SCHEMBL5403595

SCHEMBL5403595

CC(=O)c1cc(Cl)cc(C(F)(F)F)c1N

nearest known ligand 0.40

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TMPRSS4 Q9NRS4 6/20 0.40
AKR1B10 O60218 1/20 0.38
AKR1C4 P17516 1/20 0.38
AKR1C3 P42330 1/20 0.38
AKR1C2 P52895 1/20 0.38
AKR1C1 Q04828 1/20 0.38
CYP3A4 P08684 1/20 0.37
RAB9A P51151 2/20 0.36
TP53 P04637 1/20 0.36
MAPT P10636 1/20 0.36
SMN1; SMN2 Q16637 1/20 0.36
CFTR P13569 1/20 0.36
CYP1A2 P05177 1/20 0.36
CYP2D6 P10635 1/20 0.36
CYP2C19 P33261 1/20 0.36
KDM4E B2RXH2 1/20 0.35
ADRB2 P07550 2/20 0.35
ADRB1 P08588 1/20 0.35
GAA P10253 1/20 0.34
SCN9A Q15858 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
SCHEMBL9938957 0.86 MAPK14 (0.39) TMPRSS4CYP3A4RAB9ACYP1A2CYP2D6
SCHEMBL11626984 0.84 CYP3A4 (0.38) TMPRSS4AKR1B10AKR1C4AKR1C3AKR1C2
Hydrochloric Acid SCHEMBL11626989 0.83 CYP3A4 (0.49) AKR1C4AKR1C3AKR1C2AKR1C1CYP3A4
SCHEMBL19506269 0.83 ADRB2 (0.35) TMPRSS4AKR1B10AKR1C4AKR1C3AKR1C2
SCHEMBL31591119 0.82 TMPRSS4 (0.41) TMPRSS4AKR1B10AKR1C4AKR1C3AKR1C2
SCHEMBL14976789 0.81 TMPRSS4 (0.34) TMPRSS4AKR1B10AKR1C4AKR1C3AKR1C2
SCHEMBL23526580 0.81 KIF11 (0.38) TMPRSS4AKR1C3AKR1C2MAPTCFTR
SCHEMBL29945921 0.81 KIF11 (0.38) TMPRSS4AKR1C3AKR1C2MAPTCFTR
SCHEMBL23301033 0.81 CES2 (0.44) AKR1C3AKR1C2MAPTCFTRCYP2C19
SCHEMBL29656849 0.81 CES2 (0.44) AKR1C3AKR1C2MAPTCFTRCYP2C19

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7186830-B2 Tricyclic 2-pyrimidone compounds useful as HIV reverse transcriptase inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2007-03-06 US disclosed
EP-1474424-A4 TRICYCLIC 2-PYRIMIDONE COMPOUNDS USEFUL AS HIV REVERSE TRANSCRIPTASE INHIBITORS BRISTOL MYERS SQUIBB CO (US) 2005-12-28 EP disclosed
US-6844340-B2 Tricyclic 2-pyrimidone compounds useful as HIV reverse transcriptase inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2005-01-18 US disclosed
US-20040266778-A1 Tricyclic 2-pyrimidone compounds useful as HIV reverse transcriptase inhibitors TARBY CHRISTINE M 2004-12-30 US disclosed
EP-1474424-A1 TRICYCLIC 2-PYRIMIDONE COMPOUNDS USEFUL AS HIV REVERSE TRANSCRIPTASE INHIBITORS Bristol-Myers Squibb Company (US) 2004-11-10 EP disclosed
US-20030162800-A1 Tricyclic 2-pyrimidone compounds useful as HIV reverse transcriptase inhibitors BRISTOL-MYERS SQUIBB COMPANY 2003-08-28 US disclosed
WO-2003062238-A1 TRICYCLIC 2-PYRIMIDONE COMPOUNDS USEFUL AS HIV REVERSE TRANSCRIPTASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2003-07-31 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 (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-20030162800-A1 Tricyclic 2-pyrimidone compounds useful as HIV reverse transcriptase inhibitors TYMP, TYMS, DPYD TMPRSS4 128/4885AKR1B10 1608/4885AKR1C4 772/4885
US-20040266778-A1 Tricyclic 2-pyrimidone compounds useful as HIV reverse transcriptase inhibitors TYMP, TYMS, DPYD TMPRSS4 128/4885AKR1B10 1608/4885AKR1C4 772/4885

“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.