SCHEMBL3528119

SCHEMBL3528119

CC(C)COC(=O)N1CCN(c2nccc(-c3ccccc3C(F)F)n2)CC1

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
FAAH O00519 3/20 0.42
ACHE P22303 4/20 0.41
MAPT P10636 2/20 0.40
CYP1A2 P05177 2/20 0.40
CYP2C9 P11712 2/20 0.40
CYP2C19 P33261 2/20 0.40
CYP2D6 P10635 1/20 0.40
ALOX15 P16050 1/20 0.40
TSHR P16473 1/20 0.40
SMN1; SMN2 Q16637 1/20 0.40
NPSR1 Q6W5P4 1/20 0.40
HSD17B10 Q99714 1/20 0.40
HCRTR1 O43613 3/20 0.39
HCRTR2 O43614 3/20 0.39
PTPN11 Q06124 1/20 0.38
SORD Q00796 1/20 0.38
HCAR2 Q8TDS4 1/20 0.38
MEN1 O00255 3/20 0.38
KMT2A Q03164 3/20 0.38
SLC6A7 Q99884 1/20 0.38

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
SCHEMBL12991321 0.88 MAPT (0.46) FAAHACHEMAPTCYP1A2CYP2C9
SCHEMBL12991303 0.83 SORD (0.40) FAAHACHEHSD17B10HCRTR1HCRTR2
SCHEMBL12991427 0.83 CYP1A2 (0.45) FAAHMAPTCYP1A2CYP2C9CYP2C19
SCHEMBL3529053 0.83 SORD (0.40) FAAHACHEHSD17B10HCRTR1HCRTR2
SCHEMBL3531404 0.83 DRD2 (0.41) HSD17B10MEN1KMT2AALDH1A1
SCHEMBL12991312 0.81 ITGB2 (0.40) MAPTALOX15TSHRSMN1; SMN2NPSR1
SCHEMBL12991293 0.81 ITGB2 (0.51) FAAHCYP1A2CYP2C19ALOX15SMN1; SMN2
SCHEMBL3263122 0.79 KMT2A (0.40) MAPTTSHRSMN1; SMN2NPSR1HSD17B10
SCHEMBL11160876 0.78 MEN1 (0.52) MAPTCYP1A2CYP2C9CYP2C19CYP2D6
SCHEMBL3530584 0.77 PANK3 (0.59) ACHEMAPTPTPN11MEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7858786-B2 Pyrimidines and pyrazines useful as modulators of ion channels VERTEX PHARMACEUTICALS INCOROPATED (US) 2010-12-28 US disclosed
US-7858786-B2 Pyrimidines and pyrazines useful as modulators of ion channels VERTEX PHARMACEUTICALS INCOROPATED (US) 2010-12-28 US disclosed
US-7858786-B2 Pyrimidines and pyrazines useful as modulators of ion channels VERTEX PHARMACEUTICALS INCOROPATED (US) 2010-12-28 US disclosed
US-7705002-B2 Biaryls useful as modulators of ion channels VERTEX PHARMACEUTICALS INCORPORATED (US) 2010-04-27 US disclosed
US-20080090837-A1 Na channel and Ca channel antagonists; potentiation; side effects reduction; pains, epilepsy, neurodegenerative disorders, psychiatric disorders,movement disorders, neuroendocrine disorders etc.; 2-hydroxy-1-[4-[3-(2-hydroxyphenyl)phenyl]piperazin-1-yl]-4-methyl-pentan-1-one; VERTEX PHARMACEUTICALS INCORPORATED 2008-04-17 US disclosed
EP-1888549-A2 BIARYLS USEFUL AS MODULATORS OF ION CHANNELS Vertex Pharmaceuticals, Inc. (US) 2008-02-20 EP disclosed
US-20070093454-A1 Pyrimidines and pyrazines useful as modulators of ion channels VERTEX PHARMACEUTICALS INCORPORATED 2007-04-26 US disclosed
US-20070093454-A1 Pyrimidines and pyrazines useful as modulators of ion channels VERTEX PHARMACEUTICALS INCORPORATED 2007-04-26 US disclosed
US-20070093454-A1 Pyrimidines and pyrazines useful as modulators of ion channels VERTEX PHARMACEUTICALS INCORPORATED 2007-04-26 US disclosed
WO-2006124865-A2 BIARYLS DERIVATIVES USEFUL AS MODULATORS OF ION CHANNELS VERTEX PHARMACEUTICALS INCORPORATED (US) 2006-11-23 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-20080090837-A1 Na channel and Ca channel antagonists; potentiation; side effects reduction; pains, epilepsy, neurodegenerative disorders, psychiatric disorders,movement disorders, neuroendocrine disorders etc.; 2-hydroxy-1-[4-[3-(2-hydroxyphenyl)phenyl]piperazin-1-yl]-4-methyl-pentan-1-one; CACNA1B, SCN1A, CACNA1S FAAH 498/4885ACHE 238/4885MAPT 473/4885
US-20070093454-A1 Pyrimidines and pyrazines useful as modulators of ion channels KCNJ1, KCNJ2, KCNJ11 FAAH 2875/4885ACHE 1100/4885MAPT 2601/4885

“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.