SCHEMBL5505546

SCHEMBL5505546

CN(C)CCc1cn(S(=O)(=O)c2ccccc2)c2ccc(OCc3ccccc3)cc12

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
HTR6 P50406 20/20 1.00
HTR1A P08908 2/20 0.77
DRD2 P14416 2/20 0.77
HTR1D P28221 2/20 0.77
HTR1B P28222 2/20 0.77
HTR1F P30939 2/20 0.77
HTR7 P34969 2/20 0.77
DRD3 P35462 2/20 0.77
HTR1E P28566 1/20 0.77

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
SCHEMBL5499070 0.87 HTR6 (1.00) HTR6HTR1ADRD2HTR1DHTR1B
SCHEMBL29720339 0.87 HTR6 (1.00) HTR6HTR1ADRD2HTR1DHTR1B
Oxalic Acid SCHEMBL5762121 0.84 HTR6 (0.92) HTR6HTR1ADRD2HTR1DHTR1B
Oxalic Acid SCHEMBL7430614 0.83 HTR6 (0.71) HTR6HTR1ADRD2HTR1DHTR1B
SCHEMBL5504710 0.83 HTR6 (1.00) HTR6HTR1ADRD2HTR1DHTR1B
SCHEMBL5499078 0.81 HTR6 (1.00) HTR6HTR1ADRD2HTR1DHTR1B
SCHEMBL3322247 0.80 HTR6 (1.00) HTR6HTR1ADRD2HTR1DHTR1B
SCHEMBL5030681 0.80 HTR6 (0.66) HTR6HTR1ADRD2HTR1DHTR1B
SCHEMBL13940270 0.79 PPARG (0.80) HTR6HTR1ADRD2HTR1DHTR1B
SCHEMBL5498952 0.78 HTR6 (1.00) HTR6HTR1ADRD2HTR1DHTR1B

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-1438045-B1 USE OF INDOLE AND INDOLINE DERIVATIVES IN THE TREATMENT OF OBESITY OR FOR THE REDUCTION OF FOOD INTAKE BIOVITRUM AB (SE) 2007-02-14 EP claimed
US-20030139424-A1 Use BIOVITRUM AB (SE) 2003-07-24 US claimed
US-6187805-B1 TREATING CONDITION FOR WHICH SELECTIVE AGONISM OR ANTAGONISM OF 5-HT-6 RECEPTORS IS INDICATED BY ADMINISTERING COMPOUNDS SUCH AS N,N-DIMETHYL 2-(1-(BENZENESULPHONYL)-5-METHOXY-1H-INDOL-3-YL)ETHYLAMINE MERCK SHARP & DOHME LTD. (GB) 2001-02-13 US claimed
EP-1438045-B1 USE OF INDOLE AND INDOLINE DERIVATIVES IN THE TREATMENT OF OBESITY OR FOR THE REDUCTION OF FOOD INTAKE BIOVITRUM AB (SE) 2007-02-14 EP disclosed
EP-1438045-A1 USE OF INDOLE AND INDOLINE DERIVATIVES IN THE TREATMENT OF OBESITY OR FOR THE REDUCTION OF FOOD INTAKE BIOVITRUM AB (SE) 2004-07-21 EP disclosed
US-20030139424-A1 Use BIOVITRUM AB (SE) 2003-07-24 US disclosed
WO-2003035061-A1 USE OF INDOLE AND INDOLINE DERIVATIVES IN THE TREATMENT OF OBESITY OR FOR THE REDUCTION OF FOOD INTAKE BIOVITRUM AB (SE) 2003-05-01 WO disclosed
US-6187805-B1 TREATING CONDITION FOR WHICH SELECTIVE AGONISM OR ANTAGONISM OF 5-HT-6 RECEPTORS IS INDICATED BY ADMINISTERING COMPOUNDS SUCH AS N,N-DIMETHYL 2-(1-(BENZENESULPHONYL)-5-METHOXY-1H-INDOL-3-YL)ETHYLAMINE MERCK SHARP & DOHME LTD. (GB) 2001-02-13 US 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-20030139424-A1 Use TPH1, IDO1, TPH2 HTR6 25/4885HTR1A 32/4885DRD2 617/4885

“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.