Synthesis, resolution, and antiplatelet activity of 3-substituted 1 (3H ) -isobenzofuranone
- Author
- HUA YANG1 ; HU, Gao-Yun1 ; JUN CHEN1 ; YI WANG1 ; WANG, Zhong-Hua1
[1] Research Institute of Medicinal Chemistry, School of Pharmaceutical Sciences, Central South University, Changsha 410013, China - Source
Bioorganic & medicinal chemistry letters (Print). 2007, Vol 17, Num 18, pp 5210-5213, 4 p ; ref : 13 ref
- ISSN
- 0960-894X
- Scientific domain
- Biochemistry, molecular biology, biophysics; Pharmacology drugs
- Publisher
- Elsevier, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Author keyword
- 1(3H)-Isobenzofuranone Antiplatelet Specific rotation Synthesize
- Keyword (fr)
- Anticoagulant Composé aromatique Composé bicyclique Enantiomère Hétérocycle oxygène In vitro Inhibiteur thromboagrégation Lactone Racémique Relation structure activité Synthèse chimique Thrombocyte Isobenzofuran-1-one dérivé Phtalide(3-alkyl) Phtalide(3-alkylidène)
- Keyword (en)
- Anticoagulant Aromatic compound Bicyclic compound Enantiomer Oxygen heterocycle In vitro Antiplatelet agent Lactone Racemic Structure activity relation Chemical synthesis Platelet
- Keyword (es)
- Anticoagulante Compuesto aromático Compuesto bicíclico Enantiómero Heterociclo oxígeno In vitro Inhibidor tromboagregación Lactona Racémico Relación estructura actividad Síntesis química Trombocito
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B02 Pharmacology. Drug treatments / 002B02G Blood. Blood coagulation. Reticuloendothelial system
- Discipline
- Pharmacological treatments
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 19021290
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1016/j.bmcl.2007.06.082 
https://dx.doi.org/10.1016/j.bmcl.2007.06.082
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