SCHEMBL6482138

SCHEMBL6482138

NC(=O)c1cc(COc2nnc(Nc3ccc(Cl)cc3)c3ccccc23)ccn1

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDR P35968 12/20 0.60
PDGFRB P09619 3/20 0.60
KIT P10721 3/20 0.60
FLT4 P35916 3/20 0.60
MAP3K20 Q9NYL2 2/20 0.60
ILK Q13418 1/20 0.60
FLT1 P17948 7/20 0.48
CSF1R P07333 2/20 0.47
CIT O14578 1/20 0.46
EGFR P00533 1/20 0.46
HLA-A P04439 1/20 0.46
RET P07949 1/20 0.46
PDGFRA P16234 1/20 0.46
RPS6KB1 P23443 1/20 0.46
FRK P42685 1/20 0.46
CDK8 P49336 1/20 0.46
DDR1 Q08345 1/20 0.46
STK3 Q13188 1/20 0.46
PTK6 Q13882 1/20 0.46
MAP3K19 Q56UN5 1/20 0.46

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
Hydrochloric Acid SCHEMBL6479719 0.99 KDR (0.59) KDRPDGFRBKITFLT4MAP3K20
SCHEMBL6497078 0.95 KDR (0.58) KDRPDGFRBKITFLT4MAP3K20
SCHEMBL6474476 0.89 KDR (0.76) KDRPDGFRBKITFLT4MAP3K20
SCHEMBL2202245 0.88 KDR (0.57) KDRPDGFRBKITFLT4MAP3K20
SCHEMBL2200373 0.86 KDR (0.80) KDRPDGFRBKITFLT4MAP3K20
SCHEMBL6497045 0.85 KDR (0.50) KDRPDGFRBKITFLT4MAP3K20
SCHEMBL12233260 0.84 KDR (0.47) KDRPDGFRBKITFLT4MAP3K20
SCHEMBL6482081 0.84 KDR (0.69) KDRPDGFRBKITFLT4MAP3K20
SCHEMBL6482221 0.84 KDR (0.53) KDRPDGFRBKITFLT4MAP3K20
SCHEMBL6600180 0.83 KDR (0.52) KDRPDGFRBKITFLT4MAP3K20

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6903101-B1 Substituted pyridazines and fused pyridazines with angiogenesis inhibiting activity BAYER PHARMACEUTICALS CORPORATION (US) 2005-06-07 US claimed
US-20050019424-A1 Anti-angiogenesis combination therapies comprising pyridazine or pyridine derivatives BAYER HEALTHCARE LLC 2005-01-27 US claimed
EP-1467736-A2 ANTI-ANGIOGENESIS COMBINATION THERAPIES COMPRISING PYRIDAZINE OR PYRIDINE DERIVATIVES Bayer Pharmaceuticals Corporation (US) 2004-10-20 EP claimed
EP-1208096-B1 SUBSTITUTED PYRIDAZINES AND FUSED PYRIDAZINES WITH ANGIOGENESIS INHIBITING ACTIVITY BAYER AG (US) 2004-04-28 EP claimed
WO-2003059354-A2 ANTI-ANGIOGENESIS COMBINATION THERAPIES COMPRISING PYRIDAZINE OR PYRIDINE DERIVATIVES BAYER PHARMACEUTICALS CORPORATION (US) 2003-07-24 WO claimed
EP-1208096-A1 SUBSTITUTED PYRIDAZINES AND FUSED PYRIDAZINES WITH ANGIOGENESIS INHIBITING ACTIVITY Bayer Corporation (US) 2002-05-29 EP claimed
WO-2001010859-A1 SUBSTITUTED PYRIDAZINES AND FUSED PYRIDAZINES WITH ANGIOGENESIS INHIBITING ACTIVITY BAYER CORPORATION (US) 2001-02-15 WO claimed
US-6903101-B1 Substituted pyridazines and fused pyridazines with angiogenesis inhibiting activity BAYER PHARMACEUTICALS CORPORATION (US) 2005-06-07 US disclosed
EP-1208096-B1 SUBSTITUTED PYRIDAZINES AND FUSED PYRIDAZINES WITH ANGIOGENESIS INHIBITING ACTIVITY BAYER AG (US) 2004-04-28 EP 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-20050019424-A1 Anti-angiogenesis combination therapies comprising pyridazine or pyridine derivatives KDR, FLT4, FLT1 KDR 1/4885PDGFRB 7/4885KIT 44/4885

“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.