SCHEMBL3894055

SCHEMBL3894055

COc1cccc(C(=O)Cc2ccnc(F)c2)c1

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ROCK1 Q13464 3/20 0.51
▸ CYP3A4 P08684 2/20 0.51
▸ ROCK2 O75116 2/20 0.51
▸ PRKACA P17612 2/20 0.51
▸ CES2 O00748 1/20 0.48
▸ CES1 P23141 1/20 0.48
▸ NPC1 O15118 3/20 0.47
▸ RAB9A P51151 3/20 0.47
▸ POLB P06746 2/20 0.47
▸ BLM P54132 1/20 0.47
▸ SMN1; SMN2 Q16637 1/20 0.47
▸ KMT2A Q03164 2/20 0.46
▸ VNN1 O95497 1/20 0.46
▸ CDYL2 Q8N8U2 1/20 0.46
▸ CDYL Q9Y232 1/20 0.46
▸ CDY1; CDY1B Q9Y6F8 1/20 0.46
▸ PARP1 P09874 1/20 0.46
▸ HSD11B1 P28845 2/20 0.45
▸ CHRM2 P08172 1/20 0.45
▸ CHRM1 P11229 1/20 0.45

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
SCHEMBL3891876 0.83 VNN1 (0.43) SMN1; SMN2KMT2AVNN1PARP1TDP1
SCHEMBL2477853 0.82 LMNA (0.54) ROCK1CYP3A4ROCK2PRKACACES2
SCHEMBL3891730 0.82 LOXL2 (0.41) ROCK1CYP3A4ROCK2PRKACAKMT2A
SCHEMBL4313456 0.81 LOXL2 (0.47) CYP3A4CES1RAB9ASMN1; SMN2KMT2A
SCHEMBL3896447 0.80 ERCC5 (0.46) KMT2AVNN1PARP1LMNAL3MBTL1
Bromide SCHEMBL6992895 0.79 ERCC5 (0.44) KMT2AVNN1PARP1LMNAL3MBTL1
SCHEMBL4025014 0.78 DDR1 (0.52) CES2NPC1RAB9ASMN1; SMN2VNN1
SCHEMBL27572327 0.78 ALDH1A1 (0.63) CYP3A4CES2CES1NPC1RAB9A
SCHEMBL1515775 0.78 MEN1 (0.61) CES2CES1NPC1RAB9ASMN1; SMN2
SCHEMBL6276599 0.76 IDO1 (0.59) CYP3A4RAB9ASMN1; SMN2KMT2ACYP2C9

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
US-7495018-B2 Substituted 1,3-thiazole compounds, their production and use TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2009-02-24 — — US disclosed
US-20090048307-A1 5-pyridyl-1, 3-azole compounds, process for producing the same and use there of OHKAWA SHIGENORI 2009-02-19 — — US disclosed
US-7276527-B2 5-pyridyl-1,3-azole compounds, process for producing the same and use thereof TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2007-10-02 — — US disclosed
EP-1180518-B1 5-PYRIDYL-1,3-AZOLE COMPOUNDS, PROCESS FOR PRODUCING THE SAME AND USE THEREOF TAKEDA PHARMACEUTICAL (JP) 2007-01-17 — — EP disclosed
US-7101899-B1 5-pyridyl-1,3-azole compounds, process for producing the same and use thereof TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2006-09-05 — — US disclosed
US-20060135566-A1 5-pyridyl-1,3-azole compounds, process for producing the same and use thereof OHKAWA SHIGENORI 2006-06-22 — — US disclosed
US-6962933-B1 Method for inhibiting p38 MAP kinase or TNF-α production using a 1,3-thiazole TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2005-11-08 — — US disclosed
US-20050080113-A1 Medicinal compositions TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2005-04-14 — — US disclosed
US-20040097555-A1 Concomitant drugs TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2004-05-20 — — US disclosed
EP-1402900-A1 MEDICINAL COMPOSITIONS Takeda Chemical Industries, Ltd. (JP) 2004-03-31 — — EP disclosed
US-20040053973-A1 Substituted 1,3-thiazole compounds, their production and use TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2004-03-18 — — US disclosed
EP-1354603-A1 CONCOMITANT DRUGS Takeda Chemical Industries, Ltd. (JP) 2003-10-22 — — EP disclosed
EP-1268474-A2 SUBSTITUTED 1,3-THIAZOLE COMPOUNDS, THEIR PRODUCTION AND USE Takeda Chemical Industries, Ltd. (JP) 2003-01-02 — — EP disclosed
EP-1205478-A1 p38MAP KINASE INHIBITORS Takeda Chemical Industries, Ltd. (JP) 2002-05-15 — — EP disclosed
EP-1180518-A1 5-PYRIDYL-1,3-AZOLE COMPOUNDS, PROCESS FOR PRODUCING THE SAME AND USE THEREOF Takeda Chemical Industries, Ltd. (JP) 2002-02-20 — — EP disclosed
WO-2001074811-A2 SUBSTITUTED 1,3-THIAZOLE COMPOUNDS, THEIR PRODUCTION AND USE TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 2001-10-11 — — 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 (5 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-20050080113-A1 Medicinal compositions TNF, TRAF6, MMP8 ROCK1 53/4885CYP3A4 4806/4885ROCK2 102/4885
US-20060135566-A1 5-pyridyl-1,3-azole compounds, process for producing the same and use thereof ADORA3, MAPK4, MAPK3 ROCK1 923/4885CYP3A4 489/4885ROCK2 1817/4885
US-20040053973-A1 Substituted 1,3-thiazole compounds, their production and use MAPK1, MAP4K2, MAPK4 ROCK1 576/4885CYP3A4 1773/4885ROCK2 642/4885
US-20040097555-A1 Concomitant drugs TNF, CHUK, CNKSR1 ROCK1 234/4885CYP3A4 1299/4885ROCK2 224/4885
US-20090048307-A1 5-pyridyl-1, 3-azole compounds, process for producing the same and use there of ADORA3, ADORA1, MAPK3 ROCK1 1170/4885CYP3A4 500/4885ROCK2 2015/4885

“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.

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