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Structure-based design of inhibitors of purine nucleoside phosphorylase. V: 9-deazahypoxanthines

Author
NIWAS, S1 ; POORAN CHAND; PATHAK, V. P; MONTGOMERY, J. A1
[1] Southern res. inst., 55305 Birmingham AL 35255-5305, United States
Source

Journal of medicinal chemistry (Print). 1994, Vol 37, Num 15, pp 2477-2480 ; ref : 15 ref

CODEN
JMCMAR
ISSN
0022-2623
Scientific domain
Pharmacology drugs
Publisher
American Chemical Society, Washington, DC
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Activité biologique Composé bicyclique Hétérocycle azote Inhibiteur enzyme Lactame Phosphorylase Pyrrolo[3,2-d]pyrimidin-4-one(3,4-dihydro-7-hétérylméthyl) Pyrrolo[3,2-d]pyrimidin-4-one(7-arylméthyl-3,4-dihydro) Pyrrolo[3,2-d]pyrimidin-4-one(7-cyclopropylméthyl-3,4-dihydro) Enzyme Glycosyltransferases Hexosyltransferases Transferases
Keyword (en)
Biological activity Bicyclic compound Nitrogen heterocycle Enzyme inhibitor Lactam Phosphorylase Enzyme Glycosyltransferases Hexosyltransferases Transferases
Keyword (es)
Actividad biológica Compuesto bicíclico Heterociclo nitrógeno Inhibidor enzima Lactamo Phosphorylase Enzima Glycosyltransferases Hexosyltransferases Transferases
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06C Heterocyclic compounds with several n hetero atoms in the same ring, in separated rings or in fused rings

Discipline
Organic chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
4168041

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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