TN2011000636A1 - Nouveaux conjuges, leur preparation et leur application en therapeutique - Google Patents
Nouveaux conjuges, leur preparation et leur application en therapeutiqueInfo
- Publication number
- TN2011000636A1 TN2011000636A1 TNP2011000636A TN2011000636A TN2011000636A1 TN 2011000636 A1 TN2011000636 A1 TN 2011000636A1 TN P2011000636 A TNP2011000636 A TN P2011000636A TN 2011000636 A TN2011000636 A TN 2011000636A TN 2011000636 A1 TN2011000636 A1 TN 2011000636A1
- Authority
- TN
- Tunisia
- Prior art keywords
- group
- alkyl
- phenyl ring
- conjugations
- 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
- 230000008685 targeting Effects 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
- 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)
- Medicinal Preparation (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Peptides Or Proteins (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Saccharide Compounds (AREA)
Abstract
L'invention est relative à un agent de ciblage auquel est attaché au moins un dérivé de cryptophycine de formule (I) : dans laquelle : R1 représente un atome d'halogène et R2 représente un groupe -OH, un groupe acyle dérivé d'un acide aminé AA ou un groupe (C1-C4)alcanoyloxy; ou bien R1 et R2 forment ensemble un motif époxyde; AA désigne un acide aminé naturel ou non-naturel; R3 représente un groupe (C1-C6)alkyle; R4 et R5 représentent tous deux H ou forment ensemble une double liaison CH=CH entre C13 et C14; R6 et R7 représentent indépendamment l'un de l'autre H ou un groupe (C1-C6)Jalkyle; R8 et R9 représentent indépendamment l'un de l'autre H ou un groupe (C1-C6)alkyle; R10 représente au moins un substituant du noyau phényle choisi parmi : H, un groupe OH, (C1-C4)alcoxy, un atome d'halogène ou bien un groupe -NH2, -NH(C1-C6)alkyle ou -N(C1- C6)alkyle2; R11 représente au moins un substituant du noyau phényle choisi parmi H ou un groupe (C1- C4)alkyle; l'agent de ciblage et le dérivé de cryptophycine étant attachés de façon covalente, l'attachement se situant en position ortho (o), meta (m) ou para (p) du noyau phényle porteur du motif CR1.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0903170A FR2947269B1 (fr) | 2009-06-29 | 2009-06-29 | Nouveaux composes anticancereux |
| PCT/FR2010/050986 WO2011001052A1 (fr) | 2009-06-29 | 2010-05-20 | Nouveaux conjugues, leur preparation et leur application en therapeutique |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TN2011000636A1 true TN2011000636A1 (fr) | 2013-05-24 |
Family
ID=41611078
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TNP2011000636A TN2011000636A1 (fr) | 2009-06-29 | 2011-12-12 | Nouveaux conjuges, leur preparation et leur application en therapeutique |
Country Status (30)
| Country | Link |
|---|---|
| US (1) | US8952147B2 (fr) |
| EP (1) | EP2448929A1 (fr) |
| JP (1) | JP5746692B2 (fr) |
| KR (1) | KR101770584B1 (fr) |
| CN (1) | CN102482238B (fr) |
| AR (1) | AR078131A1 (fr) |
| BR (1) | BRPI1015131A2 (fr) |
| CA (1) | CA2766762C (fr) |
| CL (1) | CL2011003229A1 (fr) |
| CO (1) | CO6430462A2 (fr) |
| CR (1) | CR20110670A (fr) |
| DO (1) | DOP2011000376A (fr) |
| EA (1) | EA024627B1 (fr) |
| EC (1) | ECSP11011553A (fr) |
| FR (2) | FR2947269B1 (fr) |
| HN (1) | HN2011003414A (fr) |
| IL (1) | IL217208A (fr) |
| MA (1) | MA33465B1 (fr) |
| MX (1) | MX2011013764A (fr) |
| MY (1) | MY156684A (fr) |
| NI (1) | NI201100219A (fr) |
| NZ (1) | NZ597136A (fr) |
| PE (1) | PE20121031A1 (fr) |
| SG (2) | SG10201607595WA (fr) |
| SV (1) | SV2011004086A (fr) |
| TN (1) | TN2011000636A1 (fr) |
| TW (1) | TW201110986A (fr) |
| UY (1) | UY32745A (fr) |
| WO (1) | WO2011001052A1 (fr) |
| ZA (1) | ZA201109537B (fr) |
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| RU2595424C2 (ru) | 2009-06-03 | 2016-08-27 | Иммьюноджен, Инк. | Способы конъюгации |
| CN104945420A (zh) | 2009-06-29 | 2015-09-30 | 因塞特公司 | 作为pi3k抑制剂的嘧啶酮类 |
| US8759359B2 (en) | 2009-12-18 | 2014-06-24 | Incyte Corporation | Substituted heteroaryl fused derivatives as PI3K inhibitors |
| JP5816678B2 (ja) | 2010-04-14 | 2015-11-18 | インサイト・コーポレイションＩｎｃｙｔｅ Ｃｏｒｐｏｒａｔｉｏｎ | ＰＩ３Ｋδ阻害剤としての縮合誘導体 |
| US9062055B2 (en) | 2010-06-21 | 2015-06-23 | Incyte Corporation | Fused pyrrole derivatives as PI3K inhibitors |
| CA2822070C (fr) | 2010-12-20 | 2019-09-17 | Incyte Corporation | N-(1-(phenyl substitue)ethyl)-9h-purin-6-amines en tant qu'inhibiteurs de pi3k |
| US9108984B2 (en) | 2011-03-14 | 2015-08-18 | Incyte Corporation | Substituted diamino-pyrimidine and diamino-pyridine derivatives as PI3K inhibitors |
| WO2012135009A1 (fr) | 2011-03-25 | 2012-10-04 | Incyte Corporation | Dérivés de pyrimidine-4,6-diamine en tant qu'inhibiteurs de pi3k |
| JP6000329B2 (ja) | 2011-03-29 | 2016-09-28 | イムノゲン インコーポレーティッド | １段階の工程によるマイタンシノイド−抗体複合体の調製 |
| ES2873001T3 (es) | 2011-09-02 | 2021-11-03 | Incyte Holdings Corp | Heterociclaminas como inhibidores de PI3K |
| 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 |
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| JP6486316B2 (ja) | 2015-11-03 | 2019-03-20 | 財團法人工業技術研究院Ｉｎｄｕｓｔｒｉａｌ Ｔｅｃｈｎｏｌｏｇｙ Ｒｅｓｅａｒｃｈ Ｉｎｓｔｉｔｕｔｅ | 抗体−薬物複合体（ａｄｃ）およびそれを形成するための方法 |
| 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 |
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| EA201992667A1 (ru) * | 2017-05-10 | 2020-03-10 | Санофи | Новые пептидные линкеры и конъюгаты на основе криптофицина, их получение и их терапевтическое применение |
| WO2019030284A1 (fr) | 2017-08-09 | 2019-02-14 | Helmholtz-Zentrum für Infektionsforschung GmbH | Nouveaux dérivés de ratjadone cytotoxiques ciblés et leurs conjugués |
| SG11202005678UA (en) * | 2017-12-22 | 2020-07-29 | Univ Cornell | 18f-labeled peptide ligands useful in pet and cerenkov luminescene imaging |
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| EP4046996A1 (fr) | 2021-02-19 | 2022-08-24 | Universität Bielefeld | Composés de cryptophycine et leurs conjugués |
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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 CA CA2766762A patent/CA2766762C/fr not_active Expired - Fee Related
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- 2010-05-20 EP EP10728799A patent/EP2448929A1/fr not_active Withdrawn
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