SCHEMBL3524765

SCHEMBL3524765

Cc1nc2cc(S(=O)(=O)Cl)ccc2s1

nearest known ligand 0.66

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
POLB P06746 2/20 0.66
ALDH1A1 P00352 6/20 0.61
SMN1; SMN2 Q16637 7/20 0.53
NPC1 O15118 3/20 0.53
RAB9A P51151 3/20 0.53
PKM P14618 5/20 0.51
HSD17B10 Q99714 2/20 0.49
TP53 P04637 3/20 0.48
MAPT P10636 1/20 0.48
HPGD P15428 1/20 0.48
LMNA P02545 7/20 0.48
NPSR1 Q6W5P4 1/20 0.48
HTT P42858 5/20 0.46
GAA P10253 1/20 0.46
ALOX15 P16050 1/20 0.45
MAPK1 P28482 1/20 0.45
KMT2A Q03164 1/20 0.44
NOD2 Q9HC29 1/20 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
SCHEMBL609522 0.87 LMNA (0.57) POLBALDH1A1SMN1; SMN2NPC1RAB9A
SCHEMBL6141396 0.85 POLB (0.68) POLBALDH1A1SMN1; SMN2NPC1RAB9A
SCHEMBL84337 0.83 POLB (0.66) POLBALDH1A1SMN1; SMN2NPC1RAB9A
SCHEMBL14612413 0.83 POLB (0.66) POLBALDH1A1SMN1; SMN2NPC1RAB9A
Hydrochloric Acid SCHEMBL27712068 0.82 POLB (0.64) POLBALDH1A1SMN1; SMN2NPC1RAB9A
SCHEMBL1094692 0.81 POLB (0.44) POLBALDH1A1SMN1; SMN2NPC1RAB9A
SCHEMBL11147117 0.81 POLB (0.44) POLBALDH1A1NPC1RAB9APKM
SCHEMBL25213930 0.80 ALDH1A1 (0.57) POLBALDH1A1SMN1; SMN2RAB9APKM
SCHEMBL30991708 0.80 ALDH1A1 (0.57) POLBALDH1A1SMN1; SMN2RAB9APKM
SCHEMBL6647659 0.80 POLB (1.00) POLBALDH1A1SMN1; SMN2NPC1RAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108610301-B Chiral aromatic heterocyclic amine derivative and synthesis method and application thereof 中山大学 2021-08-31 CN disclosed
CN-108610301-A A kind of chiral fragrant miscellaneous amine derivant and its synthetic method and application 中山大学 2018-10-02 CN disclosed
US-9850382-B1 Unsymmetrical cyanine dyes and their application Ying, Laiqiang (US) 2017-12-26 US disclosed
US-8436040-B2 Method of treating conditions involving PPAR-receptors with indole compounds LABORATOIRES FOURNIER S.A. (FR) 2013-05-07 US disclosed
CN-101242833-B Pyrrolopyridine derivatives and use of same as PPAR receptor modulators FOURNIER LAB SA 2012-06-27 CN disclosed
US-20100286137-A1 Method of Treating Conditions Involving PPAR-Receptors with Indole Compounds LABORATORIES FOURNIER S.A. (FR) 2010-11-11 US disclosed
US-7795297-B2 Indole compounds, method of preparing them and uses thereof LABORATORIES FOURNIER S.A. (FR) 2010-09-14 US disclosed
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
CN-101242833-A Pyrrolopyridine derivatives and use of same as PPAR receptor modulators FOURNIER LAB SA (FR) 2008-08-13 CN disclosed
US-20080153816-A1 Indole Compounds, Method of Preparing Them and Uses Thereof LABORATOIRES FOURNIER S.A. (FR) 2008-06-26 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 (4 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 POLB 1219/4885ALDH1A1 1314/4885SMN1; SMN2 3212/4885
US-20080200495-A1 Pyrrolopyridine Compounds, Method of Making Them and Uses Thereof LIPG, PCSK9, PNLIP POLB 1293/4885ALDH1A1 1350/4885SMN1; SMN2 2484/4885
US-20080153816-A1 Indole Compounds, Method of Preparing Them and Uses Thereof LIPG, GPR119, IAPP POLB 4410/4885ALDH1A1 1607/4885SMN1; SMN2 2892/4885
US-20100286137-A1 Method of Treating Conditions Involving PPAR-Receptors with Indole Compounds GPR119, PPARA, PPARG POLB 3181/4885ALDH1A1 1453/4885SMN1; SMN2 3475/4885

“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.