SCHEMBL5597379

SCHEMBL5597379

Cc1ccc(S(=O)(=O)O)c(-c2ccccc2)c1Br

nearest known ligand 0.37

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MYC P01106 1/20 0.37
TSHR P16473 1/20 0.35
SMN1; SMN2 Q16637 1/20 0.35
MEN1 O00255 3/20 0.33
KMT2A Q03164 3/20 0.33
CASP1 P29466 1/20 0.33
EDNRB P24530 1/20 0.33
EDNRA P25101 1/20 0.33
MAOB P27338 1/20 0.33
LMNA P02545 1/20 0.32
MAPT P10636 1/20 0.32
HTT P42858 1/20 0.32
ACLY P53396 1/20 0.32
RXFP1 Q9HBX9 2/20 0.32
SUMO2 P61956 1/20 0.32
SUMO1 P63165 1/20 0.32
SENP7 Q9BQF6 1/20 0.32
SENP3 Q9H4L4 1/20 0.32
SENP2 Q9HC62 1/20 0.32
SENP1 Q9P0U3 1/20 0.32

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
SCHEMBL22444090 0.84 MYC (0.40) MYCTSHRSMN1; SMN2MEN1KMT2A
SCHEMBL2516100 0.83 MYC (0.39) MYCTSHRSMN1; SMN2MEN1KMT2A
SCHEMBL28736762 0.83 MYC (0.39) MYCTSHRSMN1; SMN2MEN1KMT2A
Iodide SCHEMBL28419660 0.83 MYC (0.39) MYCTSHRSMN1; SMN2MEN1KMT2A
SCHEMBL8523878 0.81 ELANE (0.45) MYCTSHRSMN1; SMN2KMT2ALMNA
SCHEMBL4838484 0.75 ALDH1A1 (0.49) TSHRSMN1; SMN2KMT2AMAPTPOLB
SCHEMBL20875060 0.74 ATM (0.41) MYCKMT2ACASP1EDNRAMAOB
SCHEMBL27534698 0.74 BACE1 (0.44) TSHRSMN1; SMN2LMNAMAPTPOLB
SCHEMBL30626032 0.74 FABP4 (0.44) MYCTSHRSMN1; SMN2LMNAMAPT
Ammonia Solution, Strong SCHEMBL28859729 0.73 CASP1 (0.36) MYCTSHRSMN1; SMN2CASP1MAOB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0970937-B1 POLYMER GEL AND PROCESS FOR THE ACTIVATION OF ACTIVE HYDROGEN COMPOUNDS NIPPON CATALYTIC CHEM IND (JP) 2007-07-04 EP disclosed
US-7094853-B2 Crosslinked polymer, method for manufacturing it and use thereof NIPPON SHOKUBAI CO., LTD. (JP) 2006-08-22 US disclosed
US-6914155-B2 High polymer gel and activation method for compounds containing active hydrogen NIPPON SHOKUBAI CO., LTD. (JP) 2005-07-05 US disclosed
US-20040087727-A1 Crosslinked polymer, method for manufacturing it and use thereof NIPPON SHOKUBAI CO., LTD. 2004-05-06 US disclosed
US-6646083-B2 Such as diallyldimethylammonium chloride crosslinked with 1,3-bis(N,N-diallylpiperid-1-ium-4-yl) propane dichloride; thermal stability; use as polymer catalyst for producing glycols from oxiranes; ion exchange catalyst NIPPON SHOKUBAI CO., LTD. (JP) 2003-11-11 US disclosed
US-20020028887-A1 Crosslinked polymer, method for manufacturing it and use thereof NIPPON SHOKUBAI CO., LTD. (JP) 2002-03-07 US disclosed
US-20020028872-A1 High polymer gel and activation method for compounds containing active hydrogen NIPPON SHOKUBAI CO., LTD. 2002-03-07 US disclosed
EP-1022058-A1 METHOD FOR ACTIVATING ACTIVE HYDROGEN AND ACTIVATION CATALYST Nippon Shokubai Co., Ltd. (JP) 2000-07-26 EP disclosed
EP-0970937-A1 POLYMER GEL AND PROCESS FOR THE ACTIVATION OF ACTIVE HYDROGEN COMPOUNDS Nippon Shokubai Co., Ltd. (JP) 2000-01-12 EP disclosed