SCHEMBL937568

SCHEMBL937568

CCNC(=O)c1cc(Oc2ccc(NC(=O)Nc3ccc(Cl)c(C(F)(F)F)c3)cc2)ccn1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
RAF1 P04049 12/20 1.00
KDR P35968 4/20 0.81
PDGFRB P09619 4/20 0.81
BRAF P15056 3/20 0.81
RET P07949 3/20 0.81
GSK3B P49841 2/20 0.81
ARAF P10398 2/20 0.81
RIPK2 O43353 2/20 0.81
ABCB11 O95342 2/20 0.81
ABL1 P00519 2/20 0.81
HTR1A P08908 2/20 0.81
ADORA3 P0DMS8 2/20 0.81
KIT P10721 2/20 0.81
FGFR1 P11362 2/20 0.81
PDGFRA P16234 2/20 0.81
FLT1 P17948 2/20 0.81
MAOA P21397 2/20 0.81
EPHA1 P21709 2/20 0.81
TBXA2R P21731 2/20 0.81
EPHA2 P29317 2/20 0.81

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
SCHEMBL14481765 0.93 RAF1 (0.86) RAF1KDRPDGFRBBRAFRET
SCHEMBL13471762 0.92 RAF1 (0.84) RAF1KDRPDGFRBBRAFRET
SCHEMBL2480623 0.92 RAF1 (0.84) RAF1KDRPDGFRBBRAFRET
SCHEMBL13471761 0.92 RAF1 (0.84) RAF1KDRPDGFRBBRAFRET
SCHEMBL14964383 0.91 RAF1 (0.84) RAF1KDRPDGFRBBRAFRET
SCHEMBL3707691 0.91 RAF1 (0.83) RAF1KDRPDGFRBBRAFRET
SCHEMBL22001800 0.90 RAF1 (0.82) RAF1KDRPDGFRBBRAFRET
SCHEMBL20909069 0.90 RAF1 (0.82) RAF1KDRPDGFRBBRAFRET
SCHEMBL22473654 0.90 RAF1 (0.82) RAF1KDRPDGFRBBRAFRET
Sorafenib SCHEMBL15921371 0.90 RAF1 (0.93) RAF1KDRPDGFRBBRAFRET

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2786750-A1 AGENT FOR REDUCING ADVERSE SIDE EFFECTS OF KINASE INHIBITOR Ajinomoto Co., Inc. (JP) 2014-10-08 EP claimed
EP-2324825-A1 Aryl ureas with angiogenesis inhibiting activity Bayer Healthcare LLC (US) 2011-05-25 EP claimed
US-10653684-B2 Aryl ureas with angiogenisis inhibiting activity BAYER HEALTHCARE LLC (US) 2020-05-19 US disclosed
US-20180296541-A9 ARYL UREAS WITH ANGIOGENISIS INHIBITING ACTIVITY BAYER HEALTHCARE LLC (US) 2018-10-18 US disclosed
US-9651554-B2 Molecular diagnostic methods for predicting brain metastasis of breast cancer THE METHODIST HOSPITAL RESEARCH INSTITUTE (US) 2017-05-16 US disclosed
US-20160015697-A1 ARYL UREAS WITH ANGIOGENISIS INHIBITING ACTIVITY BAYER HEALTHCARE LLC (US) 2016-01-21 US disclosed
EP-2786750-A1 AGENT FOR REDUCING ADVERSE SIDE EFFECTS OF KINASE INHIBITOR Ajinomoto Co., Inc. (JP) 2014-10-08 EP disclosed
US-8618141-B2 Aryl ureas with angiogenesis inhibiting activity BAYER HEALTHCARE LLC (US) 2013-12-31 US disclosed
EP-1478358-B1 Sorafenib tosylate for the treatment of diseases characterized by abnormal angiogenesis BAYER HEALTHCARE LLC (US) 2013-07-03 EP disclosed
US-8445687-B2 Process for the preparation of a RAF kinase inhibitor and intermediates for use in the process CIPLA LIMITED (IN) 2013-05-21 US disclosed
US-20120289552-A1 ARYL UREAS WITH ANGIOGENESIS INHIBITING ACTIVITY BAYER HEALTHCARE LLC (US) 2012-11-15 US disclosed
US-20100022467-A1 ANTI-CANCER PHOSPHONATE ANALOGS BOOJAMRA CONSTANTINE G 2010-01-28 US disclosed
US-20090068146-A1 DIARYL UREAS AND COMBINATIONS BAYER PHARMACEUTICALS CORPORATION 2009-03-12 US disclosed
US-20090012091-A1 Oximide derivatives and their therapeutical application KINAGEN, INC. (US) 2009-01-08 US disclosed
US-20090012091-A1 Oximide derivatives and their therapeutical application KINAGEN, INC. (US) 2009-01-08 US disclosed
US-7452901-B2 Anti-cancer phosphonate analogs GILEAD SCIENCES, INC. (US) 2008-11-18 US disclosed
US-20080227828-A1 Aryl Ureas With Angiogenisis Inhibiting Activity BAYER HEALTHCARE LLC 2008-09-18 US disclosed
US-7417055-B2 Kinase inhibitory phosphonate analogs GILEAD SCIENCES, INC. (US) 2008-08-26 US disclosed
EP-1636585-B1 DIARYL UREAS WITH KINASE INHIBITING ACTIVITY BAYER PHARMACEUTICALS CORP (US) 2008-01-16 EP disclosed
US-20070020704-A1 Diaryl ureas with kinase inhibiting activity BAYER HEALTHCARE LLC 2007-01-25 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 (9 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-20090012091-A1 Oximide derivatives and their therapeutical application CYP11B2, NOS2, HMOX2 RAF1 3755/4885KDR 1151/4885PDGFRB 1422/4885
US-20180296541-A9 ARYL UREAS WITH ANGIOGENISIS INHIBITING ACTIVITY FLT1, FLT4, KDR RAF1 867/4885KDR 3/4885PDGFRB 117/4885
US-20070020704-A1 Diaryl ureas with kinase inhibiting activity FLT4, FLT1, FLT3 RAF1 51/4885KDR 44/4885PDGFRB 25/4885
US-10653684-B2 Aryl ureas with angiogenisis inhibiting activity FLT1, FLT4, KDR RAF1 867/4885KDR 3/4885PDGFRB 117/4885
US-20080227828-A1 Aryl Ureas With Angiogenisis Inhibiting Activity FLT1, FLT4, KDR RAF1 867/4885KDR 3/4885PDGFRB 117/4885
US-20090068146-A1 DIARYL UREAS AND COMBINATIONS NR4A1, NAP1L4, NR4A3 RAF1 4118/4885KDR 2385/4885PDGFRB 3206/4885
US-20120289552-A1 ARYL UREAS WITH ANGIOGENESIS INHIBITING ACTIVITY FLT4, FLT1, KDR RAF1 817/4885KDR 3/4885PDGFRB 137/4885
US-20160015697-A1 ARYL UREAS WITH ANGIOGENISIS INHIBITING ACTIVITY FLT1, FLT4, KDR RAF1 867/4885KDR 3/4885PDGFRB 117/4885
US-20100022467-A1 ANTI-CANCER PHOSPHONATE ANALOGS PIK3CA, PHOSPHO1, PTEN RAF1 1304/4885KDR 1628/4885PDGFRB 644/4885

“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.