- 103628-22-4
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Novel compounds that reverse the disease phenotype in Type 2 Gaucher disease patient-derived cells
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Bioorganic and medicinal chemistry letters
(2019/12/11)
- File number:10
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- 103628-46-2
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Synthesis of 5-substituted indole derivatives, part II. Synthesis of sumatriptan through the Japp-Klingemann reaction
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Heterocycles p. 665 - 673
(2007/10/03)
- File number:10
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- 103628-48-4
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Isotope-Edited Infrared Spectroscopy for Efficient Discrimination between Pharmaceutical Salts and Cocrystals
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Molecular Pharmaceutics p. 2350 - 2358
(2017/07/12)
- File number:7
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- 103628-53-1
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Synthesis of carbon-14 labelled indolic 5HT1 receptor agonists
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Journal of labelled compounds and radiopharmaceuticals p. 1021 - 1030
(2007/10/03)
- File number:2
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- 103628-86-0
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SYNTHESE D'ETHERS ET DE THIOETHERS ALLYLIQUES FLUORES PAR CATALYSE PAR TRANSFERT DE PHASE
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Journal of Fluorine Chemistry p. 399 - 410
(2007/10/02)
- File number:17
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- 103629-71-6
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Determination of saikosaponin derivatives in Radix bupleuri and in pharmaceuticals of the Chinese multiherb remedy Xiaochaihu-tang using liquid chromatographic tandem mass spectrometry
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Analytical Chemistry p. 4208 - 4216
(2007/10/03)
- File number:2
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- 103629-72-7
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New derivatives of saikosaponins
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Chemical and Pharmaceutical Bulletin p. 3349 - 3355
(2007/10/02)
- File number:1
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- 103629-80-7
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Cnidimonins A-C, Three Types of Hybrid Dimer from Cnidium monnieri: Structural Elucidation and Semisynthesis
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Organic Letters p. 4920 - 4923
(2017/09/23)
- File number:2
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- 103630-03-1
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FLAVAN-3-OL AND PROCYANIDIN GLYCOSIDES FROM QUERCUS MIYAGII
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Phytochemistry p. 1167 - 1170
(2007/10/02)
- File number:1
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- 10363-27-6
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Cascade rearrangement of spiroepoxymethyl radicals into 2-oxocycloalkyl radicals: Evaluation of a two-carbon cycloalkanone ring expansion
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Journal of the Chemical Society. Perkin Transactions 2 (2001) p. 937 - 945
(2007/10/03)
- File number:1
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- 103633-26-7
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TLC, UV AND ACIDIC TREATMENT IN THE DIFFERENTIATION OF 5,6- AND 5,8-DIHYDROXYFLAVONES, 3-METHOXYFLAVONES AND FLAVONOLS
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Tetrahedron p. 5733 - 5740
(2007/10/02)
- File number:1
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- 103633-30-3
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Solvent responsive catalyst improves NMR sensitivity: Via efficient magnetisation transfer
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Chemical Communications p. 8467 - 8470
(2016/07/07)
- File number:12
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- 103633-59-6
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A GENERAL METHOD FOR THE SYNTHESIS OF 3,4-EPOXY-2-METHYLENEALKANOIC ACID DERIVATIVES USING DIANION OF N-PHENYL-2-(PHENYLSULFONYLMETHYL)-PROPENAMIDE
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Tetrahedron Letters p. 4751 - 4754
(2007/10/02)
- File number:2
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- 103634-03-3
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SHYNTHESIS OF (1S,5R)-KARAHANA ETHER AND (1S,5R)-KARAHANA LACTONE. THE OPTICALLY ACTIVE FORMS OF UNIQUE MONOTERPENES WITH A 6-OXABICYCLOOCTANE RING SYSTEM
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Tetrahedron p. 5487 - 5494
(2007/10/02)
- File number:3
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- 103634-10-2
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Synthesis of phosphatidylcholines containing ricinoleic acid
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Tetrahedron p. 10219 - 10227
(2007/10/03)
- File number:2
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- 103635-24-1
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METHOD FOR PREPAREING 1,3,4-OXADIAZOL UNDER SOLVENT-FREE CONDITION
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- File number:2
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- 1036378-83-2
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Highly efficient emitters of ultra-deep-blue light made from chrysene chromophores
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Journal of Materials Chemistry C p. 3833 - 3842
(2016/05/24)
- File number:28
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- 1036378-89-8
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Ultrasound assisted one-pot synthesis of benzo-fused indole-4,9-dinones from 1,4-naphthoquinone and α-aminoacetals
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Tetrahedron Letters p. 2253 - 2256
(2016/05/10)
- File number:7
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- 1036378-91-2
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Synthesis of tetrahydroisoquinolines through TiCl4-mediated cyclization and Et3SiH reduction
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Chinese Chemical Letters p. 729 - 732
(2019/10/02)
- File number:4
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- 1036380-75-2
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Selective Bisubstrate Inhibitors with Sub-nanomolar Affinity for Protein Kinase Pim-1
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ChemMedChem p. 909 - 913
(2013/07/27)
- File number:9
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- 1036381-91-5
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Inhibiting effect of trisubstituted pyrimidine derivative on protein kinase
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- File number:6
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- 1036383-21-7
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COMPOUNDS AND METHODS FOR KINASE MODULATION, AND INDICATIONS THEREFOR
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- File number:2
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- 1036383-28-4
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COMPOUNDS AND METHODS FOR KINASE MODULATION, AND INDICATIONS THEREFOR
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- File number:2
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- 1036383-29-5
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COMPOUNDS AND METHODS FOR KINASE MODULATION, AND INDICATIONS THEREFOR
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- File number:2
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- 1036383-35-3
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COMPOUNDS AND METHODS FOR KINASE MODULATION, AND INDICATIONS THEREFOR
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- File number:2
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- 1036383-41-1
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COMPOUNDS AND METHODS FOR KINASE MODULATION, AND INDICATIONS THEREFOR
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- File number:1
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- 1036383-51-3
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BICYCLIC GPR119 MODULATORS
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- File number:2
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- 103638-37-5
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Studies on organic fluorine compounds. L. Synthesis and biological activity of 2α-fluorovitamin D3
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Chemical and Pharmaceutical Bulletin p. 1568 - 1572
(2007/10/02)
- File number:1
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- 1036388-66-5
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Synthesis of Functionalized Dihydrobenzofurans by Direct Aryl C?O Bond Formation under Mild Conditions
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Angewandte Chemie - International Edition p. 11625 - 11628
(2016/10/24)
- File number:2
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- 1036388-81-4
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BICYCLIC LACTAM FACTOR VIIA INHIBITORS USEFUL AS ANTICOAGULANTS
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- File number:2
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- 1036388-85-8
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A kind of diaryl hydanto?n derivatives, its preparation method, pharmaceutical composition and application
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- File number:2
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- 1036388-91-6
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A kind of diaryl hydanto?n derivatives, its preparation method, pharmaceutical composition and application
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- File number:1
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- 1036389-05-5
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Discovery of Phenylglycine Lactams as Potent Neutral Factor VIIa Inhibitors
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ACS Medicinal Chemistry Letters p. 1077 - 1081
(2016/12/18)
- File number:3
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- 1036389-07-7
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Discovery of Phenylglycine Lactams as Potent Neutral Factor VIIa Inhibitors
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ACS Medicinal Chemistry Letters p. 1077 - 1081
(2016/12/18)
- File number:2
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- 1036389-09-9
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Discovery of Phenylglycine Lactams as Potent Neutral Factor VIIa Inhibitors
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ACS Medicinal Chemistry Letters p. 1077 - 1081
(2016/12/18)
- File number:3
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- 1036389-83-9
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Discovery of Phenylglycine Lactams as Potent Neutral Factor VIIa Inhibitors
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ACS Medicinal Chemistry Letters p. 1077 - 1081
(2016/12/18)
- File number:9
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- 1036389-86-2
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Discovery of Phenylglycine Lactams as Potent Neutral Factor VIIa Inhibitors
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ACS Medicinal Chemistry Letters p. 1077 - 1081
(2016/12/18)
- File number:7
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- 1036389-90-8
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Discovery of Phenylglycine Lactams as Potent Neutral Factor VIIa Inhibitors
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ACS Medicinal Chemistry Letters p. 1077 - 1081
(2016/12/18)
- File number:7
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- 1036389-92-0
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Discovery of Phenylglycine Lactams as Potent Neutral Factor VIIa Inhibitors
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ACS Medicinal Chemistry Letters p. 1077 - 1081
(2016/12/18)
- File number:2
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- 103-63-9
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Preparation of ionic liquid-based vilsmier reagent from novel multi-purpose dimethyl formamide-like ionic liquid and its application
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Chinese Journal of Chemistry p. 1647 - 1657
(2012/09/21)
- File number:128
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- 1036390-32-5
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Discovery of Phenylglycine Lactams as Potent Neutral Factor VIIa Inhibitors
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ACS Medicinal Chemistry Letters p. 1077 - 1081
(2016/12/18)
- File number:3
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- 103639-57-2
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Total synthesis of (-)-senepodine G and (-)-cermizine C
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Journal of Organic Chemistry p. 1039 - 1042
(2008/02/04)
- File number:7
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- 1036395-80-8
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Structure-activity relationship studies and sleep-promoting activity of novel 1-chloro-5,6,7,8-tetrahydroimidazo[1,5-a]pyrazine derivatives as dual orexin receptor antagonists. Part 2
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Bioorganic and Medicinal Chemistry Letters p. 3857 - 3863
(2013/07/27)
- File number:3
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- 1036396-21-0
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5,6,7,8-TETRAHYDRO-IMIDAZO[1,5-A]PYRAZINE DERIVATIVES
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- File number:1
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- 1036396-31-2
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TETRAHYDRO-IMIDAZO QUINOLINE COMPOSITIONS AS CBP/P300 INHIBITORS
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- File number:2
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- 1036396-40-3
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Structure-activity relationship studies and sleep-promoting activity of novel 1-chloro-5,6,7,8-tetrahydroimidazo[1,5-a]pyrazine derivatives as dual orexin receptor antagonists. Part 2
-
Bioorganic and Medicinal Chemistry Letters p. 3857 - 3863
(2013/07/27)
- File number:2
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- 1036396-43-6
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Structure-activity relationships of antitubercular nitroimidazoles. 2. determinants of aerobic activity and quantitative structure-activity relationships
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Journal of Medicinal Chemistry p. 1329 - 1344
(2009/12/07)
- File number:2
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- 1036396-64-1
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Structure-activity relationship studies and sleep-promoting activity of novel 1-chloro-5,6,7,8-tetrahydroimidazo[1,5-a]pyrazine derivatives as dual orexin receptor antagonists. Part 2
-
Bioorganic and Medicinal Chemistry Letters p. 3857 - 3863
(2013/07/27)
- File number:2
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- 1036397-17-7
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Synthesis, structure-activity relationship studies, and identification of novel 5,6,7,8-tetrahydroimidazo[1,5-a]pyrazine derivatives as dual orexin receptor antagonists. Part 1
-
Bioorganic and Medicinal Chemistry Letters p. 2212 - 2216
(2013/04/23)
- File number:2
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- 103639-82-3
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HETEROARYL COMPOUNDS AND METHODS OF USE THEREOF
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- File number:1
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