SCHEMBL8080841

SCHEMBL8080841

O=S(=O)(c1ccccc1)c1ccccc1S(=O)(=O)c1ccccc1

nearest known ligand 0.72

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTR6 P50406 6/20 0.72
KMT2A Q03164 1/20 0.59
TSHR P16473 2/20 0.55
HTT P42858 1/20 0.55
GAA P10253 2/20 0.54
POLB P06746 1/20 0.54
GFER P55789 1/20 0.54
ALDH1A1 P00352 2/20 0.50
NPSR1 Q6W5P4 1/20 0.50
HSD17B10 Q99714 1/20 0.50
TDP1 Q9NUW8 1/20 0.50
CA12 O43570 1/20 0.50
CA1 P00915 1/20 0.50
CA2 P00918 1/20 0.50
CA3 P07451 1/20 0.50
CA4 P22748 1/20 0.50
CA6 P23280 1/20 0.50
CA5A P35218 1/20 0.50
CA7 P43166 1/20 0.50
PLA2G7 Q13093 1/20 0.50

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
SCHEMBL8548164 0.90 HTR6 (0.59) HTR6KMT2ATSHRHTTGAA
SCHEMBL1516456 0.88 TSHR (0.58) HTR6KMT2ATSHRHTTGAA
SCHEMBL29469862 0.88 HTR6 (0.63) HTR6KMT2ATSHRHTTGAA
SCHEMBL31618370 0.88 HTR6 (0.57) HTR6KMT2ATSHRHTTGAA
SCHEMBL794103 0.88 HTR6 (0.63) HTR6KMT2ATSHRHTTGAA
SCHEMBL4616548 0.88 ALDH1A1 (0.58) HTR6KMT2ATSHRHTTGAA
SCHEMBL30014725 0.88 HTR6 (0.57) HTR6KMT2ATSHRHTTGAA
SCHEMBL9793431 0.87 HTR6 (0.62) HTR6KMT2ATSHRHTTGAA
Potassium Ion SCHEMBL7638087 0.86 HTR6 (0.55) HTR6KMT2ATSHRHTTGAA
SCHEMBL29121431 0.86 TSHR (0.56) HTR6KMT2ATSHRHTTGAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110183361-A ' cross ' type thermal activities delayed fluorescence material being constructed and its applying 常州大学 2019-08-30 CN claimed
US-9604941-B2 Preparation method of conjugated compound containing bis(phenylsulfonyl)benzene structure and an organic electroluminescent diode device using the conjugated compound SHENZHEN CHINA STAR OPTOELECTRONICS TECHNOLOGY CO., LTD. (CN) 2017-03-28 US claimed
US-20160322567-A1 CONJUGATED COMPOUND CONTAINING BIS(PHENYLSULFONYL)BENZENE STRUCTURE, PREPARATION METHOD AND APPLICATION THEREOF SHENZHEN CHINA STAR OPTOELECTRONICS TECHNOLOGY CO., LTD. (CN) 2016-11-03 US claimed
CN-122080034-A Polycyclic aromatic compound and organic electroluminescent element 2026-05-26 CN disclosed
CN-122059973-A Polycyclic aromatic compound, material for organic device, organic electroluminescent element, display device, and lighting device 爱思开新材料捷恩智株式会社 2026-05-19 CN disclosed
EP-4663642-A1 POLYCYCLIC AROMATIC COMPOUND Kyoto University (JP) 2025-12-17 EP disclosed
EP-4635960-A1 POLYCYCLIC AROMATIC COMPOUND Kyoto University (JP) 2025-10-22 EP disclosed
CN-120157693-A Polycyclic aromatic compound and organic electroluminescent element 爱思开新材料捷恩智株式会社 2025-06-17 CN disclosed
CN-120118107-A Polycyclic aromatic compound and organic electroluminescent element 爱思开新材料捷恩智株式会社 2025-06-10 CN disclosed
CN-119930662-A Polycyclic aromatic compound, organic electroluminescent element, display device, and lighting device 爱思开新材料捷恩智株式会社 2025-05-06 CN disclosed
CN-119504805-A Polycyclic aromatic compound, organic electroluminescent element, and display device or lighting device 国立大学法人京都大学 2025-02-25 CN disclosed
US-20160322567-A1 CONJUGATED COMPOUND CONTAINING BIS(PHENYLSULFONYL)BENZENE STRUCTURE, PREPARATION METHOD AND APPLICATION THEREOF SHENZHEN CHINA STAR OPTOELECTRONICS TECHNOLOGY CO., LTD. (CN) 2016-11-03 US disclosed
CN-104803896-A Conjugated compound containing di-(phenylsulfonyl) phenyl structure, as well as preparation method and application of conjugated compound SHENZHEN CHINA STAR OPTOELECT 2015-07-29 CN disclosed
JP-2000016979-A SUBSTITUTED DIPHENYLSULFONE-CROSSLINKED COMPOUND AND RECORDING MATERIAL PRODUCED BY USING THE COMPOUND NIPPON SODA CO LTD 2000-01-18 JP disclosed
US-5075412-A AROMATIC POLYMER IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1991-12-24 US disclosed
US-4970271-A Aromatic polymer IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1990-11-13 US disclosed
EP-0373784-A2 Aromatic polymer IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1990-06-20 EP disclosed
EP-0373783-A2 Aromatic polymer IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1990-06-20 EP disclosed
EP-0325405-A2 Aromatic polymer IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1989-07-26 EP disclosed
US-4069205-A FROM BI- OR TRI-PHENYLENE SULFIDE, AROMATIC ETHER, AND ISOPHTHALOYL OR TEREPHTHALOYL HALIDE UNIVERSITY PATENTS, INC. (US) 1978-01-17 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-20160322567-A1 CONJUGATED COMPOUND CONTAINING BIS(PHENYLSULFONYL)BENZENE STRUCTURE, PREPARATION METHOD AND APPLICATION THEREOF AOC1, DDT, KCNJ1 HTR6 2303/4885KMT2A 1670/4885TSHR 2424/4885

“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.