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Open Source Chemistry Library
/*
* Copyright (c) 1997 - 2016
* Actelion Pharmaceuticals Ltd.
* Gewerbestrasse 16
* CH-4123 Allschwil, Switzerland
*
* All rights reserved.
*
* Redistribution and use in source and binary forms, with or without
* modification, are permitted provided that the following conditions are met:
*
* 1. Redistributions of source code must retain the above copyright notice, this
* list of conditions and the following disclaimer.
* 2. Redistributions in binary form must reproduce the above copyright notice,
* this list of conditions and the following disclaimer in the documentation
* and/or other materials provided with the distribution.
* 3. Neither the name of the the copyright holder nor the
* names of its contributors may be used to endorse or promote products
* derived from this software without specific prior written permission.
*
* THIS SOFTWARE IS PROVIDED BY THE COPYRIGHT HOLDERS AND CONTRIBUTORS "AS IS" AND
* ANY EXPRESS OR IMPLIED WARRANTIES, INCLUDING, BUT NOT LIMITED TO, THE IMPLIED
* WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE ARE
* DISCLAIMED. IN NO EVENT SHALL THE COPYRIGHT OWNER OR CONTRIBUTORS BE LIABLE FOR
* ANY DIRECT, INDIRECT, INCIDENTAL, SPECIAL, EXEMPLARY, OR CONSEQUENTIAL DAMAGES
* (INCLUDING, BUT NOT LIMITED TO, PROCUREMENT OF SUBSTITUTE GOODS OR SERVICES;
* LOSS OF USE, DATA, OR PROFITS; OR BUSINESS INTERRUPTION) HOWEVER CAUSED AND
* ON ANY THEORY OF LIABILITY, WHETHER IN CONTRACT, STRICT LIABILITY, OR TORT
* (INCLUDING NEGLIGENCE OR OTHERWISE) ARISING IN ANY WAY OUT OF THE USE OF THIS
* SOFTWARE, EVEN IF ADVISED OF THE POSSIBILITY OF SUCH DAMAGE.
*
* @author Thomas Sander
*/
package com.actelion.research.gui;
import com.actelion.research.chem.*;
import com.actelion.research.chem.name.StructureNameResolver;
import com.actelion.research.gui.clipboard.IClipboardHandler;
import com.actelion.research.gui.dnd.MoleculeDragAdapter;
import com.actelion.research.gui.dnd.MoleculeDropAdapter;
import com.actelion.research.gui.dnd.MoleculeTransferable;
import com.actelion.research.gui.generic.GenericDepictor;
import com.actelion.research.gui.generic.GenericPolygon;
import com.actelion.research.gui.generic.GenericRectangle;
import com.actelion.research.gui.generic.GenericShape;
import com.actelion.research.gui.hidpi.HiDPIHelper;
import com.actelion.research.gui.swing.SwingCursorHelper;
import com.actelion.research.gui.swing.SwingDrawContext;
import com.actelion.research.util.ColorHelper;
import javax.swing.*;
import java.awt.*;
import java.awt.datatransfer.StringSelection;
import java.awt.datatransfer.Transferable;
import java.awt.dnd.*;
import java.awt.event.*;
import java.awt.geom.Rectangle2D;
import java.util.ArrayList;
public class JStructureView extends JComponent implements ActionListener,MouseListener,MouseMotionListener,StructureListener {
private static final long serialVersionUID = 0x20061113;
private static final Color DEFAULT_SELECTION_BACKGROUND = new Color(128,164,192);
private static final String ITEM_COPY = "Copy Structure";
private static final String ITEM_COPY_SMILES = "Copy Structure As SMILES-String";
private static final String ITEM_PASTE= "Paste Structure";
private static final String ITEM_PASTE_WITH_NAME = ITEM_PASTE+" or Name";
private static final String ITEM_CLEAR = "Clear Structure";
private static final long WARNING_MILLIS = 1200;
private static final int DRAG_MARGIN = 12;
private ArrayList mListener;
private String mIDCode;
private StereoMolecule mMol,mDisplayMol;
private GenericDepictor mDepictor;
private boolean mShowBorder,mAllowFragmentStatusChangeOnPasteOrDrop,mIsDraggingThis,mIsEditable,mDisableBorder,
mIsSelectable,mIsSelecting,mIsLassoSelect;
private int mChiralTextPosition,mDisplayMode;
private String[] mAtomText;
private IClipboardHandler mClipboardHandler;
protected MoleculeDropAdapter mDropAdapter = null;
protected int mAllowedDragAction;
protected int mAllowedDropAction;
private String mWarningMessage;
private int[] mAtomHiliteColor;
private float[] mAtomHiliteRadius;
private double mTextSizeFactor,mX1,mY1,mX2,mY2;
private GenericPolygon mLassoRegion;
public JStructureView() {
this(null);
}
/**
* This creates a standard structure view where the displayed molecule is
* used for D&D and clipboard transfer after removing atom colors and bond highlights.
* The default will support copy/paste and drag&drop from this view only,
* but dropping anything onto this view doesn't have an effect.
* Call setEditable(true) to allow changes through drag&drop and pasting.
* @param mol used for display, clipboard copy and d&d
*/
public JStructureView(StereoMolecule mol) {
this(mol, DnDConstants.ACTION_COPY_OR_MOVE, DnDConstants.ACTION_COPY_OR_MOVE);
}
/**
* This creates a structure view that distinguishes between displayed molecule
* and the one being used for D&D and clipboard transfer. Use this if the displayed
* molecule is structurally different, e.g. uses custom atom labels or additional
* illustrative atoms or bonds, which shall not be copied.
* Custom atom colors or highlighted bonds don't require a displayMol.
* The default will support copy/paste and drag&drop from this view only,
* but dropping anything onto this view doesn't have an effect.
* Call setEditable(true) to allow changes through drag&drop and pasting.
* @param mol used for clipboard copy and d&d; used for display if displayMol is null
* @param displayMol null if mol shall be displayed
*/
public JStructureView(StereoMolecule mol, StereoMolecule displayMol) {
this(mol, displayMol, DnDConstants.ACTION_COPY_OR_MOVE, DnDConstants.ACTION_COPY_OR_MOVE);
}
public JStructureView(int dragAction, int dropAction) {
this(null, dragAction, dropAction);
}
/**
* This creates a standard structure view where the displayed molecule is
* used for D&D and clipboard transfer after removing atom colors and bond highlights.
* The default will support copy/paste and drag&drop from this view only,
* but dropping anything onto this view doesn't have an effect.
* Call setEditable(true) to allow changes through drag&drop and pasting.
* @param mol used for display, clipboard copy and d&d
* @param dragAction
* @param dropAction
*/
public JStructureView(StereoMolecule mol, int dragAction, int dropAction) {
this(mol, null, dragAction, dropAction);
}
/**
* This creates a structure view that distinguishes between displayed molecule
* and the one being used for D&D and clipboard transfer. Use this if the displayed
* molecule is structurally different, e.g. uses custom atom labels or additional
* illustrative atoms or bonds, which shall not be copied.
* Custom atom colors or highlighted bonds don't require a displayMol.
* The default will support copy/paste and drag&drop from this view only,
* but dropping anything onto this view doesn't have an effect.
* Call setEditable(true) to allow changes through drag&drop and pasting.
* @param mol used for clipboard copy and d&d; used for display if displayMol is null
* @param displayMol null if mol shall be displayed
* @param dragAction
* @param dropAction
*/
public JStructureView(StereoMolecule mol, StereoMolecule displayMol, int dragAction, int dropAction) {
mMol = (mol == null) ? new StereoMolecule() : new StereoMolecule(mol);
mDisplayMol = (displayMol == null) ? mMol : displayMol;
mDisplayMode = AbstractDepictor.cDModeHiliteAllQueryFeatures;
mTextSizeFactor = 1.0;
mIsEditable = false;
updateBackground();
addMouseListener(this);
addMouseMotionListener(this);
initializeDragAndDrop(dragAction, dropAction);
}
public void setSelectable(boolean s) {
mIsSelectable = s;
}
@Override
public void updateUI() {
super.updateUI();
updateBackground();
}
/**
* Call this in order to get clipboard support:
* setClipboardHandler(new ClipboardHandler());
*/
public void setClipboardHandler(IClipboardHandler h) {
mClipboardHandler = h;
}
public IClipboardHandler getClipboardHandler() {
return mClipboardHandler;
}
public int getDisplayMode() {
return mDisplayMode;
}
/**
* Sets the display mode for the Depictor. The default is
* AbstractDepictor.cDModeHiliteAllQueryFeatures.
* @param mode
*/
public void setDisplayMode(int mode) {
if (mDisplayMode != mode) {
mDisplayMode = mode;
repaint();
}
}
/**
* Sets a multiplication factor to the text size of all labels. The default is 1.0.
* @param factor text size factor
*/
public void setFactorTextSize(double factor) {
mTextSizeFactor = factor;
}
public void setDisableBorder(boolean b) {
mDisableBorder = b;
}
/**
* Defines additional atom text to be displayed in top right
* position of some/all atom labels. If the atom is charged, then
* the atom text is drawn right of the atom charge.
* If using atom text make sure to update it accordingly, if atom
* indexes change due to molecule changes.
* Atom text is not supported for MODE_REACTION, MODE_MULTIPLE_FRAGMENTS or MODE_MARKUSH_STRUCTURE.
* @param atomText null or String array matching atom indexes (may contain null entries)
*/
public void setAtomText(String[] atomText) {
mAtomText = atomText;
}
public void setEnabled(boolean enable) {
if (enable != isEnabled()) {
updateBackground();
repaint();
if (mDropAdapter != null)
mDropAdapter.setActive(enable);
}
super.setEnabled(enable);
}
public boolean isEditable() {
return mIsEditable;
}
public void setEditable(boolean b) {
if (mIsEditable != b)
mIsEditable = b;
}
/**
* When fragment status change on drop is allowed then dropping a fragment (molecule)
* on a molecule (fragment) inverts the status of the view's chemical object.
* As default status changes are prohibited.
* @param allow
*/
public void setAllowFragmentStatusChangeOnPasteOrDrop(boolean allow) {
mAllowFragmentStatusChangeOnPasteOrDrop = allow;
}
/**
* If you want this structure view to also draw an atom background with specific colors for every atom,
* then you need to call this method before or just after one of the structureChanged() calls.
* @param argb if alpha < 1 then the background is mixed in accordingly
* @param radius <= 1.0; if null, then a default of 0.5 of the average bond length is used
*/
public void setAtomHighlightColors(int[] argb, float[] radius) {
mAtomHiliteColor = argb;
mAtomHiliteRadius = radius;
repaint();
}
public boolean canDrop() {
return mIsEditable && isEnabled() && !mIsDraggingThis;
}
@Override
public synchronized void paintComponent(Graphics g) {
super.paintComponent(g);
Dimension theSize = getSize();
Insets insets = getInsets();
theSize.width -= insets.left + insets.right;
theSize.height -= insets.top + insets.bottom;
if (theSize.width <= 0 || theSize.height <= 0)
return;
Graphics2D g2 = (Graphics2D)g;
g2.setRenderingHint(RenderingHints.KEY_ANTIALIASING, RenderingHints.VALUE_ANTIALIAS_ON);
g2.setRenderingHint(RenderingHints.KEY_STROKE_CONTROL, RenderingHints.VALUE_STROKE_PURE);
g2.setRenderingHint(RenderingHints.KEY_FRACTIONALMETRICS, RenderingHints.VALUE_FRACTIONALMETRICS_ON);
Color fg = g2.getColor();
Color bg = getBackground();
g2.setColor(bg);
g2.fill(new Rectangle(insets.left, insets.top, theSize.width, theSize.height));
if (mShowBorder && !mDisableBorder) {
GenericRectangle rect = mDepictor.getBoundingRect();
if (rect != null) {
g.setColor(ColorHelper.perceivedBrightness(bg) < 0.5f ? ColorHelper.brighter(bg, 0.85f) : ColorHelper.darker(bg, 0.85f));
int arc = (int)Math.min(rect.height/4, Math.min(rect.width/4, HiDPIHelper.scale(10)));
g.fillRoundRect((int)rect.x, (int)rect.y, (int)rect.width, (int)rect.height, arc, arc);
}
}
g2.setColor(fg);
if (mDisplayMol != null && mDisplayMol.getAllAtoms() != 0) {
mDepictor = new GenericDepictor(mDisplayMol);
mDepictor.setDisplayMode(mDisplayMode);
mDepictor.setFactorTextSize(mTextSizeFactor);
mDepictor.setAtomText(mAtomText);
mDepictor.setAtomHighlightColors(mAtomHiliteColor, mAtomHiliteRadius);
int bgRGB = bg.getRGB();
if (!isEnabled())
mDepictor.setOverruleColor(ColorHelper.getContrastColor(0x808080, bgRGB), bgRGB);
else
mDepictor.setForegroundColor(getForeground().getRGB(), bgRGB);
int avbl = HiDPIHelper.scale(AbstractDepictor.cOptAvBondLen);
SwingDrawContext context = new SwingDrawContext((Graphics2D)g);
mDepictor.validateView(context, new GenericRectangle(insets.left, insets.top, theSize.width,theSize.height),
AbstractDepictor.cModeInflateToMaxAVBL | mChiralTextPosition | avbl);
mDepictor.paint(context);
}
if (mWarningMessage != null) {
int fontSize = HiDPIHelper.scale(12);
g.setFont(getFont().deriveFont(Font.BOLD, (float)fontSize));
Color original = g.getColor();
g.setColor(Color.RED);
FontMetrics metrics = g.getFontMetrics();
Rectangle2D bounds = metrics.getStringBounds(mWarningMessage, g);
g.drawString(mWarningMessage, insets.left+(int)(theSize.width-bounds.getWidth())/2,
insets.top+metrics.getHeight());
g.setColor(original);
}
if (mIsSelecting) {
if (mIsLassoSelect) {
g.setColor(lassoColor());
java.awt.Polygon p = new java.awt.Polygon();
for (int i = 0; i();
mListener.add(l);
}
public void removeStructureListener(StructureListener l) {
if(mListener != null)
mListener.remove(l);
}
public void setChiralDrawPosition(int p) {
mChiralTextPosition = p;
}
@Override public void mouseClicked(MouseEvent e) {}
@Override public void mouseEntered(MouseEvent e) {}
@Override public void mouseExited(MouseEvent e) {}
@Override
public void mousePressed(MouseEvent e) {
if (handlePopupTrigger(e))
return;
if (mIsSelectable
&& (e.getModifiers() & InputEvent.BUTTON1_MASK) != 0) {
mX1 = e.getX();
mY1 = e.getY();
mIsSelecting = true;
mIsLassoSelect = !e.isAltDown();
if (mIsLassoSelect) {
mLassoRegion = new GenericPolygon();
mLassoRegion.addPoint(mX1, mY1);
mLassoRegion.addPoint(mX1, mY1);
}
}
}
@Override
public void mouseReleased(MouseEvent e) {
if (mIsSelecting) {
mIsSelecting = false;
repaint();
}
handlePopupTrigger(e);
}
@Override
public void mouseMoved(MouseEvent e) {
int x = e.getX();
int y = e.getY();
boolean isInRect = mDepictor != null
&& (mAllowedDragAction & DnDConstants.ACTION_COPY) != 0
&& shrink(mDepictor.getBoundingRect()).contains(x, y);
updateBorder(isInRect);
setCursor(SwingCursorHelper.getCursor(isInRect ? SwingCursorHelper.cHandCursor : SwingCursorHelper.cPointerCursor));
}
private GenericRectangle shrink(GenericRectangle rect) {
int margin = HiDPIHelper.scale(DRAG_MARGIN);
int marginX = Math.min(margin, (int)rect.width / 6);
int marginY = Math.min(margin, (int)rect.height / 6);
return new GenericRectangle((int)rect.x+marginX, (int)rect.y+marginY, (int)rect.width-2*marginX, (int)rect.height-2*marginY);
}
@Override public void mouseDragged(MouseEvent e) {
if (mIsSelecting) {
mX2 = e.getX();
mY2 = e.getY();
GenericShape selectedShape = null;
if (mIsLassoSelect) {
if ((Math.abs(mX2 - mLassoRegion.getX(mLassoRegion.getSize() - 1)) >= 3)
|| (Math.abs(mY2 - mLassoRegion.getY(mLassoRegion.getSize() - 1)) >= 3)) {
mLassoRegion.removeLastPoint();
mLassoRegion.addPoint(mX2, mY2);
mLassoRegion.addPoint(mX1, mY1);
selectedShape = mLassoRegion;
}
}
else {
selectedShape = new GenericRectangle(Math.min(mX1, mX2), Math.min(mY1, mY2), Math.abs(mX2 - mX1), Math.abs(mY2 - mY1));
}
if (selectedShape != null && mDepictor != null) {
for (int atom=0; atom {
try { Thread.sleep(WARNING_MILLIS); } catch (InterruptedException ie) {}
mWarningMessage = null;
repaint();
} ).start();
}
private void updateBackground() {
Color bg = UIManager.getColor(isEditable() && isEnabled() ? "TextField.background" : "TextField.inactiveBackground");
if (bg != null)
setBackground(bg);
}
private boolean handlePopupTrigger(MouseEvent e) {
if (!e.isPopupTrigger())
return false;
if (mMol != null && mClipboardHandler != null) {
JPopupMenu popup = new JPopupMenu();
JMenuItem item1 = new JMenuItem(ITEM_COPY);
item1.addActionListener(this);
item1.setEnabled(mMol.getAllAtoms() != 0);
popup.add(item1);
JMenuItem itemCopySmiles = new JMenuItem(ITEM_COPY_SMILES);
itemCopySmiles.addActionListener(this);
itemCopySmiles.setEnabled(mMol.getAllAtoms() != 0);
popup.add(itemCopySmiles);
if (mIsEditable) {
String itemText = StructureNameResolver.getInstance() == null ? ITEM_PASTE : ITEM_PASTE_WITH_NAME;
JMenuItem item2 = new JMenuItem(itemText);
item2.addActionListener(this);
popup.add(item2);
popup.addSeparator();
JMenuItem item3 = new JMenuItem(ITEM_CLEAR);
item3.addActionListener(this);
item3.setEnabled(mMol.getAllAtoms() != 0);
popup.add(item3);
}
popup.show(this, e.getX(), e.getY());
}
return true;
}
private void informListeners() {
if (mListener != null)
for (int i = 0; i getNativesForFlavors(DataFlavor[] dfs) {
// System.out.println("getNativesForFlavors " + dfs.length);
// for (int i = 0; i < dfs.length; i++)
// System.out.println(" -> " + dfs[i]);
//
return SystemFlavorMap.getDefaultFlavorMap().getNativesForFlavors(dfs);
}
public java.util.Map getFlavorsForNatives(String[] natives) {
// System.out.println("getFlavorsForNatives " + natives.length);
// for (int i = 0; i < natives.length; i++)
// System.out.println(" -> " + natives[i]);
//
return SystemFlavorMap.getDefaultFlavorMap().getFlavorsForNatives(natives);
}
public synchronized java.util.List getFlavorsForNative(String nat) {
// System.out.println("getFlavorsForNative " + nat);
return ((SystemFlavorMap)SystemFlavorMap.getDefaultFlavorMap()).getFlavorsForNative(nat);
}
public synchronized java.util.List getNativesForFlavor(DataFlavor flav) {
// System.out.println("getNativesForFlavor " + flav);
return ((SystemFlavorMap)SystemFlavorMap.getDefaultFlavorMap()).getNativesForFlavor(flav);
}
}*/
}