Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Oxford Molecular

The CAChe software packages from Oxford Molecular webpage http //www.oxmol.com/aetinfo/eduf... [Pg.2199]

Price category contact Platforms Cray, SGI, RS/6000 Contact information Oxford Molecular Group, Inc. 2105 South Bascom Ave., Suite 200 Campbell, CA 95008 (800) 876-9994 http / / www.oxmol.com/ products oxmol.com... [Pg.332]

The HyperChem program from Hypercube Inc. and UniChem from Oxford Molecular can be used as graphic interfaces to Q-Chem. At the time we conducted our tests, it was not yet available on all the platforms listed as being supported. The current version is well designed for ground- and excited-state calculations on small or large organic molecules. [Pg.340]

Oxford Molecular Ltd., the Medawar Centre, Oxford Science Park, Sandford-on-Thames, Oxford 0X4 4GA, England. [Pg.124]

Jorgensen WL, Maxwell DS, Tirado-Rives J (1996) J Am Chem Soc 118 11225 Jorgensen WL, McDonald NA (1998) Theochem - J Molec Struct 424 145 CAChe molecular moldelling program (1996) Oxford Molecular Group Inc In molecular mechanics the force field energy E is usually termed the steric energy of the molecule... [Pg.62]

G. Grassy, R. Lahana and Oxford Molecular Ltd., TSAR, Tools for Structure-Activity Relationships, User s Guide, Issue 3. Proprietary Software developed by Oxford Molecular Ltd., Oxford, UK, 1993. [Pg.418]

Photography Credits Martin Bond/Science Photo Library/Photo Researchers - Chemical Design/Science Photo Library/Photo Researchers - Oxford Molecular Biophysics Laboratory/Science Photo Library/Photo Researchers - David Parker/IMI/Univ of Birmingham/Science Photo - Library/Photo Researchers Richard Megna/Fundamental Photographs - Ed Degginger/Color-Pic, Inc - Ed Degginger/Color-Pic, Inc... [Pg.3]

G. Robert, Rhane-Poulene. Cranbury. NJ. Vanillin Gartb Roberts, FRS. Tlutrn EMI pit- and Unriersitv of Oxford. Molecular and Supermolecular Electronics... [Pg.1843]

One of the most popular applications is ChemX/ChemDiverse of Chemical Design/Oxford Molecular (now Accelrys). Details of the approaches used there are included in this review by Mason et al. [3], Another example, of an in-house pharmacophore fingerprint construction, is PharmPrint by Affymax [4, 5]. [Pg.40]

Figure 4.7 Consensus bootstrap tree of full-length amino acid sequences of insect desaturases generated with MacVector 7.0 (Oxford Molecular Limited). Branch points (internal nodes) are retained if they occur in >50 percent of resampling trees (1000 x resampling) all other nodes are collapsed. Names in bold are from the published literature names in parentheses reflect a nomenclature system for insect desaturases (proposed in Knipple ef a/.,... Figure 4.7 Consensus bootstrap tree of full-length amino acid sequences of insect desaturases generated with MacVector 7.0 (Oxford Molecular Limited). Branch points (internal nodes) are retained if they occur in >50 percent of resampling trees (1000 x resampling) all other nodes are collapsed. Names in bold are from the published literature names in parentheses reflect a nomenclature system for insect desaturases (proposed in Knipple ef a/.,...
ChemDiverse. Oxford Molecular Group, Oxford Science Park, Oxford, UK. [Pg.64]

Tsar3.11, Oxford Molecular Group, http //www.oxmol.co.uk/... [Pg.219]

This method has been used extensively in the literature for the calculation of molecular hyperpolarizabilities. The calculations employed here utilized the MOPAC and ZINDO methods within the 4.0.1 CAChe Worksystem (Oxford Molecular) software package. MNDO-AM1 method and parameterization M. J. S. Dewar and M. L. McKee, J. Am. Chem. Soc., 1977, 99, 5231. Oscillator strengths were calculated using the ZINDO method. [Pg.76]

A search for Oxford Molecular Ltd., which produces a variety of software for sequence alignment, molecular modeling of antibodies, QSAR, semiempirical molecular orbital calculations, and so on, yielded five hits in CJACS through 1993. A search for CompuDrug produced a total of two hits, one in 1990 and one in 1992. [Pg.341]

MDL Information Systems MSI companies BIOSYM Technologies Serena Software Chemical Design Ltd. Cambridge Scientific Computing Oxford Molecular Ltd. Daylight Chemical Information BioCAD Gaussian, Inc. Cache Scientific CompuDrug Wavefunction, Inc. [Pg.342]

BIOSYM Technologies Tripos, Inc, Molecular Simulations Inc. Serena Software Chemical Design Ltd. Oxford Molecular Ltd. Wavefunction, Inc. MDL Information Systems Springer-Verlag Cambridge Scientific Computing... [Pg.344]

Oxford Molecular Group (Oxford, England) acquired CAChe Scientific, Inc., from Tektronix Company. [Pg.354]


See other pages where Oxford Molecular is mentioned: [Pg.336]    [Pg.169]    [Pg.169]    [Pg.1317]    [Pg.30]    [Pg.218]    [Pg.438]    [Pg.1346]    [Pg.1354]    [Pg.1354]    [Pg.169]    [Pg.169]    [Pg.191]    [Pg.195]    [Pg.187]    [Pg.229]    [Pg.244]    [Pg.175]    [Pg.262]    [Pg.1317]    [Pg.69]    [Pg.345]    [Pg.346]    [Pg.349]    [Pg.391]    [Pg.391]    [Pg.425]    [Pg.425]   
See also in sourсe #XX -- [ Pg.30 ]

See also in sourсe #XX -- [ Pg.428 ]




SEARCH



Oxford

Oxford Molecular Group

Oxford Molecular Ltd

© 2024 chempedia.info