SCHEMBL2969168

SCHEMBL2969168

CCOC(=O)c1cnn(-c2cc(Cl)ccc2NS(=O)(=O)c2ccc(C(C)(C)C)cc2)c1

nearest known ligand 0.49

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
CCR9 P51686 16/20 0.49
HSD17B2 P37059 2/20 0.48
CCR2 P41597 1/20 0.47
KDM4E B2RXH2 1/20 0.46
ALDH1A1 P00352 1/20 0.46
LMNA P02545 1/20 0.46

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
SCHEMBL15911981 0.87 HSD17B2 (0.53) CCR9HSD17B2CCR2
SCHEMBL2969051 0.86 CCR9 (0.52) CCR9HSD17B2CCR2
SCHEMBL2971896 0.85 CCR9 (0.48) CCR9HSD17B2KDM4EALDH1A1LMNA
SCHEMBL2981286 0.85 CCR9 (0.50) CCR9HSD17B2CCR2
SCHEMBL2966174 0.84 CCR9 (0.49) CCR9HSD17B2CCR2
SCHEMBL2975523 0.83 HSD17B2 (0.56) CCR9HSD17B2
SCHEMBL2973891 0.82 MAPT (0.52) CCR9HSD17B2CCR2
SCHEMBL2970672 0.82 HSD17B2 (0.53) CCR9HSD17B2
SCHEMBL2975083 0.81 HSD17B2 (0.55) CCR9HSD17B2CCR2
SCHEMBL2972093 0.79 CCR9 (0.50) CCR9HSD17B2CCR2

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 33 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8835468-B2 N-(2-(hetaryl)aryl)arylsulfonamides and n-(2-(hetaryl)hetaryl) arylsulfonamides CHEMOCENTRYX, INC. (US) 2014-09-16 US claimed
EP-2170823-B1 N-(2-(HETARYL)ARYL)ARYLSULFONAMIDES AND N-(2-(HETARYL)HETARYL)ARYLSULFONAMIDES CHEMOCENTRYX INC (US) 2014-08-06 EP claimed
US-20120245138-A1 N-(2-(HETARYL)ARYL)ARYLSULFONAMIDES AND N-(2-(HETARYL)HETARYL ARYLSULFONAMIDES CHEMOCENTRYX, INC. (US) 2012-09-27 US claimed
US-8198309-B2 N-(2-(hetaryl)aryl) arylsulfonamides and N-(2-(hetaryl)hetaryl arylsulfonamides CHEMOCENTRYX, INC. (US) 2012-06-12 US claimed
US-20100331302-A1 N-(2-(HETARYL)ARYL) ARYLSULFONAMIDES AND N-(2-(HETARYL)HETARYL ARYLSULFONAMIDES CHEMOCENTRYX, INC. (US) 2010-12-30 US claimed
EP-2170823-A1 N-(2-(HETARYL)ARYL)ARYLSULFONAMIDES AND N-(2-(HETARYL)HETARYL)ARYLSULFONAMIDES ChemoCentryx Inc (US) 2010-04-07 EP claimed
WO-2009038847-A1 N-(2-(HETARYL)ARYL)ARYLSULFONAMIDES AND N-(2-(HETARYL)HETARYL)ARYLSULFONAMIDES CHEMOCENTRYX, INC. (US) 2009-03-26 WO claimed
US-20090005410-A1 N-(4-Chloro-2-[1,2,3]triazolo[4,5-b]pyridin-1-yl-phenyl)-4-(1-hydroxy-1-methyl-ethyl)-benzene-sulfonamide sodium salt, used as chemokine receptors antagonists, useful for treating inflammation CHEMOCENTRYX, INC. (US) 2009-01-01 US claimed
US-9409909-B2 N-(2-(hetaryl)aryl)arylsulfonamides and N-(2-(hetaryl)hetaryl)arylsulfonamides CHEMOCENTRYX, INC. (US) 2016-08-09 US disclosed
US-9409909-B2 N-(2-(hetaryl)aryl)arylsulfonamides and N-(2-(hetaryl)hetaryl)arylsulfonamides CHEMOCENTRYX, INC. (US) 2016-08-09 US disclosed
US-9409909-B2 N-(2-(hetaryl)aryl)arylsulfonamides and N-(2-(hetaryl)hetaryl)arylsulfonamides CHEMOCENTRYX, INC. (US) 2016-08-09 US disclosed
US-8835468-B2 N-(2-(hetaryl)aryl)arylsulfonamides and n-(2-(hetaryl)hetaryl) arylsulfonamides CHEMOCENTRYX, INC. (US) 2014-09-16 US disclosed
US-8835468-B2 N-(2-(hetaryl)aryl)arylsulfonamides and n-(2-(hetaryl)hetaryl) arylsulfonamides CHEMOCENTRYX, INC. (US) 2014-09-16 US disclosed
US-8835468-B2 N-(2-(hetaryl)aryl)arylsulfonamides and n-(2-(hetaryl)hetaryl) arylsulfonamides CHEMOCENTRYX, INC. (US) 2014-09-16 US disclosed
EP-2170823-A1 N-(2-(HETARYL)ARYL)ARYLSULFONAMIDES AND N-(2-(HETARYL)HETARYL)ARYLSULFONAMIDES ChemoCentryx Inc (US) 2010-04-07 EP disclosed
WO-2009038847-A1 N-(2-(HETARYL)ARYL)ARYLSULFONAMIDES AND N-(2-(HETARYL)HETARYL)ARYLSULFONAMIDES CHEMOCENTRYX, INC. (US) 2009-03-26 WO disclosed
WO-2009038847-A1 N-(2-(HETARYL)ARYL)ARYLSULFONAMIDES AND N-(2-(HETARYL)HETARYL)ARYLSULFONAMIDES CHEMOCENTRYX, INC. (US) 2009-03-26 WO disclosed
US-20090005410-A1 N-(4-Chloro-2-[1,2,3]triazolo[4,5-b]pyridin-1-yl-phenyl)-4-(1-hydroxy-1-methyl-ethyl)-benzene-sulfonamide sodium salt, used as chemokine receptors antagonists, useful for treating inflammation CHEMOCENTRYX, INC. (US) 2009-01-01 US disclosed
US-20090005410-A1 N-(4-Chloro-2-[1,2,3]triazolo[4,5-b]pyridin-1-yl-phenyl)-4-(1-hydroxy-1-methyl-ethyl)-benzene-sulfonamide sodium salt, used as chemokine receptors antagonists, useful for treating inflammation CHEMOCENTRYX, INC. (US) 2009-01-01 US disclosed
US-20090005410-A1 N-(4-Chloro-2-[1,2,3]triazolo[4,5-b]pyridin-1-yl-phenyl)-4-(1-hydroxy-1-methyl-ethyl)-benzene-sulfonamide sodium salt, used as chemokine receptors antagonists, useful for treating inflammation CHEMOCENTRYX, INC. (US) 2009-01-01 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 (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-20100331302-A1 N-(2-(HETARYL)ARYL) ARYLSULFONAMIDES AND N-(2-(HETARYL)HETARYL ARYLSULFONAMIDES CCR9, CCR2, CCR10 CCR9 1/4885HSD17B2 1177/4885CCR2 2/4885
US-20120245138-A1 N-(2-(HETARYL)ARYL)ARYLSULFONAMIDES AND N-(2-(HETARYL)HETARYL ARYLSULFONAMIDES CCR9, CCR2, CCR10 CCR9 1/4885HSD17B2 1177/4885CCR2 2/4885
US-20090005410-A1 N-(4-Chloro-2-[1,2,3]triazolo[4,5-b]pyridin-1-yl-phenyl)-4-(1-hydroxy-1-methyl-ethyl)-benzene-sulfonamide sodium salt, used as chemokine receptors antagonists, useful for treating inflammation CCR9, CCR1, CCR2 CCR9 1/4885HSD17B2 3385/4885CCR2 3/4885

“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.