SCHEMBL3529529

SCHEMBL3529529

CCc1ccc(S(=O)(=O)Nc2ccc(Cl)nc2I)cc1

nearest known ligand 0.50

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 2/20 0.49
MEN1 O00255 1/20 0.49
GAA P10253 1/20 0.49
L3MBTL1 Q9Y468 1/20 0.49
UCHL1 P09936 1/20 0.48
LMNA P02545 2/20 0.45
HTT P42858 2/20 0.45
SMN1; SMN2 Q16637 1/20 0.45
NPC1 O15118 1/20 0.44
RAB9A P51151 1/20 0.44
METAP2 P50579 2/20 0.43
CCR9 P51686 1/20 0.43
MAPT P10636 5/20 0.42
SLC40A1 Q9NP59 1/20 0.42
ALDH1A1 P00352 2/20 0.41
POLB P06746 1/20 0.41
HPGD P15428 1/20 0.41
XBP1 P17861 1/20 0.41

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
SCHEMBL3527028 0.82 CCR2 (0.48) GAAL3MBTL1LMNASMN1; SMN2MAPT
SCHEMBL3535146 0.81 SLC40A1 (0.61) KMT2AMEN1GAAMETAP2MAPT
SCHEMBL3531305 0.81 KEAP1 (0.56) KMT2AMEN1GAAL3MBTL1LMNA
SCHEMBL3530032 0.78 APP (0.42) METAP2MAPTSLC40A1ALDH1A1
SCHEMBL16235274 0.74 METAP2 (0.48) KMT2AMEN1GAAL3MBTL1LMNA
SCHEMBL3533105 0.73 SLC40A1 (0.55) KMT2AGAACCR9MAPTSLC40A1
SCHEMBL3528452 0.72 CYP2C9 (0.59) KMT2ALMNAHTTSMN1; SMN2MAPT
SCHEMBL3535998 0.72 NFE2L2 (0.61) GAALMNAHTTSLC40A1ALDH1A1
SCHEMBL3529882 0.72 GLO1 (0.54) KMT2AMEN1LMNASMN1; SMN2MAPT
SCHEMBL2227371 0.72 AKT1 (0.45) KMT2AMEN1CCR9SLC40A1

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 5 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
EP-1919474-B1 PYRROLOPYRIDINE DERIVATIVES AND USE OF SAME AS PPAR RECEPTOR MODULATORS FOURNIER LAB SA (FR) 2009-08-05 EP 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 KMT2A 2834/4885MEN1 4459/4885GAA 3439/4885
US-20080200495-A1 Pyrrolopyridine Compounds, Method of Making Them and Uses Thereof LIPG, PCSK9, PNLIP KMT2A 3514/4885MEN1 4228/4885GAA 113/4885

“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.