SCHEMBL7235014

SCHEMBL7235014

Cc1ccc(-c2nc3cc(C)ccn3c2CC(=O)O)cc1

nearest known ligand 0.65

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
RAB9A P51151 2/20 0.53
NPC1 O15118 1/20 0.53
KDM4E B2RXH2 4/20 0.52
GABRA1 P14867 2/20 0.52
GABRB2 P47870 2/20 0.52
HSD17B10 Q99714 2/20 0.52
LMNA P02545 1/20 0.52
ALB P02768 1/20 0.52
CYP3A4 P08684 1/20 0.52
CHRM1 P11229 1/20 0.52
HPGD P15428 1/20 0.52
GABRB1 P18505 1/20 0.52
GABRG2 P18507 1/20 0.52
GABRB3 P28472 1/20 0.52
GABRA3 P34903 1/20 0.52
ADRA1A P35348 1/20 0.52
OPRK1 P41145 1/20 0.52
HTR2B P41595 1/20 0.52
GABRA2 P47869 1/20 0.52
KCNH2 Q12809 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
SCHEMBL28396885 0.92 RAB9A (0.62) RAB9ANPC1KDM4ECGASALDH1A1
SCHEMBL7233460 0.91 SMN1; SMN2 (0.52) RAB9ANPC1KDM4ELMNAALB
SCHEMBL14889096 0.89 GAA (0.56) RAB9ANPC1KDM4EHSD17B10CGAS
SCHEMBL7241456 0.88 GABRA1 (0.49) KDM4EGABRA1GABRB2HSD17B10LMNA
SCHEMBL14889093 0.86 RAB9A (0.46) RAB9ANPC1KDM4EHSD17B10CGAS
SCHEMBL5630676 0.86 GABRA1 (0.72) RAB9ANPC1KDM4EGABRA1GABRB2
SCHEMBL1691295 0.85 SMN1; SMN2 (0.51) RAB9ANPC1KDM4EGABRA1GABRB2
SCHEMBL1761287 0.82 GABRA1 (0.74) RAB9ANPC1KDM4EGABRA1GABRB2
SCHEMBL7558746 0.82 KDM4E (0.45) RAB9ANPC1KDM4EHSD17B10CGAS
SCHEMBL7240481 0.81 ALOX5 (0.48) RAB9ANPC1KDM4EGABRA1GABRB2

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 9 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20020032200-A1 2-Substituted imidazo[1,2-A]pyridine derivatives NEUROGEN CORPORATION 2002-03-14 US claimed
WO-2002002557-A2 2-PHENYLIMIDAZO[1,2-A]PYRIDINE DERIVATIVES: A NEW CLASS OF GABA BRAIN RECEPTOR LIGANDS NEUROGEN CORPORATION (US) 2002-01-10 WO claimed
EP-2586780-B1 2-ARYL IMIDAZO[1,2-A]PYRIDINE-3-ACETAMIDE DERIVATIVES, PREPARATION METHODS AND USE THEREOF INST PHARMACOLOGY & TOXICOLOGY ACAD MILITARY MEDICAL SCIENCES PLA CHINA (CN) 2017-03-22 EP disclosed
US-8980887-B2 2-aryl imidazo[1,2-a]pyridine-3-acetamide derivatives, preparation methods and uses thereof INSTITUTE OF PHARMACOLOGY (CN) 2015-03-17 US disclosed
US-20130203754-A1 2-Aryl Imidazo[1,2-a]Pyridine-3-Acetamide Derivatives, Preparation Methods and Uses Thereof INSTITUTE OF PHARMACOLOGY AND TOXICOLOGY ACADEMY OF MILITARY MEDICAL SCIENCES P.L.A. CHINA (CN) 2013-08-08 US disclosed
EP-2586780-A1 2-ARYL IMIDAZO[1,2-A]PYRIDINE-3-ACETAMIDE DERIVATIVES, PREPARATION METHODS AND USE THEREOF Institute Of Pharmacology And Toxicology Academy Of Military Medical Sciences P.L.A. China (CN) 2013-05-01 EP disclosed
US-6552037-B2 An imidazo(1,2-a)Pyridine compound useful for altering the signal-transducing activity of gamma-aminobuytric acid receptor NEUROGEN CORPORATION 2003-04-22 US disclosed
US-20020032200-A1 2-Substituted imidazo[1,2-A]pyridine derivatives NEUROGEN CORPORATION 2002-03-14 US disclosed
WO-2002002557-A2 2-PHENYLIMIDAZO[1,2-A]PYRIDINE DERIVATIVES: A NEW CLASS OF GABA BRAIN RECEPTOR LIGANDS NEUROGEN CORPORATION (US) 2002-01-10 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 (2 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-20130203754-A1 2-Aryl Imidazo[1,2-a]Pyridine-3-Acetamide Derivatives, Preparation Methods and Uses Thereof TSPO, SLC6A1, TBXA2R RAB9A 2262/4885NPC1 780/4885KDM4E 3821/4885
US-20020032200-A1 2-Substituted imidazo[1,2-A]pyridine derivatives GABBR2, GABRP, GABBR1 RAB9A 2092/4885NPC1 941/4885KDM4E 3241/4885

“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.