CO6430462A2 - Nuevos conjugados, su preparación y su aplicación terapéutica - Google Patents
Nuevos conjugados, su preparación y su aplicación terapéuticaInfo
- Publication number
- CO6430462A2 CO6430462A2 CO11180696A CO11180696A CO6430462A2 CO 6430462 A2 CO6430462 A2 CO 6430462A2 CO 11180696 A CO11180696 A CO 11180696A CO 11180696 A CO11180696 A CO 11180696A CO 6430462 A2 CO6430462 A2 CO 6430462A2
- Authority
- CO
- Colombia
- Prior art keywords
- group
- alkyl
- alkyl group
- phenyl nucleus
- derivative
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D273/00—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00
- C07D273/08—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00 having two nitrogen atoms and more than one oxygen atom
-
- 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
- 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
- A61K31/495—Heterocyclic 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene
-
- 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
- C07D245/00—Heterocyclic compounds containing rings of more than seven members having two nitrogen atoms as the only ring hetero atoms
- C07D245/04—Heterocyclic compounds containing rings of more than seven members having two nitrogen atoms as the only ring hetero atoms condensed with carbocyclic rings or ring systems
- C07D245/06—Heterocyclic compounds containing rings of more than seven members having two nitrogen atoms as the only ring hetero atoms condensed with carbocyclic rings or ring systems condensed with one six-membered ring
Abstract
La invención se refiere a un agente de selección de la diana al que está unido al menos un derivado de criptoficina de la fórmula (I), en la que: R1 representa un átomo de halógeno y R2 representa un grupo -OH, un grupo acilo derivado de un aminoácido AA o un grupo alcanoiloxi(C1-C4); o bien R1 y R2 forman conjuntamente un motivo epóxido; AA indica un aminoácido natural o no natural; R3 representa un grupo alquilo(C1-C6); R4 y R5 representan los dos H o forman conjuntamente un doble enlace CH=CH entre C13 y C14; R6 y R7 representan independientemente uno de otro H o un grupo alquilo(C1-C6); R8 y R9 representan independientemente uno de otro H o un grupo alquilo(C1-C6); R10 representa al menos un sustituyente del núcleo fenilo elegido entre: H, un grupo OH, alcoxi(C1-C4), un átomo de halógeno o bien un grupo -NH2, -NHalquilo(C1-C6) o -N(alquilo(C1-C6))2; R11 representa al menos un sustituyente del núcleo fenilo elegido entre H o un grupo alquilo(C1-C4); estando unidos el agente de selección de la diana y el derivado de criptoficina de forma covalente, situándose la unión en posición orto (o), meta (m) o para (p) del núcleo fenilo portador del motivo CR1.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0903170A FR2947269B1 (fr) | 2009-06-29 | 2009-06-29 | Nouveaux composes anticancereux |
FR0905651A FR2947271B1 (fr) | 2009-06-29 | 2009-11-25 | Nouveaux composes anticancereux |
Publications (1)
Publication Number | Publication Date |
---|---|
CO6430462A2 true CO6430462A2 (es) | 2012-04-30 |
Family
ID=41611078
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CO11180696A CO6430462A2 (es) | 2009-06-29 | 2011-12-29 | Nuevos conjugados, su preparación y su aplicación terapéutica |
Country Status (30)
Country | Link |
---|---|
US (1) | US8952147B2 (es) |
EP (1) | EP2448929A1 (es) |
JP (1) | JP5746692B2 (es) |
KR (1) | KR101770584B1 (es) |
CN (1) | CN102482238B (es) |
AR (1) | AR078131A1 (es) |
BR (1) | BRPI1015131A2 (es) |
CA (1) | CA2766762C (es) |
CL (1) | CL2011003229A1 (es) |
CO (1) | CO6430462A2 (es) |
CR (1) | CR20110670A (es) |
DO (1) | DOP2011000376A (es) |
EA (1) | EA024627B1 (es) |
EC (1) | ECSP11011553A (es) |
FR (2) | FR2947269B1 (es) |
HN (1) | HN2011003414A (es) |
IL (1) | IL217208A (es) |
MA (1) | MA33465B1 (es) |
MX (1) | MX2011013764A (es) |
MY (1) | MY156684A (es) |
NI (1) | NI201100219A (es) |
NZ (1) | NZ597136A (es) |
PE (1) | PE20121031A1 (es) |
SG (2) | SG10201607595WA (es) |
SV (1) | SV2011004086A (es) |
TN (1) | TN2011000636A1 (es) |
TW (1) | TW201110986A (es) |
UY (1) | UY32745A (es) |
WO (1) | WO2011001052A1 (es) |
ZA (1) | ZA201109537B (es) |
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JP5677425B2 (ja) | 2009-06-29 | 2015-02-25 | インサイト・コーポレイションIncyte Corporation | Pi3k阻害剤としてのピリミジノン |
WO2011075643A1 (en) | 2009-12-18 | 2011-06-23 | Incyte Corporation | Substituted heteroaryl fused derivatives as pi3k inhibitors |
CA2796311A1 (en) | 2010-04-14 | 2011-10-20 | Incyte Corporation | Fused derivatives as pi3k.delta. inhibitors |
WO2011163195A1 (en) | 2010-06-21 | 2011-12-29 | Incyte Corporation | Fused pyrrole derivatives as pi3k inhibitors |
EP2655374B1 (en) | 2010-12-20 | 2019-10-23 | Incyte Holdings Corporation | N-(1-(substituted-phenyl)ethyl)-9h-purin-6-amines as pi3k inhibitors |
WO2012125629A1 (en) | 2011-03-14 | 2012-09-20 | Incyte Corporation | Substituted diamino-pyrimidine and diamino-pyridine derivatives as pi3k inhibitors |
US9126948B2 (en) | 2011-03-25 | 2015-09-08 | Incyte Holdings Corporation | Pyrimidine-4,6-diamine derivatives as PI3K inhibitors |
UA116524C2 (uk) | 2011-03-29 | 2018-04-10 | Іммуноджен, Інк. | Спосіб одержання кон'югата антитіло-майтансиноїд |
KR102507287B1 (ko) | 2011-09-02 | 2023-03-07 | 인사이트 홀딩스 코포레이션 | Pi3k 억제제로서 헤테로시클릴아민 |
AR090548A1 (es) | 2012-04-02 | 2014-11-19 | Incyte Corp | Azaheterociclobencilaminas biciclicas como inhibidores de pi3k |
RU2661083C2 (ru) | 2012-10-04 | 2018-07-11 | Иммуноджен, Инк. | Использование пвдф-мембраны для очистки конъюгатов клеточно-связывающий агент - цитотоксический агент |
ES2756526T3 (es) | 2013-07-11 | 2020-04-27 | Novartis Ag | Modificaciones de proteínas quimioenzimáticas específicas para lisina utilizando transglutaminasa microbiana |
US10077277B2 (en) | 2014-06-11 | 2018-09-18 | Incyte Corporation | Bicyclic heteroarylaminoalkyl phenyl derivatives as PI3K inhibitors |
TWI697493B (zh) * | 2014-09-03 | 2020-07-01 | 美商免疫原公司 | 細胞毒性苯并二氮呯衍生物 |
GB201416960D0 (en) | 2014-09-25 | 2014-11-12 | Antikor Biopharma Ltd | Biological materials and uses thereof |
PE20180129A1 (es) | 2015-02-27 | 2018-01-18 | Incyte Corp | Sales de inhibidor de pi3k y procesos de preparacion |
EP3069734A1 (en) | 2015-03-17 | 2016-09-21 | Exiris S.r.l. | Cryptophycin-based antibody-drug conjugates with novel self-immolative linkers |
US9988401B2 (en) | 2015-05-11 | 2018-06-05 | Incyte Corporation | Crystalline forms of a PI3K inhibitor |
US9732097B2 (en) | 2015-05-11 | 2017-08-15 | Incyte Corporation | Process for the synthesis of a phosphoinositide 3-kinase inhibitor |
TWI660741B (zh) | 2015-11-03 | 2019-06-01 | 財團法人工業技術研究院 | 抗體藥物複合物及其製造方法 |
TWI714661B (zh) * | 2015-11-05 | 2021-01-01 | 法商賽諾菲公司 | 新穎念珠藻素化合物及接合物、其製備與其治療用途 |
WO2017136769A1 (en) * | 2016-02-04 | 2017-08-10 | Eisai R&D Management Co., Ltd. | Peptide drug conjugates |
WO2018178277A1 (en) | 2017-03-29 | 2018-10-04 | Avicenna Oncology Gmbh | New targeted cytotoxic isocombretaquinoline derivatives and conjugates thereof |
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AU2018389100A1 (en) * | 2017-12-22 | 2020-07-09 | Cornell University | 18F-labeled peptide ligands useful in PET and Cerenkov luminescene imaging |
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US11911484B2 (en) | 2018-08-02 | 2024-02-27 | Dyne Therapeutics, Inc. | Muscle targeting complexes and uses thereof for treating myotonic dystrophy |
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-
2009
- 2009-06-29 FR FR0903170A patent/FR2947269B1/fr not_active Expired - Fee Related
- 2009-11-25 FR FR0905651A patent/FR2947271B1/fr not_active Expired - Fee Related
-
2010
- 2010-05-20 EA EA201270096A patent/EA024627B1/ru not_active IP Right Cessation
- 2010-05-20 MX MX2011013764A patent/MX2011013764A/es active IP Right Grant
- 2010-05-20 SG SG10201607595WA patent/SG10201607595WA/en unknown
- 2010-05-20 EP EP10728799A patent/EP2448929A1/fr not_active Withdrawn
- 2010-05-20 MY MYPI2011006289A patent/MY156684A/en unknown
- 2010-05-20 BR BRPI1015131-1A patent/BRPI1015131A2/pt not_active Application Discontinuation
- 2010-05-20 MA MA34580A patent/MA33465B1/fr unknown
- 2010-05-20 PE PE2011002178A patent/PE20121031A1/es not_active Application Discontinuation
- 2010-05-20 SG SG2011097193A patent/SG177419A1/en unknown
- 2010-05-20 CA CA2766762A patent/CA2766762C/fr not_active Expired - Fee Related
- 2010-05-20 KR KR1020117031276A patent/KR101770584B1/ko active IP Right Grant
- 2010-05-20 WO PCT/FR2010/050986 patent/WO2011001052A1/fr active Application Filing
- 2010-05-20 NZ NZ597136A patent/NZ597136A/en not_active IP Right Cessation
- 2010-05-20 JP JP2012518108A patent/JP5746692B2/ja not_active Expired - Fee Related
- 2010-05-20 CN CN201080038575.2A patent/CN102482238B/zh not_active Expired - Fee Related
- 2010-06-28 AR ARP100102290A patent/AR078131A1/es unknown
- 2010-06-28 TW TW099121094A patent/TW201110986A/zh unknown
- 2010-06-29 UY UY0001032745A patent/UY32745A/es not_active Application Discontinuation
-
2011
- 2011-12-05 DO DO2011000376A patent/DOP2011000376A/es unknown
- 2011-12-12 TN TNP2011000636A patent/TN2011000636A1/fr unknown
- 2011-12-13 CR CR20110670A patent/CR20110670A/es unknown
- 2011-12-15 SV SV2011004086A patent/SV2011004086A/es unknown
- 2011-12-19 NI NI201100219A patent/NI201100219A/es unknown
- 2011-12-20 CL CL2011003229A patent/CL2011003229A1/es unknown
- 2011-12-20 US US13/331,259 patent/US8952147B2/en not_active Expired - Fee Related
- 2011-12-23 ZA ZA2011/09537A patent/ZA201109537B/en unknown
- 2011-12-26 IL IL217208A patent/IL217208A/en not_active IP Right Cessation
- 2011-12-26 EC EC2011011553A patent/ECSP11011553A/es unknown
- 2011-12-28 HN HN2011003414A patent/HN2011003414A/es unknown
- 2011-12-29 CO CO11180696A patent/CO6430462A2/es active IP Right Grant
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