Alternatives and similar repositories for Clipboard-to-SMILES-Converter:

Users that are interested in Clipboard-to-SMILES-Converter are comparing it to the libraries listed below

• JacksonBurns / py2opsin
  Simple Python interface to OPSIN: Open Parser for Systematic IUPAC nomenclature
  ☆51Updated 3 months ago
• ghiander / novana
  Novana is a cheminformatics tool that extends the decomposition of molecules into Bemis-Murcko frameworks.
  ☆52Updated last month
• reymond-group / drfp
  An NLP-inspired chemical reaction fingerprint based on basic set arithmetic.
  ☆66Updated last week
• coleygroup / sparrow
  ☆49Updated last month
• mrodobbe / Rxn-INSIGHT
  Analyzing chemical databases and predicting reaction conditions with cheminformatics
  ☆35Updated last week
• molecularinformatics / Computational-ADME
  ☆84Updated last year
• CDDLeiden / QSPRpred
  A tool for creating Quantitative Structure Property/Activity Relationship (QSPR/QSAR) models.
  ☆68Updated last month
• mqcomplab / bitbirch
  BitBIRCH clustering algorithm
  ☆65Updated 3 weeks ago
• MolecularAI / reaction_utils
  Utilities for working with datasets of chemical reactions, reaction templates and template extraction.
  ☆71Updated 4 months ago
• osmoai / osmordred
  Mordred port in cpp
  ☆48Updated last month
• molecularinformatics / roshambo
  ☆78Updated 8 months ago
• Merck / matcher
  Matcher is a tool for understanding how chemical structure optimization problems have been solved. Matcher enables deep control over sear…
  ☆59Updated last year
• SEDenmarkLab / molli
  Molecular Library Toolbox
  ☆58Updated 3 weeks ago
• durrantlab / dimorphite_dl
  Dimorphite-DL adds hydrogen atoms to molecular representations, as appropriate for a user-specified pH range. It is a fast, accurate, acc…
  ☆30Updated last year
• Academich / reagents
  Reagent prediction with Molecular Transformer. Improvement of data for reaction product prediction in a self-supervised fashion.
  ☆24Updated 6 months ago
• PatWalters / TS
  Thompson Sampling
  ☆66Updated last week
• rdkit / UGM_2023
  Materials from the 2023 RDKit UGM
  ☆34Updated last year
• DrugBud-Suite / CADD_Vault
  ☆47Updated last month
• Laboratoire-de-Chemoinformatique / Synt-On
  Open-source tool for synthons-based library design.
  ☆79Updated 3 months ago
• JanoschMenke / metis
  Python-based GUI to collect Feedback of Chemist in Molecules
  ☆49Updated 6 months ago
• MolecularAI / Lib-INVENT
  ☆56Updated 2 years ago
• mahendra-awale / medchem_moves
  ☆45Updated 4 years ago
• HFooladi / GNNs-For-Chemists
  Implementations of different GNNs from scratch for chemists
  ☆43Updated this week
• RPirie96 / RGMolSA
  ☆34Updated last year
• czodrowskilab / Machine-learning-meets-pKa
  ☆73Updated last year
• AustinT / mol_ga
  Simple, lightweight package for genetic algorithms on molecules
  ☆54Updated 5 months ago
• chython / chython
  Library for processing molecules and reactions in python way
  ☆43Updated 2 months ago
• lich-uct / syba
  Synthetic Bayesian Classification
  ☆41Updated 4 years ago
• DrugBud-Suite / DockM8
  All in one Structure-Based Virtual Screening workflow based on the concept of consensus docking.
  ☆41Updated 2 months ago
• hutchisonlab / QupKake
  Machine Learning model for molecular micro-pKa prediction
  ☆41Updated 6 months ago