SCHEMBL1229145

SCHEMBL1229145

Cn1nccc(NC(=O)N2CCC(Oc3ccc(F)c(C(F)(F)F)c3)CC2)c1=O

nearest known ligand 0.41

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
▸ HRH1 P35367 1/20 0.41
▸ CCR3 P51677 1/20 0.41
▸ ACACB O00763 2/20 0.41
▸ HRH3 Q9Y5N1 6/20 0.40
▸ SCD O00767 1/20 0.40
▸ RBP4 P02753 2/20 0.39
▸ NTRK1 P04629 1/20 0.38
▸ KCNH2 Q12809 1/20 0.38
▸ NTRK3 Q16288 1/20 0.38
▸ NTRK2 Q16620 1/20 0.38
▸ GPR119 Q8TDV5 1/20 0.38
▸ GPR6 P46095 1/20 0.38
▸ EPHX2 P34913 3/20 0.37

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
SCHEMBL1230463 0.85 EPHX2 (0.54) HRH1CCR3SCDEPHX2
SCHEMBL1230256 0.84 SCD (0.45) SCDRBP4GPR6EPHX2
SCHEMBL1231173 0.84 SCD (0.43) SCDNTRK1KCNH2NTRK3NTRK2
SCHEMBL1231030 0.84 SCD (0.54) SCDRBP4NTRK1KCNH2NTRK3
SCHEMBL1230324 0.82 CCR3 (0.48) HRH1CCR3KCNH2
SCHEMBL1231202 0.81 GPR6 (0.45) SCDGPR6
SCHEMBL1229540 0.79 IKBKB (0.43) HRH1CCR3SCDNTRK1KCNH2
SCHEMBL1230439 0.78 SCD (0.67) HRH1CCR3SCDRBP4
SCHEMBL1230343 0.77 SCD (0.41) SCDGPR6EPHX2
SCHEMBL1231168 0.76 SCD (0.53) SCDGPR6EPHX2

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
WO-2011015629-A1 DERIVATIVES OF 2H PYRIDAZIN- 3 -ONES, THEIR PREPARATION AND THEIR USE AS SCD-1 INHIBITORS PIERRE FABRE MEDICAMENT (FR) 2011-02-10 — — WO claimed
EP-2462121-B1 DERIVATIVES OF 2H PYRIDAZIN-3-ONES, THEIR PREPARATION AND THEIR USE AS SCD-1 INHIBITORS PF MEDICAMENT (FR) 2015-02-18 — — EP disclosed
US-8946225-B2 Derivatives of 2H pyridazin-3-ones, their preparation and their use as SCD-1 inhibitors PIERRE FABRE MEDICAMENT (FR) 2015-02-03 — — US disclosed
US-8946225-B2 Derivatives of 2H pyridazin-3-ones, their preparation and their use as SCD-1 inhibitors PIERRE FABRE MEDICAMENT (FR) 2015-02-03 — — US disclosed
US-20120178678-A1 DERIVATIVES OF 2H PYRIDAZIN- 3 -ONES, THEIR PREPARATION AND THEIR USE AS SCD-1 INHIBITORS PIERRE FABRE MEDICAMENT (FR) 2012-07-12 — — US disclosed
US-20120178678-A1 DERIVATIVES OF 2H PYRIDAZIN- 3 -ONES, THEIR PREPARATION AND THEIR USE AS SCD-1 INHIBITORS PIERRE FABRE MEDICAMENT (FR) 2012-07-12 — — US disclosed
WO-2011015629-A1 DERIVATIVES OF 2H PYRIDAZIN- 3 -ONES, THEIR PREPARATION AND THEIR USE AS SCD-1 INHIBITORS PIERRE FABRE MEDICAMENT (FR) 2011-02-10 — — WO disclosed
WO-2011015629-A1 DERIVATIVES OF 2H PYRIDAZIN- 3 -ONES, THEIR PREPARATION AND THEIR USE AS SCD-1 INHIBITORS PIERRE FABRE MEDICAMENT (FR) 2011-02-10 — — 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-20120178678-A1 DERIVATIVES OF 2H PYRIDAZIN- 3 -ONES, THEIR PREPARATION AND THEIR USE AS SCD-1 INHIBITORS SCD, SCD5, CYP2S1 HRH1 1017/4885CCR3 1668/4885ACACB 446/4885

“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.

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