CO5160349A1 - Proteinas y amino acidos de sitio especifico, marcados isotopicamnete y precursores bioquimicos resultantes dos para preparar dichas proteinas, amino acidos y precurso- res bioquimicos resultantes - Google Patents

Proteinas y amino acidos de sitio especifico, marcados isotopicamnete y precursores bioquimicos resultantes dos para preparar dichas proteinas, amino acidos y precurso- res bioquimicos resultantes

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Publication number
CO5160349A1
CO5160349A1 CO00025250A CO00025250A CO5160349A1 CO 5160349 A1 CO5160349 A1 CO 5160349A1 CO 00025250 A CO00025250 A CO 00025250A CO 00025250 A CO00025250 A CO 00025250A CO 5160349 A1 CO5160349 A1 CO 5160349A1
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CO
Colombia
Prior art keywords
amino acids
results
biochemical
precurse
isotopicamnete
Prior art date
Application number
CO00025250A
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English (en)
Inventor
Stephen W Fesik
David J Augeri
Original Assignee
Abbott Lab
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.)
Filing date
Publication date
Application filed by Abbott Lab filed Critical Abbott Lab
Publication of CO5160349A1 publication Critical patent/CO5160349A1/es

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    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14Hydrolases (3)
    • C12N9/48Hydrolases (3) acting on peptide bonds (3.4)
    • C12N9/50Proteinases, e.g. Endopeptidases (3.4.21-3.4.25)
    • C12N9/64Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from animal tissue
    • C12N9/6421Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from animal tissue from mammals
    • C12N9/6489Metalloendopeptidases (3.4.24)
    • C12N9/6491Matrix metalloproteases [MMP's], e.g. interstitial collagenase (3.4.24.7); Stromelysins (3.4.24.17; 3.2.1.22); Matrilysin (3.4.24.23)
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B59/00Introduction of isotopes of elements into organic compounds ; Labelled organic compounds per se
    • C07B59/001Acyclic or carbocyclic compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/02Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C229/04Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
    • C07C229/06Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton
    • C07C229/08Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton the nitrogen atom of the amino group being further bound to hydrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K1/00General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/107General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides
    • C07K1/1072General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides by covalent attachment of residues or functional groups
    • C07K1/1075General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides by covalent attachment of residues or functional groups by covalent attachment of amino acids or peptide residues
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K1/00General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/107General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides
    • C07K1/1072General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides by covalent attachment of residues or functional groups
    • C07K1/1077General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides by covalent attachment of residues or functional groups by covalent attachment of residues other than amino acids or peptide residues, e.g. sugars, polyols, fatty acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K1/00General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/13Labelling of peptides
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P13/00Preparation of nitrogen-containing organic compounds
    • C12P13/04Alpha- or beta- amino acids
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P13/00Preparation of nitrogen-containing organic compounds
    • C12P13/04Alpha- or beta- amino acids
    • C12P13/06Alanine; Leucine; Isoleucine; Serine; Homoserine
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P13/00Preparation of nitrogen-containing organic compounds
    • C12P13/04Alpha- or beta- amino acids
    • C12P13/08Lysine; Diaminopimelic acid; Threonine; Valine
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P21/00Preparation of peptides or proteins
    • C12P21/02Preparation of peptides or proteins having a known sequence of two or more amino acids, e.g. glutathione
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/05Isotopically modified compounds, e.g. labelled
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/07Optical isomers

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Genetics & Genomics (AREA)
  • General Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Microbiology (AREA)
  • Biotechnology (AREA)
  • General Engineering & Computer Science (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Medicinal Chemistry (AREA)
  • Biophysics (AREA)
  • Analytical Chemistry (AREA)
  • Biomedical Technology (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Peptides Or Proteins (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Investigating Or Analysing Biological Materials (AREA)

Abstract

Un compuesto de la fórmula I:<EMI FILE="00025250_1" ID="1" IMF=JPEG >o la sal resultante, donde:R1 es oxigeno o NH2;R2 es seleccionada entre un grupo consistente en:<EMI FILE="00025250_2" ID="2" IMF=JPEG >donde R3 es hidrógeno o nCH3 ;el enlace de línea punteada representa un segundo enlace de valencia;m es cero o uno;y n, en cada ocurrencia es 13 ó 14;con las condiciones de que:i) cuando R1 es NH2, el segundo enlace de valencia representado por el enlace de línea punteada a R1 está ausente y el hidrógeno unido al enlace de línea punteada está presente;ii) cuando R1 es oxigeno, el segundo enlace de valencia, representado por el enlace de línea punteada a R1 está presente y el átomo de hidrógeno unido al enlace de línea punteada está ausente.iii) cuando R1 es oxigeno, R2 es B y m es cero; yiv) cuando R1 es NH2, R3 es hidrógeno o nCH3.
CO00025250A 1999-04-09 2000-04-06 Proteinas y amino acidos de sitio especifico, marcados isotopicamnete y precursores bioquimicos resultantes dos para preparar dichas proteinas, amino acidos y precurso- res bioquimicos resultantes CO5160349A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US28951799A 1999-04-09 1999-04-09

Publications (1)

Publication Number Publication Date
CO5160349A1 true CO5160349A1 (es) 2002-05-30

Family

ID=23111884

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Application Number Title Priority Date Filing Date
CO00025250A CO5160349A1 (es) 1999-04-09 2000-04-06 Proteinas y amino acidos de sitio especifico, marcados isotopicamnete y precursores bioquimicos resultantes dos para preparar dichas proteinas, amino acidos y precurso- res bioquimicos resultantes

Country Status (29)

Country Link
EP (1) EP1169282B1 (es)
JP (1) JP2002541228A (es)
KR (1) KR100708225B1 (es)
CN (1) CN1244521C (es)
AR (1) AR029747A1 (es)
AT (1) ATE296789T1 (es)
AU (1) AU777749B2 (es)
BG (1) BG106043A (es)
BR (1) BR0009664A (es)
CA (1) CA2368652C (es)
CO (1) CO5160349A1 (es)
CZ (1) CZ20013616A3 (es)
DE (1) DE60020547T2 (es)
DK (1) DK1169282T3 (es)
ES (1) ES2243251T3 (es)
HK (1) HK1044753B (es)
HU (1) HUP0200809A3 (es)
IL (2) IL145536A0 (es)
MX (1) MXPA01010183A (es)
NO (1) NO20014691L (es)
NZ (1) NZ514518A (es)
PL (1) PL350889A1 (es)
PT (1) PT1169282E (es)
SI (1) SI1169282T1 (es)
SK (1) SK14322001A3 (es)
TR (1) TR200102842T2 (es)
TW (1) TWI283659B (es)
WO (1) WO2000061525A1 (es)
ZA (1) ZA200107919B (es)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9708228B2 (en) 2010-01-06 2017-07-18 Commissariat A L'energie Atomique Et Aux Energies Alternatives Process for the specific isotopic labeling of methyl groups of Val, Leu and Ile
US10053396B2 (en) 2010-01-06 2018-08-21 Commissariat A L'energie Atomique Et Aux Energies Alternatives Process for the specific isotopic labeling of methyl groups of Val, Leu and Ile
KR101219684B1 (ko) * 2012-04-27 2013-01-10 건국대학교 산학협력단 정량적 질량분석기법을 이용한 만성골수성 백혈병의 발병 진단방법과 약제 내성 진단방법
EP2695873B1 (en) * 2012-08-08 2016-10-26 Commissariat A L'energie Atomique Et Aux Energies Alternatives Labeled chiral alpha-hydroxy ketoacid derivatives, a process for preparing said derivatives and their use
CN107793209A (zh) * 2016-08-30 2018-03-13 泰生科技香港有限公司 稳定性同位素标记植物的专用培养基、其制备方法及用途

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5698401A (en) * 1995-11-14 1997-12-16 Abbott Laboratories Use of nuclear magnetic resonance to identify ligands to target biomolecules

Also Published As

Publication number Publication date
NO20014691L (no) 2001-12-10
CN1353678A (zh) 2002-06-12
PT1169282E (pt) 2005-10-31
CN1244521C (zh) 2006-03-08
AR029747A1 (es) 2003-07-16
EP1169282A1 (en) 2002-01-09
DE60020547D1 (de) 2005-07-07
BR0009664A (pt) 2002-01-08
TWI283659B (en) 2007-07-11
KR20010108475A (ko) 2001-12-07
CA2368652C (en) 2009-11-10
IL145536A0 (en) 2002-06-30
TR200102842T2 (tr) 2002-03-21
IL145536A (en) 2010-05-31
SK14322001A3 (sk) 2002-02-05
ZA200107919B (en) 2003-03-26
HK1044753B (zh) 2006-03-24
KR100708225B1 (ko) 2007-04-17
SI1169282T1 (en) 2005-10-31
WO2000061525A1 (en) 2000-10-19
CZ20013616A3 (cs) 2002-04-17
HUP0200809A2 (en) 2002-06-29
CA2368652A1 (en) 2000-10-19
HK1044753A1 (en) 2002-11-01
AU777749B2 (en) 2004-10-28
PL350889A1 (en) 2003-02-10
HUP0200809A3 (en) 2004-11-29
DE60020547T2 (de) 2006-05-04
NO20014691D0 (no) 2001-09-27
NZ514518A (en) 2003-10-31
EP1169282B1 (en) 2005-06-01
BG106043A (en) 2002-05-31
MXPA01010183A (es) 2003-07-21
ES2243251T3 (es) 2005-12-01
AU4212100A (en) 2000-11-14
DK1169282T3 (da) 2005-10-03
JP2002541228A (ja) 2002-12-03
ATE296789T1 (de) 2005-06-15

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