CA2586915A1 - Molecules favorisant l'hematopoiese - Google Patents
Molecules favorisant l'hematopoiese Download PDFInfo
- Publication number
- CA2586915A1 CA2586915A1 CA002586915A CA2586915A CA2586915A1 CA 2586915 A1 CA2586915 A1 CA 2586915A1 CA 002586915 A CA002586915 A CA 002586915A CA 2586915 A CA2586915 A CA 2586915A CA 2586915 A1 CA2586915 A1 CA 2586915A1
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- Prior art keywords
- peptide
- amino acid
- groups
- peptides
- unit
- Prior art date
- Legal status (The legal status 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 status listed.)
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- 230000011132 hemopoiesis Effects 0.000 title description 2
- 108090000765 processed proteins & peptides Proteins 0.000 claims abstract description 388
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- 235000001014 amino acid Nutrition 0.000 claims description 141
- 150000001413 amino acids Chemical class 0.000 claims description 133
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- 108090000394 Erythropoietin Proteins 0.000 claims description 117
- 102000003951 Erythropoietin Human genes 0.000 claims description 117
- OXCMYAYHXIHQOA-UHFFFAOYSA-N potassium;[2-butyl-5-chloro-3-[[4-[2-(1,2,4-triaza-3-azanidacyclopenta-1,4-dien-5-yl)phenyl]phenyl]methyl]imidazol-4-yl]methanol Chemical compound [K+].CCCCC1=NC(Cl)=C(CO)N1CC1=CC=C(C=2C(=CC=CC=2)C2=N[N-]N=N2)C=C1 OXCMYAYHXIHQOA-UHFFFAOYSA-N 0.000 claims description 107
- 230000027455 binding Effects 0.000 claims description 58
- 238000009739 binding Methods 0.000 claims description 57
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- 238000006243 chemical reaction Methods 0.000 claims description 13
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- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 claims description 12
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- 125000003636 chemical group Chemical group 0.000 claims description 7
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- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 claims description 6
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- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 claims description 5
- 239000004475 Arginine Substances 0.000 claims description 5
- 150000008574 D-amino acids Chemical class 0.000 claims description 5
- ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical compound NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 claims description 5
- FFFHZYDWPBMWHY-VKHMYHEASA-N L-homocysteine Chemical compound OC(=O)[C@@H](N)CCS FFFHZYDWPBMWHY-VKHMYHEASA-N 0.000 claims description 5
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 claims description 5
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 claims description 5
- 150000001408 amides Chemical class 0.000 claims description 5
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 claims description 5
- 235000009697 arginine Nutrition 0.000 claims description 5
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- 229910052717 sulfur Inorganic materials 0.000 claims description 5
- RWLSBXBFZHDHHX-VIFPVBQESA-N (2s)-2-(naphthalen-2-ylamino)propanoic acid Chemical compound C1=CC=CC2=CC(N[C@@H](C)C(O)=O)=CC=C21 RWLSBXBFZHDHHX-VIFPVBQESA-N 0.000 claims description 4
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 claims description 4
- HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical compound OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 claims description 4
- AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical compound C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 0.000 claims description 4
- 230000021736 acetylation Effects 0.000 claims description 4
- 238000006640 acetylation reaction Methods 0.000 claims description 4
- 230000009435 amidation Effects 0.000 claims description 4
- 238000007112 amidation reaction Methods 0.000 claims description 4
- 150000002148 esters Chemical class 0.000 claims description 4
- 230000002265 prevention Effects 0.000 claims description 4
- IYKLZBIWFXPUCS-VIFPVBQESA-N (2s)-2-(naphthalen-1-ylamino)propanoic acid Chemical compound C1=CC=C2C(N[C@@H](C)C(O)=O)=CC=CC2=C1 IYKLZBIWFXPUCS-VIFPVBQESA-N 0.000 claims description 3
- KFHRMMHGGBCRIV-BYPYZUCNSA-N (2s)-2-azaniumyl-4-methoxybutanoate Chemical compound COCC[C@H](N)C(O)=O KFHRMMHGGBCRIV-BYPYZUCNSA-N 0.000 claims description 3
- KIUMMUBSPKGMOY-UHFFFAOYSA-N 3,3'-Dithiobis(6-nitrobenzoic acid) Chemical group C1=C([N+]([O-])=O)C(C(=O)O)=CC(SSC=2C=C(C(=CC=2)[N+]([O-])=O)C(O)=O)=C1 KIUMMUBSPKGMOY-UHFFFAOYSA-N 0.000 claims description 3
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 claims description 3
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 claims description 3
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- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- 150000001732 carboxylic acid derivatives Chemical group 0.000 claims description 3
- 125000000151 cysteine group Chemical group N[C@@H](CS)C(=O)* 0.000 claims description 3
- 229910052698 phosphorus Inorganic materials 0.000 claims description 3
- BXRNXXXXHLBUKK-UHFFFAOYSA-N piperazine-2,5-dione Chemical group O=C1CNC(=O)CN1 BXRNXXXXHLBUKK-UHFFFAOYSA-N 0.000 claims description 3
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- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 claims description 2
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 claims description 2
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 claims description 2
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- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 claims description 2
- OILAIQUEIWYQPH-UHFFFAOYSA-N cyclohexane-1,2-dione Chemical group O=C1CCCCC1=O OILAIQUEIWYQPH-UHFFFAOYSA-N 0.000 claims description 2
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- ZRALSGWEFCBTJO-UHFFFAOYSA-N guanidine group Chemical group NC(=N)N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 claims description 2
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/04—Linear peptides containing only normal peptide links
- C07K7/06—Linear peptides containing only normal peptide links having 5 to 11 amino acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/04—Linear peptides containing only normal peptide links
- C07K7/08—Linear peptides containing only normal peptide links having 12 to 20 amino acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/06—Antianaemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Molecular Biology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Immunology (AREA)
- Epidemiology (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (15)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102004054422 | 2004-11-10 | ||
DE102004054422.0 | 2004-11-10 | ||
EP04029536 | 2004-12-14 | ||
EP04029536.2 | 2004-12-14 | ||
US11/041,207 | 2005-01-25 | ||
US11/041,207 US7589063B2 (en) | 2004-12-14 | 2005-01-25 | Molecules which promote hematopoiesis |
EP05002113.8 | 2005-02-02 | ||
EP05002113 | 2005-02-02 | ||
EP05012637.4 | 2005-06-13 | ||
EP05012637 | 2005-06-13 | ||
EP05013594 | 2005-06-23 | ||
EP05013594.6 | 2005-06-23 | ||
EP05020035 | 2005-09-14 | ||
EP05020035.1 | 2005-09-14 | ||
PCT/EP2005/012075 WO2006050959A2 (fr) | 2004-11-10 | 2005-11-10 | Molecules favorisant l'hematopoiese |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2586915A1 true CA2586915A1 (fr) | 2006-05-18 |
Family
ID=36336855
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002586915A Abandoned CA2586915A1 (fr) | 2004-11-10 | 2005-11-10 | Molecules favorisant l'hematopoiese |
Country Status (7)
Country | Link |
---|---|
EP (1) | EP1812461A2 (fr) |
JP (1) | JP2008519589A (fr) |
KR (1) | KR20070092706A (fr) |
AU (1) | AU2005303887A1 (fr) |
CA (1) | CA2586915A1 (fr) |
NO (1) | NO20072856L (fr) |
WO (1) | WO2006050959A2 (fr) |
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US7589063B2 (en) | 2004-12-14 | 2009-09-15 | Aplagen Gmbh | Molecules which promote hematopoiesis |
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JP2008546732A (ja) * | 2005-06-23 | 2008-12-25 | アプラゲン ゲーエムベーハー | 多価化合物 |
JP2009529509A (ja) * | 2006-03-09 | 2009-08-20 | アプラゲン ゲーエムベーハー | 造血を促進する修飾分子 |
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CA3103105A1 (fr) | 2018-07-31 | 2020-02-06 | Amgen Inc. | Ensemble de trajet de fluide pour dispositif d'administration de medicament |
AU2019347710A1 (en) | 2018-09-24 | 2021-02-04 | Amgen Inc. | Interventional dosing systems and methods |
US12042642B2 (en) | 2018-09-28 | 2024-07-23 | Amgen Inc. | Muscle wire escapement activation assembly for a drug delivery device |
US20200101229A1 (en) | 2018-10-02 | 2020-04-02 | Amgen Inc. | Injection systems for drug delivery with internal force transmission |
WO2020072846A1 (fr) | 2018-10-05 | 2020-04-09 | Amgen Inc. | Dispositif d'administration de médicament ayant un indicateur de dose |
JP2022504769A (ja) | 2018-10-15 | 2022-01-13 | アムジエン・インコーポレーテツド | ダンピング機構を有する薬物送達装置 |
TWI846741B (zh) | 2018-10-15 | 2024-07-01 | 美商安進公司 | 用於藥物遞送裝置之平台組裝方法 |
TWI831847B (zh) | 2018-11-01 | 2024-02-11 | 美商安進公司 | 部分針頭縮回之藥物遞送裝置及其操作方法 |
WO2020091956A1 (fr) | 2018-11-01 | 2020-05-07 | Amgen Inc. | Dispositifs d'administration de médicament avec rétraction partielle de l'organe d'administration de médicament |
MA54057A (fr) | 2018-11-01 | 2022-02-09 | Amgen Inc | Dispositifs d'administration de médicament à rétraction partielle d'élément d'administration de médicament |
US20220160972A1 (en) | 2019-04-24 | 2022-05-26 | Amgen Inc. | Syringe sterilization verification assemblies and methods |
WO2021041067A2 (fr) | 2019-08-23 | 2021-03-04 | Amgen Inc. | Dispositif d'administration de médicament doté de composants configurables de mise en prise de protection d'aiguille et méthodes associées |
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WO2024094457A1 (fr) | 2022-11-02 | 2024-05-10 | F. Hoffmann-La Roche Ag | Procédé de production de compositions de glycoprotéines |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
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DE3924746A1 (de) * | 1989-07-26 | 1991-01-31 | Behringwerke Ag | Erythropoietin (epo)-peptide und dagegen gerichtete antikoerper |
JP4050314B2 (ja) * | 1995-06-07 | 2008-02-20 | オーソ ファーマシューティカル コーポレイション | エリトロポエチン受容体に結合する化合物およびペプチド |
BR0312276A (pt) * | 2002-06-28 | 2005-04-26 | Centocor Inc | Mimeticorpos ch1-removidos miméticos de epo de mamìfero, composições, métodos e usos |
-
2005
- 2005-11-10 CA CA002586915A patent/CA2586915A1/fr not_active Abandoned
- 2005-11-10 WO PCT/EP2005/012075 patent/WO2006050959A2/fr active Application Filing
- 2005-11-10 AU AU2005303887A patent/AU2005303887A1/en not_active Abandoned
- 2005-11-10 JP JP2007540582A patent/JP2008519589A/ja active Pending
- 2005-11-10 KR KR1020077012937A patent/KR20070092706A/ko not_active Application Discontinuation
- 2005-11-10 EP EP05819212A patent/EP1812461A2/fr not_active Withdrawn
-
2007
- 2007-06-05 NO NO20072856A patent/NO20072856L/no not_active Application Discontinuation
Also Published As
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EP1812461A2 (fr) | 2007-08-01 |
JP2008519589A (ja) | 2008-06-12 |
NO20072856L (no) | 2007-08-08 |
WO2006050959A3 (fr) | 2006-12-21 |
KR20070092706A (ko) | 2007-09-13 |
WO2006050959A2 (fr) | 2006-05-18 |
AU2005303887A1 (en) | 2006-05-18 |
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