SCHEMBL6356041

SCHEMBL6356041

COc1ccc(NC(=O)N2CCC(c3c[nH]c4cc(F)ccc34)CC2)cc1N1CCN(C)CC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
HTR1A P08908 5/20 0.62
HTR1D P28221 5/20 0.62
HTR1B P28222 5/20 0.62
HTR2A P28223 2/20 0.62
HTR2C P28335 2/20 0.58
HTR6 P50406 2/20 0.58
HTR7 P34969 1/20 0.58

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
SCHEMBL6346308 0.94 HTR1A (0.63) HTR1AHTR1DHTR1BHTR2AHTR2C
SCHEMBL22410939 0.90 HTR1A (0.59) HTR1AHTR1DHTR1BHTR2AHTR2C
SCHEMBL6342285 0.89 HTR1A (0.64) HTR1AHTR1DHTR1BHTR2AHTR2C
SCHEMBL7457330 0.89 HTR1A (0.60) HTR1AHTR1DHTR1BHTR2AHTR2C
Hydrochloric Acid SCHEMBL6342480 0.89 HTR1A (0.62) HTR1AHTR1DHTR1BHTR2AHTR2C
SCHEMBL6346305 0.86 DRD2 (0.50) HTR1D
SCHEMBL22411096 0.85 HTR1A (0.62) HTR1AHTR1DHTR1BHTR2AHTR2C
SCHEMBL6345386 0.85 HTR1A (0.55) HTR1AHTR1DHTR1BHTR2AHTR2C
SCHEMBL6347320 0.85 HTR1A (0.63) HTR1AHTR1DHTR1BHTR2AHTR2C
Hydrochloric Acid SCHEMBL7460111 0.84 HTR1A (0.62) HTR1AHTR1DHTR1BHTR2AHTR2C

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6509340-B1 These preparations can be employed as medicaments in human and veterinary medicine. Possible excipients are organic or inorganic substances which are suitable for enteral (e.g. oral) on the central nervous system. MERCK PATENTGESELLSCHAFT (DE) 2003-01-21 US claimed
US-20050176730-A1 Amide and urea derivatives as 5-HT reuptake inhibitors and as 5-HT 1B/1D ligands MERCK PATENT GMBH (DE) 2005-08-11 US disclosed
US-20030064995-A1 Amide and urea derivatives as 5-HT reuptake inhibitors and as5-HT1B/1D ligands MERCK PATENT GMBH (DE) 2003-04-03 US disclosed
US-6509340-B1 These preparations can be employed as medicaments in human and veterinary medicine. Possible excipients are organic or inorganic substances which are suitable for enteral (e.g. oral) on the central nervous system. MERCK PATENTGESELLSCHAFT (DE) 2003-01-21 US disclosed
EP-1140898-B1 AMIDE AND UREA DERIVATIVES AS 5-HT REUPTAKE INHIBITORS AND AS 5-HT1B/1D LIGANDS MERCK PATENT GMBH (DE) 2002-08-28 EP disclosed
EP-1140898-A1 AMIDE AND UREA DERIVATIVES AS 5-HT REUPTAKE INHIBITORS AND AS 5-HT1B/1D LIGANDS MERCK PATENT GmbH (DE) 2001-10-10 EP disclosed
WO-2000037456-A1 AMIDE AND UREA DERIVATIVES AS 5-HT REUPTAKE INHIBITORS AND AS 5-HT1B/1D LIGANDS MERCK PATENT GMBH (DE) 2000-06-29 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 (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-20050176730-A1 Amide and urea derivatives as 5-HT reuptake inhibitors and as 5-HT 1B/1D ligands HTR1B, HTR1D, HTR1A HTR1A 3/4885HTR1D 2/4885HTR1B 1/4885
US-20030064995-A1 Amide and urea derivatives as 5-HT reuptake inhibitors and as5-HT1B/1D ligands HTR5A, HTR1B, HTR1A HTR1A 3/4885HTR1D 7/4885HTR1B 2/4885

“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.