On InChI and evaluating the quality of cross-reference links.: Galgonek, Jakub; Vondrášek, Jiří
{J Cheminform 6 15 (2014).}
https://staging.inchi-trust.info

Comparative evaluation of open source software for mapping between metabolite identifiers in metabolic network reconstructions: application to Recon 2.: Haraldsdóttir, Hulda S.; Thiele, Ines; Fleming, Ronan Mt
{J Cheminform 6 2 (2014).}
https://staging.inchi-trust.info

InChI – the worldwide chemical structure identifier standard.: Heller, Stephen; McNaught, Alan; Stein, Stephen; Tchekhovskoi, Dmitrii; Pletnev, Igor
{J Cheminform 5 7 (2013).}
https://www.doi.org/10.1186/1758-2946-5-7

Applications of the InChI in cheminformatics with the CDK and Bioclipse.: Spjuth, Ola; Berg, Arvid; Adams, Samuel; Willighagen, Egon L.
{J Cheminform 5 14 (2013)}
https://doi.org/10.1186/1758-2946-5-14

MMsDusty: an Alternative InChI-Based Tool to Minimize Chemical Redundancy.: Fanton, Marco; Floris, Matteo; Cristiani, Andrea; Olla, Stefania; Medda, Ricardo; Sabbadin, Davide; Bulfone, Alessandro; Moro, Stefano
{Mol Inform 32 681-684 (2013).}
https://staging.inchi-trust.info

InChI in the wild: an assessment of InChIKey searching in Google.: Southan, Christopher
{J Cheminform 5 10 (2013).}
https://staging.inchi-trust.info

Extracting and connecting chemical structures from text sources using chemicalize.org.: Southan, Christopher; Stracz, Andras
{J Cheminform 5 20 (2013).}
https://staging.inchi-trust.info

Extending the “web of drug identity” with knowledge extracted from United States product labels.: Hassanzadeh, Oktie; Zhu, Qian; Freimuth, Robert; Boyce, Richard
{AMIA Jt Summits Transl Sci Proc 2013 64-68 (2013).}
https://staging.inchi-trust.info

CVDHD: a cardiovascular disease herbal database for drug discovery and network pharmacology.: Gu, Jiangyong; Gui, Yuanshen; Chen, Lirong; Yuan, Gu; Xu, Xiaojie
{J Cheminform 5 51 (2013).}
https://staging.inchi-trust.info

Ambit-Tautomer: An Open Source Tool for Tautomer Generation.: Kochev, Nikolay T.; Paskaleva, Vesselina H.; Jeliazkova, Nina
{Mol Inform 32 481-504 (2013).}
https://staging.inchi-trust.info

MetaboSearch: tool for mass-based metabolite identification using multiple databases.: Zhou, Bin; Wang, Jinlian; Ressom, Habtom W.
{PLoS One 7 e40096 (2012).}
10.1371/journal.pone.0040096

InChI: a user’s perspective.: Bachrach, Steven M.
{ J Cheminform 4 34 (2012).}
10.1186/1758-2946-4-34

yaInChI: modified InChI string scheme for line notation of chemical structures.: Cho, Y. S.; No, K. T.; Cho, K.-H.
{SAR QSAR Environ Res 23 237-255 (2012).}
10.1080/1062936X.2012.657677

Towards a Universal SMILES representation – A standard method to generate canonical SMILES based on the InChI.: O'Boyle, Noel M.
{J Cheminform 4 22 (2012).}
https://staging.inchi-trust.info

InChIKey collision resistance: an experimental testing.: Pletnev, Igor; Erin, Andrey; McNaught, Alan; Blinov, Kirill; Tchekhovskoi, Dmitrii; Heller, Steve
{J Cheminform 4 39 (2012).}
https://doi.org/10.1186/1758-2946-4-39

InChI: connecting and navigating chemistry.: Williams, Antony J.
{J Cheminform 4 33 (2012).}
https://staging.inchi-trust.info

Consistency of systematic chemical identifiers within and between small-molecule databases.: Akhondi, Saber A.; Kors, Jan A.; Muresan, Sorel
{J Cheminform 4 35 (2012).}
https://staging.inchi-trust.info

IUPAC International Chemical Identifier–InChI Update.:
{Chem Int -- Newsmag Iupac 31 (3) 21–21 (2009).}
https://doi.org/10.1515/ci.2009.31.3.21a

InChI 1.01: Clark, Alex M.; McEwen, Leah R.; Gedeck, Peter; Bunin, Barry A.
{Newsmag Iupac 28 (6), 23–23 (2006).}
https://doi.org/10.1515/ci.2006.28.6.23a

Enhancement of the Chemical Semantic Web through the Use of InChI Identifiers: Coles, Simon J., Day, Nick E., Murray-Rust, Peter, Rzepa, Henry S., Zhang, Yong
{Org Biomol Chem 3 (10) 1832–1834 (2005).}
https://doi.org/10.1039/b502828k