21	Cyclacel Ltd	Combination
AU2013205135B2 (en) *	2006-10-28	2015-11-05	Forum Pharmaceuticals Inc.	Inhibitors of histone deacetylase
WO2008055068A2 (en) *	2006-10-28	2008-05-08	Methylgene Inc.	Inhibitors of histone deacetylase
CN101605788A (zh) *	2006-12-11	2009-12-16	默克公司	用作铃蟾肽受体亚型-3调节剂的取代的二氮杂磺酰胺类化合物
JP2011102240A (ja) *	2008-02-29	2011-05-26	Univ Of Tokyo	三環性化合物
US8202989B2 (en)	2009-01-12	2012-06-19	Council Of Scientific And Industrial Research	One step process for the preparation of substituted 5, 10-dihydrodibenzo [b,e][1, 4]diazepine-11-ones
AU2011239537A1 (en) *	2010-04-16	2012-11-15	Curis, Inc.	Treatment of cancers having K-ras mutations
WO2012045194A1 (en) *	2010-10-09	2012-04-12	Abbott Laboratories	Benzodiazepinones as fak inhibitors for treatment of cancer
RU2519546C1 (ru) *	2013-01-16	2014-06-10	Общество С Ограниченной Ответственностью "Биоинтегратор" (Ооо "Биоинтегратор")	КОНЪЮГАТЫ И МАЛЫЕ МОЛЕКУЛЫ, ВЗАИМОДЕЙСТВУЮЩИЕ С РЕЦЕПТОРОМ CD16а
EP2958565A4 (en)	2013-02-19	2016-07-27	Icahn School Med Mount Sinai	TRICYCLIC HETEROCYCLES AS ANTICANCER AGENTS
JP2017512766A (ja)	2014-03-11	2017-05-25	アイカーンスクールオブメディスンアットマウントサイナイＩｃａｈｎＳｃｈｏｏｌｏｆＭｅｄｉｃｉｎｅａｔＭｔ．Ｓｉｎａｉ	抗癌剤としてのトリシクリル−２−アミノシクロアルカノール由来スルホンアミド
US9937180B2 (en)	2014-03-11	2018-04-10	Icahn School Of Medicine At Mount Sinai	Constrained tricyclic sulfonamides
JP2017535573A (ja) *	2014-11-25	2017-11-30	バイエルファーマアクチエンゲゼルシャフト	置換されたピリドベンゾジアゼピノン誘導体およびそれの使用
WO2016089830A1 (en)	2014-12-05	2016-06-09	Merck Sharp & Dohme Corp.	Novel tricyclic compounds as inhibitors of mutant idh enzymes
WO2016089797A1 (en)	2014-12-05	2016-06-09	Merck Sharp & Dohme Corp.	Novel tricyclic compounds as inhibitors of mutant idh enzymes
WO2016089833A1 (en)	2014-12-05	2016-06-09	Merck Sharp & Dohme Corp.	Novel tricyclic compounds as inhibitors of mutant idh enzymes
GB201510010D0 (en)	2015-06-09	2015-07-22	King S College London	PDD and BPD compounds
US20180339985A1 (en)	2015-08-21	2018-11-29	Femtogenix Limited	Pdd compounds
GB201514928D0 (en)	2015-08-21	2015-10-07	King S College London	PDD compounds
WO2017044571A1 (en) *	2015-09-09	2017-03-16	Icahn School Of Medicine At Mount Sinai	Tricyclic sultam sulfonamides as anticancer and neuroprotective agents
JP6955485B2 (ja)	2015-09-09	2021-10-27	アイカーンスクールオブメディスンアットマウントサイナイＩｃａｈｎＳｃｈｏｏｌｏｆＭｅｄｉｃｉｎｅａｔＭｔ．Ｓｉｎａｉ	抗がん剤としての複素環式の限定された三環系スルホンアミド
JP6966425B2 (ja)	2015-09-09	2021-11-17	アイカーンスクールオブメディスンアットマウントサイナイIcahn School of Medicine at Mt. Sinai	抗がん剤としての複素環式の限定された三環系スルホンアミド
CN105806973B (zh) *	2016-03-10	2019-01-18	中国医学科学院肿瘤医院	Uplc-ms/ms法测定人血浆中莎巴比星及其代谢产物m3的血药浓度
US11759450B2 (en)	2018-02-06	2023-09-19	The Board Of Trustees Of The University Of Illinois	Substituted benzothiophene analogs as selective estrogen receptor degraders
KR102301274B1 (ko) *	2019-08-05	2021-09-14	리퓨어생명과학 주식회사	히스톤 아세틸트렌스퍼라제 p300 억제용 신규 화합물 및 이를 포함하는 항섬유화 조성물
KR102243465B1 (ko) *	2019-08-05	2021-04-22	리퓨어생명과학 주식회사	히스톤 아세틸트렌스퍼라제 p300 억제용 신규 화합물 및 이를 포함하는 항섬유화 조성물
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2005
- 2005-03-15 IT IT000042 patent/IT1362675B/it active
2006
- 2006-03-07 TW TW095107553A patent/TW200719900A/zh unknown
- 2006-03-13 EP EP06708743A patent/EP1863776A1/en not_active Withdrawn
- 2006-03-13 AU AU2006222883A patent/AU2006222883A1/en not_active Abandoned
- 2006-03-13 CA CA002600521A patent/CA2600521A1/en not_active Abandoned
- 2006-03-13 MX MX2007011071A patent/MX2007011071A/es not_active Application Discontinuation
- 2006-03-13 AP AP2007004170A patent/AP2007004170A0/xx unknown
- 2006-03-13 EA EA200701969A patent/EA013015B1/ru unknown
- 2006-03-13 US US11/886,168 patent/US20080275023A1/en not_active Abandoned
- 2006-03-13 KR KR1020077023278A patent/KR20080003336A/ko not_active Withdrawn
- 2006-03-13 BR BRPI0608549-0A patent/BRPI0608549A2/pt not_active IP Right Cessation
- 2006-03-13 WO PCT/EP2006/060661 patent/WO2006097449A1/en not_active Ceased
- 2006-03-13 CN CNA2006800082490A patent/CN101142197A/zh active Pending
- 2006-03-13 JP JP2008501283A patent/JP2008533088A/ja active Pending
- 2006-03-14 AR ARP060100976A patent/AR053171A1/es not_active Application Discontinuation
- 2006-05-08 SA SA06270133A patent/SA06270133B1/ar unknown
2007
- 2007-08-23 NI NI200700222A patent/NI200700222A/es unknown
- 2007-09-10 IL IL185879A patent/IL185879A0/en unknown
- 2007-10-11 MA MA30292A patent/MA29673B1/fr unknown
- 2007-10-12 CO CO07107398A patent/CO6321131A2/es not_active Application Discontinuation
- 2007-10-12 NO NO20075229A patent/NO20075229L/no not_active Application Discontinuation
- 2007-10-12 ZA ZA200708754A patent/ZA200708754B/xx unknown

Also Published As

Publication number	Publication date
EP1863776A1 (en)	2007-12-12
EA200701969A1 (ru)	2008-02-28
MX2007011071A (es)	2007-10-08
BRPI0608549A2 (pt)	2010-01-12
TW200719900A (en)	2007-06-01
AR053171A1 (es)	2007-04-25
NI200700222A (es)	2008-07-24
CA2600521A1 (en)	2006-09-21
ITFI20050042A1 (it)	2006-09-16
EA013015B1 (ru)	2010-02-26
NO20075229L (no)	2007-11-08
MA29673B1 (fr)	2008-08-01
AP2007004170A0 (en)	2007-10-31
WO2006097449A1 (en)	2006-09-21
SA06270133B1 (ar)	2009-05-16
KR20080003336A (ko)	2008-01-07
IL185879A0 (en)	2008-01-06
US20080275023A1 (en)	2008-11-06
CO6321131A2 (es)	2011-09-20
CN101142197A (zh)	2008-03-12
JP2008533088A (ja)	2008-08-21
ZA200708754B (en)	2008-10-29
AU2006222883A1 (en)	2006-09-21

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