SCHEMBL863668

SCHEMBL863668

CNC(=O)Nc1ccc(Oc2ccnc3cc(OC)c(C(N)=O)cc23)cc1Cl

nearest known ligand 0.79

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDR P35968 19/20 0.79
PDGFRA P16234 10/20 0.79
AURKB Q96GD4 6/20 0.79
RET P07949 4/20 0.79
FLT1 P17948 4/20 0.79
FLT4 P35916 4/20 0.79
KIT P10721 4/20 0.79
PDGFRB P09619 3/20 0.79
FGFR1 P11362 3/20 0.79
ABL1 P00519 3/20 0.79
RIPK2 O43353 2/20 0.79
STK10 O94804 2/20 0.79
BCR P11274 2/20 0.79
SLC6A3 Q01959 2/20 0.79
DDR1 Q08345 2/20 0.79
MAP4K2 Q12851 2/20 0.79
PTK6 Q13882 2/20 0.79
DDR2 Q16832 2/20 0.79
RIPK3 Q9Y572 2/20 0.79
FGFR2 P21802 2/20 0.79

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
SCHEMBL23366513 0.95 KDR (0.83) KDRPDGFRAAURKBRETFLT1
SCHEMBL23366514 0.94 KDR (0.76) KDRPDGFRAAURKBRETFLT1
SCHEMBL1894042 0.92 KDR (0.67) KDRPDGFRAAURKBRETFLT1
SCHEMBL1889913 0.92 KDR (0.67) KDRPDGFRAAURKBRETFLT1
SCHEMBL1895503 0.92 KDR (0.67) KDRPDGFRAAURKBRETFLT1
SCHEMBL1890089 0.92 KDR (0.77) KDRPDGFRAAURKBRETFLT1
SCHEMBL1899422 0.91 KDR (0.67) KDRPDGFRAAURKBRETFLT1
SCHEMBL19956985 0.91 KDR (0.72) KDRPDGFRAAURKBRETFLT1
SCHEMBL2177590 0.91 KDR (0.76) KDRPDGFRAAURKBRETFLT1
SCHEMBL19072630 0.91 KDR (0.76) KDRPDGFRAAURKBRETFLT1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107305202-B HPLC method for analyzing impurities of levovatinib mesylate and preparation thereof and application of impurities as reference standard 北京睿创康泰医药研究院有限公司 2020-04-17 CN claimed
EP-2700403-B1 THERAPEUTIC AGENT FOR TUMOR EISAI R&D MAN CO LTD (JP) 2015-11-25 EP claimed
EP-2036557-B1 ANTITUMOR AGENT FOR THYROID CANCER EISAI R&D MAN CO LTD (JP) 2015-10-21 EP claimed
US-9012458-B2 Antitumor agent using compounds having kinase inhibitory effect in combination EISAI R&D MANAGEMENT CO., LTD. (JP) 2015-04-21 US claimed
US-9006240-B2 Method for assay on the effect of vascularization inhibitor EISAI R&D MANAGEMENT CO., LTD. (JP) 2015-04-14 US claimed
US-8969344-B2 Method for assay on the effect of vascularization inhibitor EISAI R&D MANAGEMENT CO., LTD. (JP) 2015-03-03 US claimed
US-8962650-B2 Therapeutic agent for tumor EISAI R&D MANAGEMENT CO., LTD. (JP) 2015-02-24 US claimed
EP-2119707-B1 COMPOSITION FOR TREATMENT OF UNDIFFERENTIATED-TYPE OF GASTRIC CANCER EISAI R&D MAN CO LTD (JP) 2015-01-14 EP claimed
EP-2700403-A1 THERAPEUTIC AGENT FOR TUMOR Eisai R&D Management Co., Ltd. (JP) 2014-02-26 EP claimed
US-20140031384-A1 THERAPEUTIC AGENT FOR TUMOR EISAI R&D MANAGEMENT CO., LTD. (JP) 2014-01-30 US claimed
EP-1964837-A1 ANTI-TUMOR AGENT FOR MULTIPLE MYELOMA Eisai R&D Management Co., Ltd. (JP) 2008-09-03 EP claimed
EP-1949902-A1 USE OF COMBINATION OF ANTI-ANGIOGENIC SUBSTANCE AND c-kit KINASE INHIBITOR Eisai R&D Management Co., Ltd. (JP) 2008-07-30 EP claimed
EP-1925676-A1 METHOD FOR ASSAY ON THE EFFECT OF VASCULARIZATION INHIBITOR Eisai R&D Management Co., Ltd. (JP) 2008-05-28 EP claimed
EP-1925941-A1 METHOD FOR PREDICTION OF THE EFFICACY OF VASCULARIZATION INHIBITOR Eisai R&D Management Co., Ltd. (JP) 2008-05-28 EP claimed
US-7253286-B2 Urea derivatives containing aromatic or heteroaromatic rings, useful as prophylactic or therapeutic agent for a disease for which angiogenesis inhibition is effective EISAI CO., LTD (JP) 2007-08-07 US claimed
EP-1797877-A1 JOINT USE OF SULFONAMIDE BASED COMPOUND WITH ANGIOGENESIS INHIBITOR Eisai Co., Ltd. (JP) 2007-06-20 EP claimed
EP-1415987-B1 NITROGENOUS AROMATIC RING COMPOUNDS AS ANTI CANCER AGENTS EISAI R&D MAN CO LTD (JP) 2007-02-28 EP claimed
US-20060135486-A1 Use of sulfonamide-including compounds in combination with angiogenesis inhibitors EISAI CO., LTD. (JP) 2006-06-22 US claimed
EP-1415987-A1 NITROGENOUS AROMATIC RING COMPOUNDS Eisai Co., Ltd. (JP) 2004-05-06 EP claimed
US-20040053908-A1 Urea derivatives containing aromatic or heteroaromatic rings, useful as prophylactic or therapeutic agent for a disease for which angiogenesis inhibition is effective EISAI R&D MANAGEMENT CO., LTD. (JP) 2004-03-18 US claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (3 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-20040053908-A1 Urea derivatives containing aromatic or heteroaromatic rings, useful as prophylactic or therapeutic agent for a disease for which angiogenesis inhibition is effective VEGFA, UACA, UTS2R KDR 22/4885PDGFRA 1572/4885AURKB 2738/4885
US-20060135486-A1 Use of sulfonamide-including compounds in combination with angiogenesis inhibitors FLT4, KDR, FLT1 KDR 2/4885PDGFRA 13/4885AURKB 1878/4885
US-20140031384-A1 THERAPEUTIC AGENT FOR TUMOR KRAS, TP53, HRAS KDR 1270/4885PDGFRA 841/4885AURKB 2760/4885

“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.