JP2005529910A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2005529910A5 JP2005529910A5 JP2004501425A JP2004501425A JP2005529910A5 JP 2005529910 A5 JP2005529910 A5 JP 2005529910A5 JP 2004501425 A JP2004501425 A JP 2004501425A JP 2004501425 A JP2004501425 A JP 2004501425A JP 2005529910 A5 JP2005529910 A5 JP 2005529910A5
- Authority
- JP
- Japan
- Prior art keywords
- hydrogen
- group
- heteroaryl
- aryl
- heteroalkyl
- 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.)
- Pending
Links
- 125000001072 heteroaryl group Chemical group 0.000 claims description 15
- 239000001257 hydrogen Substances 0.000 claims description 15
- 229910052739 hydrogen Inorganic materials 0.000 claims description 15
- 125000003118 aryl group Chemical group 0.000 claims description 14
- 125000004404 heteroalkyl group Chemical group 0.000 claims description 13
- 125000003342 alkenyl group Chemical group 0.000 claims description 9
- 125000000304 alkynyl group Chemical group 0.000 claims description 9
- 125000004103 aminoalkyl group Chemical group 0.000 claims description 9
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 9
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
- 125000002252 acyl group Chemical group 0.000 claims description 8
- 125000005001 aminoaryl group Chemical group 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- 125000003545 alkoxy group Chemical group 0.000 claims description 7
- 125000005251 aryl acyl group Chemical group 0.000 claims description 7
- 125000004104 aryloxy group Chemical group 0.000 claims description 6
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 6
- 125000005253 heteroarylacyl group Chemical group 0.000 claims description 6
- 150000002825 nitriles Chemical class 0.000 claims description 6
- 125000001424 substituent group Chemical group 0.000 claims description 6
- 125000005214 aminoheteroaryl group Chemical group 0.000 claims description 5
- -1 dichloroacetyl Chemical group 0.000 claims description 5
- 125000005553 heteroaryloxy group Chemical group 0.000 claims description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
- 150000002431 hydrogen Chemical class 0.000 claims description 4
- 125000004001 thioalkyl group Chemical group 0.000 claims description 4
- 125000005000 thioaryl group Chemical group 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims 5
- 150000001720 carbohydrates Chemical class 0.000 claims 3
- UTQNKKSJPHTPBS-UHFFFAOYSA-N 2,2,2-trichloroethanone Chemical group ClC(Cl)(Cl)[C]=O UTQNKKSJPHTPBS-UHFFFAOYSA-N 0.000 claims 1
- YQTCQNIPQMJNTI-UHFFFAOYSA-N 2,2-dimethylpropan-1-one Chemical group CC(C)(C)[C]=O YQTCQNIPQMJNTI-UHFFFAOYSA-N 0.000 claims 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims 1
- 125000005115 alkyl carbamoyl group Chemical group 0.000 claims 1
- 125000005116 aryl carbamoyl group Chemical group 0.000 claims 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 claims 1
- 125000002668 chloroacetyl group Chemical group ClCC(=O)* 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 150000003999 cyclitols Chemical group 0.000 claims 1
- 125000006239 protecting group Chemical group 0.000 claims 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims 1
- 238000003786 synthesis reaction Methods 0.000 claims 1
- 125000004044 trifluoroacetyl group Chemical group FC(C(=O)*)(F)F 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 6
- NEAQRZUHTPSBBM-UHFFFAOYSA-N 2-hydroxy-3,3-dimethyl-7-nitro-4h-isoquinolin-1-one Chemical compound C1=C([N+]([O-])=O)C=C2C(=O)N(O)C(C)(C)CC2=C1 NEAQRZUHTPSBBM-UHFFFAOYSA-N 0.000 description 4
- 229910019142 PO4 Inorganic materials 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 4
- 125000000266 alpha-aminoacyl group Chemical group 0.000 description 4
- 150000001409 amidines Chemical class 0.000 description 4
- 125000000753 cycloalkyl group Chemical group 0.000 description 4
- ZRALSGWEFCBTJO-UHFFFAOYSA-O guanidinium Chemical compound NC(N)=[NH2+] ZRALSGWEFCBTJO-UHFFFAOYSA-O 0.000 description 4
- 229910052736 halogen Inorganic materials 0.000 description 4
- 150000002367 halogens Chemical class 0.000 description 4
- 150000002466 imines Chemical class 0.000 description 4
- 235000021317 phosphate Nutrition 0.000 description 4
- 229940124530 sulfonamide Drugs 0.000 description 4
- 150000003456 sulfonamides Chemical class 0.000 description 4
- 239000002253 acid Substances 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 125000002619 bicyclic group Chemical group 0.000 description 2
- 150000001733 carboxylic acid esters Chemical class 0.000 description 2
- DMSZORWOGDLWGN-UHFFFAOYSA-N ctk1a3526 Chemical compound NP(N)(N)=O DMSZORWOGDLWGN-UHFFFAOYSA-N 0.000 description 2
- 229940042795 hydrazides for tuberculosis treatment Drugs 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 2
- 125000002950 monocyclic group Chemical group 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 150000008039 phosphoramides Chemical class 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AUPS2138A AUPS213802A0 (en) | 2002-05-03 | 2002-05-03 | Disaccharides for drug discovery |
| AUPS2138 | 2002-05-03 | ||
| PCT/AU2003/000494 WO2003093286A1 (en) | 2002-05-03 | 2003-04-24 | Disaccharides for drug discovery |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2005529910A JP2005529910A (ja) | 2005-10-06 |
| JP2005529910A5 true JP2005529910A5 (https=) | 2006-03-23 |
Family
ID=3835711
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004501425A Pending JP2005529910A (ja) | 2002-05-03 | 2003-04-24 | 薬物発見のための二糖 |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | US7875707B2 (https=) |
| EP (1) | EP1501844A4 (https=) |
| JP (1) | JP2005529910A (https=) |
| AU (1) | AUPS213802A0 (https=) |
| CA (1) | CA2483622C (https=) |
| WO (1) | WO2003093286A1 (https=) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2002952121A0 (en) | 2002-10-17 | 2002-10-31 | Alchemia Limited | Novel carbohydrate based anti-bacterials |
| US20080119373A1 (en) * | 2003-10-02 | 2008-05-22 | New York University | Receptor Specific Binder Discovery Using Intramolecular Acyl Migration Induced Dynamic Carbohydrate Library |
| WO2009155108A1 (en) * | 2008-05-30 | 2009-12-23 | Momenta Pharmaceuticals, Inc. | Saccharide structures and methods of making and using such structures |
| CN102395594A (zh) * | 2009-04-15 | 2012-03-28 | 巴斯夫欧洲公司 | 单烯键式不饱和葡基胺的制备方法 |
| CN105017193B (zh) * | 2014-04-22 | 2018-11-09 | 江苏先声药业有限公司 | 一种扎那米韦杂质的制备方法 |
| KR20200104889A (ko) | 2017-12-29 | 2020-09-04 | 글리코미메틱스, 인크. | E-셀렉틴 및 갈렉틴-3의 이종이기능성 억제제 |
| US11845771B2 (en) | 2018-12-27 | 2023-12-19 | Glycomimetics, Inc. | Heterobifunctional inhibitors of E-selectin and galectin-3 |
| CA3122321A1 (en) | 2018-12-27 | 2020-07-02 | Glycomimetics, Inc. | Galectin-3 inhibiting c-glycosides |
| CN112010995A (zh) * | 2019-05-30 | 2020-12-01 | 株式会社大赛璐 | 壳聚糖衍生物及光学异构体用分离剂 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5326867A (en) * | 1992-07-16 | 1994-07-05 | Bristol-Myers Squibb Company | Pradimic acids, amides, and pradimicin derivatives |
| AU7193494A (en) * | 1993-07-21 | 1995-02-20 | Oxford Glycosystems Ltd | Saccharides, their synthesis and use |
| WO1997034623A1 (en) * | 1996-03-21 | 1997-09-25 | Transcell Technologies, Inc. | Solid phase lipoglycopeptide library, compositions and methods |
| AU5821998A (en) * | 1997-01-13 | 1998-08-03 | Scripps Research Institute, The | Nucleic acid binders having an hydroxyamine motif |
| AUPO536797A0 (en) * | 1997-02-28 | 1997-03-20 | Alchemia Pty Ltd | Protected aminosugars |
| AU7700098A (en) | 1997-05-29 | 1998-12-30 | Incara Pharmaceutical Corp. | Carbohydrate scaffold compounds and libraries |
| US6114309A (en) | 1997-11-21 | 2000-09-05 | Incara Research Laboratories | Combinatorial library of moenomycin analogs and methods of producing same |
| WO2000064915A1 (en) | 1999-04-27 | 2000-11-02 | Advanced Medicine, Inc. | Novel disaccharide antibacterial agents |
| EP1257558A1 (en) * | 2000-01-13 | 2002-11-20 | Alchemia Pty Ltd | Methods for synthesis of alpha-d-gal (1- 3) gal-containing oligosaccharides |
| AUPR084400A0 (en) * | 2000-10-18 | 2000-11-09 | Alchemia Pty Ltd | Immunoadjuvant systems |
| AU2002952121A0 (en) * | 2002-10-17 | 2002-10-31 | Alchemia Limited | Novel carbohydrate based anti-bacterials |
-
2002
- 2002-05-03 AU AUPS2138A patent/AUPS213802A0/en not_active Abandoned
-
2003
- 2003-04-24 CA CA2483622A patent/CA2483622C/en not_active Expired - Lifetime
- 2003-04-24 JP JP2004501425A patent/JP2005529910A/ja active Pending
- 2003-04-24 EP EP20030714557 patent/EP1501844A4/en not_active Withdrawn
- 2003-04-24 WO PCT/AU2003/000494 patent/WO2003093286A1/en not_active Ceased
- 2003-04-24 US US10/513,286 patent/US7875707B2/en not_active Expired - Fee Related
-
2010
- 2010-12-17 US US12/926,913 patent/US20110201794A1/en not_active Abandoned
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2005529910A5 (https=) | ||
| AU1099302A (en) | Medicinal compositions for concominant use as anticancer atent | |
| EP1844766A3 (en) | Inhibitors against the production and release of inflammatory cytokines | |
| ATE311358T1 (de) | Immunoregulierende verbindungen, deren derivate und ihre verwendung | |
| EP1541558A4 (en) | HETEROCYCLIC COMPOUND HAVING INHIBITORY ACTIVITY OF HIV INTEGRASE | |
| SK9662000A3 (en) | Sulphonamide derivatives as prodrugs of aspartyl protease inhibitors | |
| IE831564L (en) | N-substituted imidazoles | |
| JP2005523922A5 (https=) | ||
| MX9804457A (es) | Inhibidores de las metaloproteinasas, composiciones farmaceuticas que los contienen y sus usos farmaceuticos y metodos y compuestos intermedios utiles para su preparacion. | |
| HUP0401982A2 (hu) | Indolizinszármazékok, eljárás előállításukra és a vegyületeket tartalmazó gyógyászati készítmények | |
| NO20060220L (no) | Forbindelser med inhiberene aktivitet mot natriumavhengige transportorer | |
| PL179997B1 (pl) | Nowe pochodne kwasu hydroksamowego i kwasu karboksylowego PL PL PL PL PL PL | |
| ATE33838T1 (de) | Thiazolidinderivate, ihre herstellung und diese enthaltende zusammensetzungen. | |
| WO2005092858A3 (en) | Alpha aryl or heteroaryl methyl beta piperidino propanamide compounds as orl1-receptor antagonist | |
| WO2005058884A3 (en) | Cyclopropane compounds and pharmaceutical use thereof | |
| JP2009500423A5 (https=) | ||
| JP2007500734A5 (https=) | ||
| JP2004131511A5 (https=) | ||
| JP2005526813A5 (https=) | ||
| CA2593381A1 (en) | Processes for producing 7-isoindolinequinolonecarboxylic acid derivatives and intermediates therefor, salts of 7-isoindolinequinolonecarboxylic acids, hydrates thereof, and compositions containing the same as active ingredient | |
| JP2007517900A5 (https=) | ||
| RU2002114041A (ru) | N-гуанидиноалкиламиды, их получение, их применение и содержащие их фармацевтические препараты | |
| JP2005501825A5 (https=) | ||
| DE60002558D1 (de) | Derivate der Phosphonsäure zur Inhibierung von Carboxypeptidase B | |
| JP2009505974A5 (https=) |