SCHEMBL2965338

SCHEMBL2965338

CCCCCCCCCCCCc1ccc(S(=O)(=O)OS(c2ccccc2)(c2ccccc2)c2ccccc2)cc1

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA2 P00918 3/20 0.53
SMN1; SMN2 Q16637 1/20 0.46
HTR2A P28223 2/20 0.44
CNR2 P34972 1/20 0.44
CA12 O43570 1/20 0.44
CA1 P00915 1/20 0.44
CA9 Q16790 1/20 0.44
KCNH2 Q12809 1/20 0.43
LPL P06858 3/20 0.43
LIPG Q9Y5X9 3/20 0.43
ALDH1A1 P00352 2/20 0.43
TRPV1 Q8NER1 1/20 0.43
MGLL Q99685 1/20 0.43
HAO1 Q9UJM8 1/20 0.43
ESR1 P03372 2/20 0.42
ADRA2A P08913 2/20 0.42
ADORA3 P0DMS8 2/20 0.42
TACR2 P21452 2/20 0.42
SLC6A2 P23975 2/20 0.42
SLC6A4 P31645 2/20 0.42

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
SCHEMBL2955496 1.00 CA2 (0.53) CA2SMN1; SMN2HTR2ACNR2CA12
SCHEMBL2967122 0.95 CNR2 (0.52) CA2SMN1; SMN2HTR2ACNR2CA12
SCHEMBL2966134 0.95 CNR2 (0.52) CA2SMN1; SMN2HTR2ACNR2CA12
SCHEMBL15054568 0.94 CA2 (0.53) CA2SMN1; SMN2CNR2CA12CA1
SCHEMBL2960155 0.94 CA2 (0.53) CA2SMN1; SMN2CNR2CA12CA1
SCHEMBL2964241 0.92 ALOX15B (0.46) CA2SMN1; SMN2ALDH1A1LMNA
SCHEMBL2960494 0.92 ALOX15B (0.46) CA2SMN1; SMN2ALDH1A1LMNA
SCHEMBL2963871 0.89 CNR2 (0.57) CA2SMN1; SMN2CNR2KCNH2ALDH1A1
SCHEMBL2957249 0.89 CA2 (0.53) CA2SMN1; SMN2HTR2ACNR2CA12
SCHEMBL2956228 0.89 CA2 (0.53) CA2SMN1; SMN2HTR2ACNR2CA12

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
US-7759045-B2 Chemically amplified positive resist composition SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2010-07-20 US disclosed
US-20090004601-A1 Chemically amplified positive resist composition SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2009-01-01 US disclosed
US-7214467-B2 Photosensitive resin composition FUJIFILM CORPORATION (JP) 2007-05-08 US disclosed
US-7198880-B2 Positive resist composition FUJIFILM CORPORATION (JP) 2007-04-03 US disclosed
US-7163776-B2 Positive-working resist composition FUJI PHOTO FILM CO., LTD. (JP) 2007-01-16 US disclosed
US-7160666-B2 Photosensitive resin composition FUJI PHOTO FILM CO., LTD. (JP) 2007-01-09 US disclosed
US-6893794-B2 Chemical amplification type positive resist composition SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2005-05-17 US disclosed
EP-1480079-A2 Photosensitive resin composition FUJI PHOTO FILM CO., LTD. (JP) 2004-11-24 EP disclosed
US-6811947-B2 RESIN, WHICH IS DECOMPOSED BY THE ACTION OF AN ACID TO INCREASE SOLUBILITY IN AN ALKALI DEVELOPING SOLUTION FUJI PHOTO FILM CO., LTD. (JP) 2004-11-02 US disclosed
US-20040018445-A1 Chemical amplification type positive resist composition SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2004-01-29 US disclosed
US-20040009430-A1 Photosensitive resin composition FUJI PHOTO FILM CO., LTD. 2004-01-15 US disclosed
EP-1376232-A1 Photosensitive resin composition FUJI PHOTO FILM CO., LTD. (JP) 2004-01-02 EP disclosed
US-20030232277-A1 Positive resist composition FUJI PHOTO FILM CO., LTD. 2003-12-18 US disclosed
US-20030219679-A1 Positive-working resist composition FUJI PHOTO FILM CO., LTD. 2003-11-27 US disclosed
US-20030203308-A1 Photosensitive resin composition FUJI PHOTO FILM CO., LTD. 2003-10-30 US disclosed
US-20030194641-A1 Positive resist composition FUJI PHOTO FILM CO., LTD. 2003-10-16 US disclosed
US-20030068573-A1 Chemical amplification type positive resist composition SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2003-04-10 US disclosed