SCHEMBL2887160

SCHEMBL2887160

COc1ccc(-c2ccc3nncn3n2)cc1

nearest known ligand 0.58

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
POLB P06746 4/20 0.58
KDM4E B2RXH2 8/20 0.53
MAPT P10636 3/20 0.53
L3MBTL1 Q9Y468 2/20 0.51
SMN1; SMN2 Q16637 2/20 0.47
MET P08581 1/20 0.47
TDP1 Q9NUW8 3/20 0.46
ALDH1A1 P00352 3/20 0.46
MAPK1 P28482 1/20 0.46
PKM P14618 1/20 0.44
PPARG P37231 1/20 0.44
NR2E3 Q9Y5X4 1/20 0.44
NCOR2 Q9Y618 1/20 0.44
ALDH1A3 P47895 1/20 0.44
HTT P42858 1/20 0.44

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
SCHEMBL936663 0.83 TDP1 (0.50) POLBKDM4EMAPTL3MBTL1SMN1; SMN2
SCHEMBL26538921 0.82 KDM4E (0.49) POLBKDM4EMAPTL3MBTL1SMN1; SMN2
SCHEMBL10806026 0.82 KDM4E (0.57) POLBKDM4EMAPTL3MBTL1SMN1; SMN2
SCHEMBL935922 0.82 SCN5A (0.60) POLBKDM4EMAPTSMN1; SMN2TDP1
SCHEMBL5806164 0.80 TDP1 (0.54) POLBKDM4EMAPTSMN1; SMN2TDP1
SCHEMBL11626523 0.79 KDM4E (0.58) POLBKDM4EMAPTL3MBTL1SMN1; SMN2
SCHEMBL11629082 0.79 KDM4E (0.53) POLBKDM4EMAPTL3MBTL1SMN1; SMN2
SCHEMBL2887969 0.79 KDM4E (0.57) POLBKDM4EMAPTL3MBTL1SMN1; SMN2
SCHEMBL11628950 0.79 KDM4E (0.53) POLBKDM4EMAPTL3MBTL1SMN1; SMN2
SCHEMBL11626405 0.78 KDM4E (0.53) POLBKDM4EMAPTL3MBTL1SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7645756-B2 6-[4-(3-piperidin-1-ylpropoxy)-phenyl]-[1,2,4]triazolo[4,3-b]pyridazine; has histamine-H3 receptor antagonistic effect or a histamine-H3 receptor inverse-agonistic effect; for metabolic system, circulatory system or nervous system diseases BANYU PHARMACEUTICAL CO. LTD. (JP) 2010-01-12 US disclosed
US-20070167453-A1 Nitrogenous fused heteroaromatic ring derivative MSD K.K. (JP) 2007-07-19 US disclosed
EP-1719756-A1 NITROGENOUS FUSED HETEROAROMATIC RING DERIVATIVE BANYU PHARMACEUTICAL CO., LTD. (JP) 2006-11-08 EP 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 (1 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-20070167453-A1 Nitrogenous fused heteroaromatic ring derivative HRH3, HRH2, HRH4 POLB 4606/4885KDM4E 4024/4885MAPT 3450/4885

“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.