SCHEMBL4707592

SCHEMBL4707592

CC(=O)c1c(-c2ccccc2)nn(C(C)C)c(=O)c1Nc1ccc(C(=O)O)cc1

nearest known ligand 0.70

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ PDE4B Q07343 2/20 0.70
▸ CSF1R P07333 1/20 0.43
▸ FGFR1 P11362 1/20 0.43
▸ FLT1 P17948 1/20 0.43
▸ KDR P35968 1/20 0.43
▸ CSNK1A1 P48729 1/20 0.43
▸ CDK8 P49336 1/20 0.43
▸ GSK3A P49840 1/20 0.43
▸ GSK3B P49841 1/20 0.43
▸ CDK5 Q00535 1/20 0.43
▸ PRKCQ Q04759 1/20 0.43
▸ LRRK2 Q5S007 1/20 0.43
▸ CLK4 Q9HAZ1 1/20 0.43
▸ DYRK1B Q9Y463 1/20 0.43
▸ MEN1 O00255 3/20 0.41
▸ KMT2A Q03164 3/20 0.41
▸ SMN1; SMN2 Q16637 1/20 0.41
▸ RXRA P19793 1/20 0.41
▸ NR4A2 P43354 1/20 0.41
▸ NPC1 O15118 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
SCHEMBL4902161 0.87 PDE4B (0.57) PDE4BCSF1RFGFR1FLT1KDR
SCHEMBL4708113 0.85 PDE4B (0.74) PDE4BCSF1RFGFR1FLT1KDR
SCHEMBL4707413 0.84 PDE4B (0.50) PDE4BCSF1RFGFR1FLT1KDR
SCHEMBL4708408 0.84 PDE4B (0.50) PDE4BCSF1RFGFR1FLT1KDR
SCHEMBL4707471 0.83 PDE4B (0.72) PDE4BCSF1RFGFR1FLT1KDR
SCHEMBL4708354 0.83 PDE4B (1.00) PDE4BCSF1RFGFR1FLT1KDR
SCHEMBL4707163 0.82 PDE4B (0.48) PDE4BCSF1RFGFR1FLT1KDR
SCHEMBL4705814 0.82 PDE4B (0.48) PDE4BCSF1RFGFR1FLT1KDR
SCHEMBL4706077 0.81 PDE4B (0.81) PDE4BCSF1RFGFR1FLT1KDR
SCHEMBL4708005 0.81 ALDH1A1 (0.48) PDE4BCSF1RFGFR1FLT1KDR

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 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
EP-1503992-A1 PYRIDAZIN-3(2H)-ONE DERIVATIVES AS PDE4 INHIBITORS Almirall Prodesfarma, S.A. (ES) 2005-02-09 — — EP disclosed
WO-2003097613-A1 PYRIDAZIN-3(2H)-ONE DERIVATIVES AS PDE4 INHIBITORS ALMIRALL PRODESFARMA SA (ES) 2003-11-27 — — 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 (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 3/4885CSF1R 4118/4885FGFR1 2580/4885
US-20060052379-A1 Pyridazin-3(2h)-one derivatives as pde4 inhibitors PDE4A, PDE3A, PDE4B PDE4B 3/4885CSF1R 4118/4885FGFR1 2580/4885

“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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