SCHEMBL5778843

SCHEMBL5778843

C(#Cc1ccc2ccccc2n1)c1ccccc1

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GRM5 P41594 10/20 0.62
KCNH2 Q12809 3/20 0.62
TTR P02766 1/20 0.61
NPC1 O15118 2/20 0.52
RAB9A P51151 2/20 0.52
SMN1; SMN2 Q16637 2/20 0.52
CYP1A2 P05177 2/20 0.52
KDM4E B2RXH2 1/20 0.52
MEN1 O00255 1/20 0.52
ALDH1A1 P00352 1/20 0.52
TP53 P04637 1/20 0.52
CYP3A4 P08684 1/20 0.52
CYP2D6 P10635 1/20 0.52
CYP2C9 P11712 1/20 0.52
PKM P14618 1/20 0.52
HPGD P15428 1/20 0.52
ALOX15 P16050 1/20 0.52
CYP2C19 P33261 1/20 0.52
THPO P40225 1/20 0.52
KMT2A Q03164 1/20 0.52

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
SCHEMBL12884286 0.94 GRM5 (0.65) GRM5KCNH2TTRNPC1RAB9A
SCHEMBL15422868 0.85 TTR (0.68) GRM5KCNH2TTRNPC1RAB9A
SCHEMBL21858065 0.85 GRM5 (0.56) GRM5KCNH2TTRNPC1RAB9A
SCHEMBL484570 0.85 GRM5 (0.56) GRM5KCNH2TTRNPC1RAB9A
SCHEMBL12884290 0.85 TTR (0.62) GRM5KCNH2TTRCYP1A2ALDH1A1
SCHEMBL15877809 0.83 GRM5 (0.59) GRM5KCNH2TTRCYP1A2CYP3A4
SCHEMBL15877543 0.82 GRM5 (0.56) GRM5KCNH2TTRNCF1NOS2
SCHEMBL2808633 0.81 TTR (0.55) GRM5KCNH2TTRNPC1RAB9A
SCHEMBL2808776 0.81 TTR (0.62) GRM5KCNH2TTRNPC1RAB9A
SCHEMBL4713149 0.81 TTR (0.55) GRM5KCNH2TTRCA12CA9

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 21 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8946431-B2 2-(substituted ethynyl)quinoline derivatives as mGLUr5 antagonists KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY (KR) 2015-02-03 US claimed
US-20140206876-A1 2-(Substituted ethynyl)quinoline Derivatives as mGLUr5 Antagonists KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY (KR) 2014-07-24 US claimed
US-9879004-B2 Substituted acetylene derivatives and their use as positive allosteric modulators of mGluR4 MERCK PATENT GMBH (DE) 2018-01-30 US disclosed
US-9815788-B2 Anti-angiogenic compounds THE PROVOST, FELLOWS, FOUNDATION SCHOLARS, AND THE OTHER MEMBERS OF BOARD, OF THE COLLEGE OF THE HOLY AND UNDIVIDED TRINITY OF QUEEN ELIZABETH NEAR DUBLIN (IE) 2017-11-14 US disclosed
US-9815788-B2 Anti-angiogenic compounds THE PROVOST, FELLOWS, FOUNDATION SCHOLARS, AND THE OTHER MEMBERS OF BOARD, OF THE COLLEGE OF THE HOLY AND UNDIVIDED TRINITY OF QUEEN ELIZABETH NEAR DUBLIN (IE) 2017-11-14 US disclosed
US-20170050930-A1 ANTI-ANGIOGENIC COMPOUNDS UNIVERSITY COLLEGE DUBLIN NATIONAL UNIVERSITY OF IRELAND, DUBLIN (IE) 2017-02-23 US disclosed
US-20170050930-A1 ANTI-ANGIOGENIC COMPOUNDS UNIVERSITY COLLEGE DUBLIN NATIONAL UNIVERSITY OF IRELAND, DUBLIN (IE) 2017-02-23 US disclosed
US-9388138-B2 Anti-angiogenic compounds UNIVERSITY COLLEGE DUBLIN NATIONAL UNIVERSITY OF IRELAND, DUBLIN (IE) 2016-07-12 US disclosed
US-9388138-B2 Anti-angiogenic compounds UNIVERSITY COLLEGE DUBLIN NATIONAL UNIVERSITY OF IRELAND, DUBLIN (IE) 2016-07-12 US disclosed
US-20150376182-A1 Substituted Acetylene Derivatives and their Use as Positive Allosteric Modulators of mGluR4 MERCK PATENT GMBH (DE) 2015-12-31 US disclosed
EP-2953933-A1 SUBSTITUTED ACETYLENE DERIVATIVES AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR4 Merck Patent GmbH (DE) 2015-12-16 EP disclosed
US-20150218100-A1 ANTI-ANGIOGENIC COMPOUNDS UNIVERSITY COLLEGE DUBLIN NATIONAL UNIVERSITY OF IRELAND, DUBLIN (IE) 2015-08-06 US disclosed
US-8946431-B2 2-(substituted ethynyl)quinoline derivatives as mGLUr5 antagonists KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY (KR) 2015-02-03 US disclosed
WO-2014121883-A1 SUBSTITUTED ACETYLENE DERIVATIVES AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR4 MERCK PATENT GMBH (DE) 2014-08-14 WO disclosed
US-20140206876-A1 2-(Substituted ethynyl)quinoline Derivatives as mGLUr5 Antagonists KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY (KR) 2014-07-24 US disclosed
EP-1032393-B1 QUINOLINE-CONTAINING ALPHA-KETOAMIDE CYSTEINE AND SERINE PROTEASE INHIBITORS CEPHALON INC (US) 2006-08-09 EP disclosed
EP-1032393-A4 QUINOLINE-CONTAINING ALPHA-KETOAMIDE CYSTEINE AND SERINE PROTEASE INHIBITORS CEPHALON INC (US) 2002-06-12 EP disclosed
EP-1032393-A1 QUINOLINE-CONTAINING $g(a)-KETOAMIDE CYSTEINE AND SERINE PROTEASE INHIBITORS CEPHALON, INC. (US) 2000-09-06 EP disclosed
US-6083944-A ENZYME INHIBITORS; TREATMENT OF VARIOUS DEBILITATING DISORDERS CEPHALON, INC. (US) 2000-07-04 US disclosed
WO-1999017775-A1 QUINOLINE-CONTAINING α-KETOAMIDE CYSTEINE AND SERINE PROTEASE INHIBITORS CEPHALON INC. (US) 1999-04-15 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 (4 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-20150376182-A1 Substituted Acetylene Derivatives and their Use as Positive Allosteric Modulators of mGluR4 GRM4, GRIA4, GRIK4 GRM5 6/4885KCNH2 2236/4885TTR 4837/4885
US-20170050930-A1 ANTI-ANGIOGENIC COMPOUNDS VEGFA, FLT4, VHL GRM5 3709/4885KCNH2 4753/4885TTR 1646/4885
US-20150218100-A1 ANTI-ANGIOGENIC COMPOUNDS VEGFA, FLT4, VHL GRM5 3709/4885KCNH2 4753/4885TTR 1646/4885
US-20140206876-A1 2-(Substituted ethynyl)quinoline Derivatives as mGLUr5 Antagonists GRM5, GRIK5, GRIA4 GRM5 1/4885KCNH2 1318/4885TTR 3319/4885

“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.