SCHEMBL4813338

SCHEMBL4813338

CCn1cc(Cc2ccc(C(=O)NCc3cnc(C)cn3)cc2-c2ccc(C)cc2C(=O)OCc2ccccc2)c2ccc(C#N)cc21

nearest known ligand 0.40

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
P2RX3 P56373 13/20 0.40
P2RX2 Q9UBL9 13/20 0.40
ROCK2 O75116 1/20 0.37
PTGER4 P35408 1/20 0.35
TSHR P16473 1/20 0.34
MAPK1 P28482 1/20 0.34
IDO1 P14902 1/20 0.34
EGLN1 Q9GZT9 1/20 0.34

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
SCHEMBL4815675 0.89 ROCK2 (0.42) ROCK2PTGER4TSHRMAPK1
SCHEMBL4816122 0.89 P2RX3 (0.43) P2RX3P2RX2ROCK2PTGER4EGLN1
SCHEMBL4811266 0.88 PTGER4 (0.36) ROCK2PTGER4TSHRMAPK1
SCHEMBL4815141 0.86 PTGER4 (0.34) ROCK2PTGER4TSHRMAPK1
SCHEMBL4812930 0.86 PLA2G4A (0.41) TSHRMAPK1
SCHEMBL4814044 0.86 P2RX3 (0.37) P2RX3P2RX2ROCK2
SCHEMBL4815680 0.85 PTPRC (0.37) PTGER4TSHRMAPK1
SCHEMBL4812944 0.83 PLA2G4A (0.38) TSHRMAPK1
SCHEMBL4815505 0.83 TSHR (0.36) TSHRMAPK1
SCHEMBL4817901 0.82 ROCK2 (0.41) ROCK2TSHRMAPK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7417063-B2 Bicyclic heterocycles useful as serine protease inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2008-08-26 US disclosed
EP-1740538-A4 BICYCLIC HETEROCYCLES USEFUL AS SERINE PROTEASE INHIBITORS BRISTOL MYERS SQUIBB CO (US) 2007-12-19 EP disclosed
EP-1740538-A2 BICYCLIC HETEROCYCLES USEFUL AS SERINE PROTEASE INHIBITORS Bristol-Myers Squibb Company (US) 2007-01-10 EP disclosed
WO-2005099709-A2 BICYCLIC HETEROCYCLES USEFUL AS SERINE PROTEASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2005-10-27 WO disclosed
US-20050228000-A1 of the coagulation cascade or contact activation system: thrombin, factor Xa, factor XIa, factor IXa, factor VIIa or plasma kallikrein; e.g. -(6-carbamimidoyl-1H-indol-3-ylmethyl)-4-methoxy-biphenyl-2-carboxylic acid; anticoagulant, antiinflammatory agent BRISTOL-MYERS SQUIBB COMPANY 2005-10-13 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-20050228000-A1 of the coagulation cascade or contact activation system: thrombin, factor Xa, factor XIa, factor IXa, factor VIIa or plasma kallikrein; e.g. -(6-carbamimidoyl-1H-indol-3-ylmethyl)-4-methoxy-biphenyl-2-carboxylic acid; anticoagulant, antiinflammatory agent F12, F11, F2 P2RX3 1152/4885P2RX2 1535/4885ROCK2 1511/4885

“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.