All chiral are missed with `CC1(C)[C@]2(CC[C@@]3(C)[C@]4([H])[C@@H](O)[C@]5([H])O3)[C@@](C1)([H])[C@]5([H])[C@]4([H])O2`
- Dominant language
- C++
- Stars
- 406
- Forks
- 134
- Avg merge
- 2d 11h
- Merged PRs (30d)
- 24
Description
**Steps to Reproduce**
paste smiles `CC1(C)[C@]2(CC[C@@]3(C)[C@]4([H])[C@@H](O)[C@]5([H])O3)[C@@](C1)([H])[C@]5([H])[C@]4([H])O2`
**Actual behavior**
rander in ketcher
**Expected behavior**
should be like
**Screenshots**
**Desktop (please complete the following information):**
- OS: iMac 14.6.1 (23G93)
- Browser chrome 128.0.6613.121
- Version 2.15.1
**Ketcher version** [e.g. v2.4.2].
2.15.1, also confirm same behavior in latest demo page
Contributor guide
No contributing guide indexed for this repository
Research direction
Reproduce the issue in the latest Ketcher demo using the supplied SMILES, then compare the rendered stereochemistry with the expected image. Trace the molecule-rendering entry point responsible for chiral centers; done means all chiral centers in this structure are rendered as expected.
Written by the indexing model from the issue text.
Assessment
- Tech stack
- cpp
- Domain
- computer-graphics
- Issue type
- Bug
- Difficulty
- 4/5
- Estimated time
- 3-5 days
- Activity status
- Stale
- Clarity
- Mostly clear
- Newbie friendliness
- 35/100