메뉴 건너뛰기




Volumn 1, Issue , 2008, Pages 302-319

Molecular Shape Analysis

Author keywords

[No Author keywords available]

Indexed keywords

MOLECULAR SHAPES;

EID: 84955653943     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1002/9783527618279.ch10     Document Type: Chapter
Times cited : (12)

References (72)
  • 5
    • 0035978673 scopus 로고    scopus 로고
    • F. Weinhold, Nature, 2001, 411, 539-541.
    • (2001) Nature , vol.411 , pp. 539-541
    • Weinhold, F.1
  • 13
    • 0001219854 scopus 로고    scopus 로고
    • The Prediction of the 3D Structure of Organic Molecules from Their Infrared Spectra
    • M. C. Hemmer, V. Steinhauer, J. Gasteiger, The Prediction of the 3D Structure of Organic Molecules from Their Infrared Spectra, in Vibrational Spectroscopy, 19, 1999, 151-164.
    • (1999) Vibrational Spectroscopy , vol.19 , pp. 151-164
    • Hemmer, M.C.1    Steinhauer, V.2    Gasteiger, J.3
  • 15
    • 0001761498 scopus 로고
    • Distance Geometry in Molecular Modeling
    • K. B. Lipkowitz, D. B. Boyd (Eds.), VCH, Weinheim, Germany
    • J. M. Blaney, J. S. Dixon, Distance Geometry in Molecular Modeling, in Reviews in Computational Chemistry, Vol. 5, K. B. Lipkowitz, D. B. Boyd (Eds.), VCH, Weinheim, Germany 1994.
    • (1994) Reviews in Computational Chemistry , vol.5
    • Blaney, J.M.1    Dixon, J.S.2
  • 21
    • 84955678782 scopus 로고    scopus 로고
    • Multiresolution Molecular Shapes, TICAM report #99-42
    • L. Bajaj, V. Pascucci, A. Shamir, R. Holt, A. Netravali, Multiresolution Molecular Shapes, TICAM report #99-42, http://www.ticam.utexas.edu/ CCV/ projects/ Angstrom/ shape.html.
    • Bajaj, L.1    Pascucci, V.2    Shamir, A.3    Holt, R.4    Netravali, A.5
  • 22
    • 0011525709 scopus 로고    scopus 로고
    • Molecular Surfaces: A Review
    • M. L. Connolly, Molecular Surfaces: A Review, http://www.netsci.org/Science/ Compchemffeature 14.html
    • Connolly, M.L.1
  • 26
    • 84955715148 scopus 로고    scopus 로고
    • R. R. Gabdoulline, http://www.embl-heidelberg.de/~gabdoull/ads/ introduction.html.
    • Gabdoulline, R.R.1
  • 28
    • 80052413272 scopus 로고    scopus 로고
    • Application of the "shape signatures" approach to ligand- and receptor-based drug design
    • Washington DC
    • R. J. Zauhar, W. J. Welsh, Application of the "shape signatures" approach to ligand- and receptor-based drug design, 200th ACS Natl. Meet., Washington DC, 2000.
    • (2000) 200th ACS Natl. Meet
    • Zauhar, R.J.1    Welsh, W.J.2
  • 30
    • 84955654143 scopus 로고    scopus 로고
    • Protein surface segmentation using fuzzy logic
    • W. Heiden, F.Brickmann, Protein surface segmentation using fuzzy logic, http://www.pc.chemie.tu-darmstadt.de/research/fuzzy/ segment_right.shtml
    • Heiden, W.1    Brickmann, F.2
  • 43
    • 84903808242 scopus 로고    scopus 로고
    • When There is No Receptor Crystal Structure: Building Useful Models of Receptor Sites
    • D. E. Walters, When There is No Receptor Crystal Structure: Building Useful Models of Receptor Sites, http:// www.netsci.org/ Science/ Compchem/ feature03.html.
    • Walters, D.E.1
  • 48
    • 0000676724 scopus 로고
    • Application of Various Steric Constants to Quantitative Structure-Activity Relationships
    • M. Charton, I. Motoc (Eds.), Akademie, Berlin
    • T. Fujita, H. Iwamura, Application of Various Steric Constants to Quantitative Structure-Activity Relationships, in Steric Effects in Drug Design, M. Charton, I. Motoc (Eds.), Akademie, Berlin, 1983.
    • (1983) Steric Effects in Drug Design
    • Fujita, T.1    Iwamura, H.2
  • 52
    • 84890244523 scopus 로고    scopus 로고
    • 2
    • Release 4.5 June, Documentation, MSI, Theory QSAR + descriptors
    • 2, Release 4.5 June 2000, Documentation, MSI, Theory QSAR + descriptors, http://www. accelrys.com/doc/.
    • (2000)
  • 55
    • 0041496732 scopus 로고
    • Molecular Recognition: The Measurement and Search for Molecular Similarity in Ligand-Receptor Interaction
    • M. A. Johnson, G. M. Maggiora (Eds.), Wiley, New York
    • P. M. Dean, Molecular Recognition: The Measurement and Search for Molecular Similarity in Ligand-Receptor Interaction, in Concepts and Applications of Molecular Similarity M. A. Johnson, G. M. Maggiora (Eds.), Wiley, New York, 1990.
    • (1990) Concepts and Applications of Molecular Similarity
    • Dean, P.M.1
  • 61
    • 84955742895 scopus 로고    scopus 로고
    • Shape Analysis, ECC
    • P. G. Mezey, Shape Analysis, ECC.
    • Mezey, P.G.1
  • 62
    • 0347248495 scopus 로고
    • The application of molecular topology to drug design - topological descriptions of molecular shape
    • P. M. Dean (Ed.), Blackie, Glasgow
    • D. C. Whitney, M. G. Ford, The application of molecular topology to drug design - topological descriptions of molecular shape, in Molecular Similarity in Drug Design, P. M. Dean (Ed.), Blackie, Glasgow, 1995.
    • (1995) Olecular Similarity in Drug Design
    • Whitney, D.C.1    Ford, M.G.2
  • 64
    • 84955709245 scopus 로고    scopus 로고
    • Shapes of small molecules and proteins, Network Science
    • M. L. Connolly, Shapes of small molecules and proteins, Network Science, http://www.netsci.org/ Science/ Compchem/feature14h.html.
    • Connolly, M.L.1
  • 65
    • 0344942117 scopus 로고    scopus 로고
    • Shape Analysis of Molecular Surfaces
    • B. S. Duncan, A. J. Olson, Shape Analysis of Molecular Surfaces, http:// www.scripps.edu/pub/olson-web/papers/ shape/ shape.html.
    • Duncan, B.S.1    Olson, A.J.2
  • 70
    • 35248869048 scopus 로고    scopus 로고
    • A new method for evaluating the structural similarity of proteins using geometric morphometries in Currents
    • Frontiers Science Series No. 30, S. Miyano, R. Shamir, T. Takagi (Eds.), Universal Academy Press, Tokyo
    • D. C. Adams, and G. J. P. Naylor, A new method for evaluating the structural similarity of proteins using geometric morphometries in Currents in Computational Molecular Biology, Frontiers Science Series No. 30, S. Miyano, R. Shamir, T. Takagi (Eds.), Universal Academy Press, Tokyo, 2000.
    • (2000) Computational Molecular Biology
    • Adams, D.C.1    Naylor, G.J.P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.