- 870653-45-5
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Design of PAP-1, a selective small molecule Kv1.3 blocker, for the suppression of effector memory t cells in autoimmune diseases
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Molecular Pharmacology p. 1254 - 1270
(2007/10/03)
- File number:2
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- 87066-94-2
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2-[(2-Aminobenzyl)sulfinyl]-1-(2-pyridyl)-1,4,5,6- tetrahydrocyclopent[d]imidazoles as a novel class of gastric H+/K+-ATPase inhibitors
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Journal of Medicinal Chemistry p. 596 - 604
(2007/10/03)
- File number:4
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- 870703-68-7
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Halogen-lithium exchange between substituted dihalobenzenes and butyllithium: Application to the regioselective synthesis of functionalized bromobenzaldehydes
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Tetrahedron p. 6590 - 6595
(2007/10/03)
- File number:1
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- 870703-95-0
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Novel hybrid molecules of isoxazole chalcone derivatives: Synthesis and study of In Vitro cytotoxic activities
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Letters in drug design and discovery p. 576 - 582
(2018/06/06)
- File number:2
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- 870717-93-4
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Rational Design of Original Fused-Cycle Selective Inhibitors of Tryptophan 2,3-Dioxygenase
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Journal of Medicinal Chemistry p. 10967 - 10980
(2021/08/24)
- File number:2
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- 870-72-4
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Synthese d'α-Hydroxysulfinates
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Tetrahedron p. 2469 - 2476
(2007/10/02)
- File number:7
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- 870-73-5
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2-β-D-RIBOFURANOSYLBENZOXAZOLE FROM 2,5-ANHYDRO-D-ALLONOIMIDATE, AND 1,3-DIMETHYL-8-β-D-RIBOFURANOSYLXANTHINE FROM 2,5-ANHYDRO-D-ALLONO-THIOIMIDATES AND -DITHIOATES
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Carbohydrate Research p. 271 - 284
(2007/10/02)
- File number:18
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- 870774-25-7
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NAPHTHALENE DERIVATIVE, MATERIAL FOR ORGANIC ELECTROLUMINESCENCE DEVICE, AND ORGANIC ELECTROLUMINESCENCE DEVICE USING THE SAME
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- File number:3
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- 870774-29-1
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Scyllo-inositol as a convenient protecting group for aryl boronic acids in Suzuki-Miyaura cross-coupling reactions
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Tetrahedron Letters p. 720 - 724
(2014/01/23)
- File number:4
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- 870779-02-5
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Synthetic chemistry-led creation of a difluorinated biaryl ether non-nucleoside reverse transcriptase inhibitor
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Organic and Biomolecular Chemistry p. 3431 - 3433
(2008/09/19)
- File number:1
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- 870-78-0
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SUBSTITUTED HETEROCYCLIC INHIBITORS OF LYSINE BIOSYNTHESIS VIA THE DIAMINOPIMELATE PATHWAY
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- File number:1
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- 87-08-1
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New Oxidatively Removable Carboxy Protecting Groups
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Tetrahedron Letters p. 2027 - 2030
(2007/10/02)
- File number:34
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- 870812-94-5
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N-sulfonylcarboximidamide apoptosis promoters
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- File number:3
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- 870822-88-1
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A novel series of 4-methyl substituted pyrazole derivatives as potent glucagon receptor antagonists: Design, synthesis and evaluation of biological activities
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Bioorganic and Medicinal Chemistry p. 1896 - 1908
(2018/03/12)
- File number:6
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- 870823-08-8
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Discovery of a novel glucagon receptor antagonist N-[(4-{(1 S)-1-[3-(3, 5-dichlorophenyl)-5-(6-methoxynaphthalen-2-yl)-1 H -pyrazol-1-yl]ethyl}phenyl) carbonyl]-β-alanine (MK-0893) for the treatment of type II diabetes
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Journal of Medicinal Chemistry p. 6137 - 6148
(2012/09/07)
- File number:2
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- 870837-18-6
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Quinazolinones as γ-secretase modulators
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Bioorganic and Medicinal Chemistry Letters p. 773 - 776
(2011/03/18)
- File number:18
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- 870837-70-0
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Cation Radical Accelerated Nucleophilic Aromatic Substitution via Organic Photoredox Catalysis
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Journal of the American Chemical Society p. 16100 - 16104
(2017/11/22)
- File number:5
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- 870843-42-8
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ONE-POT METHODS FOR PREPARING CINNAMIDE DERIVATIVES
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- File number:3
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- 87087-35-2
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Perfluoro-tagged, phosphine-free palladium nanoparticles supported on silica gel: Application to alkynylation of aryl halides, Suzuki-Miyaura cross-coupling, and Heck reactions under aerobic conditions
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Green Chemistry p. 150 - 158
(2010/05/18)
- File number:7
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- 870888-46-3
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Synthesis, structure-activity relationships, and characterization of novel nonsteroidal and selective androgen receptor modulators
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Journal of Medicinal Chemistry p. 7186 - 7191
(2010/07/04)
- File number:2
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- 870-93-9
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Crystal-facet-dependent denitrosylation: Modulation of NO release from S-nitrosothiols by Cu2O polymorphs
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Chemical Science p. 5308 - 5318
(2019/05/29)
- File number:13
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- 87095-74-7
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A Bioinspired Strategy for the Enantioselective Synthesis of Bicyclic Oxygen Heterocycles
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Organic Letters
(2020/04/02)
- File number:2
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- 870997-82-3
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Design and evaluation of novel 8-oxo-pyridopyrimidine Jak1/2 inhibitors
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Bioorganic and Medicinal Chemistry Letters p. 5923 - 5930
(2013/10/22)
- File number:1
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- 87100-15-0
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Ruthenium-Catalyzed Anti-Markovnikov Selective Hydroboration of Olefins
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ACS Catalysis p. 5950 - 5954
(2017/09/15)
- File number:86
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- 87100-28-5
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Photochemical Radical C–H Halogenation of Benzyl N-Methyliminodiacetyl (MIDA) Boronates: Synthesis of α-Functionalized Alkyl Boronates
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Angewandte Chemie - International Edition p. 3454 - 3458
(2020/12/17)
- File number:69
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- 871024-38-3
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Design, synthesis, and evaluation of 5-methyl-4-phenoxy-5H-pyrrolo[3,2-d] pyrimidine derivatives: Novel VEGFR2 kinase inhibitors binding to inactive kinase conformation
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Bioorganic and Medicinal Chemistry p. 7260 - 7273
(2010/11/18)
- File number:7
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- 87-10-5
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Identification of halosalicylamide derivatives as a novel class of allosteric inhibitors of HCV NS5B polymerase
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Bioorganic and Medicinal Chemistry Letters p. 3173 - 3177
(2009/04/11)
- File number:8
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- 87109-10-2
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Aqueous Suzuki Coupling Reactions of Basic Nitrogen-Containing Substrates in the Absence of Added Base and Ligand: Observation of High Yields under Acidic Conditions
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Journal of Organic Chemistry p. 8520 - 8529
(2016/09/28)
- File number:12
-
- 871101-87-0
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Discovery of A-893, A New Cell-Active Benzoxazinone Inhibitor of Lysine Methyltransferase SMYD2
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ACS Medicinal Chemistry Letters p. 695 - 700
(2015/06/30)
- File number:4
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- 871115-32-1
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Synthesis and antibacterial evaluation of a novel series of rifabutin-like spirorifamycins
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Bioorganic and Medicinal Chemistry Letters p. 1181 - 1184
(2007/10/03)
- File number:5
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- 871125-68-7
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Neosilyllithium-Catalyzed Hydroboration of Alkynes and Alkenes in the Presence of Pinacolborane (HBpin)
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European Journal of Inorganic Chemistry
(2021/11/13)
- File number:13
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- 871130-18-6
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Synthesis, resolution, and determination of absolute configuration of a vaulted 2,2′-binaphthol and a vaulted 3,3′-biphenanthrol (VAPOL)
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Journal of the American Chemical Society p. 3392 - 3405
(2007/10/03)
- File number:2
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- 87120-72-7
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Potent small molecule Hedgehog agonists induce VEGF expression in vitro
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Bioorganic and medicinal chemistry p. 6465 - 6481,17
(2012/12/11)
- File number:53
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- 871224-19-0
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5-Aryl-1,3,4-oxadiazol-2-ylthioalkanoic Acids: A Highly Potent New Class of Inhibitors of Rho/Myocardin-Related Transcription Factor (MRTF)/Serum Response Factor (SRF)-Mediated Gene Transcription as Potential Antifibrotic Agents for Scleroderma
-
Journal of Medicinal Chemistry p. 4350 - 4369
(2019/05/08)
- File number:6
-
- 871224-64-5
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Stereoselective total synthesis of almorexant
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Tetrahedron Letters p. 3157 - 3159
(2014/05/20)
- File number:7
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- 871224-68-9
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5,6,7,8-TETRAHYDRO-IMIDAZO[1,5-A]PYRAZINE DERIVATIVES
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- File number:8
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- 871231-45-7
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Functionalization of (2S)-Isopropyl-5-iodo-2,3-dihydro-4(H)-pyrimidin-4- ones by a Suzuki-Miyaura Cross-Coupling Reaction Using Aryltrifluoroborate Salts: Convenient Enantioselective Preparation of α-Substituted β-Amino Acids
-
European Journal of Organic Chemistry p. 6393 - 6403
(2011/02/21)
- File number:4
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- 871254-61-4
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Novel 1H-pyrazolo[3,4-d]pyrimidin-6-amino derivatives as potent selective Janus kinase 3 (JAK3) inhibitors. Evaluation of their improved effect for the treatment of rheumatoid arthritis
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Bioorganic Chemistry
(2020/03/17)
- File number:9
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- 871269-12-4
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Rational Design and Synthesis of Selective PRMT4 Inhibitors: A New Chemotype for Development of Cancer Therapeutics**
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ChemMedChem p. 1116 - 1125
(2021/03/08)
- File number:5
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- 87129-32-6
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Resolution of (R, S)-ethyl-2-(4-hydroxyphenoxy) propanoate using lyophilized mycelium of Aspergillus oryzae WZ007
-
Journal of Molecular Catalysis B: Enzymatic p. 62 - 66
(2013/10/01)
- File number:7
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- 871329-65-6
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Design and synthesis of 1H-pyrazolo[3,4-b]pyridines targeting mitogen-activated protein kinase kinase 4 (MKK4) - A promising target for liver regeneration
-
European Journal of Medicinal Chemistry
(2021/04/05)
- File number:2
-
- 871329-83-8
-
6-Phenyl-1H-imidazo[4,5-c]pyridine-4-carbonitrile derivatives
-
- File number:2
-
- 871332-97-7
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One-pot synthesis of arylboronic acids and aryl trifluoroborates by Ir-catalyzed borylation of arenes
-
Organic Letters p. 757 - 760
(2007/10/03)
- File number:2
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- 871353-25-2
-
STK4 INHIBITORS FOR TREATMENT OF HEMATOLOGIC MALIGNANCIES
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- File number:8
-
- 87-13-8
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Discovery of Benzimidazole–Quinolone Hybrids as New Cleaving Agents toward Drug-Resistant Pseudomonas aeruginosa DNA
-
ChemMedChem p. 1004 - 1017
(2018/04/30)
- File number:33
-
- 87150-13-8
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Is NMR fragment screening fine-tuned to assess druggability of protein-protein interactions?
-
ACS Medicinal Chemistry Letters p. 23 - 28
(2014/02/14)
- File number:18
-
- 871502-87-3
-
Bioorthogonal double-fluorogenic siliconrhodamine probes for intracellular super-resolution microscopy
-
Chemical Communications p. 6696 - 6699
(2017/07/10)
- File number:17
-