SCHEMBL254106

SCHEMBL254106

CS(=O)(=O)N(c1ccccn1)S(C)(=O)=O

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.57
CYP2D6 P10635 1/20 0.44
CYP2C19 P33261 1/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
TSHR P16473 1/20 0.42
ATM Q13315 1/20 0.42
NPSR1 Q6W5P4 2/20 0.40
MAPT P10636 1/20 0.40
KDM4E B2RXH2 1/20 0.39
LMNA P02545 1/20 0.39
TDP1 Q9NUW8 1/20 0.39
POLB P06746 1/20 0.38
CHRM2 P08172 1/20 0.38
ADRA2A P08913 1/20 0.38
ADRA2B P18089 1/20 0.38
ADRA2C P18825 1/20 0.38
DRD1 P21728 1/20 0.38
SLC6A2 P23975 1/20 0.38
HTR2A P28223 1/20 0.38
SLC6A4 P31645 1/20 0.38

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
SCHEMBL761379 0.82 ALDH1A1 (0.56) ALDH1A1CYP2D6CYP2C19SMN1; SMN2TSHR
SCHEMBL17258671 0.77 ALDH1A1 (0.69) ALDH1A1CYP2D6CYP2C19SMN1; SMN2TSHR
SCHEMBL1133044 0.76 LMNA (0.51) ALDH1A1CYP2D6CYP2C19SMN1; SMN2TSHR
SCHEMBL5706368 0.75 ALDH1A1 (0.41) ALDH1A1CYP2D6CYP2C19SMN1; SMN2TSHR
SCHEMBL306348 0.75 ALDH1A1 (0.41) ALDH1A1CYP2D6CYP2C19SMN1; SMN2TSHR
SCHEMBL29443546 0.75 ALDH1A1 (0.41) ALDH1A1CYP2D6CYP2C19SMN1; SMN2TSHR
SCHEMBL5630877 0.72 BRD4 (0.48) ALDH1A1CYP2D6CYP2C19SMN1; SMN2TSHR
SCHEMBL17353090 0.72 ALDH1A1 (0.46) ALDH1A1CYP2D6CYP2C19SMN1; SMN2TSHR
SCHEMBL15550676 0.71 ALDH1A1 (0.49) ALDH1A1CYP2D6CYP2C19SMN1; SMN2TSHR
SCHEMBL21314513 0.71 SLC22A12 (0.40) ALDH1A1SMN1; SMN2KDM4EHTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2009016663-A1 AMPHIPHILIC DEXTRIN CONJUGATES AND THEIR USE IN PHARMACEUTICAL FORMULATIONS AS COMPLEXING AGENTS FOR HYDROPHOBIC DRUGS TO IMPROVE THE AQUEOUS SOLUBILITY AND CONSEQUENTLY THE THERAPEUTIC EFFICACY OF THE COMPLEXED DRUGS ISTITUTO GIANNINA GASLINI (IT) 2009-02-05 WO claimed
WO-2005059005-A1 MOISTURE CURABLE HIGH STRENGTH, FLEXIBLE RTV ORGANIC COPOLYMER COMPOSITIONS AND METHODS OF PREPARATION HENKEL CORPORATION (US) 2005-06-30 WO claimed
EP-3430013-A1 CARBAPENEM COMPOUNDS Orchid Pharma Limited (IN) 2019-01-23 EP disclosed
WO-2017158616-A1 CARBAPENEM COMPOUNDS ORCHID PHARMA LTD. (IN) 2017-09-21 WO disclosed
EP-3122347-A1 CELASTROL AND DERIVATIVES FOR THE TREATMENT OF OBESITY The Children's Medical Center Corporation (US) 2017-02-01 EP disclosed
WO-2015148802-A1 CELASTROL AND DERIVATIVES FOR THE TREATMENT OF OBESITY THE CHILDREN'S MEDICAL CENTER CORPORATION (US) 2015-10-01 WO disclosed
EP-2588465-A1 SGC STIMULATORS Ironwood Pharmaceuticals, Inc. (US) 2013-05-08 EP disclosed
WO-2012003405-A1 SGC STIMULATORS IRONWOOD PHARMACEUTICALS, INC. (US) 2012-01-05 WO disclosed
WO-2011104540-A1 ONE STEP PROCESS FOR THE PREPARATION OF CAPECITABINE GENERICS [UK] LIMITED (GB) 2011-09-01 WO disclosed
EP-2238102-A1 NOVEL SEMI-SYNTHETIC GLYCOPEPTIDES AS ANTIBACTERIAL AGENTS Lead Therapeutics, Inc. (US) 2010-10-13 EP disclosed
WO-2009085562-A1 NOVEL SEMI-SYNTHETIC GLYCOPEPTIDES AS ANTIBACTERIAL AGENTS LEAD THERAPEUTICS, INC. (US) 2009-07-09 WO disclosed
EP-0828710-A1 PROCESS FOR THE PREPARATION OF (THIO-)CARBONIC/CARBAMIC ACID 2-PYRROLIDONYL-3-ESTERS, THIO ESTERS AND AMIDES ZENECA LIMITED (GB) 1998-03-18 EP disclosed
WO-1998002191-A2 CATIONIC AMPHIPHILE COMPOSITIONS FOR INTRACELLULAR DELIVERY OF THERAPEUTIC MOLECULES GENZYME CORPORATION (US) 1998-01-22 WO disclosed
WO-1996039132-A1 N,N-DISULFONYLATED AMINOBENZENE CARBOXYLIC ACIDS AND THE USE THEREOF AS THROMBIN INHIBITORS 3-DIMENSIONAL PHARMACEUTICALS, INC. (US) 1996-12-12 WO disclosed
WO-1996037466-A1 PROCESS FOR THE PREPARATION OF (THIO-)CARBONIC/CARBAMIC ACID 2-PYRROLIDONYL-3-ESTERS, THIO ESTERS AND AMIDES ZENECA LIMITED (GB) 1996-11-28 WO disclosed
EP-0638082-A1 MACROCYCLIC IMMUNOMODULATORS ABBOTT LABORATORIES (US) 1995-02-15 EP disclosed
EP-0638082-A4 MACROCYCLIC IMMUNOMODULATORS. ABBOTT LAB (US) 1994-06-09 EP disclosed
EP-0590022-A1 IMIDAZO 1,5-a]QUINOXALINES PHARMACIA & UPJOHN COMPANY (US) 1994-04-06 EP disclosed
WO-1993004680-A1 MACROCYCLIC IMMUNOMODULATORS ABBOTT LABORATORIES (US) 1993-03-18 WO disclosed
WO-1993004679-A1 MACROCYCLIC IMMUNOMODULATORS ABBOTT LABORATORIES (US) 1993-03-18 WO disclosed