SCHEMBL4329670

SCHEMBL4329670

CC(=O)NC(=S)Nc1ccc(Oc2ccnc(NC(=O)NCCCN3CCOCC3)c2)cc1Cl.c1cc2cc-2c1

nearest known ligand 0.47

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 1/20 0.47
LMNA P02545 4/20 0.43
KMT2A Q03164 2/20 0.43
SMN1; SMN2 Q16637 2/20 0.43
CA12 O43570 1/20 0.43
CA1 P00915 1/20 0.43
CA2 P00918 1/20 0.43
CA9 Q16790 1/20 0.43
ALDH1A1 P00352 3/20 0.43
KDM4E B2RXH2 2/20 0.43
GAA P10253 1/20 0.43
HTT P42858 1/20 0.41
MAPT P10636 1/20 0.41
KDR P35968 1/20 0.40
RAF1 P04049 1/20 0.40
MDM2 Q00987 1/20 0.40

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
SCHEMBL4326479 0.93 KDR (0.41) L3MBTL1LMNAKMT2AKDM4EHTT
SCHEMBL4329648 0.86 L3MBTL1 (0.49) L3MBTL1LMNAKMT2ASMN1; SMN2ALDH1A1
SCHEMBL4330567 0.83 MAPK14 (0.38) ALDH1A1KDR
SCHEMBL4326460 0.80 KDR (0.42) L3MBTL1KMT2AALDH1A1KDM4EKDR
SCHEMBL4333183 0.80 CA12 (0.48) LMNAKMT2ASMN1; SMN2CA12CA1
SCHEMBL14366283 0.79 KDR (0.47) L3MBTL1LMNAKMT2ASMN1; SMN2CA12
SCHEMBL4323368 0.79 KDR (0.51) LMNAKMT2ASMN1; SMN2CA12CA1
SCHEMBL4333756 0.72 MAPT (0.45) LMNAKMT2AALDH1A1KDM4EHTT
SCHEMBL14366284 0.72 MET (0.48) MAPTKDR
SCHEMBL4330370 0.72 MAPT (0.48) LMNAKMT2AHTTMAPTKDR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1719762-B1 NOVEL PYRIDINE DERIVATIVE AND PYRIMIDINE DERIVATIVE (1) EISAI R&D MAN CO LTD (JP) 2012-06-27 EP disclosed
US-7531532-B2 Hepatocyte growth factor receptor inhibitors; Antitumor agents, anticarcinogenic agents, angiogenesis inhibitors; pyrimidine derivatives like Pyrrolidine-1-carboxylic acid [6-(2-fluoro-4-{3-[2-(4-fluorophenyl)acetyl]thioureido}phenoxy)pyrimidin-4-yl]amide EISAI R&D MANAGEMENT CO., LTD. (JP) 2009-05-12 US disclosed
US-20070270421-A1 Novel pyridine Derivative and Pyrimidine Derivative (1) EISAI R&D MANAGEMENT CO., LTD. (JP) 2007-11-22 US disclosed
EP-1719763-A1 NOVEL PYRIDINE DERIVATIVE AND PYRIMIDINE DERIVATIVE (2) Eisai Co., Ltd. (JP) 2006-11-08 EP disclosed
EP-1719762-A1 NOVEL PYRIDINE DERIVATIVE AND PYRIMIDINE DERIVATIVE (1) Eisai Co., Ltd. (JP) 2006-11-08 EP disclosed
US-20050277652-A1 Novel pyridine derivative and pyrimidine derivative EISAI CO., LTD. (JP) 2005-12-15 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 (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-20070270421-A1 Novel pyridine Derivative and Pyrimidine Derivative (1) HGF, MET, FLT1 L3MBTL1 1054/4885LMNA 4875/4885KMT2A 4095/4885
US-20050277652-A1 Novel pyridine derivative and pyrimidine derivative HGF, MET, HDGF L3MBTL1 1338/4885LMNA 4870/4885KMT2A 4080/4885

“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.