SCHEMBL4794728

SCHEMBL4794728

CC1(C)COC(c2c[c]ccc2)=N1

nearest known ligand 0.50

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 1/20 0.50
HRH3 Q9Y5N1 4/20 0.42
HTT P42858 2/20 0.41
LMNA P02545 2/20 0.41
MAPT P10636 1/20 0.41
CYP2D6 P10635 1/20 0.40
ATM Q13315 2/20 0.39
ALDH1A1 P00352 1/20 0.39
IL2 P60568 1/20 0.34
ROCK1 Q13464 1/20 0.33

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
SCHEMBL8488526 0.80 KDM4E (0.51) KDM4EHRH3HTTLMNAMAPT
SCHEMBL342910 0.79 KDM4E (0.59) KDM4EHRH3HTTLMNAMAPT
SCHEMBL471881 0.78 KDM4E (0.62) KDM4EHRH3HTTLMNAMAPT
Hydrochloric Acid SCHEMBL11553058 0.78 KDM4E (0.58) KDM4EHRH3HTTLMNAMAPT
SCHEMBL471858 0.77 KDM4E (0.60) KDM4EHRH3HTTLMNAMAPT
Hydrochloric Acid SCHEMBL4777692 0.76 KDM4E (0.56) KDM4EHRH3HTTLMNAMAPT
SCHEMBL10837608 0.76 KDM4E (0.56) KDM4EHRH3HTTLMNAMAPT
Hydrochloric Acid SCHEMBL4777694 0.76 KDM4E (0.56) KDM4EHRH3HTTLMNAMAPT
SCHEMBL20410843 0.75 KDM4E (0.59) KDM4EHRH3HTTLMNAMAPT
SCHEMBL4792824 0.74 HRH3 (0.43) KDM4EHRH3HTTLMNAMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1991530-A1 CINNOLINE DERIVATIVES AS PHOSPHODIESTERASE 10 INHIBITORS Amgen Inc. (US) 2008-11-19 EP claimed
US-20070265256-A1 Phosphodiesterase 10 inhibitors AMGEN INC. 2007-11-15 US claimed
WO-2007098169-A1 CINNOLINE DERIVATIVES AS PHOSPHODIESTERASE 10 INHIBITORS AMGEN INC. (US) 2007-08-30 WO claimed
EP-1991530-A1 CINNOLINE DERIVATIVES AS PHOSPHODIESTERASE 10 INHIBITORS Amgen Inc. (US) 2008-11-19 EP disclosed
US-20070265256-A1 Phosphodiesterase 10 inhibitors AMGEN INC. 2007-11-15 US disclosed
WO-2007098169-A1 CINNOLINE DERIVATIVES AS PHOSPHODIESTERASE 10 INHIBITORS AMGEN INC. (US) 2007-08-30 WO disclosed
CN-1070173-C Benzoylguanidine derivatives as medicaments FUJISAWA PHARMACEUTICAL CO (JP) 2001-08-29 CN disclosed
CN-1158606-A Benzoylguanidine derivatives as medicaments FUJISAWA PHARMACEUTICAL CO (JP) 1997-09-03 CN disclosed
CN-1022184-C Process for preparing (1 H-imidzol-1-ylmethyl) substituted benzotriazole derivatives JANSSEN PHARMACEUTICA NV (BE) 1993-09-22 CN disclosed
EP-0293978-B1 (1H-AZOL-1-YLMETHYL)SUBSTITUTED BENZOTRIAZOLE DERIVATIVES JANSSEN PHARMACEUTICA N.V. (BE) 1993-09-15 EP disclosed
CN-88103408-A Process for preparing (1H-oxazol-1-ylmethyl) substituted benzotriazole derivatives 1988-12-14 CN 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-20070265256-A1 Phosphodiesterase 10 inhibitors PDE7A, PDE7B, PDE10A KDM4E 2328/4885HRH3 4562/4885HTT 1809/4885

“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.