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Molecules with Multiple Chiral Centers02:25

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Molecules that possess multiple chiral centers can afford a large number of stereoisomers. For instance, while some molecules like 2-butanol have one chiral center, defined as a tetrahedral carbon atom with four different substituents attached, several molecules like butane-2,3-diol have multiple chiral centers. A simple formula to predict the number of stereoisomers possible for a molecule with n chiral centers is 2n. However, there can be a lower number where some of the stereoisomers are...
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Chirality is a term that describes the lack of mirror symmetry in an object. In other words, chiral objects cannot be superposed on their mirror images. For example, our feet are chiral, as the mirror image of the left foot, the right foot, cannot be superposed on the left foot.
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The concept of prochirality leads to the nomenclature of the individual faces of a molecule and plays a crucial role in the enantioselective reaction. It is a concept where two or more achiral molecules react to produce chiral products. A typical process is the reaction of an achiral ketone to generate a chiral alcohol. Here, the achiral reactant reacts with an achiral reducing agent, sodium borohydride, to generate an equimolar mixture of the chiral enantiomers of the product. For example, an...
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Chirality is most prevalent in carbon-based tetrahedral compounds, but this important facet of molecular symmetry extends to sp3-hybridized nitrogen, phosphorus and sulfur centers, including trivalent molecules with lone pairs. Here, the lone pair behaves as a functional group in addition to the other three substituents to form an analogous tetrahedral center that can be chiral.
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Learning to draw Fischer projections of molecules and understanding their relevance plays a crucial role in the visual depiction of organic molecules. A Fischer projection is a two-dimensional projection on a planar surface to simplify the three-dimensional wedge–dash representation of molecules. This is especially helpful in the case of molecules with multiple chiral centers that can be difficult to draw. Here, all the bonds of interest are represented as horizontal or vertical lines.
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Chirality is the most intriguing yet essential facet of nature, governing life’s biochemical processes and precision. It can be observed from a snail shell pattern in a macroscopic world to an amino acid, the minutest building block of life. Most of the snails around the world have right-coiled shells because of the intrinsic chirality in their genes. All the amino acids present in the human body exist in an enantiomerically pure state, except for glycine - the sole achiral amino acid.
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A Micropatterning Assay for Measuring Cell Chirality
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Identifying Chirality in Line Drawings of Molecules Using Imbalanced Dataset Sampler for a Multilabel Classification

Yong En Kok1, Simon Woodward2, Ender Özcan3

  • 1Computer Vision Laboratory, School of Computer Science, University of Nottingham, Nottingham, NG81BB, UK.

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Summary
This summary is machine-generated.

This study introduces a deep learning approach for identifying molecular chirality, achieving 90% accuracy in binary classification and improving multilabel classification performance by 2% with a novel sampling method.

Keywords:
ChiralityClassificationConvolutional Neural NetworkDeep LearningImage Recognition

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Area of Science:

  • Computational Chemistry
  • Machine Learning
  • Cheminformatics

Background:

  • Chirality is crucial in chemistry and biology, but its automated recognition from molecular structures is challenging.
  • Existing machine-readable molecular representations may not fully capture chirality information.
  • Deep learning advances offer potential for automatic chemical structure recognition, yet chirality discovery remains understudied.

Purpose of the Study:

  • To develop and evaluate deep learning models for classifying molecule chirality (achiral/chiral) and chirality types (none/centre/axial/planar).
  • To address data imbalance issues in multilabel chirality classification using a novel sampling technique.
  • To investigate the interpretability of deep learning models in predicting chirality based on structural elements.

Main Methods:

  • Pretraining deep neural networks on the ChEMBL+ dataset (79,641 molecules).
  • Fine-tuning models for binary and multilabel chirality classification tasks.
  • Implementing a Formulated Imbalanced Dataset Sampler (FIDS) to handle imbalanced label combinations in multilabel classification.
  • Conducting 10-fold cross-validation on a manually curated CHIRAL dataset (1,142 molecules).

Main Results:

  • Achieved up to 90% accuracy in binary chirality classification.
  • The multilabel classification task, enhanced by FIDS, showed an overall performance increase from 87% to 89%.
  • Accuracy per label combination in the multilabel task improved by up to 50% with FIDS.
  • Heatmap analysis demonstrated the models' ability to predict chirality based on specific molecular locations.

Conclusions:

  • Deep learning models can effectively classify molecular chirality and chirality types.
  • The proposed FIDS method significantly improves performance in imbalanced multilabel chirality classification.
  • The study highlights the potential of deep learning for interpretable chirality prediction, linking predictions to specific structural features.