SCHEMBL2568784

SCHEMBL2568784

Cc1ccc(CN2CCN(C(=O)COCC3CCCCN3S(=O)(=O)c3c(Cl)cccc3Cl)CC2)cc1

nearest known ligand 0.45

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 1/20 0.45
LMNA P02545 4/20 0.44
ALDH1A1 P00352 4/20 0.44
TSHR P16473 2/20 0.44
SMN1; SMN2 Q16637 6/20 0.43
MAPT P10636 1/20 0.42
USP2 O75604 1/20 0.42
ATM Q13315 2/20 0.41
KDM4E B2RXH2 3/20 0.41
MEN1 O00255 2/20 0.40
KMT2A Q03164 2/20 0.40
FKBP1A P62942 1/20 0.40
OPRM1 P35372 1/20 0.40
OPRK1 P41145 1/20 0.40

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
SCHEMBL2563588 0.97 L3MBTL1 (0.46) L3MBTL1LMNAALDH1A1TSHRSMN1; SMN2
SCHEMBL2565189 0.93 LMNA (0.43) LMNAALDH1A1SMN1; SMN2USP2ATM
SCHEMBL2564519 0.92 ALDH1A1 (0.50) LMNAALDH1A1TSHRSMN1; SMN2USP2
SCHEMBL2568311 0.91 ALDH1A1 (0.43) LMNAALDH1A1SMN1; SMN2MAPTUSP2
SCHEMBL2564995 0.91 OPRK1 (0.43) LMNAALDH1A1SMN1; SMN2USP2KDM4E
SCHEMBL2569878 0.90 LMNA (0.44) LMNAALDH1A1SMN1; SMN2USP2KDM4E
SCHEMBL2569991 0.90 ALDH1A1 (0.48) LMNAALDH1A1TSHRSMN1; SMN2USP2
SCHEMBL2564531 0.89 SMN1; SMN2 (0.46) LMNAALDH1A1TSHRSMN1; SMN2USP2
SCHEMBL2563798 0.89 ALDH1A1 (0.44) LMNAALDH1A1SMN1; SMN2MAPTUSP2
SCHEMBL2567631 0.88 SMN1; SMN2 (0.42) LMNAALDH1A1SMN1; SMN2USP2ATM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2066659-B1 SUBSTITUTED SULFONAMIDE DERIVATIVES GRUENENTHAL GMBH (DE) 2013-08-28 EP claimed
EP-2383267-A1 Substituted sulfonamide derivatives Grünenthal GmbH (DE) 2011-11-02 EP claimed
US-20100317644-A1 Substituted Sulfonamide Compounds GRUENENTHAL GMBH (DE) 2010-12-16 US claimed
US-20080153843-A1 SUBSTITUTED SULFONAMIDE COMPOUNDS GRUENENTHAL GMBH (DE) 2008-06-26 US claimed
EP-2066659-B1 SUBSTITUTED SULFONAMIDE DERIVATIVES GRUENENTHAL GMBH (DE) 2013-08-28 EP disclosed
US-8435978-B2 Substituted sulfonamide compounds GRUENENTHAL GMBH (DE) 2013-05-07 US disclosed
EP-2383267-A1 Substituted sulfonamide derivatives Grünenthal GmbH (DE) 2011-11-02 EP disclosed
US-20100324009-A1 Substituted Sulfonamide Compounds GRUENENTHAL GMBH (DE) 2010-12-23 US disclosed
US-20100317644-A1 Substituted Sulfonamide Compounds GRUENENTHAL GMBH (DE) 2010-12-16 US disclosed
EP-2066659-A1 SUBSTITUTED SULFONAMIDE DERIVATIVES Grünenthal GmbH (DE) 2009-06-10 EP disclosed
US-20080153843-A1 SUBSTITUTED SULFONAMIDE COMPOUNDS GRUENENTHAL GMBH (DE) 2008-06-26 US disclosed
WO-2008040492-A1 SUBSTITUTED SULFONAMIDE DERIVATIVES Grünenthal GmbH (DE) 2008-04-10 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 (3 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-20100317644-A1 Substituted Sulfonamide Compounds SULT2A1, STS, SULT1A1 L3MBTL1 4648/4885LMNA 2964/4885ALDH1A1 1535/4885
US-20100324009-A1 Substituted Sulfonamide Compounds SULT2A1, STS, SULT1A1 L3MBTL1 4648/4885LMNA 2964/4885ALDH1A1 1535/4885
US-20080153843-A1 SUBSTITUTED SULFONAMIDE COMPOUNDS SULT2A1, STS, SULT1A1 L3MBTL1 4648/4885LMNA 2964/4885ALDH1A1 1535/4885

“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.