SCHEMBL2584583

SCHEMBL2584583

NC(=O)c1cccc(F)c1C(F)(F)F

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PARP1 P09874 3/20 0.44
CES2 O00748 3/20 0.44
CES1 P23141 3/20 0.44
BCHE P06276 1/20 0.44
ALB P02768 1/20 0.41
MAPT P10636 2/20 0.41
ALDH1A1 P00352 2/20 0.41
KDM4E B2RXH2 1/20 0.41
HPGD P15428 1/20 0.41
TSHR P16473 1/20 0.41
HSD17B10 Q99714 1/20 0.41
PDPK1 O15530 1/20 0.41
PDK2 Q15119 1/20 0.41
SCN9A Q15858 1/20 0.40
SLC6A2 P23975 1/20 0.40
SLC6A4 P31645 1/20 0.40
PBRM1 Q86U86 1/20 0.40
HTT P42858 1/20 0.40
ALOX15 P16050 1/20 0.39
DGAT1 O75907 1/20 0.39

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
SCHEMBL27722750 0.88 PARP1 (0.49) PARP1MAPTALDH1A1KDM4EHPGD
SCHEMBL17030746 0.83 CES2 (0.42) PARP1CES2CES1BCHEALB
SCHEMBL1259459 0.82 ALB (0.57) CES2CES1BCHEALBMAPT
SCHEMBL31388520 0.82 ALB (0.57) CES2CES1BCHEALBMAPT
SCHEMBL4446378 0.82 CES2 (0.45) CES2CES1BCHEALBMAPT
SCHEMBL634076 0.81 PARP1 (0.47) PARP1MAPTALDH1A1KDM4EHPGD
SCHEMBL30554614 0.81 PARP1 (0.47) PARP1MAPTALDH1A1KDM4EHPGD
SCHEMBL937001 0.81 ALDH1A1 (0.59) CES2CES1BCHEALBMAPT
SCHEMBL29789811 0.81 ALDH1A1 (0.59) CES2CES1BCHEALBMAPT
Hydrochloric Acid SCHEMBL7069187 0.79 PARP1 (0.46) PARP1MAPTALDH1A1KDM4EHPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-101006052-A Pyrrole derivatives as pharmaceutical agents EXELIXIS INC (US) 2007-07-25 CN claimed
CN-106661035-B The Pyrazolopyrimidine derivative of inhibitor as bruton's tyrosine kinase 洛克索肿瘤学股份有限公司 2019-11-19 CN disclosed
CN-105985319-B Aryl phthalazine compound and its preparation method and application 复旦大学 2019-02-26 CN disclosed
CN-102781963-B Functional modified NAv1.7 antibodies UCB医药有限公司 2018-02-16 CN disclosed
CN-102597002-B The antibody of ion channel UCB医药有限公司 2017-08-22 CN disclosed
CN-106661035-A Pyrazolopyrimidine derivatives as inhibitors of bruton's tyrosine kinase 莱德克斯制药公共有限公司 2017-05-10 CN disclosed
CN-102573994-B Novel bicyclic urea compounds MERCK PATENT GMBH 2015-06-24 CN disclosed
EP-2049478-B1 SUBSTITUTED N-PHENYLMETHYL -5-OXO-PROLINE-2-AMIDES AS P2X7-RECEPTOR ANTAGONISTS AND THEIR METHODS OF USE GLAXO GROUP LTD (GB) 2012-05-30 EP disclosed
CN-101511787-B Substituted N-phenylmethyl-5-oxo-proline-2-amides as P2X 7-receptor antagonists and methods of their use GLAXO GROUP LTD. (GB) 2011-11-30 CN disclosed
US-8048907-B2 Receptor antagonists and their methods of use GLAXO GROUP LIMITED (GB) 2011-11-01 US disclosed
US-20100144829-A1 Novel Receptor Antagonists and Their Methods of Use GLAXO GROUP LIMITED 2010-06-10 US disclosed
US-7718693-B2 Receptor antagonists and their methods of use GLAXO GROUP LIMITED (GB) 2010-05-18 US disclosed
CN-101511787-A Substituted N-phenylmethyl-5-oxo-proline-2-amides as P2X 7-receptor antagonists and methods of their use GLAXO GROUP LTD (GB) 2009-08-19 CN disclosed
WO-2009074518-A1 COMBINATIONS OF PROLINAMIDE P2X7 MODULATORS WITH FURTHER THERAPEUTIC AGENTS GLAXO GROUP LIMITED (GB) 2009-06-18 WO disclosed
EP-2049478-A1 SUBSTITUTED N-PHENYLMETHYL -5-OXO-PROLINE-2-AMIDES AS P2X7-RECEPTOR ANTAGONISTS AND THEIR METHODS OF USE Glaxo Group Limited (GB) 2009-04-22 EP disclosed
WO-2008003697-A1 SUBSTITUTED N-PHENYLMETHYL -5-OXO-PROLINE-2-AMIDES AS P2X7-RECEPTOR ANTAGONISTS AND THEIR METHODS OF USE GLAXO GROUP LIMITED (GB) 2008-01-10 WO disclosed
US-20080009541-A1 Novel Receptor Antagonists and Their Methods of Use GLAXO GROUP LIMITED (GB) 2008-01-10 US disclosed
CN-101006052-A Pyrrole derivatives as pharmaceutical agents EXELIXIS INC (US) 2007-07-25 CN disclosed
US-20060211739-A1 Use of selective P2X7 receptor antagonists ABBOTT LABORATORIES 2006-09-21 US disclosed
WO-2006086229-A1 THE USE OF SELECTIVE P2X7 RECEPTOR ANTAGONISTS ABBOTT LABORATORIES (US) 2006-08-17 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 (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-20080009541-A1 Novel Receptor Antagonists and Their Methods of Use P2RX7, P2RX3, P2RX1 PARP1 2650/4885CES2 3816/4885CES1 2950/4885
US-20100144829-A1 Novel Receptor Antagonists and Their Methods of Use P2RX7, P2RX3, P2RX1 PARP1 2650/4885CES2 3816/4885CES1 2950/4885
US-20060211739-A1 Use of selective P2X7 receptor antagonists P2RX1, P2RX3, P2RX7 PARP1 2161/4885CES2 2986/4885CES1 2030/4885

“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.