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**Is your feature request related to a problem? Please describe.**
The use of wavy wedge bonds may create some confusion when compared to the actual dashed 'down' stereochemistry bonds:
3. Click on 'Save as' button
4. Click on '…
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_Scenario 1_
When structure has Generic S-Group, saved structure does not have brackets
**Steps to reproduce:**
1. Execute /v2/indigo/render
struct
[sstruct.zip](https://github.com/epam/Indigo/…
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The file `cistrans.smi` is missing cases where the bond stereochemistry is indicated to an explicit hydrogen atom, e.g. `FC(/[H])=C/I`, which has been a source of bugs (sometimes on downstream proces…
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RIght, so in openSMILES chirality is very elaborate [1]. I suggest supporting only tetrahedral chiralities, i.e. `@` and `@@` specifications, and later on E/Z chirality. This issue will be just about …
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# Variability of PMI descriptors | RDKit blog
Which is more important, stereochemistry or conformational variability
[https://greglandrum.github.io/rdkit-blog/3d/questions/2022/06/22/variability-of-…
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There is a text overlap of A and is.
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There is a text overlay in Chapter 3 Figure 1b.
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I'm getting this error when assigning partial charges using openeye's am1bccelf1 via the openff-toolkit:
```
def gen_charges(smc):
offmol = smc.to_openff()
offmol.assign_partial_charges(…
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Is there a way perceive the R/S stereochemistry from a structure with marked bonds?
[test_stereo.mol.txt](https://github.com/user-attachments/files/17157917/test_stereo.mol.txt)
For example, read …