sameAs
P1343
A facile preparation of 1-(6-hydroxyindol-1-yl)-2,2-dimethylpropan-1-oneChemistry of Fluorinated Carbon Acids: Synthesis, Physicochemical Properties, and CatalysisRadical-Mediated Three-Component Reaction: A Study toward the Total Synthesis of ResiniferatoxinDevelopment and leading-edge application of innovative photoaffinity labelingSynthesis of natural products with polycyclic systemsDevelopment of new methods in organic synthesis and their applications to the synthesis of biologically interesting natural productsEffective use of heterologous hosts for characterization of biosynthetic enzymes allows production of natural products and promotes new natural product discoveryDesign and synthesis of peptidomimetic factor VIIa inhibitorsPeptide based interleukin-1 beta converting enzyme (ICE) inhibitors: synthesis, structure activity relationships and crystallographic study of the ICE-inhibitor complexNew Approaches to Drug Discovery for Combating MRSAEnvironmental Behaviors and Toxicities of Polycyclic Aromatic Hydrocarbons and Nitropolycyclic Aromatic HydrocarbonsDegranulation Inhibitors from Medicinal Plants in Antigen-Stimulated Rat Basophilic Leukemia (RBL-2H3) CellsSearch for Anti-angiogenic Substances from Natural SourcesSearch for Inhibitors of the Ubiquitin-Proteasome System from Natural Sources for Cancer TherapyBio-active Natural Products with TRAIL-Resistance Overcoming ActivityMedicinal Chemistry Focusing on Aggregation of Amyloid-βTerpenoid Composition and Base Sequences of Ligularia virgaurea (Asteraceae) Grown in the Hengduan Mountain Area in China and a Comment on Drawing StructuresCyclooxygenase inhibitors derived from thalidomideA highly diastereoselective pinacol coupling reaction of aldehydes and ketones using low-valence niobium generated from Nb(V)Antitumor-promoting constituents from Chaenomeles sinensis KOEHNE and their activities in JB6 mouse epidermal cellsMicrowave drying of granules containing a moisture-sensitive drug: a promising alternative to fluid bed and hot air oven dryingMathematical algorithms applied to the multi-linear regression functions for the multicomponent determination of pharmaceutical dosage form containing three-component mixturesAsymmetric synthesis by the intramolecular haloetherification reaction of ene acetal: discrimination of prochiral dienes in cyclohexane systemsTransformation of arctiin to estrogenic and antiestrogenic substances by human intestinal bacteriaRegioselective nucleophilic addition of methoxybenzene derivatives to the beta-carbon of p-benzoquinone mono O,S-acetalCharacterization of physical state of mannitol after freeze-drying: effect of acetylsalicylic acid as a second crystalline cosoluteControl release effects of binders used in pills of traditional Chinese medicine herbsPreparation and evaluation of combination tablet containing incompatible active ingredientsStructural and thermodynamic behavior of eukaryotic initiation factor 4E in supramolecular formation with 4E-binding protein 1 and mRNA cap analogue, studied by spectroscopic methodsRepandiol, a new cytotoxic diepoxide from the mushrooms Hydnum repandum and H. repandum var. albumRussuphelin A, a new cytotoxic substance from the mushroom Russula subnigricans HongoMedicinal flowers. III. Marigold. (1): hypoglycemic, gastric emptying inhibitory, and gastroprotective principles and new oleanane-type triterpene oligoglycosides, calendasaponins A, B, C, and D, from Egyptian Calendula officinalisIsolation and characterization of a novel membrane glycoprotein of 85,000 molecular weight from rat liver lysosomesThe total structure of viomycin by sequential analysisVariation in chemical composition and antibacterial activities of essential oils from two species of Houttuynia THUNBSynthesis of tripeptide chloromethyl ketones and examination of their inhibitory effects on plasmin and plasma kallikreinDiscovery of a structurally novel opioid kappa-agonist derived from 4,5-epoxymorphinanPartial purification, and some properties and reactivities of cetraxate benzyl ester hydrochloride-hydrolyzing enzymeEvaluation of isonicotinoyl-gamma-aminobutyric acid (GABA) and nicotinoyl-GABA as pro-drugs of GABAQuantitative structure-activity relationships for calmodulin inhibitors
P1433
Q22330799-4775987D-FF79-45FA-A54E-3F5431C9A7C4Q26795442-5BDB23D1-50DA-4A42-ABFA-D0C72516EAEAQ26800161-B151149F-078F-445D-A99C-68CD358C9F61Q26824918-D81D62C2-5BE1-42C1-9B88-3BA0E96513D7Q26859225-25FB1CBD-90EC-401A-ADA1-82A9F05562C4Q26991648-89604E95-D16E-44C6-A5C2-7DB191B6889EQ27022271-DA0585FC-26AE-4FBA-A146-8EFD0E6D4D6CQ27658841-9D1CFD1B-5D30-473D-8B33-C2B7F7D08325Q27766888-6E747436-CCE0-4873-8F22-B9109D875FFBQ28068866-E35F102B-98BD-4BBE-A15C-759B3A9A0FAAQ28069903-E165051F-DD3F-4083-887A-B83CC976846AQ28073138-8A8E9B46-B5D0-4831-956D-4A9CCCA68E66Q28073334-12D8A096-94E9-4674-8124-05B4FD1F516AQ28075103-2F6816CE-4D98-4A3B-8156-388498D13BF4Q28076566-0F92E18A-4B7D-439E-B3A8-1A44755D1B68Q28076589-E7BF5479-899E-4A9B-A486-492EF4D19E40Q28077616-0F5188C0-096B-43F9-BB4A-42FB95856A9EQ28165198-77D744ED-0007-43D6-8142-B06C9B8219C0Q28167082-7A826A21-0584-4028-99E1-B1BBFE6657D4Q28182068-7E1C056D-3193-4D95-8383-DE7E2504F768Q28182650-5DE70E8E-74AD-4F4B-BEB7-F1C38A04C443Q28185996-708B7C03-B2ED-4D6C-9833-D63A10A4CF19Q28186011-CF279429-338C-41F0-9B88-1B69E0B1F07CQ28188387-ABFADB1C-311E-433B-9264-948B10971A3DQ28191982-B6B3E08F-0427-4886-B49D-2384A0E0BCD0Q28193092-FA27758C-680A-4EEC-87EE-2E96026D1978Q28194908-C3BFDBA7-72B3-4BF5-9F3D-948596037203Q28196629-F27DE837-DC12-419D-B8EB-B567870B2D83Q28199115-F38D82BA-54CB-4E8F-8A9C-F669F44C3E58Q28203917-7A3F5F2C-DF3F-407D-BB20-0EC5B1EC4FD6Q28203929-8FE3D9CB-E608-4DCF-A4C4-19E238FBC262Q28206631-CDB525C4-3254-44A8-8170-E99B3FF3B5EAQ28239726-2BBFCD74-8A0D-4EF0-8C87-0CD99B34876FQ28240139-1197198A-CFB9-4D22-ABA2-F18EBA563F01Q28250248-2AB88957-5D15-44F2-AD89-2119C1D93F2BQ28250287-93514F78-0FD8-46D5-95FB-F6D9E34E4D5EQ28264679-15AB9193-A2AB-43BF-B16B-EDA536899C18Q28266769-C5E919A6-A410-4F4E-953D-4B975BA0AAFDQ28270005-2CB442AE-0324-4187-8331-3389E14F585CQ28271015-B6F017B8-9422-4145-8CAB-E6633B242CE0
P1433
description
Wissenschaftliche Fachzeitschrift
@de
czasopismo naukowe
@pl
revista científica
@es
revue scientifique
@fr
rivista scientifica
@it
scientific journal
@en
vědecký časopis
@cs
wetenschappelijk tijdschrift
@nl
науковий журнал
@uk
مجلة
@ar
name
Chemical & Pharmaceutical Bulletin
@ast
Chemical & Pharmaceutical Bulletin
@da
Chemical & Pharmaceutical Bulletin
@de
Chemical & Pharmaceutical Bulletin
@en
Chemical & Pharmaceutical Bulletin
@es
Chemical & Pharmaceutical Bulletin
@fi
Chemical & Pharmaceutical Bulletin
@fr
Chemical & Pharmaceutical Bulletin
@it
Chemical & Pharmaceutical Bulletin
@nb
Chemical & Pharmaceutical Bulletin
@nl
type
label
Chemical & Pharmaceutical Bulletin
@ast
Chemical & Pharmaceutical Bulletin
@da
Chemical & Pharmaceutical Bulletin
@de
Chemical & Pharmaceutical Bulletin
@en
Chemical & Pharmaceutical Bulletin
@es
Chemical & Pharmaceutical Bulletin
@fi
Chemical & Pharmaceutical Bulletin
@fr
Chemical & Pharmaceutical Bulletin
@it
Chemical & Pharmaceutical Bulletin
@nb
Chemical & Pharmaceutical Bulletin
@nl
altLabel
Chemical and Pharmaceutical Bulletin
@en
prefLabel
Chemical & Pharmaceutical Bulletin
@ast
Chemical & Pharmaceutical Bulletin
@da
Chemical & Pharmaceutical Bulletin
@de
Chemical & Pharmaceutical Bulletin
@en
Chemical & Pharmaceutical Bulletin
@es
Chemical & Pharmaceutical Bulletin
@fi
Chemical & Pharmaceutical Bulletin
@fr
Chemical & Pharmaceutical Bulletin
@it
Chemical & Pharmaceutical Bulletin
@nb
Chemical & Pharmaceutical Bulletin
@nl
P3181
P4616
P1055
P1058
P1156
P1277
P1476
Chemical & Pharmaceutical Bulletin
@en
P236
P3181
P407
P495
P571
1953-01-01T00:00:00Z