SCHEMBL3593317

SCHEMBL3593317

CN(C(=O)O)C1CCN(Cc2ccc(Cl)cc2)CC1

nearest known ligand 0.56

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
SIGMAR1 Q99720 3/20 0.55
CHRM2 P08172 2/20 0.55
CHRM3 P20309 2/20 0.55
DRD2 P14416 2/20 0.55
HTR2A P28223 2/20 0.55
HTR2C P28335 2/20 0.55
HTR2B P41595 2/20 0.55
KCNH2 Q12809 1/20 0.55
CCR5 P51681 1/20 0.55
LSS P48449 2/20 0.53
DRD4 P21917 1/20 0.52
OPRM1 P35372 1/20 0.52
MEN1 O00255 1/20 0.51
KMT2A Q03164 1/20 0.51

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
Hydrochloric Acid SCHEMBL3592267 0.99 SIGMAR1 (0.54) SIGMAR1CHRM2CHRM3DRD2HTR2A
SCHEMBL784863 0.88 SIGMAR1 (0.68) SIGMAR1CHRM2CHRM3DRD2HTR2A
SCHEMBL3605410 0.88 ALDH1A1 (0.53) SIGMAR1CHRM2CHRM3DRD2HTR2A
SCHEMBL13478881 0.86 KCNH2 (0.56) SIGMAR1CHRM2CHRM3DRD2HTR2A
SCHEMBL3942391 0.86 CHRM4 (0.62) SIGMAR1CHRM2CHRM3DRD2HTR2A
SCHEMBL3599854 0.81 CCR5 (0.58) CHRM2KCNH2CCR5LSS
SCHEMBL12274497 0.81 KCNH2 (0.62) SIGMAR1DRD2HTR2AHTR2CHTR2B
SCHEMBL3936632 0.80 MCHR1 (0.69) SIGMAR1DRD2HTR2AHTR2CHTR2B
SCHEMBL1220330 0.80 OPRM1 (0.59) SIGMAR1CHRM2CHRM3DRD2HTR2A
SCHEMBL3817982 0.80 OPRM1 (0.59) SIGMAR1CHRM2CHRM3DRD2HTR2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1720550-B1 DERIVATIVES OF PIPERIDINYLALKYLCARBAMATES, PREPARATION METHOD THEREOF AND USE OF SAME AS FAAH ENZYME INHIBITORS SANOFI AVENTIS (FR) 2009-04-15 EP claimed
US-20100279998-A1 PIPERIDINYLALKYLCARBAMATE DERIVATIVES, METHODS FOR THEIR PREPARATION AND THE THERAPEUTIC USE THEREOF AS FATTY ACID AMIDO HYDROLASE ENZYME INHIBITORS SANOFI-AVENTIS (FR) 2010-11-04 US disclosed
EP-1720550-B1 DERIVATIVES OF PIPERIDINYLALKYLCARBAMATES, PREPARATION METHOD THEREOF AND USE OF SAME AS FAAH ENZYME INHIBITORS SANOFI AVENTIS (FR) 2009-04-15 EP disclosed
EP-1720550-A1 DERIVATIVES OF PIPERIDINYLALKYLCARBAMATES, PREPARATION METHOD THEREOF AND USE OF SAME AS FAAH ENZYME INHIBITORS Sanofi-Aventis (FR) 2006-11-15 EP disclosed
WO-2005089759-A1 DERIVATIVES OF PIPERIDINYLALKYLCARBAMATES, PREPARATION METHOD THEREOF AND USE OF SAME AS FAAH ENZYME INHIBITORS SANOFI-AVENTIS (FR) 2005-09-29 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 (1 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-20100279998-A1 PIPERIDINYLALKYLCARBAMATE DERIVATIVES, METHODS FOR THEIR PREPARATION AND THE THERAPEUTIC USE THEREOF AS FATTY ACID AMIDO HYDROLASE ENZYME INHIBITORS FAAH, FAAH2, CNR2 SIGMAR1 2487/4885CHRM2 3417/4885CHRM3 1790/4885

“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.