SCHEMBL136405

SCHEMBL136405

CN1CCN(c2nc(N)c(-c3cc(Cl)cc(Cl)c3Cl)c(C(F)(F)F)n2)CC1

nearest known ligand 0.61

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
KCNK2 O95069 1/20 0.61
SCN2A Q99250 1/20 0.61
HRH4 Q9H3N8 8/20 0.46
HTR3A P46098 2/20 0.46
KMT2A Q03164 1/20 0.43
HTR6 P50406 6/20 0.42
DRD2 P14416 5/20 0.42
HTR7 P34969 5/20 0.42
HTR2A P28223 4/20 0.42
HTR1A P08908 1/20 0.39
HRH3 Q9Y5N1 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
SCHEMBL5070744 0.93 KCNK2 (0.54) KCNK2SCN2AHRH4HTR3AKMT2A
SCHEMBL8842601 0.86 PIK3CA (0.46) KCNK2SCN2A
SCHEMBL7277240 0.85 SCN2A (0.44) KCNK2SCN2AHRH4HTR3A
SCHEMBL7273354 0.83 HRH4 (0.50) KCNK2SCN2AHRH4HTR3AKMT2A
SCHEMBL134764 0.83 KCNK2 (0.67) KCNK2SCN2AHRH4HTR3AKMT2A
Sipatrigine SCHEMBL135888 0.76 SCN2A (1.00) KCNK2SCN2AHRH4HTR3AKMT2A
Sipatrigine SCHEMBL29421474 0.76 SCN2A (1.00) KCNK2SCN2AHRH4HTR3AKMT2A
SCHEMBL170312 0.76 SCN2A (0.43) KCNK2SCN2AKMT2AHTR2AHTR1A
SCHEMBL7382696 0.75 KCNK2 (0.61) KCNK2SCN2AHRH4HTR3AHTR6
SCHEMBL6049502 0.73 SCN2A (0.39) KCNK2SCN2AKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0727213-B9 Substituted phenylpyrimidine derivatives, useful in the treatment or prevention of CNS disorders WELLCOME FOUND (GB) 2007-11-07 EP claimed
EP-0727213-B1 Substituted phenylpyrimidine derivatives, useful in the treatment or prevention of CNS disorders WELLCOME FOUND (GB) 2005-10-26 EP claimed
US-20040229873-A1 Treatment of neurodegenerative conditions BTG INTERNATIONAL LIMITED (GB) 2004-11-18 US claimed
US-5712276-A TREATING NERVOUS SYSTEM DISORDERS GLAXO WELLCOME INC. (US) 1998-01-27 US claimed
US-5684005-A PHENYLPYRIMIDINE COMPOUNDS AS INHIBITORS OF EXCITATORY AMINO ACID GLUTAMATE GLAXO WELLCOME INC. (US) 1997-11-04 US claimed
EP-0372934-A2 Pharmacologically active CNS compounds THE WELLCOME FOUNDATION LIMITED (GB) 1990-06-13 EP claimed
US-20140079757-A1 ORAL DRUG DELIVERY FORMULATIONS BROWN RUDNICK LLP 2014-03-20 US disclosed
WO-2012028963-A2 COMPOSITIONS INCLUDING A SODIUM CHANNEL BLOCKER AND A B VITAMIN MOLECULE AND METHODS OF USE THEREOF MS THERAPEUTICS LIMITED (GB) 2012-03-08 WO disclosed
US-20120058097-A1 COMPOSITIONS INCLUDING A SODIUM CHANNEL BLOCKER AND A B VITAMIN MOLECULE AND METHODS OF USE THEREOF MS THERAPEUTICS LIMITED (GB) 2012-03-08 US disclosed
EP-1325916-B1 Piperazinyl-substituted phenyl pyrimidine derivatives useful in the treatment or prevention of disorders of the central nervous system WELLCOME FOUND (GB) 2008-01-23 EP disclosed
EP-0727213-B9 Substituted phenylpyrimidine derivatives, useful in the treatment or prevention of CNS disorders WELLCOME FOUND (GB) 2007-11-07 EP disclosed
EP-1681058-A2 Pharmacologically active cns compounds THE WELLCOME FOUNDATION LIMITED (GB) 2006-07-19 EP disclosed
EP-0727213-B1 Substituted phenylpyrimidine derivatives, useful in the treatment or prevention of CNS disorders WELLCOME FOUND (GB) 2005-10-26 EP disclosed
CN-1119099-A Method for preparing pharmacologically active CNS composition WELLCOME FOUND (GB) 1996-03-27 CN disclosed
CN-1117046-A Method for preparing pharmaceutically active CNS compounds WELLCOME FOUND (GB) 1996-02-21 CN disclosed
CN-1115756-A Method for preparing pharmaceutically active CNS compounds WELLCOME FOUND (GB) 1996-01-31 CN disclosed
EP-0679645-A1 Pharmacologically active CNS pyridmidin compounds THE WELLCOME FOUNDATION LIMITED (GB) 1995-11-02 EP disclosed
US-5136080-A Intermediates for glutamate inhibitors BURROUGHS WELLCOME CO. (US) 1992-08-04 US disclosed
EP-0459819-A2 Pharmacologically active CNS compound THE WELLCOME FOUNDATION LIMITED (GB) 1991-12-04 EP disclosed
EP-0372934-A2 Pharmacologically active CNS compounds THE WELLCOME FOUNDATION LIMITED (GB) 1990-06-13 EP 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-20120058097-A1 COMPOSITIONS INCLUDING A SODIUM CHANNEL BLOCKER AND A B VITAMIN MOLECULE AND METHODS OF USE THEREOF CACNA1B, KCNMB1, KCNB2 KCNK2 103/4885SCN2A 25/4885HRH4 3061/4885
US-20040229873-A1 Treatment of neurodegenerative conditions CHRM2, CHRNA3, CHRNA2 KCNK2 136/4885SCN2A 63/4885HRH4 58/4885
US-20140079757-A1 ORAL DRUG DELIVERY FORMULATIONS PGF, MMP1, MMP26 KCNK2 3641/4885SCN2A 4830/4885HRH4 2946/4885

“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.