shows molecule SMILES
clears the editing area (or the current molecule, if structure contains several parts)
starts new molecule component (when multipart option or reaction input are enabled)
delete mode (click on atom or bond to delete it)
deletes functional group - choose this option and then click bond connecting the group with the main skeleton
starts atom numbering or reaction mapping (when this option is enabled)
query atom / SMARTS (when this option is enabled)
switches between allowed charged states on clicked atom
reaction input (when reactions are enabled)
undo
redo
next ring will be added as a spiro ring
version information and link to the help page
input stereo bond, click existing stereo bond to cycle through possible types (up, dowm, orientation)
powerful chain tool, allows creation of various chains and rings; click single bond to change it to double
allows input of inorganic atoms or atoms in nonstandard valence state (in this case enter the atom symbol enclosed in [], for example the carbene carbon will be [C])
opens functional group popup menu
move selected atom useful when drawing crowded structures (visible when enabled in options)
Rings are added connected by a single bond (when not added to a terminal atom); if you want to add a spiro ring press Shift when adding it. An alternative way to add a spiro ring (that may be used also on touch devices) is to press the icon; the next ring will be then added as spiro.
With single bond selected, a click on existing single bond changes it to double.
With the powerful chain tool you can draw chains, saturated rings and by clicking on single bond change it to a double bond.
Molecule may be moved by "dragging" free space and rotated by pressing also the Shift key.
If you are using JSME often, learn the following shortcuts. They will speed-up your editing considerably.
ESC returns to the standard editing state (carbon, single bond)
d or Del starts delete mode
atoms C, N, O, P, S, F, L (for Cl), B (for Br), I, H, R
bonds - for single bond, = for double bond
rings 3..8 for 3 to 8 membered rings, 1 for phenyl and 0 for furyl
groups a - COOH, y - NO2, z - SO3H, t - tert. butyl, ft - CF3
appears in the menu. To mark an atom the "numbering mode" must be on, selected by clicking the 123 button. The atom number is chosen by pressing respective keys on your keyboard (i.e. 2 or 12); then atom(s) must be clicked. To delete the number pres 0 at your keyboard and then click the atom.
appears in the menu. A new molecule may be started only after clicking this button, then selecting a proper template (atom, ring or bond) and clicking free space in the drawing area. Without clicking the NEW button first clicking the free space has the same effect as in the standard mode (i.e moving or rotation of the last touched molecule). In the multipart mode the button deletes the last touched molecule.
, and appear in the menu and arrow appears also in the drawing area.
Now simply draw reactant(s), product(s) and modulator(s) (modulators have to be above the arrow) as explained in the description of input of multipart structures.
The arrow button enables simplified input of reactions. After clicking it, the reactant will be copied to the product (including atom numbering, if any).
(when enabled in the options) launches a query window that allows creation of SMARTS atom or bond queries by combining various atom attributes. Select the SMARTS options in this panel and then click the respective atom or bond in the molecule.
On supported touch devices, the menu can be opened by “touch and hold” on the surface of the editor.
Keyboard shortcuts Ctrl C (for copy) and Ctrl V (for paste) are supported on most browsers.
