ECSP11011553A - Nuevos conjugados, su preparación y su aplicación terapéutica - Google Patents
Nuevos conjugados, su preparación y su aplicación terapéuticaInfo
- Publication number
- ECSP11011553A ECSP11011553A EC2011011553A ECSP11011553A ECSP11011553A EC SP11011553 A ECSP11011553 A EC SP11011553A EC 2011011553 A EC2011011553 A EC 2011011553A EC SP11011553 A ECSP11011553 A EC SP11011553A EC SP11011553 A ECSP11011553 A EC SP11011553A
- Authority
- EC
- Ecuador
- Prior art keywords
- group
- alkyl
- alkyl group
- phenyl nucleus
- preparation
- Prior art date
Links
- 230000001225 therapeutic effect Effects 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- 150000001413 amino acids Chemical class 0.000 abstract 2
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- PSNOPSMXOBPNNV-VVCTWANISA-N cryptophycin 1 Chemical class C1=C(Cl)C(OC)=CC=C1C[C@@H]1C(=O)NC[C@@H](C)C(=O)O[C@@H](CC(C)C)C(=O)O[C@H]([C@H](C)[C@@H]2[C@H](O2)C=2C=CC=CC=2)C/C=C/C(=O)N1 PSNOPSMXOBPNNV-VVCTWANISA-N 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
- 239000004593 Epoxy Substances 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 125000004423 acyloxy group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
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 or sparfloxacin
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicinal Preparation (AREA)
- Peptides Or Proteins (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Saccharide Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
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
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 |
---|---|
ECSP11011553A true ECSP11011553A (es) | 2012-01-31 |
Family
ID=41611078
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EC2011011553A ECSP11011553A (es) | 2009-06-29 | 2011-12-26 | 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) | SG177419A1 (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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AR084366A1 (es) | 2010-12-20 | 2013-05-08 | Incyte Corp | N-(1-(fenil sustituido)etil)-9h-purin-6-aminas como inhibidores de pi3k |
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WO2012135009A1 (en) | 2011-03-25 | 2012-10-04 | Incyte Corporation | Pyrimidine-4,6-diamine derivatives as pi3k inhibitors |
KR20220009505A (ko) | 2011-03-29 | 2022-01-24 | 이뮤노젠 아이엔씨 | 일-단계 방법에 의한 메이탄시노이드 항체 접합체의 제조 |
BR122019020716B1 (pt) | 2011-09-02 | 2021-02-17 | Incyte Holdings Corporation | heterociclilaminas como inibidores de pi3k e composição farmacêutica que as compreende |
AR090548A1 (es) | 2012-04-02 | 2014-11-19 | Incyte Corp | Azaheterociclobencilaminas biciclicas como inhibidores de pi3k |
SG11201502429YA (en) | 2012-10-04 | 2015-04-29 | Immunogen Inc | Use of a pvdf membrane to purify cell-binding agent cytotoxic agent conjugates |
CN105593238B (zh) | 2013-07-11 | 2020-09-08 | 诺华股份有限公司 | 使用微生物转谷氨酰胺酶进行赖氨酸特异性化学酶法蛋白质修饰 |
US10077277B2 (en) | 2014-06-11 | 2018-09-18 | Incyte Corporation | Bicyclic heteroarylaminoalkyl phenyl derivatives as PI3K inhibitors |
CR20170111A (es) * | 2014-09-03 | 2017-05-23 | Immunogen Inc | Derivados de benzodiazepina citotóxicos |
GB201416960D0 (en) | 2014-09-25 | 2014-11-12 | Antikor Biopharma Ltd | Biological materials and uses thereof |
MD3262046T2 (ro) | 2015-02-27 | 2021-03-31 | Incyte Corp | Săruri de inhibitori ai PI3K și procedee pentru prepararea lor |
EP3069734A1 (en) * | 2015-03-17 | 2016-09-21 | Exiris S.r.l. | Cryptophycin-based antibody-drug conjugates with novel self-immolative linkers |
US9732097B2 (en) | 2015-05-11 | 2017-08-15 | Incyte Corporation | Process for the synthesis of a phosphoinositide 3-kinase inhibitor |
WO2016183063A1 (en) | 2015-05-11 | 2016-11-17 | Incyte Corporation | Crystalline forms of a pi3k inhibitor |
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MA50764A (fr) | 2017-05-10 | 2020-03-18 | Sanofi Sa | Linkers peptidiques et conjugués de cryptophycine, utiles en thérapie, et leur préparation |
EP3665161B1 (en) | 2017-08-09 | 2023-09-27 | Helmholtz-Zentrum für Infektionsforschung GmbH | New targeted cytotoxic ratjadone derivatives and conjugates thereof |
CA3085600A1 (en) * | 2017-12-22 | 2019-06-27 | Cornell University | 18f-labeled peptide ligands useful in pet and cerenkov luminescene imaging |
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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
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2010
- 2010-05-20 CN CN201080038575.2A patent/CN102482238B/zh not_active Expired - Fee Related
- 2010-05-20 MX MX2011013764A patent/MX2011013764A/es active IP Right Grant
- 2010-05-20 MY MYPI2011006289A patent/MY156684A/en unknown
- 2010-05-20 KR KR1020117031276A patent/KR101770584B1/ko active IP Right Grant
- 2010-05-20 PE PE2011002178A patent/PE20121031A1/es not_active Application Discontinuation
- 2010-05-20 JP JP2012518108A patent/JP5746692B2/ja not_active Expired - Fee Related
- 2010-05-20 EA EA201270096A patent/EA024627B1/ru not_active IP Right Cessation
- 2010-05-20 CA CA2766762A patent/CA2766762C/fr not_active Expired - Fee Related
- 2010-05-20 NZ NZ597136A patent/NZ597136A/en not_active IP Right Cessation
- 2010-05-20 EP EP10728799A patent/EP2448929A1/fr not_active Withdrawn
- 2010-05-20 WO PCT/FR2010/050986 patent/WO2011001052A1/fr active Application Filing
- 2010-05-20 BR BRPI1015131-1A patent/BRPI1015131A2/pt not_active Application Discontinuation
- 2010-05-20 SG SG2011097193A patent/SG177419A1/en unknown
- 2010-05-20 MA MA34580A patent/MA33465B1/fr unknown
- 2010-05-20 SG SG10201607595WA patent/SG10201607595WA/en unknown
- 2010-06-28 TW TW099121094A patent/TW201110986A/zh unknown
- 2010-06-28 AR ARP100102290A patent/AR078131A1/es 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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