SCHEMBL772458

SCHEMBL772458

COc1ccc2c(c1)OCCn1c-2c(C2CCCCC2)c2ccc(C(=O)N[C@@H](Cc3ccc(O)c(Cl)c3)C(=O)O)cc21

nearest known ligand 0.41

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
NR1I2 O75469 5/20 0.41
CYP3A4 P08684 3/20 0.41
CYP2C9 P11712 1/20 0.41
CYP2C19 P33261 1/20 0.41
KCNH2 Q12809 7/20 0.39
SCN5A Q14524 2/20 0.39
CA2 P00918 4/20 0.38
SCN9A Q15858 1/20 0.37
CA1 P00915 1/20 0.37
PRKCA P17252 1/20 0.37
MMP12 P39900 1/20 0.37
ALB P02768 1/20 0.37
IL2 P60568 1/20 0.37
ITGB3 P05106 1/20 0.36
ITGA2B P08514 1/20 0.36

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
SCHEMBL772414 0.95 NR1I2 (0.40) NR1I2CYP3A4CYP2C9CYP2C19KCNH2
SCHEMBL771810 0.92 KCNH2 (0.42) NR1I2CYP3A4CYP2C9CYP2C19KCNH2
SCHEMBL774073 0.90 NR1I2 (0.41) NR1I2CYP3A4CYP2C9CYP2C19KCNH2
SCHEMBL773883 0.90 KCNH2 (0.42) NR1I2CYP3A4CYP2C9CYP2C19KCNH2
SCHEMBL3784315 0.90 KCNH2 (0.42) NR1I2CYP3A4CYP2C9CYP2C19KCNH2
SCHEMBL3780892 0.89 KCNH2 (0.41) NR1I2CYP3A4CYP2C9CYP2C19KCNH2
SCHEMBL3783427 0.89 ROCK2 (0.42) NR1I2CYP3A4CYP2C9CYP2C19KCNH2
SCHEMBL774091 0.88 KCNH2 (0.41) NR1I2CYP3A4CYP2C9CYP2C19KCNH2
SCHEMBL3783819 0.88 ITGB3 (0.41) NR1I2CYP3A4CYP2C9CYP2C19KCNH2
SCHEMBL3789253 0.88 ITGB3 (0.41) NR1I2CYP3A4CYP2C9CYP2C19KCNH2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20120070409-A1 TETRACYCLIC FUSED HETEROCYCLIC COMPOUND AND USE THEREOF AS HCV POLYMERASE INHIBITOR JAPAN TOBACCO INC. (JP) 2012-03-22 US disclosed
US-7977331-B1 Tetracyclic fused heterocyclic compound and use thereof as HCV polymerase inhibitor JAPAN TOBACCO INC. (JP) 2011-07-12 US disclosed
US-7977331-B1 Tetracyclic fused heterocyclic compound and use thereof as HCV polymerase inhibitor JAPAN TOBACCO INC. (JP) 2011-07-12 US disclosed
US-7977331-B1 Tetracyclic fused heterocyclic compound and use thereof as HCV polymerase inhibitor JAPAN TOBACCO INC. (JP) 2011-07-12 US disclosed
EP-2206715-A1 Fused heterotetracyclic compounds and use thereof as hcv polymerase inhibitor Japan Tobacco, Inc. (JP) 2010-07-14 EP disclosed
EP-1719773-B1 FUSED HETEROTETRACYCLIC COMPOUNDS AND USE TEHREOF AS HCV POLYMERASE INHIBITOR JAPAN TOBACCO INC (JP) 2009-04-15 EP disclosed
US-20070049593-A1 Tetracyclic fused heterocyclic compound and use thereof as HCV polymerase inhibitor JAPAN TOBACCO INC. (JP) 2007-03-01 US disclosed
EP-1719773-A1 FUSED HETEROTETRACYCLIC COMPOUNDS AND USE TEHREOF AS HCV POLYMERASE INHIBITOR Japan Tobacco, Inc. (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 (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-20070049593-A1 Tetracyclic fused heterocyclic compound and use thereof as HCV polymerase inhibitor POLI, TERT, ZC3HAV1 NR1I2 1189/4885CYP3A4 1341/4885CYP2C9 976/4885
US-20120070409-A1 TETRACYCLIC FUSED HETEROCYCLIC COMPOUND AND USE THEREOF AS HCV POLYMERASE INHIBITOR POLI, TERT, ZC3HAV1 NR1I2 1189/4885CYP3A4 1341/4885CYP2C9 976/4885

“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.