SCHEMBL3689081

SCHEMBL3689081

CCOC(=O)c1sc2c(Cl)cccc2c1C

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 7/20 0.53
MAPK1 P28482 2/20 0.53
KDM4E B2RXH2 2/20 0.53
L3MBTL1 Q9Y468 1/20 0.53
CDC7 O00311 3/20 0.49
DBF4 Q9UBU7 3/20 0.49
GRM6 O15303 1/20 0.45
PDE4A P27815 1/20 0.45
PDE4B Q07343 1/20 0.45
PDE4C Q08493 1/20 0.45
PDE4D Q08499 1/20 0.45
MCL1 Q07820 1/20 0.45
PFKFB3 Q16875 1/20 0.45
PFKFB4 Q16877 1/20 0.45
MAPT P10636 5/20 0.44
NPC1 O15118 4/20 0.44
RAB9A P51151 4/20 0.44
KMT2A Q03164 4/20 0.44
LMNA P02545 3/20 0.44
MEN1 O00255 2/20 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
SCHEMBL15619156 0.85 PFKFB4 (0.55) ALDH1A1MAPK1KDM4EMCL1PFKFB3
SCHEMBL1850633 0.83 MAPT (0.44) ALDH1A1KDM4EL3MBTL1CDC7DBF4
SCHEMBL17434058 0.83 PDE10A (0.48) ALDH1A1MAPK1KDM4EL3MBTL1CDC7
SCHEMBL17433936 0.81 PDE10A (0.47) ALDH1A1KDM4EL3MBTL1CDC7DBF4
SCHEMBL17433833 0.81 PDE10A (0.48) ALDH1A1KDM4EL3MBTL1CDC7DBF4
SCHEMBL2897560 0.80 MCL1 (0.52) MAPK1MCL1PFKFB3PFKFB4KMT2A
SCHEMBL17433957 0.80 PDE10A (0.49) ALDH1A1KDM4EL3MBTL1CDC7DBF4
SCHEMBL17434007 0.79 PDE10A (0.48) ALDH1A1MAPK1KDM4EL3MBTL1MAPT
SCHEMBL17433942 0.79 PDE10A (0.48) ALDH1A1KDM4EL3MBTL1CDC7DBF4
SCHEMBL1850127 0.79 GPR35 (0.48) ALDH1A1KDM4EL3MBTL1CDC7DBF4

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-7655641-B2 Sulfonamide derivatives as PPAR modulators ELI LILLY AND COMPANY (US) 2010-02-02 US disclosed
US-7655641-B2 Sulfonamide derivatives as PPAR modulators ELI LILLY AND COMPANY (US) 2010-02-02 US disclosed
EP-1597248-B1 SULFONAMIDE DERIVATIVES AS PPAR MODULATORS LILLY CO ELI (US) 2007-12-26 EP disclosed
EP-1597248-B1 SULFONAMIDE DERIVATIVES AS PPAR MODULATORS LILLY CO ELI (US) 2007-12-26 EP disclosed
US-20060217433-A1 Sulfonamide derivatives as ppar modulators ELI LILLY AND COMPANY (US) 2006-09-28 US disclosed
EP-1597248-A2 SULFONAMIDE DERIVATIVES AS PPAR MODULATORS ELI LILLY AND COMPANY (US) 2005-11-23 EP disclosed
WO-2004073606-A2 SULFONAMIDE DERIVATIVES AS PPAR MODULATORS ELI LILLY AND COMPANY (US) 2004-09-02 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-20060217433-A1 Sulfonamide derivatives as ppar modulators PPARD, PPARA, PPARG ALDH1A1 1050/4885MAPK1 2241/4885KDM4E 3238/4885

“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.