- combinatorial drug design
- Макаров: комбинаторный дизайн лекарственный веществ
Универсальный англо-русский словарь. Академик.ру. 2011.
combinatorial drug design
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Combinatorial chemistry — involves the rapid synthesis or the computer simulation of a large number of different but structurally related molecules or materials. It is especially common in CADD (Computer aided drug design) and can be done online with web based software,… … Wikipedia
Drug discovery — In the fields of medicine, biotechnology and pharmacology, drug discovery is the process by which drugs are discovered and/or designed. In the past most drugs have been discovered either by identifying the active ingredient from traditional… … Wikipedia
Drug discovery hit to lead — Early drug discovery involves several phases from target identification to preclinical development. The identification of small molecule modulators of protein function and the process of transforming these into high content lead series are key… … Wikipedia
Central Drug Research Institute — The Central Drug Research Institute (CDRI) is one of the first laboratories to be established in India right after its independence. CDRI is among the thirty nine laboratories that are functioning under the aegis of the council of scientific and… … Wikipedia
pharmaceutical industry — Producers of pharmaceuticals, substances used in the diagnosis, treatment, and prevention of disease and the modification of organic functions. The earliest records of medicinal plants and minerals are those of the ancient Chinese, Hindu, and… … Universalium
Chemical biology — is a scientific discipline spanning the fields of chemistry and biology that involves the application of chemical techniques and tools, often compounds produced through synthetic chemistry, to the study and manipulation of biological systems.… … Wikipedia
Stratégies pour franchir la barrière hémato-encéphalique — Traduction à relire … Wikipédia en Français
Druglikeness — is a qualitative concept used in drug design for how druglike a substance is with respect to factors like bioavailability. It is estimated from the molecular structure before the substance is even synthesized and tested. A druglike molecule has… … Wikipedia
Relación cuantitativa estructura actividad — Saltar a navegación, búsqueda {La relación cuantitativa estructura actividad (en inglés, Quantitative structure activity relationship, QSAR, o bien, quantitative structure property relationship, QSPR, es el proceso por el cual la estructura… … Wikipedia Español
Enzyme inhibitor — Enzyme inhibitors are molecules that bind to enzymes and decrease their activity. Since blocking an enzyme s activity can kill a pathogen or correct a metabolic imbalance, many drugs are enzyme inhibitors. They are also used as herbicides and… … Wikipedia
Medicinal chemistry — Pharmaceutical chemistry redirects here. For the subject being offered to the GCE A level students in Singapore, see H3 Pharmaceutical Chemistry. Medicinal chemistry and pharmaceutical chemistry are disciplines at the intersection of chemistry,… … Wikipedia
