SCHEMBL694648

SCHEMBL694648

CNC(=O)c1cc(Oc2ccc(N(C(N)=O)c3ccc(Cl)c(C(F)(F)F)c3)cc2)ccn1

nearest known ligand 0.67

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
RAF1 P04049 15/20 0.67
BRAF P15056 9/20 0.67
KDR P35968 5/20 0.67
RET P07949 3/20 0.67
RIPK2 O43353 2/20 0.67
ABCB11 O95342 2/20 0.67
ABL1 P00519 2/20 0.67
HTR1A P08908 2/20 0.67
PDGFRB P09619 2/20 0.67
ADORA3 P0DMS8 2/20 0.67
KIT P10721 2/20 0.67
FGFR1 P11362 2/20 0.67
PDGFRA P16234 2/20 0.67
FLT1 P17948 2/20 0.67
MAOA P21397 2/20 0.67
EPHA1 P21709 2/20 0.67
TBXA2R P21731 2/20 0.67
EPHA2 P29317 2/20 0.67
TTK P33981 2/20 0.67
EPHX2 P34913 2/20 0.67

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 SCHEMBL1702120 0.99 RAF1 (0.66) RAF1BRAFKDRRETRIPK2
Hydrochloric Acid SCHEMBL1702492 0.98 RAF1 (0.65) RAF1BRAFKDRRETRIPK2
SCHEMBL1702479 0.96 RAF1 (0.63) RAF1BRAFKDRRETRIPK2
Sulfuric Acid SCHEMBL2043327 0.96 RAF1 (0.63) RAF1BRAFKDRRETRIPK2
Maleic Acid SCHEMBL1702367 0.95 RAF1 (0.61) RAF1BRAFKDRRETRIPK2
SCHEMBL2045624 0.94 RAF1 (0.60) RAF1BRAFKDRRETRIPK2
SCHEMBL14481187 0.94 RAF1 (0.59) RAF1BRAFKDRRETRIPK2
Sorafenib SCHEMBL16699243 0.93 RAF1 (0.81) RAF1BRAFKDRRETRIPK2
SCHEMBL5079975 0.93 RAF1 (0.69) RAF1BRAFKDRRETRIPK2
SCHEMBL6012038 0.92 RAF1 (0.61) RAF1BRAFKDRRETRIPK2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2786750-B2 AGENT FOR REDUCING ADVERSE SIDE EFFECTS OF KINASE INHIBITOR EA PHARMA CO LTD (JP) 2023-06-28 EP claimed
US-20230141981-A1 NOVEL COMPOUNDS AND COMPOSITION FOR TARGETED THERAPY OF KIDNEY-ASSOCIATED CANCERS Shanghai MICURX Pharmaceuticals Co., Ltd. (CN) 2023-05-11 US claimed
US-20200155594-A1 HORNERIN: A NOVEL NON-VEGF MEDIATED ANGIOGENIC PROTEIN EXPRESSED IN BOTH HUMAN AND MOUSE ANGIOGENIC ENDOTHELIAL CELLS AND HUMAN PANCREATIC CANCER CELLS UNIVERSITY OF VIRGINIA PATENT FOUNDATION (US) 2020-05-21 US claimed
US-20180169067-A1 COMBINATION DRUG THERAPIES FOR CANCER AND METHODS OF MAKING AND USING THEM VICUS THERAPEUTICS LLC (US) 2018-06-21 US claimed
WO-2018075865-A1 COMPOSITIONS FOR THE TREATMENT OF NEURODEGENERATIVE DISEASES Glialogix, Inc. (US) 2018-04-26 WO claimed
US-9889120-B2 Combination drug therapies for cancer and methods of making and using them VICUS THERAPEUTICS, LLC (US) 2018-02-13 US claimed
US-20170202806-A1 COMBINATION DRUG THERAPIES FOR CANCER AND METHODS OF MAKING AND USING THEM VICUS THERAPEUTICS LLC (US) 2017-07-20 US claimed
US-20170165240-A1 NEW STRATEGIES FOR TREATING MELANOMA Université Libre de Bruxelles (BE) 2017-06-15 US claimed
US-20160228513-A1 TREATMENT OF MELANOMA WITH INTERFERON-BETA AND RAS-RAF-MEK-ERK INHIBITOR COMBINATION THERAPY BIOGEN MA INC. (US) 2016-08-11 US claimed
EP-2786750-B1 AGENT FOR REDUCING ADVERSE SIDE EFFECTS OF KINASE INHIBITOR AJINOMOTO KK (JP) 2016-06-08 EP claimed
EP-2298311-B1 w-Carboxy aryl substituted diphenyl ureas as p38 kinase inhibitors BAYER HEALTHCARE LLC (US) 2012-05-09 EP claimed
WO-2012052757-A1 TUMOUR PHENOTYPE PATIENT SELECTION METHOD ASTRAZENECA AB (SE) 2012-04-26 WO claimed
EP-2440531-A2 POLYMORPHS OF 4-[4-[[4-CHLORO-3-(TRIFLUOROMETHYL)PHENYL]CARBAMOYLAMINO]PHENOXY]-N-METHYL-PYRIDINE-2-CARBOXAMIDE Ratiopharm GmbH (DE) 2012-04-18 EP claimed
US-20120082647-A1 INTERFERON-BETA FOR USE AS MONOTHERAPY OR IN COMBINATION WITH OTHER CANCER THERAPIES BIOGEN MA INC. 2012-04-05 US claimed
WO-2010142678-A2 POLYMORPHS OF 4-[4-[[4-CHLORO-3-(TRIFLUOROMETHYL)PHENYL]CARBAMOYLAMINO]PHENOXY]-N-METHYL-PYRIDINE-2-CARBOXAMIDE RATIOPHARM GMBH (DE) 2010-12-16 WO claimed
US-20080108672-A1 Omega-Carboxyaryl Substituted Diphenyl Ureas As Raf Kinase Inhibitors BAYER HEALTHCARE LLC 2008-05-08 US claimed
US-20070031338-A1 Embolized cryoablation for treatment of tumors ZABINSKI PETER P 2007-02-08 US claimed
CN-1625602-A Method for selecting drug sensitivity decision factor and method for predetermining drug sensitivity using the selected factor HOFFMANN LA ROCHE (CH) 2005-06-08 CN claimed
US-20020042517-A1 Omega-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors BAYER CORPORATION 2002-04-11 US claimed
US-20010034447-A1 Omega-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors BAYER HEALTHCARE LLC 2001-10-25 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 (5 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-20080108672-A1 Omega-Carboxyaryl Substituted Diphenyl Ureas As Raf Kinase Inhibitors BRAF, RAF1, ARAF RAF1 2/4885BRAF 1/4885KDR 567/4885
US-20170165240-A1 NEW STRATEGIES FOR TREATING MELANOMA TP53, BRAF, TP53BP1 RAF1 5/4885BRAF 2/4885KDR 1139/4885
US-20010034447-A1 Omega-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors BRAF, RAF1, ARAF RAF1 2/4885BRAF 1/4885KDR 567/4885
US-20020042517-A1 Omega-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors BRAF, RAF1, ARAF RAF1 2/4885BRAF 1/4885KDR 567/4885
US-20230141981-A1 NOVEL COMPOUNDS AND COMPOSITION FOR TARGETED THERAPY OF KIDNEY-ASSOCIATED CANCERS GLS, ATP6V1B1, KRAS RAF1 37/4885BRAF 42/4885KDR 277/4885

“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.