SCHEMBL5201820

SCHEMBL5201820

Nc1ccc(O[C@H]2CCCNC2)cc1

nearest known ligand 0.57

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
ROCK1 Q13464 6/20 0.57
ROCK2 O75116 2/20 0.57
KCNH2 Q12809 1/20 0.57
CHRNB2 P17787 3/20 0.56
CHRNA4 P43681 3/20 0.56
PRKX P51817 1/20 0.51
PRKCE Q02156 1/20 0.51
PRKCD Q05655 1/20 0.51
PRKD1 Q15139 1/20 0.51
CHEK2 O96017 1/20 0.47
PRKCZ Q05513 2/20 0.47
HTR1A P08908 1/20 0.43
SLC6A2 P23975 1/20 0.43
PARP1 P09874 1/20 0.43
HRH1 P35367 1/20 0.42

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
SCHEMBL3634171 1.00 ROCK1 (0.57) ROCK1ROCK2KCNH2CHRNB2CHRNA4
SCHEMBL7000861 0.89 PRKCZ (0.56) ROCK1ROCK2KCNH2CHRNB2CHRNA4
SCHEMBL3133920 0.89 PRKCZ (0.56) ROCK1ROCK2KCNH2CHRNB2CHRNA4
SCHEMBL4067092 0.89 PRKCZ (0.56) ROCK1ROCK2KCNH2CHRNB2CHRNA4
Hydrochloric Acid SCHEMBL3127582 0.87 PRKCZ (0.54) ROCK1ROCK2KCNH2CHRNB2CHRNA4
SCHEMBL3809688 0.84 CHRNB2 (0.63) ROCK1ROCK2KCNH2CHRNB2CHRNA4
SCHEMBL3153942 0.84 CHRNB2 (0.55) ROCK1ROCK2KCNH2CHRNB2CHRNA4
SCHEMBL19582779 0.84 CHRNB2 (0.55) ROCK1ROCK2KCNH2CHRNB2CHRNA4
SCHEMBL18689816 0.84 CHRNB2 (0.55) ROCK1ROCK2KCNH2CHRNB2CHRNA4
SCHEMBL3158901 0.84 CHRNB2 (0.55) ROCK1ROCK2KCNH2CHRNB2CHRNA4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1795192-A2 1-Substituted imidazole derivatives as nos inhibitors Bayer Schering Pharma Aktiengesellschaft (DE) 2007-06-13 EP disclosed
US-7202263-B2 N-heterocyclic derivatives as NOS inhibitors SCHERING AKTIENGESELLSCHAFT (DE) 2007-04-10 US disclosed
EP-1501504-B1 1-SUBSTITUTED IMIDAZOLE DERIVATIVES AS NOS INHIBITORS SCHERING AG (DE) 2007-02-07 EP disclosed
US-20060094725-A1 N-heterocyclic derivatives as NOS inhibitors SCHERING AKTIENGESELLSCHAFT (DE) 2006-05-04 US disclosed
US-6982259-B2 N-heterocyclic derivatives as NOS inhibitors SCHERING AKTIENGESELLSCHAFT (DE) 2006-01-03 US disclosed
EP-1501504-A1 1-SUBSTITUTED IMIDAZOLE DERIVATIVES AS NOS INHIBITORS SCHERING AKTIENGESELLSCHAFT (DE) 2005-02-02 EP disclosed
US-20040023950-A1 N-heterocyclic derivatives as NOS inhibitors SCHERING AKTIENGESELLSCHAFT (DE) 2004-02-05 US disclosed
WO-2003092678-A1 1-SUBSTITUTED IMIDAZOLE DERIVATIVES AS NOS INHIBITORS SCHERING AKTIENGESELLSCHAFT (DE) 2003-11-13 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-20060094725-A1 N-heterocyclic derivatives as NOS inhibitors NOS1, NOS2, NOS3 ROCK1 579/4885ROCK2 1519/4885KCNH2 2322/4885
US-20040023950-A1 N-heterocyclic derivatives as NOS inhibitors NOS1, NOS2, NOS3 ROCK1 394/4885ROCK2 898/4885KCNH2 1939/4885

“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.