SCHEMBL10196941

SCHEMBL10196941

O=c1c(Cc2ccc(I)cc2)nc2c(Cc3ccccc3)[nH]c(-c3ccc(O)cc3)cn1-2

nearest known ligand 0.39

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
▸ ABCB1 P08183 1/20 0.39
▸ MTOR P42345 1/20 0.35
▸ CDC7 O00311 2/20 0.34
▸ ALDH1A1 P00352 2/20 0.34
▸ ADORA3 P0DMS8 2/20 0.34
▸ ADORA1 P30542 2/20 0.34
▸ PARP1 P09874 2/20 0.33
▸ XDH P47989 1/20 0.33
▸ LTB4R Q15722 1/20 0.33
▸ AKT2 P31751 2/20 0.33
▸ AKT1 P31749 1/20 0.33
▸ KDM4E B2RXH2 1/20 0.33
▸ HTT P42858 1/20 0.33
▸ TDP1 Q9NUW8 1/20 0.33
▸ ADORA2A P29274 2/20 0.33
▸ ADORA2B P29275 1/20 0.33
▸ MET P08581 1/20 0.32

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL64690 0.95 ABCB1 (0.42) ABCB1MTORCDC7ALDH1A1ADORA3
SCHEMBL12293879 0.95 ABCB1 (0.42) ABCB1MTORCDC7ALDH1A1ADORA3
SCHEMBL954434 0.94 ABCB1 (0.41) ABCB1MTORCDC7ALDH1A1ADORA3
SCHEMBL2680751 0.93 ABCB1 (0.40) ABCB1CDC7ALDH1A1ADORA3ADORA1
SCHEMBL13401854 0.90 ABCB1 (0.39) ABCB1MTORCDC7ALDH1A1ADORA3
SCHEMBL20841761 0.90 ABCB1 (0.39) ABCB1CDC7ALDH1A1ADORA3ADORA1
SCHEMBL20841749 0.90 ABCB1 (0.39) ABCB1MTORCDC7ALDH1A1ADORA3
SCHEMBL10196888 0.90 ABCB1 (0.39) ABCB1CDC7ALDH1A1ADORA3ADORA1
SCHEMBL10196893 0.90 ABCB1 (0.39) ABCB1MTORCDC7ALDH1A1ADORA3
SCHEMBL29887519 0.89 CDC7 (0.43) ABCB1MTORCDC7ALDH1A1ADORA3

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 19 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9645128-B2 Substituted imidazo[1,2-A]pyrazines for measuring a transcription activity JNC CORPORATION (JP) 2017-05-09 — — US disclosed
US-9645128-B2 Substituted imidazo[1,2-A]pyrazines for measuring a transcription activity JNC CORPORATION (JP) 2017-05-09 — — US disclosed
US-20160281129-A1 LUMINESCENT SUBSTRATE FOR USE IN ARTIFICIAL BIOLUMINESCENT ENZYME NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY (JP) 2016-09-29 — — US disclosed
US-20160281129-A1 LUMINESCENT SUBSTRATE FOR USE IN ARTIFICIAL BIOLUMINESCENT ENZYME NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY (JP) 2016-09-29 — — US disclosed
US-20150344936-A1 COELENTERAZINE ANALOGS AND MANUFACTURING METHOD THEREOF TOKYO INSTITUTE OF TECHNOLOGY (JP) 2015-12-03 — — US disclosed
US-20150344936-A1 COELENTERAZINE ANALOGS AND MANUFACTURING METHOD THEREOF TOKYO INSTITUTE OF TECHNOLOGY (JP) 2015-12-03 — — US disclosed
US-9151739-B2 Coelenterazine analogs and manufacturing method thereof JNC CORPORATION (JP) 2015-10-06 — — US disclosed
US-9151739-B2 Coelenterazine analogs and manufacturing method thereof JNC CORPORATION (JP) 2015-10-06 — — US disclosed
US-20140296521-A1 COELENTERAZINE ANALOGS AND MANUFACTURING METHOD THEREOF JNC CORP (JP) 2014-10-02 — — US disclosed
US-20140296521-A1 COELENTERAZINE ANALOGS AND MANUFACTURING METHOD THEREOF JNC CORP (JP) 2014-10-02 — — US disclosed
US-8765921-B2 Coelenterazine analogs and manufacturing method thereof JNC CORPORATION (JP) 2014-07-01 — — US disclosed
US-8765921-B2 Coelenterazine analogs and manufacturing method thereof JNC CORPORATION (JP) 2014-07-01 — — US disclosed
US-20140024058-A1 COELENTERAZINE ANALOGS AND MANUFACTURING METHOD THEREOF TOKYO INSTITUTE OF TECHNOLOGY (JP) 2014-01-23 — — US disclosed
US-20140024058-A1 COELENTERAZINE ANALOGS AND MANUFACTURING METHOD THEREOF TOKYO INSTITUTE OF TECHNOLOGY (JP) 2014-01-23 — — US disclosed
US-8546568-B2 Coelenterazine analogs and manufacturing method thereof JNC CORPORATION (JP) 2013-10-01 — — US disclosed
US-8546568-B2 Coelenterazine analogs and manufacturing method thereof JNC CORPORATION (JP) 2013-10-01 — — US disclosed
US-20120035070-A1 COELENTERAZINE ANALOGS AND MANUFACTURING METHOD THEREOF TOKYO INSTITUTE OF TECHNOLOGY (JP) 2012-02-09 — — US disclosed
US-20120035070-A1 COELENTERAZINE ANALOGS AND MANUFACTURING METHOD THEREOF TOKYO INSTITUTE OF TECHNOLOGY (JP) 2012-02-09 — — US disclosed
WO-2010090319-A1 COELENTERAZINE ANALOGS AND MANUFACTURING METHOD THEREOF チッソ株式会社 (JP) 2010-08-12 — — WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (3 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20140296521-A1 COELENTERAZINE ANALOGS AND MANUFACTURING METHOD THEREOF GLB1, CEL, SI ABCB1 1068/4885MTOR 4256/4885CDC7 2192/4885
US-20160281129-A1 LUMINESCENT SUBSTRATE FOR USE IN ARTIFICIAL BIOLUMINESCENT ENZYME GALC, GUSB, GLB1 ABCB1 3205/4885MTOR 3508/4885CDC7 3588/4885
US-20120035070-A1 COELENTERAZINE ANALOGS AND MANUFACTURING METHOD THEREOF GLB1, CEL, SI ABCB1 1068/4885MTOR 4256/4885CDC7 2192/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.

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