SCHEMBL4707672

SCHEMBL4707672

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

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PDE4B Q07343 1/20 0.47
RAB9A P51151 4/20 0.43
SMN1; SMN2 Q16637 3/20 0.43
POLB P06746 3/20 0.41
NPC1 O15118 3/20 0.41
AURKA O14965 1/20 0.41
RPS6KB1 P23443 1/20 0.41
MEN1 O00255 3/20 0.40
KMT2A Q03164 3/20 0.40
KDM4E B2RXH2 3/20 0.40
ALDH1A1 P00352 1/20 0.40
MAPT P10636 1/20 0.40
AKR1B1 P15121 1/20 0.40
RXFP1 Q9HBX9 1/20 0.39
TDP1 Q9NUW8 1/20 0.39
RIPK1 Q13546 1/20 0.39
PKM P14618 1/20 0.39
LMNA P02545 1/20 0.39
HPGD P15428 1/20 0.39
ACHE P22303 1/20 0.39

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
SCHEMBL4706418 0.88 PDE4B (0.60) PDE4BRAB9ASMN1; SMN2POLBKDM4E
SCHEMBL4706084 0.81 PDE4B (0.62) PDE4BRAB9ASMN1; SMN2POLBNPC1
SCHEMBL4058811 0.80 PDE4B (0.70) PDE4BRAB9ASMN1; SMN2POLBNPC1
SCHEMBL4678300 0.80 PDE4B (0.53) PDE4BRAB9ASMN1; SMN2POLBNPC1
SCHEMBL4707603 0.79 PDE4B (0.55) PDE4BSMN1; SMN2KDM4EALDH1A1MAPT
SCHEMBL4708343 0.79 PDE4B (0.56) PDE4BSMN1; SMN2MEN1KMT2AMAPT
SCHEMBL4706645 0.78 PDE4B (0.56) PDE4BSMN1; SMN2POLBMEN1KMT2A
SCHEMBL6185709 0.78 PDE4B (0.47) PDE4BSMN1; SMN2POLBMAPTRXFP1
SCHEMBL1652702 0.77 PDE4B (0.52) PDE4BRAB9ASMN1; SMN2POLBNPC1
SCHEMBL4707865 0.77 PDE4B (0.62) PDE4BRAB9ASMN1; SMN2POLBNPC1

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
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
EP-1503992-A1 PYRIDAZIN-3(2H)-ONE DERIVATIVES AS PDE4 INHIBITORS Almirall Prodesfarma, S.A. (ES) 2005-02-09 EP claimed
WO-2003097613-A1 PYRIDAZIN-3(2H)-ONE DERIVATIVES AS PDE4 INHIBITORS ALMIRALL PRODESFARMA SA (ES) 2003-11-27 WO 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 3/4885RAB9A 2162/4885SMN1; SMN2 2927/4885
US-20060052379-A1 Pyridazin-3(2h)-one derivatives as pde4 inhibitors PDE4A, PDE3A, PDE4B PDE4B 3/4885RAB9A 2162/4885SMN1; 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.