- 885276-59-5
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Fragment-based drug discovery of potent and selective MKK3/6 inhibitors
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Bioorganic and Medicinal Chemistry Letters p. 1086 - 1089
(2016/06/28)
- File number:3
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- 885276-99-3
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Photoinduced Trifluoromethylation of Arenes and Heteroarenes Catalyzed by High-Valent Nickel Complexes
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Angewandte Chemie - International Edition p. 24620 - 24629
(2021/10/08)
- File number:4
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- 885277-08-7
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Desulfonative Suzuki–Miyaura Coupling of Sulfonyl Fluorides
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Angewandte Chemie - International Edition p. 25307 - 25312
(2021/10/25)
- File number:3
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- 885278-53-5
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Synthesis of 3-indazolecarboxylic esters and amides via Pd-catalyzed carbonylation of 3-iodoindazoles
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Synthesis p. 3089 - 3098
(2011/10/13)
- File number:2
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- 885279-16-3
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Design, synthesis, and biological activity evaluation of 2-(benzo[b]thiophen-2-yl)-4-phenyl-4,5-dihydrooxazole derivatives as broad-spectrum antifungal agents
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European Journal of Medicinal Chemistry
(2021/11/22)
- File number:3
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- 885280-30-8
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Indium powder as the reducing agent in the synthesis of 2-amino-1,1′-biphenyls
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Tetrahedron Letters p. 1224 - 1226
(2016/03/01)
- File number:2
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- 885280-92-2
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PHARMACOLOGICALLY ACTIVE GUANIDINE COMPOUNDS
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- File number:2
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- 885281-30-1
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SPIROCYCLE COMPOUNDS AND METHODS OF MAKING AND USING SAME
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- File number:2
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- 88529-79-7
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Regioselective synthesis of ethyl pyrazolecarboxylates from ethyl 3-[(dimethylamino)methylidene]pyruvate and diethyl 3-[(dimethylamino)methylidene]-2-oxosuccinate. Isolation of ethyl 4,5-dihydro-1-heteroaryl-5-hydroxy-1H-pyrazole-5-carboxylates as stable intermediates in the pyrazole ring formation
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Journal of Heterocyclic Chemistry p. 487 - 498
(2007/10/03)
- File number:5
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- 885326-88-5
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POSITIVE ALLOSTERIC MODULATORS OF THE MUSCARINIC ACETYLCHOLINE RECEPTOR M1
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- File number:4
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- 885465-97-4
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The synthesis and SAR study of phenylalanine-derived (Z)-5-arylmethylidene rhodanines as anti-methicillin-resistant Staphylococcus aureus (MRSA) compounds
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Bioorganic and Medicinal Chemistry Letters p. 5523 - 5527
(2013/10/01)
- File number:2
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- 88546-96-7
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COUMARINS OF MERRILLIA CALOXYLON
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Phytochemistry p. 657 - 659
(2007/10/02)
- File number:2
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- 885518-46-7
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4,6-Substituted-1H-Indazoles as potent IDO1/TDO dual inhibitors
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Bioorganic and Medicinal Chemistry p. 1087 - 1098
(2019/02/19)
- File number:6
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- 885519-21-1
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The design and synthesis of indazole and pyrazolopyridine based glucokinase activators for the treatment of Type 2 diabetes mellitus
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Bioorganic and Medicinal Chemistry Letters p. 7100 - 7105
(2013/01/15)
- File number:7
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- 88552-21-0
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REDUCTION OF α-PYRONE DERIVATIVES WITH BORANE-METHYLSULFIDE COMPLEX
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Heterocycles p. 2445 - 2450
(2007/10/02)
- File number:3
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- 885523-43-3
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Synthesis of substituted 4-(1H-indol-6-yl)-1H-indazoles as potential PDK1 inhibitors
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Tetrahedron p. 318 - 326
(2014/01/06)
- File number:2
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- 885524-81-2
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Virtual screening and structure-based discovery of indole acylguanidines as potent β-secretase (BACE1) inhibitors
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Molecules p. 5706 - 5722
(2013/06/27)
- File number:4
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- 88552-69-6
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Synthesis of some novel substituted purine derivatives as potential anticancer, anti-HIV-1 and antimicrobial agents
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Archiv der Pharmazie p. 185 - 194
(2008/02/09)
- File number:3
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- 885588-14-7
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3-ARYLAMINO PYRIDINE DERIVATIVES
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- File number:7
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- 885618-31-5
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Synthesis and cytotoxic activity of novel 2,6-disubstituted-4-mor- pholinothieno[3,2-d]pyrimidines as potent anti-tumor agents
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Chinese Chemical Letters p. 703 - 706
(2012/07/16)
- File number:35
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- 885672-81-1
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Novel and potent small-molecule urotensin II receptor agonists
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Bioorganic and Medicinal Chemistry p. 4657 - 4665
(2009/12/06)
- File number:4
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- 885685-70-1
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PITUITARY ADENYLATE CYCLASE ACTIVATING PEPTIDE (PACAP) RECEPTOR (VPAC2) AGONISTS AND THEIR PHARMACOLOGICAL METHODS OF USE
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- File number:12
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- 88569-32-8
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Quinolone nucleosides: 6,7-dihalo-N-β- and α-glycosyl-1,4-dihydro-4- oxo-quinoline-3-carboxylic acids and derivatives. Synthesis, antimicrobial and antiviral activity
-
Nucleosides and Nucleotides p. 2255 - 2266
(2007/10/03)
- File number:7
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- 88569-66-8
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N-SUBSTITUTED DERIVATIVES OF (ALPHA)-MERCAPTO ALKYLAMINES, THEIR PREPARATION PROCESS AND THE INTERMEDIATES OBTAINED, THEIR USE AS MEDICAMENTS AND THE COMPOSITIONS CONTAINING THEM
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- File number:6
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- 885698-94-2
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METHODS OF TREATING LIVER FIBROSIS USING CALPAIN INHIBITORS
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- File number:4
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- 88571-77-1
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Optimization of diarylthiazole B-Raf inhibitors: Identification of a compound endowed with high oral antitumor activity, mitigated hERG inhibition, and low paradoxical effect
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ChemMedChem p. 276 - 295
(2015/02/05)
- File number:7
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- 88584-09-2
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In the search for new anticancer drugs, VI. Structural modifications of cyclophosphamide
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Zeitschrift fur Naturforschung, Teil B: Anorganische Chemie, Organische Chemie p. 1146 - 1155
(2007/10/02)
- File number:2
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- 885950-48-1
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Tetrahydroquinoline derivatives as potent and selective factor XIa inhibitors
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Journal of Medicinal Chemistry p. 955 - 969
(2014/03/21)
- File number:4
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- 885951-15-5
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2-Aminomethyl piperidines as novel urotensin-II receptor antagonists
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Bioorganic and Medicinal Chemistry Letters p. 2860 - 2864
(2008/12/22)
- File number:3
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- 88625-24-5
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Benzoxaborole Antimalarial Agents. Part 4. Discovery of Potent 6-(2-(Alkoxycarbonyl)pyrazinyl-5-oxy)-1,3-dihydro-1-hydroxy-2,1-benzoxaboroles
-
Journal of Medicinal Chemistry p. 5344 - 5354
(2015/08/03)
- File number:4
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- 886361-38-2
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2-CYCLOPROPYL-THIAZOLE DERIVATIVES
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- File number:5
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- 886361-78-0
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Cross-coupling study of iodo/chloropyridines and 2-chloroquinoline with atom-economic triarylbismuth reagents under Pd-catalysis
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Tetrahedron p. 338 - 349
(2015/03/04)
- File number:2
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- 886364-57-4
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2,2′-Bipyridine-α,α′-trifluoromethyl-diol ligand: Synthesis and application in the asymmetric Et2Zn alkylation of aldehydes
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Chemical Communications p. 11025 - 11028
(2021/11/03)
- File number:3
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- 886364-82-5
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Asymmetric Biocatalytic Synthesis of Fluorinated Pyridines through Transesterification or Transamination: Computational Insights into the Reactivity of Transaminases
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Advanced Synthesis and Catalysis p. 279 - 291
(2017/02/05)
- File number:5
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- 886364-94-9
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NOVEL COMPOUNDS AS ANTAGONISTS OR INVERSE AGONISTS FOR OPIOID RECEPTORS
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- File number:3
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- 886365-06-6
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7-AZAINDOLE INHIBITORS OF CRAC
-
- File number:5
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- 88636-52-6
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Rhodium(III)-catalyzed C4-amidation of indole-oximes with dioxazolones: Via C-H activation
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Organic and Biomolecular Chemistry p. 7922 - 7931
(2020/11/02)
- File number:19
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- 886365-47-5
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Identification of novel 7-amino-5-methyl-1,6-naphthyridin-2(1H)-one derivatives as potent PI3K/mTOR dual inhibitors
-
Bioorganic and Medicinal Chemistry Letters p. 790 - 793
(2014/02/14)
- File number:6
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- 886367-24-4
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Synthesis of Methyl 7,9-Dimethyl-5-oxo-2,3,4,5-tetrahydro-1 H -benzo[ b ]azepine-1-carboxylate and Its Analogues
-
Synthesis p. 2463 - 2470
(2014/11/08)
- File number:2
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- 886370-56-5
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A stereoselective approach to both 3,4-trans-disubstituted pyrrolidin-2-ones and pyrrolidines. A convenient synthesis of (3R,4R)-4-benzyl-3-pyrrolidinecarboxylic acid
-
Heterocycles p. 2485 - 2498
(2007/10/03)
- File number:4
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- 886370-75-8
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Discovery of Pyrazolopyridones as a Novel Class of Gyrase B Inhibitors Using Structure Guided Design
-
ACS Medicinal Chemistry Letters p. 374 - 378
(2016/05/19)
- File number:4
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- 88642-46-0
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SYNTHESIS OF (4E,8E,2S,3R,2'R)-N-2'-HYDROXYHEXADECANOYL-1-O-β-D-GLUCOPYRANOSYL-9-METHYL-4,8-SPHINGADIENINE, THE FRUITING-INDUCING CEREBROSIDE IN A BASIDIOMYCETE SCHIZOPHYLLUM COMMUNE
-
Tetrahedron p. 2379 - 2386
(2007/10/02)
- File number:3
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- 886498-84-6
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Synthesis of aryl ketones by palladium(II)-catalyzed decarboxylative addition of benzoic acids to nitriles
-
Angewandte Chemie - International Edition p. 7733 - 7737
(2011/01/05)
- File number:4
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- 886498-94-8
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SUBSTITUTED NAPHTHYRIDINES AND THEIR USE AS SYK KINASE INHIBITORS
-
- File number:2
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- 886499-50-9
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A step toward direct fullerene synthesis: C60 fullerene precursors with fluorine in key positions
-
Tetrahedron p. 8587 - 8593
(2010/11/18)
- File number:2
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- 886502-22-3
-
NOVEL CURCUMIN DERIVATIVE
-
- File number:2
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- 886505-43-7
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Design of a versatile and improved precatalyst scaffold for palladium-catalyzed cross-coupling: (η3-1-tBu-indenyl)2(μ-Cl)2Pd2
-
ACS Catalysis p. 3680 - 3688
(2015/06/16)
- File number:4
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- 886506-63-4
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Discovery of N-(3-fluorophenyl)-1-[(4-([(35)-3-methyl-1-piperazinyl]methyl) phenyl)acetyl]-4-piperidinamine (GSK962040), the first small molecule motilin receptor agonist clinical candidate
-
Journal of Medicinal Chemistry p. 1180 - 1189
(2010/01/16)
- File number:7
-