SCHEMBL9909085

SCHEMBL9909085

Bc1ccc2[nH]nc(C)c2c1

nearest known ligand 0.46

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
ADORA2A P29274 2/20 0.46
ADORA2B P29275 2/20 0.46
CYP1A2 P05177 1/20 0.43
JAK2 O60674 4/20 0.40
MAP2K4 P45985 6/20 0.39
MAPK1 P28482 5/20 0.38
MAPKAPK3 Q16644 4/20 0.38
MAPK6 Q16659 4/20 0.38
MAPKAPK2 P49137 3/20 0.38
MAPKAPK5 Q8IW41 2/20 0.38
MKNK1 Q9BUB5 1/20 0.38
GSK3B P49841 1/20 0.37
PDPK1 O15530 1/20 0.36
NTRK1 P04629 1/20 0.36
ITK Q08881 2/20 0.35

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
SCHEMBL10131378 0.84 ADORA2A (0.46) ADORA2AADORA2BCYP1A2JAK2MAP2K4
SCHEMBL12222 0.79 MAP2K4 (0.57) ADORA2AADORA2BCYP1A2JAK2MAP2K4
SCHEMBL29769133 0.79 MAP2K4 (0.57) ADORA2AADORA2BCYP1A2JAK2MAP2K4
SCHEMBL14404116 0.78 JAK2 (0.60) JAK2MAPK1GSK3BPDPK1NTRK1
SCHEMBL24149246 0.76 ADORA2A (0.46) ADORA2AADORA2BCYP1A2JAK2MAP2K4
SCHEMBL13122049 0.76 FADS1 (0.49) ADORA2AADORA2BCYP1A2JAK2
SCHEMBL23062796 0.76 MAP2K4 (0.53) ADORA2AADORA2BCYP1A2JAK2MAP2K4
SCHEMBL8045852 0.76 ITK (0.46) ADORA2AADORA2BCYP1A2MAP2K4GSK3B
SCHEMBL24610364 0.76 ADORA2A (0.46) ADORA2AADORA2BCYP1A2JAK2MAP2K4
SCHEMBL182633 0.76 JAK2 (0.63) ADORA2AADORA2BCYP1A2JAK2MAP2K4

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
WO-2016150800-A1 USP7 INHIBITOR COMPOUNDS AND METHODS OF USE F. HOFFMANN-LA ROCHE AG (CH) 2016-09-29 WO disclosed
US-8198456-B2 e.g. 1,4-dihydro-4-(1H-indazol-5-yl)-2,6-dimethyl-3,5-pyridinedicarbonitrile; c-Met tyrosine kinase inhibitor; antitumor agent; lung, liver, gastric and breast solid tumors; pancreatic cancer, glioma, and hepatocellular carcinoma BAYER INTELLECTUAL PROPERTY GMBH (DE) 2012-06-12 US disclosed
US-20080176833-A1 DIHYDROPYRIDINE DERIVATIVES AS USEFUL AS PROTEIN KINASE INHIBITORS BAYER INTELLECTUAL PROPERTY GMBH (DE) 2008-07-24 US 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-20080176833-A1 DIHYDROPYRIDINE DERIVATIVES AS USEFUL AS PROTEIN KINASE INHIBITORS MET, DMPK, RET ADORA2A 4255/4885ADORA2B 4325/4885CYP1A2 3348/4885

“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.