SCHEMBL379165

SCHEMBL379165

COC(=O)/C=C/c1cccc(F)c1NC(=O)Nc1cc(C(F)(F)F)ccc1OC

nearest known ligand 0.47

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
RAF1 P04049 7/20 0.47
KDM4E B2RXH2 7/20 0.46
MEN1 O00255 3/20 0.46
KMT2A Q03164 3/20 0.46
MAPK14 Q16539 1/20 0.44
HPGD P15428 3/20 0.43
MAOB P27338 1/20 0.43
MAPT P10636 6/20 0.43
LMNA P02545 3/20 0.43
NPSR1 Q6W5P4 2/20 0.43
ALDH1A1 P00352 3/20 0.43
GAA P10253 1/20 0.43
BRAF P15056 1/20 0.42
POLB P06746 1/20 0.42
L3MBTL1 Q9Y468 1/20 0.41
KDR P35968 1/20 0.41
CYP1A2 P05177 1/20 0.41
CYP2D6 P10635 1/20 0.41
CYP2C19 P33261 1/20 0.41

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
SCHEMBL28799154 1.00 RAF1 (0.47) RAF1KDM4EMEN1KMT2AMAPK14
SCHEMBL30667504 1.00 RAF1 (0.47) RAF1KDM4EMEN1KMT2AMAPK14
SCHEMBL15229756 1.00 RAF1 (0.47) RAF1KDM4EMEN1KMT2AMAPK14
SCHEMBL8793664 0.93 RAF1 (0.45) RAF1KDM4EMEN1KMT2AMAPK14
SCHEMBL4534203 0.92 RAF1 (0.47) RAF1KDM4EMEN1KMT2AMAPK14
SCHEMBL27145420 0.92 RAF1 (0.47) RAF1KDM4EMEN1KMT2AMAPK14
SCHEMBL4534200 0.92 RAF1 (0.47) RAF1KDM4EMEN1KMT2AMAPK14
SCHEMBL8746798 0.92 KDM4E (0.49) RAF1KDM4EMEN1KMT2AMAPK14
SCHEMBL12056332 0.88 KDM4E (0.45) KDM4EMEN1KMT2AHPGDMAOB
SCHEMBL379266 0.83 RAF1 (0.46) RAF1KDM4EMAPK14HPGDMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116874436-A Preparation method of letromycin intermediate 济宁学院 2023-10-13 CN claimed
EP-1893587-B1 METHOD FOR PRODUCING DIHYDROQUINAZOLINES AICURIS GMBH & CO KG (DE) 2012-01-25 EP claimed
US-8084604-B2 Process for the preparation of dihydroquinazolines Aicuris GmbH & Co., KG (DE) 2011-12-27 US claimed
CN-117700339-A Preparation method of letromycin intermediate 江苏正济药业股份有限公司 2024-03-15 CN disclosed
CN-116874436-A Preparation method of letromycin intermediate 济宁学院 2023-10-13 CN disclosed
US-9890128-B2 Process for making substituted quinazoline compounds MERCK SHARP & DOHME CORP. (US) 2018-02-13 US disclosed
US-9890128-B2 Process for making substituted quinazoline compounds MERCK SHARP & DOHME CORP. (US) 2018-02-13 US disclosed
US-20160311781-A1 PROCESS FOR MAKING SUBSTITUTED QUINAZOLINE COMPOUNDS MERCK SHARP & DOHME LLC 2016-10-27 US disclosed
US-20160311781-A1 PROCESS FOR MAKING SUBSTITUTED QUINAZOLINE COMPOUNDS MERCK SHARP & DOHME LLC 2016-10-27 US disclosed
WO-2015088931-A1 PROCESS FOR MAKING SUBSTITUTED QUINAZOLINE COMPOUNDS MERCK SHARP & DOHME CORP. (US) 2015-06-18 WO disclosed
US-8816075-B2 Process for the preparation of dihydroquinazolines AICURIS GMBH & CO. KG (DE) 2014-08-26 US disclosed
EP-1893587-B1 METHOD FOR PRODUCING DIHYDROQUINAZOLINES AICURIS GMBH & CO KG (DE) 2012-01-25 EP disclosed
EP-1893587-B1 METHOD FOR PRODUCING DIHYDROQUINAZOLINES AICURIS GMBH & CO KG (DE) 2012-01-25 EP disclosed
US-8084604-B2 Process for the preparation of dihydroquinazolines Aicuris GmbH & Co., KG (DE) 2011-12-27 US disclosed
US-8084604-B2 Process for the preparation of dihydroquinazolines Aicuris GmbH & Co., KG (DE) 2011-12-27 US disclosed
US-8084604-B2 Process for the preparation of dihydroquinazolines Aicuris GmbH & Co., KG (DE) 2011-12-27 US disclosed
US-20090221822-A1 Process for the Preparation of Dihydroquinazolines BAYER HEALTHCARE AG (DE) 2009-09-03 US disclosed
US-20090221822-A1 Process for the Preparation of Dihydroquinazolines BAYER HEALTHCARE AG (DE) 2009-09-03 US disclosed
EP-1893587-A1 METHOD FOR PRODUCING DIHYDROQUINAZOLINES Bayer HealthCare AG (DE) 2008-03-05 EP disclosed
WO-2006133822-A1 METHOD FOR PRODUCING DIHYDROQUINAZOLINES BAYER HEALTHCARE AG (DE) 2006-12-21 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 (2 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-20160311781-A1 PROCESS FOR MAKING SUBSTITUTED QUINAZOLINE COMPOUNDS CYP3A5, TPMT, MCM5 RAF1 1666/4885KDM4E 1211/4885MEN1 359/4885
US-20090221822-A1 Process for the Preparation of Dihydroquinazolines QDPR, DHPS, DHX15 RAF1 2551/4885KDM4E 1466/4885MEN1 2627/4885

“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.