SCHEMBL465090

SCHEMBL465090

O=C1C=C(S(=O)(=O)O)C(=O)c2ccccc21.[NaH]

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 5/20 0.48
MAPK1 P28482 5/20 0.48
CDC25B P30305 4/20 0.48
ALDH1A1 P00352 3/20 0.48
CDC25A P30304 3/20 0.48
MEN1 O00255 3/20 0.48
KMT2A Q03164 3/20 0.48
LMNA P02545 3/20 0.48
SMN1; SMN2 Q16637 3/20 0.48
BLM P54132 3/20 0.48
IDO1 P14902 2/20 0.48
CYP3A4 P08684 2/20 0.48
HPGD P15428 2/20 0.48
PLIN1 O60240 2/20 0.48
MAOA P21397 2/20 0.48
PLIN5 Q00G26 2/20 0.48
ABHD5 Q8WTS1 2/20 0.48
NR1I2 O75469 1/20 0.48
USP2 O75604 1/20 0.48
GSR P00390 1/20 0.48

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
SCHEMBL191617 0.98 MAPT (0.50) MAPTMAPK1CDC25BALDH1A1CDC25A
SCHEMBL30094883 0.98 MAPT (0.50) MAPTMAPK1CDC25BALDH1A1CDC25A
Hydrochloric Acid SCHEMBL27483886 0.96 MAPT (0.48) MAPTMAPK1CDC25BALDH1A1CDC25A
Ammonia Solution, Strong SCHEMBL11426289 0.96 MAPT (0.48) MAPTMAPK1CDC25BALDH1A1CDC25A
SCHEMBL8972948 0.96 MAPT (0.48) MAPTMAPK1CDC25BALDH1A1CDC25A
SCHEMBL7740059 0.96 CDC25B (0.48) MAPTMAPK1CDC25BALDH1A1CDC25A
SCHEMBL1520492 0.96 MAPT (0.48) MAPTMAPK1CDC25BALDH1A1CDC25A
SCHEMBL27661392 0.91 MAPT (0.44) MAPTMAPK1CDC25BALDH1A1CDC25A
SCHEMBL28427715 0.91 MAPT (0.44) MAPTMAPK1CDC25BALDH1A1CDC25A
Hydrochloric Acid SCHEMBL27872709 0.89 MAPT (0.43) MAPTMAPK1CDC25BALDH1A1CDC25A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113637503-B Bimetallic FMG desulfurizing agent for wet oxidation desulfurization 曲靖大为焦化制供气有限公司 2023-10-20 CN claimed
CN-113637503-A Bimetallic FMG desulfurizer for wet oxidation desulfurization 曲靖大为焦化制供气有限公司 2021-11-12 CN claimed
US-5324815-A Polyaniline NITTO DENKO CORPORATION (JP) 1994-06-28 US claimed
US-4874589-A Method for desulfurization of sulfur or hydrogen sulfide-containing gases UTB UMWELTTECHNIK BUCHS AG (CH) 1989-10-17 US claimed
CN-112570033-B Wet desulphurization catalyst, desulphurization solution and preparation method thereof 宁波中科远东催化工程技术有限公司 2022-05-17 CN disclosed
CN-113637503-A Bimetallic FMG desulfurizer for wet oxidation desulfurization 曲靖大为焦化制供气有限公司 2021-11-12 CN disclosed
CN-112570033-A Wet desulphurization catalyst, desulphurization solution and preparation method thereof 宁波中科远东催化工程技术有限公司 2021-03-30 CN disclosed
CN-112138723-A Desulfurization catalyst and preparation method thereof 田作林 2020-12-29 CN disclosed
CN-110446542-A Wet desulfurization method for gas containing hydrogen sulfide NIPPON STEEL & SUMITOMO METAL CORP 2019-11-12 CN disclosed
US-8440846-B2 Direct epoxidation process LYONDELL CHEMICAL TECHNOLOGY, L.P. (US) 2013-05-14 US disclosed
EP-2146359-B1 Solid electrolytic capacitor and method for producing the same MURATA MANUFACTURING CO (JP) 2012-05-16 EP disclosed
WO-2012044827-A1 DIRECT EPOXIDATION PROCESS LYONDELL CHEMICAL TECHNOLOGY, L.P. (US) 2012-04-05 WO disclosed
US-4693881-A Simultaneous separation and conversion to sulfur of H2 S T-THERMAL, INC. (US) 1987-09-15 US disclosed
EP-0018635-B1 CONTROL OF THIOSULFATE IN WET DESULFURIZATION PROCESS SOLUTIONS FMC Corporation (US) 1985-01-16 EP disclosed
US-4367212-A Control of thiosulfate in wet desulfurization process solutions FMC CORPORATION (US) 1983-01-04 US disclosed
EP-0018635-A2 Control of thiosulfate in wet desulfurization process solutions FMC Corporation (US) 1980-11-12 EP disclosed
US-4199553-A HYDROGEN SULFIDE AND HYDROGEN CYANIDE KAWADA TATSUYA 1980-04-22 US disclosed
US-4178861-A Method for the delignification of lignocellulosic material in an amine delignifying liquor containing a quinone or hydroquinone compound AUSTRALIAN PAPER MANUFACTURERS LIMITED (AU) 1979-12-18 US disclosed
US-4176125-A Process for producing 1,4-dihydroanthraquinone KAWASAKI KASEI CHEMICALS LTD. (JP) 1979-11-27 US disclosed
US-3937795-A OXIDATION CATALYSTS, CHELATE COMPOUNDS, QUINONES AND HYDROQUINONES, ABSORPTION 3937795 3937795 NEW WORLD BUSINESS CORPORATION, A CA CORP. 1976-02-10 US disclosed