SCHEMBL1194672

SCHEMBL1194672

N#Cc1cc(Oc2c([N+](=O)[O-])ccc(F)c2F)cc(C(F)F)c1

nearest known ligand 0.37

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
EPAS1 Q99814 6/20 0.37
VCAM1 P19320 4/20 0.36
MERTK Q12866 1/20 0.36
MAPT P10636 1/20 0.35
VEGFA P15692 3/20 0.34
HSPB1 P04792 1/20 0.33
ATM Q13315 1/20 0.32
TDP1 Q9NUW8 1/20 0.32
TRPV4 Q9HBA0 1/20 0.32
ALDH1A1 P00352 1/20 0.31
HIF1A Q16665 1/20 0.31

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
SCHEMBL4268207 0.89 VCAM1 (0.42) EPAS1VCAM1MERTKMAPTHSPB1
SCHEMBL3636393 0.85 MAPT (0.39) VCAM1MERTKMAPTHSPB1ATM
SCHEMBL3016476 0.85 VCAM1 (0.44) EPAS1VCAM1MERTKMAPTVEGFA
SCHEMBL13581462 0.82 HSPB1 (0.35) EPAS1VCAM1MAPTHSPB1ATM
SCHEMBL3638340 0.82 VCAM1 (0.36) EPAS1VCAM1MERTKMAPTHSPB1
Valine SCHEMBL5207123 0.79 SMN1; SMN2 (0.35) EPAS1VCAM1MERTKMAPTTRPV4
SCHEMBL13492243 0.75 MAPT (0.42) EPAS1VCAM1MERTKMAPTHSPB1
SCHEMBL3035964 0.75 CYP3A4 (0.48) EPAS1VCAM1MERTKMAPTVEGFA
SCHEMBL3640707 0.74 MAPT (0.44) EPAS1VCAM1MERTKMAPTALDH1A1
SCHEMBL12135916 0.73 MAPT (0.37) EPAS1VCAM1MERTKMAPTHSPB1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2164835-A2 PROCESS FOR PREPARING TRIAZOLONES F. Hoffmann-Roche AG (CH) 2010-03-24 EP claimed
US-20090012304-A1 preparation of intermediates 3-[3-(4-methyl-5-methylsulfanyl-4H-[1,2,4]triazol-3-ylmethyl)phenoxy]-5-difluoromethyl-benzonitrile derivatives; for making enzyme inhibitors of HIV-1 reverse transcriptase, treating AIDS and HIV-1 syndromes ROCHE PALO ALTO LLC 2009-01-08 US claimed
WO-2008145563-A2 PROCESS FOR PREPARING TRIAZOLONES F. HOFFMANN-LA ROCHE AG (CH) 2008-12-04 WO claimed
EP-2164835-B1 PROCESS FOR PREPARING TRIAZOLONES HOFFMANN LA ROCHE (CH) 2012-12-12 EP disclosed
US-7906540-B2 Antivirals for HIV and AIDS; compounds are 2-1,2,4-triazolin-5-ones, substituted with aryl(oxy)methyl or benzylamino at position 3; use in combination with antivirals; treating drug resistance infections ROCHE PALO ALTO LLC (US) 2011-03-15 US disclosed
US-7893276-B2 Process for preparing triazolones ROCHE PALO ALTO LLC (US) 2011-02-22 US disclosed
US-20100280256-A1 PROCESS FOR PREPARING TRIAZOLONES LEE GARY M 2010-11-04 US disclosed
US-7745634-B2 Process for preparing triazolones ROCHE PALO ALTO LLC (US) 2010-06-29 US disclosed
EP-2164835-A2 PROCESS FOR PREPARING TRIAZOLONES F. Hoffmann-Roche AG (CH) 2010-03-24 EP disclosed
EP-2142520-A1 NON-NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS F. Hoffmann-Roche AG (CH) 2010-01-13 EP disclosed
US-20090012304-A1 preparation of intermediates 3-[3-(4-methyl-5-methylsulfanyl-4H-[1,2,4]triazol-3-ylmethyl)phenoxy]-5-difluoromethyl-benzonitrile derivatives; for making enzyme inhibitors of HIV-1 reverse transcriptase, treating AIDS and HIV-1 syndromes ROCHE PALO ALTO LLC 2009-01-08 US disclosed
WO-2008145563-A2 PROCESS FOR PREPARING TRIAZOLONES F. HOFFMANN-LA ROCHE AG (CH) 2008-12-04 WO disclosed
WO-2008119662-A1 NON-NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS F. HOFFMANN-LA ROCHE AG (CH) 2008-10-09 WO disclosed
US-20080249151-A1 Non-nucleoside reverse transcriptase inhibitors ROCHE PALO ALTO LLC 2008-10-09 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 (3 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-20100280256-A1 PROCESS FOR PREPARING TRIAZOLONES CYP51A1, TNKS, TNKS2 EPAS1 1711/4885VCAM1 4746/4885MERTK 2521/4885
US-20080249151-A1 Non-nucleoside reverse transcriptase inhibitors QTRT1, RTF1, REV1 EPAS1 3074/4885VCAM1 2102/4885MERTK 4331/4885
US-20090012304-A1 preparation of intermediates 3-[3-(4-methyl-5-methylsulfanyl-4H-[1,2,4]triazol-3-ylmethyl)phenoxy]-5-difluoromethyl-benzonitrile derivatives; for making enzyme inhibitors of HIV-1 reverse transcriptase, treating AIDS and HIV-1 syndromes POLRMT, TYMS, POLR1G EPAS1 1428/4885VCAM1 2150/4885MERTK 3417/4885

“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.