SCHEMBL4706435

SCHEMBL4706435

CCn1nc(-c2ccccc2)c(C(C)=O)c(Nc2cccc(C(=O)O)c2)c1=O

nearest known ligand 0.79

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PDE4B Q07343 1/20 0.79
L3MBTL1 Q9Y468 1/20 0.44
SMN1; SMN2 Q16637 1/20 0.43
AKR1C4 P17516 1/20 0.43
AKR1C3 P42330 1/20 0.43
AKR1C2 P52895 1/20 0.43
AKR1C1 Q04828 1/20 0.43
RHOA P61586 1/20 0.42
GSK3B P49841 2/20 0.42
CSF1R P07333 1/20 0.41
FGFR1 P11362 1/20 0.41
FLT1 P17948 1/20 0.41
KDR P35968 1/20 0.41
CSNK1A1 P48729 1/20 0.41
CDK8 P49336 1/20 0.41
GSK3A P49840 1/20 0.41
CDK5 Q00535 1/20 0.41
PRKCQ Q04759 1/20 0.41
LRRK2 Q5S007 1/20 0.41
CLK4 Q9HAZ1 1/20 0.41

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
SCHEMBL4710128 0.95 PDE4B (0.74) PDE4BSMN1; SMN2
SCHEMBL4674510 0.93 PDE4B (0.69) PDE4BL3MBTL1SMN1; SMN2AKR1C4AKR1C3
SCHEMBL4706065 0.92 PDE4B (0.70) PDE4BSMN1; SMN2GSK3BCSF1RFGFR1
SCHEMBL6167638 0.92 PDE4B (0.68) PDE4BL3MBTL1SMN1; SMN2AKR1C4AKR1C3
SCHEMBL4709867 0.91 PDE4B (0.69) PDE4BSMN1; SMN2GSK3BCSF1RFGFR1
SCHEMBL4706611 0.90 PDE4B (0.68) PDE4BSMN1; SMN2GSK3BCSF1RFGFR1
SCHEMBL4708040 0.90 PDE4B (0.72) PDE4BSMN1; SMN2GSK3BCSF1RFGFR1
SCHEMBL6166894 0.89 PDE4B (0.64) PDE4BL3MBTL1SMN1; SMN2AKR1C4AKR1C3
SCHEMBL4706123 0.89 PDE4B (0.71) PDE4BSMN1; SMN2GSK3BCSF1RFGFR1
SCHEMBL4708354 0.89 PDE4B (1.00) PDE4BSMN1; SMN2GSK3BCSF1RFGFR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7459453-B2 Pyridazin-3(2H)-one derivatives as PDE4 inhibitors LABORATORIOS ALMIRALL, S.A. (ES) 2008-12-02 US claimed
US-20060052379-A1 Pyridazin-3(2h)-one derivatives as pde4 inhibitors LABORATORIOS ALMIRALL, S.A. (ES) 2006-03-09 US claimed
US-7459453-B2 Pyridazin-3(2H)-one derivatives as PDE4 inhibitors LABORATORIOS ALMIRALL, S.A. (ES) 2008-12-02 US disclosed
US-20080269235-A1 PYRIDAZIN-3 (2H) -ONE DERIVATIVES AS PDE4 INHIBITORS DAL PIAZ VITTORIO 2008-10-30 US disclosed
US-20060052379-A1 Pyridazin-3(2h)-one derivatives as pde4 inhibitors LABORATORIOS ALMIRALL, S.A. (ES) 2006-03-09 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 (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-20080269235-A1 PYRIDAZIN-3 (2H) -ONE DERIVATIVES AS PDE4 INHIBITORS PDE4A, PDE3A, PDE4B PDE4B 3/4885L3MBTL1 4850/4885SMN1; SMN2 2927/4885
US-20060052379-A1 Pyridazin-3(2h)-one derivatives as pde4 inhibitors PDE4A, PDE3A, PDE4B PDE4B 3/4885L3MBTL1 4850/4885SMN1; SMN2 2927/4885

“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.