SCHEMBL3528969

SCHEMBL3528969

CC(C)(OCc1cc2nc(Cl)ccc2n1S(=O)(=O)c1cccc2ccccc12)C(=O)O

nearest known ligand 0.47

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
PPARG P37231 4/20 0.47
PPARA Q07869 2/20 0.47
SLC16A3 O15427 11/20 0.40
MCTS1 Q9ULC4 8/20 0.38
SLC16A1 P53985 8/20 0.36
KDM4E B2RXH2 1/20 0.36
ALDH1A1 P00352 1/20 0.36
HSD17B10 Q99714 1/20 0.36
NR1I2 O75469 1/20 0.36
HTR6 P50406 2/20 0.35
HTT P42858 1/20 0.35

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
SCHEMBL3534366 0.88 SLC16A3 (0.38) SLC16A3MCTS1SLC16A1
SCHEMBL3528148 0.88 PPARG (0.48) PPARGPPARASLC16A3MCTS1SLC16A1
SCHEMBL3530329 0.87 MAPT (0.43) SLC16A3SLC16A1KDM4EALDH1A1HTR6
SCHEMBL3530590 0.82 PPARG (0.39) PPARGPPARASLC16A3MCTS1SLC16A1
SCHEMBL3530092 0.82 PPARG (0.50) PPARGPPARASLC16A3MCTS1SLC16A1
SCHEMBL3530102 0.82 PPARG (0.63) PPARGPPARAKDM4EALDH1A1NR1I2
SCHEMBL3531617 0.80 PPARG (0.48) PPARGPPARASLC16A3MCTS1SLC16A1
SCHEMBL3533511 0.80 NOD1 (0.41) PPARGPPARASLC16A3MCTS1SLC16A1
SCHEMBL3532413 0.80 PPARG (0.41) PPARGPPARASLC16A3MCTS1SLC16A1
SCHEMBL3530970 0.80 PPARG (0.72) PPARGPPARA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7728002-B2 Use of pyrrolopyridine compounds for activating PPAR receptors and treatment of conditions involving such receptors LABORATOIRES FOURNIER S.A. (FR) 2010-06-01 US disclosed
US-20090239856-A1 Use of Pyrrolopyridine Compounds for Activating PPAR Receptors and Treatment of Conditions Involving Such Receptors LABORATOIRES FOURNIER S.A. (FR) 2009-09-24 US disclosed
US-7557122-B2 Pyrrolopyridine compounds, method of making them and uses thereof LABORATOIRES FOURNIER S.A. (FR) 2009-07-07 US disclosed
US-20080200495-A1 Pyrrolopyridine Compounds, Method of Making Them and Uses Thereof LABORATOIRES FOURNIER S.A. (FR) 2008-08-21 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 (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-20090239856-A1 Use of Pyrrolopyridine Compounds for Activating PPAR Receptors and Treatment of Conditions Involving Such Receptors PPARD, PPARA, PPARG PPARG 3/4885PPARA 2/4885SLC16A3 2283/4885
US-20080200495-A1 Pyrrolopyridine Compounds, Method of Making Them and Uses Thereof LIPG, PCSK9, PNLIP PPARG 335/4885PPARA 168/4885SLC16A3 2244/4885

“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.