SCHEMBL5225964

SCHEMBL5225964

Fc1ccc(Cn2c(N3CCC(CNc4nccc(OCc5ccccc5)n4)CC3)nc3ccccc32)cc1

nearest known ligand 0.55

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
▸ HRH1 P35367 19/20 0.55
▸ CYP2D6 P10635 17/20 0.55
▸ KCNH2 Q12809 10/20 0.55
▸ CHRM1 P11229 8/20 0.54
▸ HTR3A P46098 1/20 0.53
▸ CYP3A4 P08684 1/20 0.51
▸ ADRA2A P08913 1/20 0.49
▸ HTR2B P41595 1/20 0.49
▸ PDE4D Q08499 1/20 0.49
▸ PDE3A Q14432 1/20 0.49

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
SCHEMBL6273031 0.85 HRH1 (0.59) HRH1CYP2D6KCNH2CHRM1HTR3A
SCHEMBL5229019 0.83 HRH1 (0.60) HRH1CYP2D6KCNH2CHRM1HTR3A
SCHEMBL5225966 0.81 HRH1 (0.77) HRH1CYP2D6KCNH2CHRM1HTR3A
SCHEMBL5229030 0.80 HRH1 (0.54) HRH1CYP2D6KCNH2CHRM1HTR3A
SCHEMBL15568527 0.77 HRH1 (0.66) HRH1CYP2D6KCNH2CHRM1HTR3A
SCHEMBL9371586 0.77 HRH1 (0.61) HRH1CYP2D6KCNH2CHRM1HTR3A
SCHEMBL10337877 0.76 HRH1 (0.74) HRH1CYP2D6KCNH2CHRM1HTR3A
SCHEMBL10337965 0.76 HTR3A (0.47) HRH1CYP2D6KCNH2CHRM1HTR3A
SCHEMBL15568200 0.76 HRH1 (0.62) HRH1CYP2D6KCNH2CHRM1HTR3A
SCHEMBL15568620 0.75 HRH1 (0.63) HRH1CYP2D6KCNH2CHRM1HTR3A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1564212-B1 PROCESS AND INTERMEDIATES FOR OBTAINING 1-(1H-BENZIMIDAZOL-2-YL)-4-(PYRIMIDIN-2-YLAMINO)PIPERIDINE DERIVATIVES RAGACTIVES SL (ES) 2007-12-12 — — EP claimed
US-20050228006-A1 Process and intermediates for obtaining 1-(1H-benzimidazol-2-YL)-4-(2-aminopyrimidine)piperidine derivatives RAGACTIVES, S.L. 2005-10-13 — — US claimed
EP-1564212-A1 METHOD AND INTERMEDIA USED TO OBTAIN DERIVATIVES OF 1-(1H- BENZIMIDAZOLE-2-YL)-4-(2-AMINOPYRIMIDINE)PIPERIDINE Ragactives, S.L. (ES) 2005-08-17 — — EP claimed
EP-1564212-B1 PROCESS AND INTERMEDIATES FOR OBTAINING 1-(1H-BENZIMIDAZOL-2-YL)-4-(PYRIMIDIN-2-YLAMINO)PIPERIDINE DERIVATIVES RAGACTIVES SL (ES) 2007-12-12 — — EP disclosed
US-20050228006-A1 Process and intermediates for obtaining 1-(1H-benzimidazol-2-YL)-4-(2-aminopyrimidine)piperidine derivatives RAGACTIVES, S.L. 2005-10-13 — — US disclosed
EP-1564212-A1 METHOD AND INTERMEDIA USED TO OBTAIN DERIVATIVES OF 1-(1H- BENZIMIDAZOLE-2-YL)-4-(2-AMINOPYRIMIDINE)PIPERIDINE Ragactives, S.L. (ES) 2005-08-17 — — 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 (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-20050228006-A1 Process and intermediates for obtaining 1-(1H-benzimidazol-2-YL)-4-(2-aminopyrimidine)piperidine derivatives IL2, IL4, IL4I1 HRH1 37/4885CYP2D6 177/4885KCNH2 609/4885

“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.

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