SCHEMBL2965334

SCHEMBL2965334

CCCCCCCCCCCCc1ccc(S(=O)(=O)[O-])cc1.c1ccc([S+](c2ccccc2)c2ccccc2)cc1

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA2 P00918 3/20 0.54
KCNH2 Q12809 2/20 0.51
LMNA P02545 2/20 0.51
HIF1A Q16665 2/20 0.51
CYP2D6 P10635 1/20 0.51
CYP2C9 P11712 1/20 0.51
TSHR P16473 1/20 0.51
CYP2C19 P33261 1/20 0.51
HTT P42858 1/20 0.51
SMN1; SMN2 Q16637 1/20 0.47
HTR2A P28223 2/20 0.46
CNR2 P34972 1/20 0.45
CA12 O43570 1/20 0.45
CA1 P00915 1/20 0.45
CA9 Q16790 1/20 0.45
ALDH1A1 P00352 3/20 0.44
ESR1 P03372 2/20 0.44
ADRA2A P08913 2/20 0.44
ADORA3 P0DMS8 2/20 0.44
TACR2 P21452 2/20 0.44

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
SCHEMBL2955495 1.00 CA2 (0.54) CA2KCNH2LMNAHIF1ACYP2D6
SCHEMBL2960150 0.94 CA2 (0.54) CA2KCNH2LMNAHIF1ACYP2D6
SCHEMBL2966132 0.93 KCNH2 (0.58) CA2KCNH2LMNAHIF1ACYP2D6
SCHEMBL2967119 0.93 KCNH2 (0.58) CA2KCNH2LMNAHIF1ACYP2D6
SCHEMBL2964238 0.90 ALOX15B (0.46) CA2KCNH2LMNAHIF1ACYP2D6
SCHEMBL2960491 0.90 ALOX15B (0.46) CA2KCNH2LMNAHIF1ACYP2D6
SCHEMBL2963870 0.87 CNR2 (0.57) CA2KCNH2LMNAHIF1ACYP2D6
SCHEMBL2956226 0.87 LMNA (0.62) CA2KCNH2LMNAHIF1ACYP2D6
SCHEMBL2957248 0.87 LMNA (0.62) CA2KCNH2LMNAHIF1ACYP2D6
SCHEMBL28417025 0.86 CA2 (0.54) CA2KCNH2LMNAHIF1ACYP2D6

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