SCHEMBL3532199

SCHEMBL3532199

CC(OCc1cc2nc(Cl)ccc2n1S(=O)(=O)c1ccc2nc(N)sc2c1)C(=O)O

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PPARG P37231 6/20 0.53
PPARD Q03181 5/20 0.53
PPARA Q07869 3/20 0.53
ALDH1A1 P00352 3/20 0.41
HPGD P15428 2/20 0.41
MAPT P10636 2/20 0.41
VDR P11473 1/20 0.41
GFER P55789 1/20 0.41
GPR55 Q9Y2T6 1/20 0.41
KMT2A Q03164 2/20 0.40
LMNA P02545 2/20 0.40
HSD17B10 Q99714 2/20 0.40
KDM4E B2RXH2 1/20 0.40
PKM P14618 1/20 0.40
CYP3A4 P08684 2/20 0.40
CYP2C9 P11712 2/20 0.40
CYP2D6 P10635 1/20 0.39
MEN1 O00255 1/20 0.35
TP53 P04637 1/20 0.35
P2RX3 P56373 1/20 0.34

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
SCHEMBL3533574 0.87 POLB (0.48) PPARGPPARDPPARAALDH1A1KMT2A
SCHEMBL3533939 0.86 PPARG (0.53) PPARGPPARDPPARAALDH1A1PKM
SCHEMBL3531264 0.84 PPARG (0.50) PPARGPPARDPPARAALDH1A1
SCHEMBL3532175 0.83 PPARG (0.43) PPARGPPARDPPARAALDH1A1HPGD
SCHEMBL3531610 0.83 PPARG (0.43) PPARGPPARDPPARAALDH1A1HPGD
SCHEMBL3531013 0.83 PPARG (0.43) PPARGPPARDPPARAALDH1A1HPGD
SCHEMBL3530572 0.83 PPARG (0.69) PPARGPPARDPPARAALDH1A1HPGD
SCHEMBL3531746 0.81 PPARG (0.78) PPARGPPARDPPARAALDH1A1HPGD
SCHEMBL3526787 0.79 PPARG (0.69) PPARGPPARDPPARAGPR55KMT2A
SCHEMBL3530671 0.76 PPARG (0.48) PPARGPPARDPPARAALDH1A1PKM

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 3/4885PPARD 1/4885PPARA 2/4885
US-20080200495-A1 Pyrrolopyridine Compounds, Method of Making Them and Uses Thereof LIPG, PCSK9, PNLIP PPARG 335/4885PPARD 55/4885PPARA 168/4885

“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.