|
|
|
|
| LEADER |
00000pam a2200000 a 4500 |
| 001 |
in00004502917 |
| 005 |
20191203131626.0 |
| 008 |
060125s2006 gw a b 001 0 eng |
| 015 |
|
|
|a GBA643470
|2 bnb
|
| 016 |
7 |
|
|a 013455829
|2 Uk
|
| 020 |
|
|
|a 3527310762
|
| 020 |
|
|
|a 9783527310760
|
| 024 |
3 |
|
|a 9783527310760
|
| 029 |
1 |
|
|a YDXCP
|b 2423487
|
| 035 |
|
|
|a (OCoLC)ocm67873889
|
| 035 |
|
|
|z (UtOrBLW)41624
|
| 035 |
|
|
|a 59481
|
| 040 |
|
|
|a UKM
|c UKM
|d BAKER
|d YDXCP
|d TMV
|d UtOrBLW
|
| 042 |
|
|
|a ukblsr
|
| 049 |
|
|
|a TMVM
|c 1
|
| 060 |
|
4 |
|a QV 744
|b C541 2006
|
| 082 |
0 |
4 |
|a 615.19
|2 22
|
| 245 |
0 |
0 |
|a Chirality in drug research /
|c edited by Eric Francotte and Wolfgang Lindner.
|
| 264 |
|
1 |
|a Weinheim :
|b Wiley-VCH,
|c [2006]
|
| 264 |
|
4 |
|c ©2006
|
| 300 |
|
|
|a xix, 351 pages :
|b illustrations, portrait ;
|c 25 cm.
|
| 336 |
|
|
|a text
|2 rdacontent
|b txt
|
| 337 |
|
|
|a unmediated
|2 rdamedia
|
| 338 |
|
|
|a volume
|2 rdacarrier
|b nc
|
| 490 |
1 |
|
|a Methods and principles in medicinal chemistry ;
|v 33
|
| 504 |
|
|
|a Includes bibliographical references and index.
|
| 505 |
0 |
|
|a Chiral drugs from a historical point of view -- Stereoselective synthesis of drugs - an industrial perspective -- Aspects of chirality in natural products drug discovery -- Biotransformation methods for preparing chiral drugs and drug intermediates -- Resolution of chiral drugs and drug intermediates by crystallisation -- Isolation and production of optically pure drugs by enantioselective chromatography -- Stereoselective chromatographic methods for drug analysis -- Capillary electrophoresis coupled to mass spectrometry for chiral drugs analysis -- Powerful chiral molecular tools for preparation of enantiopure alcohols and simultaneous determination of their absolute configurations by X-ray crystallography and/or ¹H NMR anisotropy methods -- Keywords in chirality modeling molecular modeling of chirality - software and literature research on chirality in modeling, chirality in docking, chiral ligand - receptor interaction and symmetry
|
| 650 |
|
0 |
|a Drugs
|x Research.
|
| 650 |
|
0 |
|a Drug development.
|
| 650 |
|
0 |
|a Chirality.
|
| 650 |
|
2 |
|a Drug Design.
|
| 650 |
|
2 |
|a Molecular Conformation.
|
| 650 |
|
2 |
|a Stereoisomerism.
|
| 700 |
1 |
|
|a Francotte, Eric.
|
| 700 |
1 |
|
|a Lindner, W.
|q (Wolfgang)
|
| 830 |
|
0 |
|a Methods and principles in medicinal chemistry ;
|v 33.
|
| 999 |
|
|
|a MARS
|
| 999 |
f |
f |
|s 5c623636-6b4a-374c-b175-308c61f8b56b
|i 16f8c470-67a3-32ff-93f1-be2f6e699986
|t 0
|
| 952 |
f |
f |
|p ric
|a Texas A&M University
|b Rellis Campus
|c Joint Library Facility
|d Remote Storage
|t 0
|e QV 744 C541 2006
|h National Library of Medicine classification
|i unmediated -- volume
|m 323890192935B
|
| 998 |
f |
f |
|a QV 744 C541 2006
|t 0
|l Remote Storage
|