TWC
BioSearch
Discount Research Software Agent
A Utility for Assistance in Mass Spectral Interpretation
Draw Chemical Structures on Screen Quickly and Easily
Fragment Structures on Screen Using Either Manual or Automated Routines
Compare Predicted Fragmentations with Observed Mass Spectra
Instantly Calculate & Display Isotopic Profiles of Molecules or Fragment Ions
Calculate Possible Elemental Compositions for a Given Mass
To begin using MSC, one would generally first draw a structure. The MSC drawing editor is designed to be very simple and easy to use, and a variety of preformed rings, functional groups and other structures are available to assist in this process. For example, the structure of nicotine can be drawn on screen in seconds in just six steps. This compound was drawn by placing two preformed rings on screen, then adding the bond, two N atoms and the methyl group as added objects.
The structure could be saved to disk, then converted to cotinine by adding =O in one step to form the lactam structure. The two structures shown here could thus be drawn and saved for later use by using just 7 steps and in less than 30 seconds.
Once a structure has been drawn, it can be analyzed in a number of ways. The most fundamental operation is manual fragmentation. This is done just as you would do using paper and pencil, but with electronic speed and accuracy. For example, to examine a homolytic break of the bond linking the two ring structures of nicotine, you would simply draw a line through the bond using the mouse; the program will instantly calculate and display the resulting two fragment masses. The display is color-coded to clearly link the fragment atoms with the associated mass.
This instant manual fragmentation process is interactive and can be repeated as often as desired. Manual fragmentation draws upon your knowledge of likely fragmentation routes to focus your time and effort on the most likely possibilities. There are three different manual fragmentation modes available including a ‘free-form’ option to accommodate any sort of fragmentation you might wish to examine. Multiple and sub-fragmentations of compounds can also be examined, and the display can be instantly switched between nominal and accurate mass resolution.
Autofragmentation results are only a mouse-click away. In the screen shown below, nicotine has been autofragmented by MSC and the user has selected mass 39 in the fragment list ... this automatically redraws the structure with the three atoms present in the fragment (C3H3) indicated on screen. This process of identifying specific fragments in the structure can be repeated as often as desired. These results can also be directly compared with the actual mass spectrum, either imported as an ASCII file or recreated within MSC; also, fragment isotope profiles can be instantly calculated and displayed; additional possible fragments including major rearrangement products such as McLafferty or tropylium ions can be identified; etc.
Once a molecule has been autofragmented, it can also be compared with an observed mass spectrum by choosing the ‘Match’ option button. This enables you to essentially overlay the projected and observed spectra, match predicted and observed isotopic profiles for the molecular ion, and calculate an overall ‘Match Index’ for the actual and predicted spectra.
MSC also includes utilities for determining Isotopic Profiles, for calculating possible elemental compositions given a mass, and for importing user spectral data in a variety of text formats, or creating spectral files directly from data entered onto an internal ‘spreadsheet’.
The screen on the right demonstrates the Isotopic Abundance utility. The user has drawn the structure of dioxin (TCDD) and then clicked on the Isotopic Abundance menu item. MSC automatically incorporated the elemental composition for the TCDD structure, carried out the calculations, and instantly displayed the window shown here displaying the theoretical profile in both text and bar graph form. Compositions can also be entered and edited directly, and additional options such as to display the results in accurate mass form are available.
The screen below shows the Elemental Composition utility. You can enter a mass and tolerance, select the elements to be considered (with additional constraints if desired such as to specify the range of an element to include, or only show possible molecular ions, etc.), and then click on the ‘Calculate’ button to have MSC calculate all possible elemental compositions.
MSC Features
All modules support C, H, O, N, Cl, F, Br, I, S, P, B, Si and the major stable isotopes.
Both nominal and accurate mass values are supported.
Multiple valence states are supported by all elements.
Results can be printed, or copied to other programs via the Windows clipboard.
MSC imports ASCII mass/intensity files in a number of formats, & displays spectra.
MOLfile import/export is supported for most structures.
A complete On-line Help system with Tutorials is included.
Ask TWC BioSearch for a Demonstration Version.
For enhanced features see Mass Spec
Calculator Pro!
This is an excellent companion for the
NIST Mass Spectral Search Program for
Windows!
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section
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