SCHEMBL3882895

SCHEMBL3882895

Cc1ccccc1SSc1ccccc1

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 2/20 0.57
HPGD P15428 1/20 0.57
SMN1; SMN2 Q16637 1/20 0.57
MGLL Q99685 1/20 0.57
HSD17B10 Q99714 1/20 0.57
ACHE P22303 3/20 0.41
TSHR P16473 2/20 0.41
MCHR1 Q99705 1/20 0.38
L3MBTL1 Q9Y468 1/20 0.38
APOBEC3G Q9HC16 2/20 0.37
MEN1 O00255 1/20 0.37
KMT2A Q03164 1/20 0.37
NPSR1 Q6W5P4 1/20 0.37
POLB P06746 1/20 0.37
HAO1 Q9UJM8 1/20 0.36
ALDH1A1 P00352 2/20 0.33
HTR1A P08908 2/20 0.33
HTR3A P46098 2/20 0.33
MAPK1 P28482 1/20 0.33
CA1 P00915 1/20 0.33

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
SCHEMBL29722832 1.00 MAPT (0.57) MAPTHPGDSMN1; SMN2MGLLHSD17B10
SCHEMBL57312 0.87 ACHE (0.53) MAPTACHETSHRMCHR1APOBEC3G
SCHEMBL29468536 0.87 ACHE (0.53) MAPTACHETSHRMCHR1APOBEC3G
SCHEMBL29411690 0.87 ACHE (0.53) MAPTACHETSHRMCHR1APOBEC3G
SCHEMBL575922 0.86 MAPT (0.40) MAPTHPGDSMN1; SMN2MGLLHSD17B10
SCHEMBL4231323 0.85 ACHE (0.50) MAPTACHETSHRMCHR1APOBEC3G
SCHEMBL9193703 0.85 MAPT (0.50) MAPTHPGDSMN1; SMN2MGLLHSD17B10
SCHEMBL2876479 0.78 L3MBTL1 (0.50) MAPTACHETSHRL3MBTL1HAO1
SCHEMBL29580858 0.78 L3MBTL1 (0.50) MAPTACHETSHRL3MBTL1HAO1
SCHEMBL10702121 0.77 ACHE (0.47) MAPTHPGDACHETSHRMCHR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107722049-A A kind of preparation and its application of novel ionic double-core schiff bases titanium complex 山西医科大学 2018-02-23 CN claimed
CN-105085341-B N-substituted amide derivative and preparation method thereof 西南石油大学 2017-03-22 CN claimed
CN-105085341-A N-substituted amide derivative and preparation method thereof UNIV SOUTHWEST PETROLEUM 2015-11-25 CN claimed
CN-104496870-A Catalytic synthesis method of sulfur-containing carboxylic acid compound and sulfur-containing amide compound UNIV HUNAN 2015-04-08 CN claimed
US-5153305-A From diaryl disulfide; mild conditions using organometallic catalyst RESEARCH INSTITUTE FOR PRODUCTION DEVELOPMENT (JP) 1992-10-06 US claimed
US-12100809-B2 Non-aqueous liquid electrolyte and non-aqueous liquid electrolyte secondary battery MITSUBISHI CHEMICAL CORPORATION (JP) 2024-09-24 US disclosed
US-20220149436-A1 NON-AQUEOUS LIQUID ELECTROLYTE AND NON-AQUEOUS LIQUID ELECTROLYTE SECONDARY BATTERY MITSUBISHI CHEMICAL CORPORATION (JP) 2022-05-12 US disclosed
US-11283107-B2 Non-aqueous liquid electrolyte and non-aqueous liquid electrolyte secondary battery MITSUBISHI CHEMICAL CORPORATION (JP) 2022-03-22 US disclosed
EP-3621141-A1 NON-AQUEOUS LIQUID ELECTROLYTE AND NON-AQUEOUS LIQUID ELECTROLYTE SECONDARY BATTERY MITSUBISHI CHEMICAL CORPORATION (JP) 2020-03-11 EP disclosed
US-20190229372-A1 NON-AQUEOUS LIQUID ELECTROLYTE AND NON-AQUEOUS LIQUID ELECTROLYTE SECONDARY BATTERY MITSUBISHI CHEMICAL CORPORATION (JP) 2019-07-25 US disclosed
CN-110015981-A A kind of synthetic method of (the iodo- 2- aryl of 2-) ethyl aryl ethers derivative 丽水学院 2019-07-16 CN disclosed
US-10333172-B2 Non-aqueous liquid electrolyte and non-aqueous liquid electrolyte secondary battery MITSUBISHI CHEMICAL CORPORATION (JP) 2019-06-25 US disclosed
EP-2012386-A1 NONAQUEOUS ELECTROLYTE SOLUTION AND NONAQUEOUS ELECTROLYTE SECONDARY BATTERY Mitsubishi Chemical Corporation (JP) 2009-01-07 EP disclosed
EP-0402481-B1 PRODUCTION OF POLYARYLENE THIOETHER PROD DEV RES INST (JP) 1995-10-25 EP disclosed
US-5290911-A Forming polymers by catalytic oxidative coupling RESEARCH INSTITUTE FOR PRODUCTION DEVELOPMENT (JP) 1994-03-01 US disclosed
US-5153305-A From diaryl disulfide; mild conditions using organometallic catalyst RESEARCH INSTITUTE FOR PRODUCTION DEVELOPMENT (JP) 1992-10-06 US disclosed
US-4983720-A Process for preparing a polyarylene thioether IDEMITSU PETROCHEMICAL CO., LTD. (JP) 1991-01-08 US disclosed
EP-0402481-A1 PRODUCTION OF POLYARYLENE THIOETHER RESEARCH INSTITUTE FOR PRODUCTION DEVELOPMENT (JP) 1990-12-19 EP disclosed
US-4931542-A Process for preparing a polyarylene thioether IDEMITSU PETROCHEMICAL COMPANY, LIMITED (JP) 1990-06-05 US disclosed
EP-0281036-A2 A process for preparing a polyarylene thioether IDEMITSU PETROCHEMICAL CO. LTD. (JP) 1988-09-07 EP disclosed