SCHEMBL14832292

SCHEMBL14832292

Oc1cc(C(F)(F)F)ccc1-c1cccnc1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CNR1 P21554 1/20 0.56
CNR2 P34972 1/20 0.56
CYP11B1 P15538 6/20 0.55
CYP11B2 P19099 6/20 0.55
NPC1 O15118 1/20 0.51
DGAT1 O75907 1/20 0.50
KCNH2 Q12809 1/20 0.50
NPY5R Q15761 2/20 0.49
ALOX5AP P20292 2/20 0.49
FEN1 P39748 2/20 0.49
S1PR1 P21453 1/20 0.48
KDR P35968 1/20 0.47
CYP19A1 P11511 1/20 0.47
CYP17A1 P05093 1/20 0.47
CYP3A4 P08684 1/20 0.47
KIF11 P52732 1/20 0.46
HTR2B P41595 1/20 0.46
HTR6 P50406 1/20 0.46
ERN1 O75460 1/20 0.46
PDK2 Q15119 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
SCHEMBL30545136 1.00 CNR1 (0.56) CNR1CNR2CYP11B1CYP11B2NPC1
Formic Acid SCHEMBL30412981 0.93 CYP11B1 (0.50) CNR1CNR2CYP11B1CYP11B2NPC1
SCHEMBL5990332 0.89 CYP11B1 (0.51) CNR1CNR2CYP11B1CYP11B2NPC1
SCHEMBL15989428 0.84 CYP11B1 (0.53) CYP11B1CYP11B2NPC1DGAT1KCNH2
SCHEMBL31359600 0.83 CNR1 (0.63) CNR1CNR2CYP11B1CYP11B2NPC1
SCHEMBL15009839 0.81 CYP11B1 (0.50) CYP11B1CYP11B2NPC1DGAT1KCNH2
SCHEMBL9809559 0.80 ALOX5 (0.55) CNR1CNR2ALOX5APFEN1KIF11
SCHEMBL23326178 0.80 CYP11B1 (0.62) CYP11B1CYP11B2NPC1DGAT1KCNH2
SCHEMBL29775352 0.80 CYP11B1 (0.62) CYP11B1CYP11B2NPC1DGAT1KCNH2
SCHEMBL26133012 0.78 IL1B (0.57) CNR1CNR2CYP11B1CYP11B2NPC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4419532-A1 FUSED BICYCLIC HETEROARYL COMPOUNDS USEFUL AS NLRP3 INHIBITORS F. Hoffmann-La Roche AG (CH) 2024-08-28 EP disclosed
CN-116635029-A REV-ERB agonists 圣路易斯大学 2023-08-22 CN disclosed
WO-2023066825-A1 FUSED BICYCLIC HETEROARYL COMPOUNDS USEFUL AS NLRP3 INHIBITORS F. HOFFMANN-LA ROCHE AG (CH) 2023-04-27 WO disclosed
US-10799510-B2 Derivatives of 6-substituted triazolopyridazines as Rev-Erb agonists GENFIT (FR) 2020-10-13 US disclosed
US-20170296548-A1 DERIVATIVES OF 6-SUBSTITUTED TRIAZOLOPYRIDAZINES AS REV-ERB AGONISTS GENFIT (FR) 2017-10-19 US disclosed
US-9586963-B2 Derivatives of 6-substituted triazolopyridazines as Rev-Erb agonists GENFIT (FR) 2017-03-07 US disclosed
US-20150038503-A1 DERIVATIVES OF 6-SUBSTITUTED TRIAZOLOPYRIDAZINES AS REV-ERB AGONISTS GENFIT (FR) 2015-02-05 US disclosed
EP-2760866-A1 DERIVATIVES OF 6-SUBSTITUTED TRIAZOLOPYRIDAZINES AS REV-ERB AGONISTS Genfit (FR) 2014-08-06 EP disclosed
WO-2013045519-A1 DERIVATIVES OF 6-SUBSTITUTED TRIAZOLOPYRIDAZINES AS REV-ERB AGONISTS GENFIT (FR) 2013-04-04 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 (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-10799510-B2 Derivatives of 6-substituted triazolopyridazines as Rev-Erb agonists NR1D1, NR1D2, PER2 CNR1 202/4885CNR2 381/4885CYP11B1 50/4885
US-20170296548-A1 DERIVATIVES OF 6-SUBSTITUTED TRIAZOLOPYRIDAZINES AS REV-ERB AGONISTS NR1D1, NR1D2, PER2 CNR1 202/4885CNR2 381/4885CYP11B1 50/4885
US-20150038503-A1 DERIVATIVES OF 6-SUBSTITUTED TRIAZOLOPYRIDAZINES AS REV-ERB AGONISTS NR1D1, NR1D2, PER2 CNR1 202/4885CNR2 381/4885CYP11B1 50/4885

“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.