SCHEMBL4249339

SCHEMBL4249339

O=C(Nc1ccc(-n2nc(-c3cccnc3)cc2C(F)(F)F)nc1)c1ccc(Cl)cc1

nearest known ligand 0.84

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
EPHX2 P34913 11/20 0.84
NAMPT P43490 1/20 0.52
CRACR2A Q9BSW2 2/20 0.51
CYP11B1 P15538 1/20 0.51
CYP11B2 P19099 1/20 0.51
ORAI1 Q96D31 1/20 0.51
ABL1 P00519 1/20 0.49
PDGFRB P09619 1/20 0.49
BCR P11274 1/20 0.49
PDGFRA P16234 1/20 0.49
ALOX5 P09917 1/20 0.48
TBXAS1 P24557 1/20 0.48
SLC6A3 Q01959 1/20 0.48
SIGMAR1 Q99720 1/20 0.48
PPARG P37231 1/20 0.47
KMT2A Q03164 1/20 0.47
TDP1 Q9NUW8 1/20 0.47
NR2E3 Q9Y5X4 1/20 0.47
NCOR2 Q9Y618 1/20 0.47
LMNA P02545 1/20 0.46

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
SCHEMBL4249684 0.93 EPHX2 (0.81) EPHX2CRACR2AABL1ALOX5TBXAS1
SCHEMBL4257269 0.92 EPHX2 (0.89) EPHX2CRACR2AABL1BCRALOX5
SCHEMBL4248491 0.92 EPHX2 (1.00) EPHX2NAMPTCRACR2AABL1PDGFRB
SCHEMBL4248369 0.91 EPHX2 (0.82) EPHX2CRACR2AABL1BCRKMT2A
SCHEMBL4245798 0.91 EPHX2 (0.91) EPHX2CRACR2AALOX5TBXAS1SLC6A3
SCHEMBL4250442 0.89 EPHX2 (0.79) EPHX2CRACR2AABL1ALOX5TBXAS1
SCHEMBL4252824 0.89 EPHX2 (0.80) EPHX2ABL1
SCHEMBL4255008 0.88 EPHX2 (0.80) EPHX2CRACR2AALOX5TBXAS1SLC6A3
SCHEMBL4249945 0.88 EPHX2 (0.83) EPHX2CRACR2ACYP11B1CYP11B2ABL1
SCHEMBL4250527 0.87 EPHX2 (0.84) EPHX2CRACR2AABL1BCRKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20090227588-A1 Substituted pyrazole compounds useful as soluble epoxide hyrolase inhibitors FLECK ROMAN WOLFGANG 2009-09-10 US disclosed
US-20090227588-A1 Substituted pyrazole compounds useful as soluble epoxide hyrolase inhibitors FLECK ROMAN WOLFGANG 2009-09-10 US disclosed
US-20090227588-A1 Substituted pyrazole compounds useful as soluble epoxide hyrolase inhibitors FLECK ROMAN WOLFGANG 2009-09-10 US disclosed
WO-2007067836-A2 SUBSTITUTED PYRAZOLE COMPOUNDS USEFUL AS SOLUBLE EPOXIDE HYDROLASE INHIBITORS BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2007-06-14 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 (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-20090227588-A1 Substituted pyrazole compounds useful as soluble epoxide hyrolase inhibitors EPHX1, EPHX2, EPX EPHX2 2/4885NAMPT 1672/4885CRACR2A 3167/4885

“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.