SCHEMBL970334

SCHEMBL970334

Ic1ccc(-c2cn3ccccc3n2)cc1

nearest known ligand 0.73

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
RAB9A P51151 12/20 0.73
NPC1 O15118 11/20 0.73
KDM4E B2RXH2 9/20 0.73
POLB P06746 1/20 0.73
GFER P55789 3/20 0.71
PKM P14618 5/20 0.67
EPHX2 P34913 1/20 0.67
HDAC6 Q9UBN7 1/20 0.63
MEN1 O00255 1/20 0.62
GAA P10253 1/20 0.62
MIF P14174 1/20 0.62
KMT2A Q03164 1/20 0.62
ALDH1A1 P00352 7/20 0.61
SMN1; SMN2 Q16637 7/20 0.61
MAPK1 P28482 3/20 0.61
HPGD P15428 3/20 0.58
NFKB1 P19838 2/20 0.58
NFKB2 Q00653 2/20 0.58
RELA Q04206 2/20 0.58
PTGS1 P23219 1/20 0.57

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
SCHEMBL13325909 0.93 RAB9A (0.83) RAB9ANPC1KDM4EPOLBGFER
SCHEMBL13325938 0.91 RAB9A (0.80) RAB9ANPC1KDM4EPOLBGFER
SCHEMBL13325735 0.87 RAB9A (0.75) RAB9ANPC1KDM4EPOLBGFER
SCHEMBL31154574 0.87 RAB9A (0.74) RAB9ANPC1KDM4EPOLBGFER
SCHEMBL29080554 0.87 RAB9A (0.74) RAB9ANPC1KDM4EPOLBGFER
SCHEMBL966793 0.87 RAB9A (0.74) RAB9ANPC1KDM4EPOLBGFER
SCHEMBL25343703 0.85 RAB9A (0.72) RAB9ANPC1KDM4EPOLBGFER
SCHEMBL3304334 0.84 RAB9A (0.97) RAB9ANPC1KDM4EPOLBGFER
SCHEMBL6388717 0.84 RAB9A (0.71) RAB9ANPC1KDM4EPOLBGFER
SCHEMBL972536 0.84 RAB9A (1.00) RAB9ANPC1KDM4EPOLBGFER

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114892187-B Method for electrochemically synthesizing imidazole polycyclic aromatic compounds 南京工业大学 2023-08-22 CN disclosed
CN-112538087-B Synthesis method of imidazopyridine compound 温州大学新材料与产业技术研究院 2021-10-15 CN disclosed
EP-2752415-B1 Fluorinated ligands for targeting peripheral benzodiazepine receptors AUSTRALIAN NUCLEAR SCIENCE & TECH ORGANISATION (AU) 2017-10-11 EP disclosed
US-20160050895-A1 TRANSGENIC NON-HUMAN ORGANISMS WITH NON-FUNCTIONAL TSPO GENES THE UNIVERSITY OF SYDNEY (AU) 2016-02-25 US disclosed
EP-2971007-A1 TRANSGENIC NON-HUMAN ORGANISMS WITH NON-FUNCTIONAL TSPO GENES AUSTRALIAN NUCLEAR SCIENCE AND TECHNOLOGY ORGANISATION (AU) 2016-01-20 EP disclosed
WO-2014138791-A1 TRANSGENIC NON-HUMAN ORGANISMS WITH NON-FUNCTIONAL TSPO GENES AUSTRALIAN NUCLEAR SCIENCE AND TECHNOLOGY ORGANISATION (AU) 2014-09-18 WO disclosed
EP-2752415-A1 Fluorinated ligands for targeting peripheral benzodiazepine receptors AUSTRALIAN NUCLEAR SCIENCE & TECHNOLOGY ORGANISATION (AU) 2014-07-09 EP disclosed
US-7867629-B2 Nitrogenous heterocyclic derivative and organic electroluminescent element employing the same IDEMITSU KOSAN CO., LTD. (JP) 2011-01-11 US disclosed
US-20100209345-A1 Fluorinated Ligands for Targeting Peripheral Benzodiazepine Receptors AUSTRALIAN NUCLEAR SCIENCE & TECHNOLOGY ORGANISATION 2010-08-19 US disclosed
US-20040204443-A1 Method for inducing pain relief using imidazo[1,2-a]pyridine derivatives ZAKS ARTHUR (US) 2004-10-14 US disclosed
WO-2004066930-A2 METHOD FOR INDUCING PAIN RELIEF USING IMIDAZO[1,2-A]PYRIDINE DERIVATIVES ZAKS ARTHUR (US) 2004-08-12 WO disclosed
EP-1071684-B1 IMIDAZO 1,2-a]PYRIDINES AS PERIPHERAL BENZODIAZEPINE RECEPTOR BINDING AGENTS AUSTRALIAN NUCLEAR SCIENCE TEC (AU) 2004-03-17 EP disclosed
US-6379649-B1 USEFUL FOR DIAGNOSIS AND TREATMENT, INCLUDING RADIOTHERAPY, OF DISORDERS THAT ARE CHARACTERIZED BY AN ABNORMAL DENSITY OF PERIPHERAL BENZODIAZEPINE RECEPTORS; NERVE SYSTEM DISPORDERS AUSTRALIAN NUCLEAR SCIENCE & TECHNOLOGY ORGANISATION (AU) 2002-04-30 US disclosed
EP-1071684-A4 IMIDAZO 1,2-a]PYRIDINES AS PERIPHERAL BENZODIAZEPINE RECEPTOR BINDING AGENTS AUSTRALIAN NUCLEAR SCIENCE TEC (AU) 2001-10-04 EP disclosed
EP-1071684-A1 IMIDAZO 1,2-a]PYRIDINES AS PERIPHERAL BENZODIAZEPINE RECEPTOR BINDING AGENTS AUSTRALIAN NUCLEAR SCIENCE & TECHNOLOGY ORGANISATION (AU) 2001-01-31 EP disclosed
WO-1999051594-A1 IMIDAZO[1,2-a]PYRIDINES AS PERIPHERAL BENZODIAZEPINE RECEPTOR BINDING AGENTS AUSTRALIAN NUCLEAR SCIENCE & TECHNOLOGY ORGANISATION (AU) 1999-10-14 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-20100209345-A1 Fluorinated Ligands for Targeting Peripheral Benzodiazepine Receptors GABRA6, GABRA1, GABRA2 RAB9A 1716/4885NPC1 524/4885KDM4E 3090/4885
US-20040204443-A1 Method for inducing pain relief using imidazo[1,2-a]pyridine derivatives P2RY1, ITPR1, P2RX3 RAB9A 1094/4885NPC1 939/4885KDM4E 1409/4885

“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.