SCHEMBL1777673

SCHEMBL1777673

c1ccc2nc(N3CCN(CC4CCCN(C5CC5)C4)CC3)ccc2c1

nearest known ligand 0.63

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HRH3 Q9Y5N1 10/20 0.63
CCR2 P41597 3/20 0.49
HTR3E A5X5Y0 2/20 0.47
KDM4E B2RXH2 2/20 0.47
HTR3B O95264 2/20 0.47
ALDH1A1 P00352 2/20 0.47
CYP1A2 P05177 2/20 0.47
HTR3A P46098 2/20 0.47
HTR3D Q70Z44 2/20 0.47
HTR3C Q8WXA8 2/20 0.47
THPO P40225 1/20 0.47
HRH4 Q9H3N8 1/20 0.47
NPC1 O15118 2/20 0.45
RAB9A P51151 2/20 0.45
HTR1A P08908 2/20 0.44
USP2 O75604 1/20 0.44
ADRB1 P08588 1/20 0.44
CYP3A4 P08684 1/20 0.44
HTR2C P28335 1/20 0.44
MAPK1 P28482 1/20 0.44

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
SCHEMBL1777668 1.00 HRH3 (0.63) HRH3CCR2HTR3EKDM4EHTR3B
SCHEMBL12603436 1.00 HRH3 (0.63) HRH3CCR2HTR3EKDM4EHTR3B
SCHEMBL13648942 0.83 HRH3 (0.67) HRH3HTR3EKDM4EHTR3BALDH1A1
SCHEMBL1778611 0.81 HRH3 (0.49) HRH3CCR2HTR3EKDM4EHTR3B
SCHEMBL12603434 0.81 HRH3 (0.49) HRH3CCR2HTR3EKDM4EHTR3B
SCHEMBL1778333 0.79 KDM4E (0.51) HRH3HTR3EKDM4EHTR3BALDH1A1
SCHEMBL13648831 0.79 HRH3 (1.00) HRH3HTR3EKDM4EHTR3BALDH1A1
Hydrochloric Acid SCHEMBL4198254 0.77 HRH3 (0.97) HRH3HTR3EKDM4EHTR3BALDH1A1
SCHEMBL3970736 0.76 HRH3 (1.00) HRH3HTR3EKDM4EHTR3BALDH1A1
Hydrochloric Acid SCHEMBL27602136 0.76 HRH3 (0.94) HRH3HTR3EKDM4EHTR3BALDH1A1

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
US-7943768-B2 Piperazine compounds useful as antagonists of C-C chemokines (Ccr2b and CcrS) for the treatment of inflammatory diseases ASTRAZENECA AB (SE) 2011-05-17 US disclosed
CN-101384582-A Piperazine compounds useful as antagonists of C-C chemokines (CCR2B and CCR5) for the treatment of inflammatory diseases ASTRAZENECA AB (SE) 2009-03-11 CN disclosed
US-20080287453-A1 Piperazine Compounds Useful as Antagonists of C-C Chemokines (Ccr2b and Ccr5) for the Treatment of Inflammatory Diseases ASTRAZENECA AB (SE) 2008-11-20 US disclosed
EP-1966187-A1 PIPERAZINE COMPOUNDS USEFUL AS ANTAGONISTS OF C-C CHEMOKINES (CCR2B AND CCR5) FOR THE TREATMENT OF INFLAMMATORY DISEASES AstraZeneca AB (SE) 2008-09-10 EP disclosed
WO-2007071952-A1 PIPERAZINE COMPOUNDS USEFUL AS ANTAGONISTS OF C-C CHEMOKINES (CCR2B AND CCR5) FOR THE TREATMENT OF INFLAMMATORY DISEASES ASTRAZENECA AB (SE) 2007-06-28 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-20080287453-A1 Piperazine Compounds Useful as Antagonists of C-C Chemokines (Ccr2b and Ccr5) for the Treatment of Inflammatory Diseases CCR2, CCR5, CCL2 HRH3 283/4885CCR2 1/4885HTR3E 881/4885

“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.