SCHEMBL2064679

SCHEMBL2064679

[O]S(=O)(=O)c1ccc(OS(=O)(=O)c2ccc3ccccc3c2)cc1

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 3/20 0.59
TDP1 Q9NUW8 3/20 0.59
LMNA P02545 2/20 0.59
HTT P42858 1/20 0.59
SMN1; SMN2 Q16637 1/20 0.59
GAA P10253 1/20 0.55
MAPK1 P28482 1/20 0.55
MEN1 O00255 2/20 0.48
KMT2A Q03164 2/20 0.48
KDM4E B2RXH2 1/20 0.48
ALDH1A1 P00352 1/20 0.48
MAPT P10636 1/20 0.48
ENPP1 P22413 4/20 0.48
ENPP3 O14638 3/20 0.48
ENPP2 Q13822 2/20 0.48
CA1 P00915 1/20 0.47
CA2 P00918 1/20 0.47
CA9 Q16790 1/20 0.47
MAOB P27338 1/20 0.47
APEX1 P27695 1/20 0.46

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
SCHEMBL2473745 0.87 L3MBTL1 (0.60) L3MBTL1TDP1LMNAHTTSMN1; SMN2
SCHEMBL28296929 0.87 L3MBTL1 (0.75) L3MBTL1TDP1LMNAHTTSMN1; SMN2
SCHEMBL22558337 0.85 L3MBTL1 (0.62) L3MBTL1TDP1LMNAHTTSMN1; SMN2
SCHEMBL2064683 0.85 L3MBTL1 (0.58) L3MBTL1TDP1LMNAHTTSMN1; SMN2
SCHEMBL2065832 0.82 TDP1 (0.67) L3MBTL1TDP1LMNAHTTSMN1; SMN2
SCHEMBL294027 0.81 LMNA (0.65) L3MBTL1LMNASMN1; SMN2MEN1KMT2A
SCHEMBL9479161 0.81 SNCA (0.59) L3MBTL1TDP1LMNAHTTSMN1; SMN2
SCHEMBL8520162 0.81 L3MBTL1 (0.54) L3MBTL1TDP1LMNAHTTSMN1; SMN2
SCHEMBL29930612 0.80 L3MBTL1 (0.60) L3MBTL1TDP1LMNAHTTSMN1; SMN2
SCHEMBL6746327 0.80 L3MBTL1 (0.65) L3MBTL1TDP1LMNAHTTSMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8148053-B2 DNA sequenceing, biochemical immobilization, and genetic diagnosis; forming monomolecular film using (alkoxyalkoxy)alkylsilane(triol and/or halide) such as 10-(methoxymethoxy)dodecyltrimethoxysilane which forms hydroxyl groups when exposed to acid; forming polysulfonates; radiation with high energy beams SHIN-ETSU CHEMICAL CO., LTD. (JP) 2012-04-03 US disclosed
US-7494760-B2 Photoacid generators, chemically amplified resist compositions, and patterning process SHIN-ETSU CHEMICAL CO., LTD. (JP) 2009-02-24 US disclosed
US-20080233309-A1 Method for manufacturing substrate for making microarray SHIN-ETSU CHEMICAL CO., LTD. (JP) 2008-09-25 US disclosed
US-20070287096-A1 Photoacid generators, chemically amplified resist compositions, and patterning process SHIN-ETSU CHEMICAL CO., LTD. 2007-12-13 US disclosed
US-6916591-B2 Photoacid generators, chemically amplified resist compositions, and patterning process SHIN-ETSU CHEMICAL CO., LTD. (JP) 2005-07-12 US disclosed
US-20030215738-A1 Photoacid generators, chemically amplified resist compositions, and patterning process SHIN-ETSU CHEMICAL CO., LTD. (JP) 2003-11-20 US 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 (1 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-20030215738-A1 Photoacid generators, chemically amplified resist compositions, and patterning process CCNH, PAH, POLH L3MBTL1 3023/4885TDP1 2871/4885LMNA 2395/4885

“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.