SCHEMBL4977459

SCHEMBL4977459

Cc1cccc(C(=O)Nc2cccc(C(F)(F)F)c2)c1NCc1ccncc1

nearest known ligand 0.73

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
KDR P35968 11/20 0.73
FLT1 P17948 5/20 0.73
KIT P10721 3/20 0.73
CSF1R P07333 2/20 0.73
ABL1 P00519 1/20 0.73
EGFR P00533 1/20 0.73
PDGFRB P09619 1/20 0.73
FLT4 P35916 1/20 0.73
RXFP1 Q9HBX9 4/20 0.60
DDR1 Q08345 1/20 0.55
DDR2 Q16832 1/20 0.55
SMO Q99835 1/20 0.53
MAPK14 Q16539 2/20 0.52
P2RX1 P51575 2/20 0.52
LCK P06239 1/20 0.51
SRC P12931 1/20 0.51

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
SCHEMBL29356168 0.84 KDR (1.00) KDRFLT1KITCSF1RABL1
SCHEMBL4976103 0.84 KDR (1.00) KDRFLT1KITCSF1RABL1
SCHEMBL427615 0.82 KDR (0.84) KDRFLT1KITCSF1RABL1
Hydrochloric Acid SCHEMBL447740 0.82 KDR (0.83) KDRFLT1KITCSF1RABL1
SCHEMBL4979871 0.80 KDR (0.77) KDRFLT1KITCSF1RABL1
SCHEMBL5964886 0.79 KDR (0.72) KDRFLT1KITCSF1RABL1
SCHEMBL427738 0.79 KDR (0.68) KDRFLT1KITCSF1RABL1
SCHEMBL4979592 0.79 KDR (0.74) KDRFLT1KITCSF1RABL1
SCHEMBL12544169 0.77 RXFP1 (0.88) RXFP1P2RX1
SCHEMBL4981385 0.76 KDR (0.68) KDRFLT1KITCSF1RABL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20040198782-A1 N-aryl (THIO) anthranilic acid amide derivatives, their preparation and their use as VEGF receptor tyrosine kinase inhibitors ALTMANN KARL-HEINZ (CH) 2004-10-07 US claimed
CN-1152014-C N-aryl (thio) anthranilic acid amide derivatives, their prepn. and their use as VEGF receptor tyrosine kinase inhibitors ��˹��ŵ�� 2004-06-02 CN claimed
US-6448277-B2 ANTITUOR AGENTS, ANTICARCINOGENIC AGENTS NOVARTIS AG (CH) 2002-09-10 US claimed
US-20020019414-A1 N-aryl(thio)anthranilic acid amide derivatives, their preparation and their use as VEGF receptor tyrosine kinase inhibitors NOVARTIS AG (CH) 2002-02-14 US claimed
CN-1331680-A N-aryl (thio) anthranilic acid amide derivatives, their prepn. and their use as VEGF receptor tyrosine kinase inhibitors NOVARTIS AG (CH) 2002-01-16 CN claimed
US-20080085902-A1 Combination Of A Vegf Receptor Inhibitor Or With A Chemotherapeutic Agent BOLD GUIDO 2008-04-10 US disclosed
US-20060074112-A1 N-aryl (thio) anthranilic acid amide derivatives, their preparation and their use as VEGF receptor tyrosine kinase inhibitors ALTMANN KARL-HEINZ 2006-04-06 US disclosed
US-7002022-B2 N-Aryl (thio) anthranilic acid amide derivatives, their preparation and their use as VEGF NOVARTIS AG (CH) 2006-02-21 US disclosed
US-6878720-B2 VEGF receptor tyrosine kinase inhibitors NOVARTIS AG (CH) 2005-04-12 US disclosed
US-20040198782-A1 N-aryl (THIO) anthranilic acid amide derivatives, their preparation and their use as VEGF receptor tyrosine kinase inhibitors ALTMANN KARL-HEINZ (CH) 2004-10-07 US disclosed
CN-1152014-C N-aryl (thio) anthranilic acid amide derivatives, their prepn. and their use as VEGF receptor tyrosine kinase inhibitors ��˹��ŵ�� 2004-06-02 CN disclosed
US-20030064992-A1 N-aryl (thio) anthranilic acid amide derivatives, their preparation and their use as VEGF receptor tyrosine kinase inhibitors ALTMANN KARL-HEINZ (CH) 2003-04-03 US disclosed
US-20020187942-A1 Method for producing beta-D-ribofuranose derivatives or optical isomers thereof AJINOMOTO CO., INC. (JP) 2002-12-12 US disclosed
US-6448277-B2 ANTITUOR AGENTS, ANTICARCINOGENIC AGENTS NOVARTIS AG (CH) 2002-09-10 US disclosed
US-20020019414-A1 N-aryl(thio)anthranilic acid amide derivatives, their preparation and their use as VEGF receptor tyrosine kinase inhibitors NOVARTIS AG (CH) 2002-02-14 US disclosed
CN-1331680-A N-aryl (thio) anthranilic acid amide derivatives, their prepn. and their use as VEGF receptor tyrosine kinase inhibitors NOVARTIS AG (CH) 2002-01-16 CN 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 (6 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-20080085902-A1 Combination Of A Vegf Receptor Inhibitor Or With A Chemotherapeutic Agent VEGFA, FLT1, FLT4 KDR 4/4885FLT1 2/4885KIT 95/4885
US-20030064992-A1 N-aryl (thio) anthranilic acid amide derivatives, their preparation and their use as VEGF receptor tyrosine kinase inhibitors AXL, TYRO3, NR2E3 KDR 4/4885FLT1 6/4885KIT 1200/4885
US-20060074112-A1 N-aryl (thio) anthranilic acid amide derivatives, their preparation and their use as VEGF receptor tyrosine kinase inhibitors NR2E3, AXL, FLT1 KDR 6/4885FLT1 3/4885KIT 1240/4885
US-20020187942-A1 Method for producing beta-D-ribofuranose derivatives or optical isomers thereof DERA, RNGTT, DUT KDR 2680/4885FLT1 2727/4885KIT 4460/4885
US-20020019414-A1 N-aryl(thio)anthranilic acid amide derivatives, their preparation and their use as VEGF receptor tyrosine kinase inhibitors AXL, TYRO3, KDR KDR 3/4885FLT1 6/4885KIT 1055/4885
US-20040198782-A1 N-aryl (THIO) anthranilic acid amide derivatives, their preparation and their use as VEGF receptor tyrosine kinase inhibitors AXL, TYRO3, NR2E3 KDR 4/4885FLT1 6/4885KIT 1176/4885

“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.