SCHEMBL972687

SCHEMBL972687

Cc1cccc(NS(=O)(=O)c2ccc(Cl)cc2)c1C(=O)Nc1ccc(S(=O)(=O)N2CCSCC2)cc1

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GPR27 Q9NS67 3/20 0.52
LMNA P02545 2/20 0.49
SMN1; SMN2 Q16637 1/20 0.49
KMT2A Q03164 6/20 0.47
MEN1 O00255 5/20 0.47
NPC1 O15118 1/20 0.47
ALDH1A1 P00352 5/20 0.46
ABCC9 O60706 1/20 0.46
ABCC8 Q09428 1/20 0.46
KCNJ11 Q14654 1/20 0.46
KCNJ8 Q15842 1/20 0.46
GAA P10253 3/20 0.45
MAPT P10636 2/20 0.45
USP2 O75604 2/20 0.45
KDM4E B2RXH2 1/20 0.44
POLB P06746 1/20 0.44
BLM P54132 1/20 0.44
CTDSP1 Q9GZU7 1/20 0.44
APOBEC3G Q9HC16 1/20 0.44
L3MBTL1 Q9Y468 1/20 0.43

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
SCHEMBL971693 0.92 LMNA (0.52) GPR27LMNASMN1; SMN2KMT2AMEN1
SCHEMBL492078 0.91 ALDH1A1 (0.55) GPR27LMNASMN1; SMN2KMT2AMEN1
SCHEMBL491583 0.82 ALDH1A1 (0.55) GPR27LMNASMN1; SMN2KMT2AMEN1
SCHEMBL491092 0.81 SLC10A2 (0.57) GPR27LMNASMN1; SMN2KMT2AMEN1
SCHEMBL492309 0.81 SLC10A6 (0.61) GPR27LMNASMN1; SMN2KMT2AMEN1
Hydrochloric Acid SCHEMBL971595 0.81 SLC10A2 (0.56) GPR27LMNASMN1; SMN2KMT2AMEN1
SCHEMBL491824 0.80 KMT2A (0.49) GPR27LMNASMN1; SMN2KMT2AMEN1
SCHEMBL12585305 0.80 ALDH1A1 (0.57) GPR27LMNASMN1; SMN2KMT2AMEN1
SCHEMBL29382580 0.78 ALDH1A1 (0.59) GPR27LMNASMN1; SMN2KMT2AMEN1
SCHEMBL422152 0.78 ALDH1A1 (0.59) GPR27LMNASMN1; SMN2KMT2AMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2207541-B1 USE OF SULFONYL-SUBSTITUTED 2-SULFONYLAMINOBENZOIC ACID N-PHENYLAMIDES IN THE TREATMENT OF PAIN SANOFI AVENTIS DEUTSCHLAND (DE) 2014-10-29 EP disclosed
US-8518998-B2 Use of sulfonyl-substituted 2-sulfonylaminobenzoic acid N-phenylamides in the treatment of pain SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2013-08-27 US disclosed
CN-101815514-B Use of sulfonyl-substituted 2-sulfonylaminobenzoic acid N-phenylamides in the treatment of pain SANOFI AVENTIS DEUTSCHLAND 2012-05-09 CN disclosed
US-20110021505-A1 Use of sulfonyl-substituted 2-sulfonylaminobenzoic acid N-phenylamides in the treatment of pain SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2011-01-27 US disclosed
CN-101815514-A Use of sulfonyl-substituted 2-sulfonylaminobenzoic acid N-phenylamides in the treatment of pain SANOFI AVENTIS DEUTSCHLAND 2010-08-25 CN disclosed
EP-2207541-A1 USE OF SULFONYL-SUBSTITUTED 2-SULFONYLAMINOBENZOIC ACID N-PHENYLAMIDES IN THE TREATMENT OF PAIN Sanofi-Aventis Deutschland GmbH (DE) 2010-07-21 EP disclosed
WO-2009043495-A1 USE OF SULFONYL-SUBSTITUTED 2-SULFONYLAMINOBENZOIC ACID N-PHENYLAMIDES IN THE TREATMENT OF PAIN SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2009-04-09 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-20110021505-A1 Use of sulfonyl-substituted 2-sulfonylaminobenzoic acid N-phenylamides in the treatment of pain SCN1A, SCN2A, CACNA1A GPR27 1930/4885LMNA 2591/4885SMN1; SMN2 157/4885

“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.