SCHEMBL2968121

SCHEMBL2968121

NS(=O)(=O)c1ccccc1N1CCOCC1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 2/20 0.50
MAPT P10636 2/20 0.50
MEN1 O00255 1/20 0.50
NPC1 O15118 1/20 0.50
RAB9A P51151 1/20 0.50
KMT2A Q03164 1/20 0.50
TDP1 Q9NUW8 1/20 0.50
CA2 P00918 10/20 0.49
CA1 P00915 8/20 0.49
CA12 O43570 8/20 0.49
CA9 Q16790 7/20 0.49
LMNA P02545 2/20 0.47
NSD2 O96028 1/20 0.47
CA7 P43166 3/20 0.46
PKM P14618 1/20 0.46
TSHR P16473 1/20 0.46
ALOX15 P16050 1/20 0.45
HSD17B10 Q99714 1/20 0.45
POLB P06746 1/20 0.43
HTR6 P50406 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
SCHEMBL4059759 0.84 CA2 (0.50) L3MBTL1MAPTNPC1CA2CA1
SCHEMBL7011722 0.83 MAPT (0.50) L3MBTL1MAPTMEN1NPC1RAB9A
SCHEMBL6867989 0.83 MAPT (0.50) L3MBTL1MAPTMEN1NPC1RAB9A
SCHEMBL25284343 0.82 MAPT (0.47) L3MBTL1MAPTMEN1NPC1RAB9A
Hydrochloric Acid SCHEMBL11538427 0.81 KEAP1 (0.52) L3MBTL1MAPTNPC1CA2CA1
SCHEMBL31527700 0.81 KEAP1 (0.52) L3MBTL1MAPTNPC1CA2CA1
SCHEMBL14900132 0.80 MAPT (0.44) L3MBTL1MAPTMEN1NPC1RAB9A
SCHEMBL4261189 0.79 HTR6 (0.67) CA2CA1CA12CA9LMNA
SCHEMBL30564805 0.79 MAPT (0.47) L3MBTL1MAPTMEN1NPC1RAB9A
SCHEMBL10942684 0.79 MAPT (0.59) L3MBTL1MAPTMEN1NPC1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2000023444-A1 5,7-DISUBSTITUTED-4-AMINOPYRIDO[2,3-D]PYRIMIDINE COMPOUNDS ABBOTT LABORATORIES (US) 2000-04-27 WO claimed
US-12559455-B2 Compound as a UBR box domain ligand AUTOTAC INC. (KR) 2026-02-24 US disclosed
US-20230174470-A1 COMPOUND AS A UBR BOX DOMAIN LIGAND AUTOTAC INC. (KR) 2023-06-08 US disclosed
US-10752640-B2 Compounds active towards bromodomains NUEVOLUTION A/S (DK) 2020-08-25 US disclosed
US-20170349607-A1 COMPOUNDS ACTIVE TOWARDS BROMODOMAINS NUEVOLUTION A/S (DK) 2017-12-07 US disclosed
EP-3174868-A1 COMPOUNDS ACTIVE TOWARDS BROMODOMAINS Nuevolution A/S (DK) 2017-06-07 EP disclosed
US-9409909-B2 N-(2-(hetaryl)aryl)arylsulfonamides and N-(2-(hetaryl)hetaryl)arylsulfonamides CHEMOCENTRYX, INC. (US) 2016-08-09 US disclosed
WO-2016016316-A1 COMPOUNDS ACTIVE TOWARDS BROMODOMAINS NUEVOLUTION A/S (DK) 2016-02-04 WO disclosed
US-8835468-B2 N-(2-(hetaryl)aryl)arylsulfonamides and n-(2-(hetaryl)hetaryl) arylsulfonamides CHEMOCENTRYX, INC. (US) 2014-09-16 US disclosed
US-20120245138-A1 N-(2-(HETARYL)ARYL)ARYLSULFONAMIDES AND N-(2-(HETARYL)HETARYL ARYLSULFONAMIDES CHEMOCENTRYX, INC. (US) 2012-09-27 US disclosed
US-20100331302-A1 N-(2-(HETARYL)ARYL) ARYLSULFONAMIDES AND N-(2-(HETARYL)HETARYL ARYLSULFONAMIDES CHEMOCENTRYX, INC. (US) 2010-12-30 US disclosed
US-20100234364-A1 CCR2 INHIBITORS AND METHODS OF USE THEREOF CHEMOCENTRYX, INC. 2010-09-16 US disclosed
US-7776877-B2 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) 2010-08-17 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-6617357-B2 Administering to a patient for inhibiting cyclic nucleotide phosphodiesterases (PDEs) activity, a benzenesulfonamide compound SMITHKLINE BEECHAM CORPORATION 2003-09-09 US disclosed
US-20020156064-A1 Compounds and their use as PDE inhibitors SMITHKLINE BEECHAM CORP 2002-10-24 US disclosed
WO-2000023444-A1 5,7-DISUBSTITUTED-4-AMINOPYRIDO[2,3-D]PYRIMIDINE COMPOUNDS ABBOTT LABORATORIES (US) 2000-04-27 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 (9 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 L3MBTL1 3262/4885MAPT 4750/4885MEN1 4798/4885
US-20120245138-A1 N-(2-(HETARYL)ARYL)ARYLSULFONAMIDES AND N-(2-(HETARYL)HETARYL ARYLSULFONAMIDES CCR9, CCR2, CCR10 L3MBTL1 3262/4885MAPT 4750/4885MEN1 4798/4885
US-20020156064-A1 Compounds and their use as PDE inhibitors PDE3A, PDE2A, PDE5A L3MBTL1 4316/4885MAPT 2761/4885MEN1 2589/4885
US-20100234364-A1 CCR2 INHIBITORS AND METHODS OF USE THEREOF CCR2, CCR9, CCR1 L3MBTL1 2377/4885MAPT 4415/4885MEN1 4867/4885
US-20230174470-A1 COMPOUND AS A UBR BOX DOMAIN LIGAND UBR4, UBQLN2, UBTF L3MBTL1 1141/4885MAPT 235/4885MEN1 3583/4885
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 L3MBTL1 3008/4885MAPT 3899/4885MEN1 4848/4885
US-20170349607-A1 COMPOUNDS ACTIVE TOWARDS BROMODOMAINS BRD4, BRD3, BRDT L3MBTL1 2388/4885MAPT 575/4885MEN1 3579/4885
US-12559455-B2 Compound as a UBR box domain ligand UBR4, UBTF, UBQLN1 L3MBTL1 1436/4885MAPT 1338/4885MEN1 4497/4885
US-10752640-B2 Compounds active towards bromodomains BRD4, BRD3, BRDT L3MBTL1 2388/4885MAPT 575/4885MEN1 3579/4885

“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.