SCHEMBL6444671

SCHEMBL6444671

CC(=S)N1CCOC(c2ccc(Oc3ccc(Cl)cc3)cc2)C1

nearest known ligand 0.44

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
CNR2 P34972 1/20 0.44
PDE10A Q9Y233 1/20 0.39
PDK1 Q15118 1/20 0.38
ALDH1A1 P00352 2/20 0.38
PHGDH O43175 2/20 0.38
HPGD P15428 1/20 0.38
TSHR P16473 1/20 0.38
MGLL Q99685 1/20 0.38
HSD17B10 Q99714 1/20 0.38
MEN1 O00255 1/20 0.38
KMT2A Q03164 1/20 0.38
PDE2A O00408 1/20 0.37
RXRB P28702 1/20 0.36
USP2 O75604 1/20 0.36
DRD3 P35462 2/20 0.36

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
SCHEMBL5028958 0.92 ALDH1A1 (0.43) PDE10AALDH1A1PHGDHHPGDTSHR
SCHEMBL6243985 0.88 CNR2 (0.42) CNR2PDK1PHGDHPDE2A
SCHEMBL5028952 0.84 ALDH1A1 (0.44) CNR2ALDH1A1HPGDMEN1KMT2A
SCHEMBL19049367 0.76 PHGDH (0.42) PDE10APHGDHPDE2A
SCHEMBL2295521 0.75 PDE10A (0.43) PDE10APDE2A
SCHEMBL2293809 0.75 PDE10A (0.43) PDE10APDE2A
SCHEMBL6444675 0.75 CNR2 (0.56) CNR2RXRBDRD3
SCHEMBL5029162 0.74 AKR1C3 (0.41)
SCHEMBL23222307 0.74 PHGDH (0.43) PDE10APHGDHHSD17B10PDE2ADRD3
SCHEMBL3375071 0.74 USP30 (0.44) PDE10APHGDHPDE2A

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-1226128-B1 NEW PYRIMIDINE-2,4,6-TRIONE DERIVATIVES, PROCESSES FOR THEIR PRODUCTION AND PHARMACEUTICAL AGENTS CONTAINING THESE COMPOUNDS HOFFMANN LA ROCHE (CH) 2005-02-23 EP disclosed
US-6716845-B2 Barbituric acid derivatives HOFFMANN-LA ROCHE INC. 2004-04-06 US disclosed
EP-1383746-A2 NEW PYRIMIDINE-2,4,6-TRIONE DERIVATIVES, PROCESSES FOR THEIR PRODUCTION AND PHARMACEUTICAL AGENTS CONTAINING THESE COMPOUNDS F. HOFFMANN-LA ROCHE AG (CH) 2004-01-28 EP disclosed
US-6498252-B1 Pyrimidine-2,4,6-trione derivatives, processes for their production and pharmaceutical agents containing these compounds HOFFMANN-LA ROCHE INC. 2002-12-24 US disclosed
US-20020187991-A1 Barbituric acid derivatives F. HOFFMANN-LA ROCHE AG (CH) 2002-12-12 US disclosed
WO-2002079170-A2 PYRIMIDINE-2,4,6-TRIONE DERIVATIVES, PROCESSES FOR THEIR PRODUCTION AND PHARMACEUTICAL AGENTS CONTAINING THEM F. HOFFMANN-LA ROCHE AG (CH) 2002-10-10 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-20020187991-A1 Barbituric acid derivatives GABBR1, GABBR2, TUBB6 CNR2 2063/4885PDE10A 919/4885PDK1 208/4885

“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.