SCHEMBL5207914

SCHEMBL5207914

COC(=O)c1ccc(OC)c2nc(C(F)(F)F)ccc12

nearest known ligand 0.65

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PDE4B Q07343 19/20 0.65
PDE4A P27815 8/20 0.65
PDE4C Q08493 8/20 0.65
PDE4D Q08499 8/20 0.65
PDE11A Q9HCR9 2/20 0.64
PDE10A Q9Y233 1/20 0.50
TUBB4A P04350 1/20 0.50
TUBB P07437 1/20 0.50
TUBA3C P0DPH7 1/20 0.50
TUBA1B P68363 1/20 0.50
TUBA4A P68366 1/20 0.50
TUBB4B P68371 1/20 0.50
TUBB3 Q13509 1/20 0.50
TUBB2A Q13885 1/20 0.50
TUBB8 Q3ZCM7 1/20 0.50
TUBA3E Q6PEY2 1/20 0.50
TUBA1A Q71U36 1/20 0.50
TUBA1C Q9BQE3 1/20 0.50
TUBB6 Q9BUF5 1/20 0.50
TUBB2B Q9BVA1 1/20 0.50

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
SCHEMBL2671425 0.88 PDE4B (0.63) PDE4BPDE4APDE4CPDE4DPDE11A
SCHEMBL3119101 0.88 PDE4B (0.63) PDE4BPDE4APDE4CPDE4DPDE11A
SCHEMBL8275008 0.86 PDE4B (0.61) PDE4BPDE4APDE4CPDE4DPDE11A
SCHEMBL4704186 0.86 PDE4B (0.64) PDE4BPDE4APDE4CPDE4DPDE11A
SCHEMBL2847332 0.85 PDE4B (0.60) PDE4BPDE4APDE4CPDE4DPDE11A
SCHEMBL2839762 0.84 PDE4B (0.59) PDE4BPDE4APDE4CPDE4DPDE11A
SCHEMBL13354230 0.84 PDE4B (0.59) PDE4BPDE4APDE4CPDE4DPDE11A
SCHEMBL2842068 0.83 PDE4B (0.58) PDE4BPDE4APDE4CPDE4DPDE11A
SCHEMBL13918308 0.82 PDE4B (0.62) PDE4BPDE4APDE4CPDE4DPDE11A
SCHEMBL8274723 0.81 PDE4B (0.56) PDE4BPDE4APDE4CPDE4DPDE11A

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
EP-1664024-B1 SYNTHESIS OF QUINOLINE 5-CARBOXAMIDES USEFUL FOR THE PREPARATION OF PDE IV INHIBITORS SCHERING CORP (US) 2007-07-11 EP disclosed
EP-1664024-B1 SYNTHESIS OF QUINOLINE 5-CARBOXAMIDES USEFUL FOR THE PREPARATION OF PDE IV INHIBITORS SCHERING CORP (US) 2007-07-11 EP disclosed
US-7129357-B2 Synthesis of quinoline 5-carboxamides useful for the preparation of PDE IV inhibitors SCHERING CORPORATION (US) 2006-10-31 US disclosed
EP-1664024-A1 SYNTHESIS OF QUINOLINE 5-CARBOXAMIDES USEFUL FOR THE PREPARATION OF PDE IV INHIBITORS SCHERING CORPORATION (US) 2006-06-07 EP disclosed
US-20050124655-A1 Synthesis of quinoline 5-carboxamides useful for the preparation of PDE IV inhibitors SCHERING CORPORATION 2005-06-09 US disclosed
WO-2005028471-A1 SYNTHESIS OF QUINOLINE 5-CARBOXAMIDES USEFUL FOR THE PREPARATION OF PDE IV INHIBITORS SCHERING CORPORATION (US) 2005-03-31 WO disclosed
WO-2005028471-A1 SYNTHESIS OF QUINOLINE 5-CARBOXAMIDES USEFUL FOR THE PREPARATION OF PDE IV INHIBITORS SCHERING CORPORATION (US) 2005-03-31 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 (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-20050124655-A1 Synthesis of quinoline 5-carboxamides useful for the preparation of PDE IV inhibitors PDE3B, PDE4A, PDE5A PDE4B 6/4885PDE4A 2/4885PDE4C 8/4885

“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.