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ReactionClassifier

imported

therapeutics/reactionclassifier

Fast, lightweight reaction classification with high granularity

Machine-generated from the listed sources and not yet reviewed by a human.

ReactionClassifier project image
GitHub preview card for schwallergroup/ReactionClassifier. Served by its origin, not stored here, and not covered by this registry’s licence.
record
Category
Therapeutics
Subcategory
unknown
License
MIT(osi)
Status
active
Maturity
deployed
Organization
schwallergroup
Country
unknown
Homepage
unknown
Documentation
unknown
Tags
cheminformatics · cheminformatics-software · organic-chemistry · reaction-classification · reaction-smiles
Regulatory
unknown
built by · 1

Top contributors by commit count, from the project’s public repository. Avatars are served by their origin, not stored here. To be removed from this list, open an issue.

similar by tags

Computed from shared tags, weighted so a rare tag counts for more than a common one. These are suggestions, not curated relationships.

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    Deterministic classification, naming, and analysis of chemical reactions

  • SMILESAugmentationcheminformatics · reaction-smiles

    SMILES, SELFIES and Reaction SMILES augmentation using RDKit

  • BARSICcheminformatics · cheminformatics-software

    DDL SQL code to create a set of user-defined functions in Snowflake to enable chemical structure queries (exact structure, substructure, superstructure, similarity), chemistry data file import and…

  • bbleancheminformatics · cheminformatics-software

    BitBIRCH-Lean, a memory-efficient implementation of BitBIRCH designed for high-throughput clustering of huge molecular libraries

  • BChemXtractWebcheminformatics · cheminformatics-software

    Parse CDX and CDXML files directly in the browser. Extract structures and reactions with InChI, SMILES, RInChI, and formulas. Export instantly to JSON, SDF/Mol, TSV, and images—no installation or…

  • logD_predictorcheminformatics · cheminformatics-software

    Prediction of CHI logD from ¹H/¹³C NMR spectra and molecular fingerprints using ML and deep learning.

sources
  1. api.github.com/repos/schwallergroup/ReactionClassifier
    retrieved 2026-08-05 · via github-api

    Machine-imported from GitHub search. Last push 2026-07-13, 26 stars, license reported as MIT. Category and schematic were assigned by keyword heuristics and are unreviewed.

Not yet verified by a human. Correct this record →

machine-readable

/v1/entries/11.json→ .entries["reactionclassifier"]

Entries are sharded 64 ways by a stable hash of the id, so a consumer can find any record without an index.