SCHEMBL3690288

SCHEMBL3690288

Cc1c(S(=O)(=O)Cl)sc2cccc(Cl)c12

nearest known ligand 0.41

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
MCL1 Q07820 3/20 0.41
MAPK1 P28482 2/20 0.41
ALDH1A1 P00352 4/20 0.40
KDM4E B2RXH2 1/20 0.40
L3MBTL1 Q9Y468 1/20 0.40
OGG1 O15527 1/20 0.38
MAPT P10636 2/20 0.37
PFKFB4 Q16877 3/20 0.32
SLC9A1 P19634 2/20 0.32
MEN1 O00255 1/20 0.32
KMT2A Q03164 1/20 0.32
RXFP1 Q9HBX9 1/20 0.32
USP2 O75604 1/20 0.32
LMNA P02545 1/20 0.32
TSHR P16473 1/20 0.32
PFKFB3 Q16875 2/20 0.32
PARP1 P09874 1/20 0.31

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
SCHEMBL788101 0.85 PKM (0.33) ALDH1A1MAPTSLC9A1MEN1KMT2A
SCHEMBL787663 0.74 HSD11B1 (0.43) MCL1ALDH1A1KDM4EL3MBTL1MAPT
SCHEMBL788498 0.73 PFKFB4 (0.54) MCL1ALDH1A1PFKFB4PFKFB3PARP1
SCHEMBL12095433 0.71 MAPK1 (0.42) MCL1MAPK1ALDH1A1KDM4EL3MBTL1
SCHEMBL15619314 0.70 MCL1 (0.71) MCL1MAPK1ALDH1A1KDM4EL3MBTL1
SCHEMBL31568860 0.69 MAPK1 (0.53) MCL1MAPK1ALDH1A1KDM4EL3MBTL1
SCHEMBL3689291 0.68 NPSR1 (0.37) L3MBTL1PFKFB4PFKFB3
SCHEMBL18869413 0.67 MAPK1 (0.53) MCL1MAPK1ALDH1A1KDM4EL3MBTL1
SCHEMBL11762263 0.67 ALDH1A1 (0.52) ALDH1A1MAPTMEN1KMT2AUSP2
SCHEMBL15619321 0.67 MAPK1 (0.56) MCL1MAPK1ALDH1A1KDM4EL3MBTL1

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
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
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-0946539-A1 SULPHONAMIDE DERIVATIVES, PROCESS FOR THEIR PREPARATION, AND THEIR USE AS MEDICAMENTS SMITHKLINE BEECHAM PLC (GB) 1999-10-06 EP disclosed
WO-1998027081-A1 SULPHONAMIDE DERIVATIVES, PROCESS FOR THEIR PREPARATION, AND THEIR USE AS MEDICAMENTS SMITHKLINE BEECHAM PLC (GB) 1998-06-25 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 MCL1 4406/4885MAPK1 2241/4885ALDH1A1 1050/4885

“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.