SCHEMBL3084639

SCHEMBL3084639

Cc1ccc(C(=O)Nc2cccc(C(F)(F)F)c2)cc1C(N)=O

nearest known ligand 0.71

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPK14 Q16539 8/20 0.71
KIT P10721 7/20 0.71
KDR P35968 7/20 0.71
LCK P06239 5/20 0.71
SRC P12931 2/20 0.71
CSF1R P07333 3/20 0.69
DDR2 Q16832 3/20 0.66
MAPT P10636 2/20 0.65
DDR1 Q08345 2/20 0.63
EPHB2 P29323 1/20 0.63
MEN1 O00255 1/20 0.62
HTT P42858 1/20 0.62
RAB9A P51151 1/20 0.62
KMT2A Q03164 1/20 0.62
KCNK3 O14649 1/20 0.60
KCNK9 Q9NPC2 1/20 0.60
BTK Q06187 2/20 0.59
BRAF P15056 1/20 0.59
RXFP1 Q9HBX9 2/20 0.59
KDM4E B2RXH2 1/20 0.59

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
SCHEMBL3074483 0.90 LCK (0.71) MAPK14KITKDRLCKSRC
SCHEMBL15987528 0.89 KIT (0.72) MAPK14KITKDRLCKSRC
SCHEMBL12858514 0.86 MAPT (0.74) MAPK14KITKDRLCKSRC
SCHEMBL2313285 0.85 MAPT (0.68) MAPK14KITKDRLCKSRC
SCHEMBL1264375 0.84 MAPT (0.74) MAPK14KITKDRLCKSRC
SCHEMBL20467572 0.84 MAPT (0.70) MAPK14KITKDRLCKSRC
SCHEMBL2951430 0.83 LCK (1.00) MAPK14KITKDRLCKSRC
SCHEMBL24070816 0.83 MAPT (0.65) MAPK14KITKDRLCKSRC
SCHEMBL30211957 0.83 MAPT (0.65) MAPK14KITKDRLCKSRC
SCHEMBL2949699 0.83 MAPK14 (0.78) MAPK14KITKDRLCKSRC

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 32 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7795273-B2 Pyrazolo[1,5-a]pyridine-3-carboxylic acids as EphB and VEGFR2 kinase inhibitors NOVARTIS AG (CH) 2010-09-14 US claimed
US-20100093821-A1 3-Amino-pyrazole-4-carboxamide derivatives useful as inhibitors of protein kinases HOLZER PHILIPP 2010-04-15 US claimed
US-7589101-B2 Compounds and compositions as protein kinase inhibitors IRM LLC (BM) 2009-09-15 US claimed
EP-2079745-A1 3-AMINOCARBONYI-SUBSTITUTED FUSED PYRAZOLO-DERIVATIVES AS PROTEIN KINASE MODULATORS Novartis AG (CH) 2009-07-22 EP claimed
EP-2079702-A1 3-AMINO-PYRAZOLE-4-CARBOXAMIDE DERIVATIVES USEFUL AS INHIBITORS OF PROTEIN KINASES Novartis AG (CH) 2009-07-22 EP claimed
US-20090105250-A1 COMPOUNDS AND COMPOSITIONS AS PROTEIN KINASE INHIBITORS IRM LLC (BM) 2009-04-23 US claimed
US-20080300245-A1 Pyrazolo[1,5-A]Pyridine-3-Carboxylic Acids as Ephb and Vegfr2 Kinase Inhibitors IMBACH PATRICIA 2008-12-04 US claimed
US-20080287432-A1 Compounds and Compositions as Protein Kinase Inhibitors IRM LLC (BM) 2008-11-20 US claimed
EP-1963316-A2 PYRAZOLO[1,5-A]PYRIDINE-3-CARBOXYLIC ACIDS AS EPHB AND VEGFR2 KINASE INHIBITORS Novartis AG (CH) 2008-09-03 EP claimed
EP-1919924-A2 COMPOUNDS AND COMPOSITIONS AS PROTEIN KINASE INHIBITORS IRM, LLC (BM) 2008-05-14 EP claimed
WO-2008052974-A1 3-AMINO-PYRAZOLE-4-CARBOXAMIDE DERIVATIVES USEFUL AS INHIBITORS OF PROTEIN KINASES NOVARTIS AG (CH) 2008-05-08 WO claimed
WO-2008052964-A1 3-AMINOCARBONYI-SUBSTITUTED FUSED PYRAZOLO-DERIVATIVES AS PROTEIN KINASE MODULATORS NOVARTIS AG (CH) 2008-05-08 WO claimed
EP-1918291-A1 3-Aminocarbonyl-substituted fused pyrazolo-derivatives as protein kinase modulators Novartis AG (CH) 2008-05-07 EP claimed
EP-1841431-A2 COMPOUNDS AND COMPOSITIONS AS PROTEIN KINASE INHIBITORS IRM, LLC (BM) 2007-10-10 EP claimed
WO-2007065664-A2 PYRAZOLO[1,5-A]PYRIDINE-3-CARBOXYLIC ACIDS AS EPHB AND VEGFR2 KINASE INHIBITORS NOVARTIS AG (CH) 2007-06-14 WO claimed
WO-2007022268-A2 COMPOUNDS AND COMPOSITIONS AS PROTEIN KINASE INHIBITORS IRM LLC (BM) 2007-02-22 WO claimed
WO-2006081172-A2 COMPOUNDS AND COMPOSITIONS AS PROTEIN KINASE INHIBITORS IRM LLC (BM) 2006-08-03 WO claimed
US-7795273-B2 Pyrazolo[1,5-a]pyridine-3-carboxylic acids as EphB and VEGFR2 kinase inhibitors NOVARTIS AG (CH) 2010-09-14 US disclosed
WO-2007022268-A2 COMPOUNDS AND COMPOSITIONS AS PROTEIN KINASE INHIBITORS IRM LLC (BM) 2007-02-22 WO disclosed
WO-2006081172-A2 COMPOUNDS AND COMPOSITIONS AS PROTEIN KINASE INHIBITORS IRM LLC (BM) 2006-08-03 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 (4 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-20090105250-A1 COMPOUNDS AND COMPOSITIONS AS PROTEIN KINASE INHIBITORS ABL1, BCR, PDGFRB MAPK14 461/4885KIT 683/4885KDR 172/4885
US-20080287432-A1 Compounds and Compositions as Protein Kinase Inhibitors AURKC, PTK2B, FRK MAPK14 442/4885KIT 115/4885KDR 78/4885
US-20080300245-A1 Pyrazolo[1,5-A]Pyridine-3-Carboxylic Acids as Ephb and Vegfr2 Kinase Inhibitors EPHB2, EPHB1, EPHB3 MAPK14 143/4885KIT 133/4885KDR 7/4885
US-20100093821-A1 3-Amino-pyrazole-4-carboxamide derivatives useful as inhibitors of protein kinases MAP4K2, MAP4K3, MAP4K1 MAPK14 47/4885KIT 699/4885KDR 1705/4885

“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.