CO4960642A1 - PROTEIN INHIBITORS FARNESIL TRANSFERASAS PROTEINOFARNESIL TRANSFERASE INHIBITORS AND COMPOSITION - Google Patents
PROTEIN INHIBITORS FARNESIL TRANSFERASAS PROTEINOFARNESIL TRANSFERASE INHIBITORS AND COMPOSITIONInfo
- Publication number
- CO4960642A1 CO4960642A1 CO97028769A CO97028769A CO4960642A1 CO 4960642 A1 CO4960642 A1 CO 4960642A1 CO 97028769 A CO97028769 A CO 97028769A CO 97028769 A CO97028769 A CO 97028769A CO 4960642 A1 CO4960642 A1 CO 4960642A1
- Authority
- CO
- Colombia
- Prior art keywords
- inhibitors
- transferasas
- proteinofarnesil
- farnesil
- composition
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06191—Dipeptides containing heteroatoms different from O, S, or N
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/04—Drugs for genital or sexual disorders; Contraceptives for inducing labour or abortion; Uterotonics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06139—Dipeptides with the first amino acid being heterocyclic
- C07K5/06147—Dipeptides with the first amino acid being heterocyclic and His-amino acid; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Abstract
La presente invención se refiere a compuestos de ácidocarbámico y propionamida que son inhibidores de enzima proteinofarnesiltransferasa, que tienen la Fórmuladonde:R21 es hidrógeno o alquilo C1 -C6 ;RQ esn es 0 ó 1;A es -CORa , -CO2 Ra´ , -CONHRa´ , -CSRa , -C(S)ORa´ , -C(S)NHRa´, -SO2 Ra , -CONRa Ra ",Ra , Ra´ y Ra" son independientemente alquilo C1 -C6 , -(CH2 )m -cicloalquilo, -(CH2 )m -arilo o -(CH2 )m -heteroarilo;cada m es independientemente de 0 a 3;R1 , R2 y R4 son independientemente hidrógeno o alquilo C1 -C6 ;R3 es , -(CH2 )m -heteroarilo,-(CH2 )m -(CH2 )m -naftilo, -(CH2 )m -(heteroarilo sustituido con Rb ), o alquilo C1 -C6 ;t es 2 a 6; ...The present invention relates to carbamic acid and propionamide compounds which are proteinophanesyltransferase enzyme inhibitors, having the Formula where: R21 is hydrogen or C1-C6 alkyl; RQ is 0 or 1; A is -CORa, -CO2 Ra ', - CONHRa´, -CSRa, -C (S) ORa´, -C (S) NHRa´, -SO2 Ra, -CONRa Ra ", Ra, Ra´ and Ra" are independently C1-C6 alkyl, - (CH2) m -cycloalkyl, - (CH2) m -aryl or - (CH2) m -heteroaryl; each m is independently 0 to 3; R1, R2 and R4 are independently hydrogen or C1-C6 alkyl; R3 is, - (CH2) m -heteroaryl, - (CH2) m - (CH2) m -naphthyl, - (CH2) m - (heteroaryl substituted with Rb), or C1-C6 alkyl; t is 2 to 6; ...
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US1611096P | 1996-05-22 | 1996-05-22 | |
US3366296P | 1996-12-17 | 1996-12-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
CO4960642A1 true CO4960642A1 (en) | 2000-09-25 |
Family
ID=26688183
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CO97028769A CO4960642A1 (en) | 1996-05-22 | 1997-05-26 | PROTEIN INHIBITORS FARNESIL TRANSFERASAS PROTEINOFARNESIL TRANSFERASE INHIBITORS AND COMPOSITION |
Country Status (18)
Country | Link |
---|---|
EP (1) | EP0938494A1 (en) |
JP (1) | JP2000511527A (en) |
CN (1) | CN1219174A (en) |
AU (1) | AU728477B2 (en) |
BG (1) | BG102936A (en) |
BR (1) | BR9709354A (en) |
CA (1) | CA2253934A1 (en) |
CO (1) | CO4960642A1 (en) |
CZ (1) | CZ376498A3 (en) |
EA (1) | EA199801031A1 (en) |
EE (1) | EE9800408A (en) |
GE (1) | GEP20012500B (en) |
IL (1) | IL126833A0 (en) |
NO (1) | NO985405L (en) |
NZ (1) | NZ332712A (en) |
PL (1) | PL330120A1 (en) |
SK (1) | SK161098A3 (en) |
WO (1) | WO1997044350A1 (en) |
Families Citing this family (65)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6090948A (en) * | 1996-01-30 | 2000-07-18 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
US6028201A (en) * | 1996-01-30 | 2000-02-22 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
EP0944387A1 (en) * | 1996-01-30 | 1999-09-29 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
US5981562A (en) * | 1996-01-30 | 1999-11-09 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
US5968965A (en) * | 1996-01-30 | 1999-10-19 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
US6300501B1 (en) | 1996-05-22 | 2001-10-09 | Warner-Lambert Company | Histidine-(N-benzyl glycinamide) inhibitors of protein farnesyl transferase |
WO1998046625A1 (en) * | 1997-04-11 | 1998-10-22 | Warner-Lambert Company | Dipeptide inhibitors of protein farnesyltransferase |
US6737410B1 (en) | 1997-04-11 | 2004-05-18 | Warner-Lambert Company | Inhibitors of protein farnesyl transferase |
US20030069231A1 (en) | 1999-10-12 | 2003-04-10 | Klaus Rudolf | Modified aminoacids, pharmaceuticals containing these compounds and method for their production |
BR9909961A (en) * | 1998-04-27 | 2000-12-26 | Warner Lambert Co | Alkyl and alkenyl functionalized derivatives of glycinamides as farnesyl transferase inhibitors |
US6316436B1 (en) | 1998-12-08 | 2001-11-13 | Merck & Co., Inc. | Inhibitors of prenyl-protein transferase |
AU2477400A (en) | 1998-12-08 | 2000-06-26 | Merck & Co., Inc. | Inhibitors of prenyl-protein transferase |
WO2001051494A1 (en) | 2000-01-12 | 2001-07-19 | Merck & Co., Inc. | Inhibitors of prenyl-protein transferase |
JP2002188646A (en) * | 2000-12-20 | 2002-07-05 | Nsk Ltd | Rolling bearing and bearing device |
US7595312B2 (en) | 2002-10-25 | 2009-09-29 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Selected CGRP antagonists, processes for preparing them and their use as pharmaceutical compositions |
WO2005049589A2 (en) * | 2003-10-14 | 2005-06-02 | Cadila Healthcare Limited | Heterocyclic compounds for the treatment of hyperlipidemia, diabetes, obesity and similar diseases |
DE102004015723A1 (en) | 2004-03-29 | 2005-10-20 | Boehringer Ingelheim Pharma | Selected CGRP antagonists, process for their preparation and their use as pharmaceuticals |
WO2006123182A2 (en) | 2005-05-17 | 2006-11-23 | Merck Sharp & Dohme Limited | Cyclohexyl sulphones for treatment of cancer |
GB0603041D0 (en) | 2006-02-15 | 2006-03-29 | Angeletti P Ist Richerche Bio | Therapeutic compounds |
WO2008039327A2 (en) | 2006-09-22 | 2008-04-03 | Merck & Co., Inc. | Method of treatment using fatty acid synthesis inhibitors |
US20110218176A1 (en) | 2006-11-01 | 2011-09-08 | Barbara Brooke Jennings-Spring | Compounds, methods, and treatments for abnormal signaling pathways for prenatal and postnatal development |
AU2008204380B2 (en) | 2007-01-10 | 2013-08-15 | Msd Italia S.R.L. | Amide substituted indazoles as poly(ADP-ribose)polymerase (PARP) inhibitors |
CN101679266B (en) | 2007-03-01 | 2015-05-06 | 诺华股份有限公司 | PIM kinase inhibitors and methods of their use |
BRPI0812159A2 (en) | 2007-05-21 | 2017-05-02 | Novartis Ag | csf-1r inhibitors, compositions and methods of use |
US8389553B2 (en) | 2007-06-27 | 2013-03-05 | Merck Sharp & Dohme Corp. | 4-carboxybenzylamino derivatives as histone deacetylase inhibitors |
EP2413932A4 (en) | 2009-04-01 | 2012-09-19 | Merck Sharp & Dohme | Inhibitors of akt activity |
JP6073677B2 (en) | 2009-06-12 | 2017-02-01 | デイナ ファーバー キャンサー インスティチュート,インコーポレイテッド | Fused heterocyclic compounds and their use |
BR112012008849A2 (en) | 2009-10-14 | 2015-09-22 | Schering Corp | compound, pharmaceutical composition, and use of a compound |
CA2784807C (en) | 2009-12-29 | 2021-12-14 | Dana-Farber Cancer Institute, Inc. | Type ii raf kinase inhibitors |
BR112012023021A2 (en) | 2010-03-16 | 2016-05-31 | Dana Farber Cancer Inst Inc | indazole compounds and their uses |
EP2584903B1 (en) | 2010-06-24 | 2018-10-24 | Merck Sharp & Dohme Corp. | Novel heterocyclic compounds as erk inhibitors |
JP6043285B2 (en) | 2010-08-02 | 2016-12-14 | サーナ・セラピューティクス・インコーポレイテッドSirna Therapeutics,Inc. | RNA interference-mediated inhibition of catenin (cadherin-binding protein) β1 (CTNNB1) gene expression using small interfering nucleic acids (siNA) |
HUE044815T2 (en) | 2010-08-17 | 2019-11-28 | Sirna Therapeutics Inc | RNA INTERFERENCE MEDIATED INHIBITION OF HEPATITIS B VIRUS (HBV) GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACID (siNA) |
EP2608669B1 (en) | 2010-08-23 | 2016-06-22 | Merck Sharp & Dohme Corp. | NOVEL PYRAZOLO[1,5-a]PYRIMIDINE DERIVATIVES AS mTOR INHIBITORS |
EP2613782B1 (en) | 2010-09-01 | 2016-11-02 | Merck Sharp & Dohme Corp. | Indazole derivatives useful as erk inhibitors |
WO2012036997A1 (en) | 2010-09-16 | 2012-03-22 | Schering Corporation | Fused pyrazole derivatives as novel erk inhibitors |
US9260471B2 (en) | 2010-10-29 | 2016-02-16 | Sirna Therapeutics, Inc. | RNA interference mediated inhibition of gene expression using short interfering nucleic acids (siNA) |
WO2012087772A1 (en) | 2010-12-21 | 2012-06-28 | Schering Corporation | Indazole derivatives useful as erk inhibitors |
US20140045847A1 (en) | 2011-04-21 | 2014-02-13 | Piramal Enterprises Limited | Crystalline form of a salt of a morpholino sulfonyl indole derivative and a process for its preparation |
WO2013063214A1 (en) | 2011-10-27 | 2013-05-02 | Merck Sharp & Dohme Corp. | Novel compounds that are erk inhibitors |
WO2013074986A1 (en) | 2011-11-17 | 2013-05-23 | Dana-Farber Cancer Institute, Inc. | Inhibitors of c-jun-n-terminal kinase (jnk) |
EP3919620A1 (en) | 2012-05-02 | 2021-12-08 | Sirna Therapeutics, Inc. | Short interfering nucleic acid (sina) compositions |
US9233979B2 (en) | 2012-09-28 | 2016-01-12 | Merck Sharp & Dohme Corp. | Compounds that are ERK inhibitors |
US10112927B2 (en) | 2012-10-18 | 2018-10-30 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinase 7 (CDK7) |
US9758522B2 (en) | 2012-10-19 | 2017-09-12 | Dana-Farber Cancer Institute, Inc. | Hydrophobically tagged small molecules as inducers of protein degradation |
WO2014063054A1 (en) | 2012-10-19 | 2014-04-24 | Dana-Farber Cancer Institute, Inc. | Bone marrow on x chromosome kinase (bmx) inhibitors and uses thereof |
BR112015012295A8 (en) | 2012-11-28 | 2023-03-14 | Merck Sharp & Dohme | USE OF A WEE1 INHIBITOR, E, KIT TO IDENTIFY A PATIENT WITH CANCER |
BR112015013611A2 (en) | 2012-12-20 | 2017-11-14 | Merck Sharp & Dohme | compound and pharmaceutical composition |
EP2951180B1 (en) | 2013-01-30 | 2018-05-02 | Merck Sharp & Dohme Corp. | 2,6,7,8 substituted purines as hdm2 inhibitors |
EP3041938A1 (en) | 2013-09-03 | 2016-07-13 | Moderna Therapeutics, Inc. | Circular polynucleotides |
WO2015058126A1 (en) | 2013-10-18 | 2015-04-23 | Syros Pharmaceuticals, Inc. | Heteroaromatic compounds useful for the treatment of prolferative diseases |
JP6491202B2 (en) | 2013-10-18 | 2019-03-27 | デイナ ファーバー キャンサー インスティチュート,インコーポレイテッド | Polycyclic inhibitors of cyclin dependent kinase 7 (CDK 7) |
US9862688B2 (en) | 2014-04-23 | 2018-01-09 | Dana-Farber Cancer Institute, Inc. | Hydrophobically tagged janus kinase inhibitors and uses thereof |
WO2015164614A1 (en) | 2014-04-23 | 2015-10-29 | Dana-Farber Cancer Institute, Inc. | Janus kinase inhibitors and uses thereof |
JO3589B1 (en) | 2014-08-06 | 2020-07-05 | Novartis Ag | Protein kinase c inhibitors and methods of their use |
AU2015371251B2 (en) | 2014-12-23 | 2020-06-11 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinase 7 (CDK7) |
WO2016160617A2 (en) | 2015-03-27 | 2016-10-06 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinases |
EP3307728A4 (en) | 2015-06-12 | 2019-07-17 | Dana Farber Cancer Institute, Inc. | Combination therapy of transcription inhibitors and kinase inhibitors |
EP3347018B1 (en) | 2015-09-09 | 2021-09-01 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinases |
JOP20190055A1 (en) | 2016-09-26 | 2019-03-24 | Merck Sharp & Dohme | Anti-cd27 antibodies |
JP7160833B2 (en) | 2017-04-13 | 2022-10-25 | サイロパ ビー.ブイ. | anti-SIRP alpha antibody |
WO2019094311A1 (en) | 2017-11-08 | 2019-05-16 | Merck Sharp & Dohme Corp. | Prmt5 inhibitors |
WO2019148412A1 (en) | 2018-02-01 | 2019-08-08 | Merck Sharp & Dohme Corp. | Anti-pd-1/lag3 bispecific antibodies |
EP3833667B1 (en) | 2018-08-07 | 2024-03-13 | Merck Sharp & Dohme LLC | Prmt5 inhibitors |
WO2020033282A1 (en) | 2018-08-07 | 2020-02-13 | Merck Sharp & Dohme Corp. | Prmt5 inhibitors |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5352705A (en) * | 1992-06-26 | 1994-10-04 | Merck & Co., Inc. | Inhibitors of farnesyl protein transferase |
EP0725650A4 (en) * | 1993-09-30 | 1999-02-03 | Merck & Co Inc | Inhibitors of farnesyl-protein transferase |
KR100362338B1 (en) * | 1993-11-05 | 2003-04-08 | 워너-램버트 캄파니 | Protein: Substituted Di- and Tripeptide Inhibitors of Farnesyl Transferase |
US5571792A (en) * | 1994-06-30 | 1996-11-05 | Warner-Lambert Company | Histidine and homohistidine derivatives as inhibitors of protein farnesyltransferase |
-
1997
- 1997-04-29 PL PL97330120A patent/PL330120A1/en unknown
- 1997-04-29 GE GEAP19974612A patent/GEP20012500B/en unknown
- 1997-04-29 BR BR9709354A patent/BR9709354A/en not_active Application Discontinuation
- 1997-04-29 EE EE9800408A patent/EE9800408A/en unknown
- 1997-04-29 EP EP97922365A patent/EP0938494A1/en not_active Withdrawn
- 1997-04-29 AU AU28058/97A patent/AU728477B2/en not_active Ceased
- 1997-04-29 WO PCT/US1997/006591 patent/WO1997044350A1/en not_active Application Discontinuation
- 1997-04-29 CZ CZ983764A patent/CZ376498A3/en unknown
- 1997-04-29 NZ NZ332712A patent/NZ332712A/en unknown
- 1997-04-29 IL IL12683397A patent/IL126833A0/en unknown
- 1997-04-29 CN CN97194835A patent/CN1219174A/en active Pending
- 1997-04-29 SK SK1610-98A patent/SK161098A3/en unknown
- 1997-04-29 EA EA199801031A patent/EA199801031A1/en unknown
- 1997-04-29 JP JP09542369A patent/JP2000511527A/en not_active Abandoned
- 1997-04-29 CA CA002253934A patent/CA2253934A1/en not_active Abandoned
- 1997-05-26 CO CO97028769A patent/CO4960642A1/en unknown
-
1998
- 1998-11-19 BG BG102936A patent/BG102936A/en unknown
- 1998-11-20 NO NO985405A patent/NO985405L/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
SK161098A3 (en) | 2000-06-12 |
AU728477B2 (en) | 2001-01-11 |
CN1219174A (en) | 1999-06-09 |
CZ376498A3 (en) | 1999-02-17 |
GEP20012500B (en) | 2001-07-25 |
PL330120A1 (en) | 1999-04-26 |
EP0938494A1 (en) | 1999-09-01 |
NO985405L (en) | 1999-01-19 |
CA2253934A1 (en) | 1997-11-27 |
JP2000511527A (en) | 2000-09-05 |
EA199801031A1 (en) | 1999-06-24 |
NO985405D0 (en) | 1998-11-20 |
EE9800408A (en) | 1999-06-15 |
BR9709354A (en) | 1999-08-10 |
IL126833A0 (en) | 1999-08-17 |
WO1997044350A1 (en) | 1997-11-27 |
AU2805897A (en) | 1997-12-09 |
NZ332712A (en) | 2000-07-28 |
BG102936A (en) | 1999-09-30 |
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