SCHEMBL2396708

SCHEMBL2396708

CCCCc1nccn1C.Cc1ccc(S(=O)(=O)O)cc1

nearest known ligand 0.50

Known targets — ChEMBL curated mechanism

ABL1BMXBRAFBTKCHRNA4CHRNB2CSNK1EEGFRERBB2F10FLT1FLT3FLT4IGF1RINSRITKJAK3KDRKITOPRM1PARP1PARP2PDGFRBPIK3CDRAF1RETSLC18A2TECTXKdacAdacBdacCftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
TSHR P16473 3/20 0.50
KDM4E B2RXH2 2/20 0.43
ALDH1A1 P00352 3/20 0.43
LMNA P02545 2/20 0.43
TDP1 Q9NUW8 2/20 0.43
MAPT P10636 1/20 0.43
HTT P42858 1/20 0.43
SMN1; SMN2 Q16637 1/20 0.43
L3MBTL1 Q9Y468 1/20 0.43
KCNA5 P22460 2/20 0.40
APLNR P35414 4/20 0.39
CYP2D6 P10635 1/20 0.37
CD4 P01730 2/20 0.36
POLB P06746 1/20 0.36
NPSR1 Q6W5P4 1/20 0.36
AGTR1 P30556 1/20 0.36
ALB P02768 1/20 0.36
CYP2C9 P11712 1/20 0.36
CNR2 P34972 1/20 0.36

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
SCHEMBL29402099 0.93 TSHR (0.53) TSHRKDM4EALDH1A1LMNATDP1
SCHEMBL29036131 0.89 TSHR (0.49) TSHRKDM4EALDH1A1LMNATDP1
Quinoline SCHEMBL27810303 0.88 ALDH1A1 (0.47) TSHRKDM4EALDH1A1LMNATDP1
SCHEMBL28879101 0.88 TSHR (0.48) TSHRKDM4EALDH1A1LMNATDP1
SCHEMBL5091012 0.87 TSHR (0.54) TSHRKDM4EALDH1A1LMNATDP1
Sulfuric Acid SCHEMBL62247 0.85 FDPS (0.43) TSHRALDH1A1HTTL3MBTL1APLNR
Sulfuric Acid SCHEMBL27798882 0.85 FDPS (0.43) TSHRALDH1A1HTTL3MBTL1APLNR
SCHEMBL29859619 0.84 ALDH1A1 (0.46) TSHRKDM4EALDH1A1LMNATDP1
SCHEMBL1274385 0.83 FDPS (0.42) TSHRALDH1A1APLNRPOLBAGTR1
SCHEMBL29859863 0.81 ALDH1A1 (0.46) TSHRKDM4EALDH1A1LMNATDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116082540-B Synthesis process of low-volatile odorless polyvinyl butyral resin powder 江苏奥天利新材料有限公司 2023-09-26 CN claimed
CN-114849786-B Imidazole sulfonic acid ionic liquid-based palladium phosphine complex catalyst for synthesizing methyl propionate through ethylene hydro-methyl esterification 中国科学院过程工程研究所 2023-09-05 CN claimed
CN-116283634-A Aromatic diamine chain extender containing ester group and preparation method thereof 江苏湘园化工有限公司 2023-06-23 CN claimed
CN-116082540-A Synthesis process of low-volatile odorless polyvinyl butyral resin powder 江苏奥天利新材料有限公司 2023-05-09 CN claimed
CN-114849786-A Imidazole sulfonic acid ionic liquid based palladium-phosphine complex catalyst for synthesizing methyl propionate by ethylene methyl hydrogen esterification 中国科学院过程工程研究所 2022-08-05 CN claimed
CN-114849786-B Imidazole sulfonic acid ionic liquid-based palladium phosphine complex catalyst for synthesizing methyl propionate through ethylene hydro-methyl esterification 中国科学院过程工程研究所 2023-09-05 CN disclosed
CN-116283634-A Aromatic diamine chain extender containing ester group and preparation method thereof 江苏湘园化工有限公司 2023-06-23 CN disclosed
CN-116178315-A Method for efficiently converting chitosan into 5-hydroxymethylfurfural by using sulfonated ionic liquid 集美大学 2023-05-30 CN disclosed
CN-114849786-A Imidazole sulfonic acid ionic liquid based palladium-phosphine complex catalyst for synthesizing methyl propionate by ethylene methyl hydrogen esterification 中国科学院过程工程研究所 2022-08-05 CN disclosed
US-9399613-B2 Direct carbon dioxide hydrogenation to formic acid in acidic media ECOLE POLYTECHNIQUE FEDERALE DE LAUSANNE (EPFL) (CH) 2016-07-26 US disclosed
US-20160016875-A1 DIRECT CARBON DIOXIDE HYDROGENATION TO FORMIC ACID IN ACIDIC MEDIA ECOLE POLYTECHNIQUE FEDERALE DE LAUSANNE (EPFL) EPFL-TTO (CH) 2016-01-21 US disclosed
EP-2767530-A1 Direct carbon dioxide hydrogenation to formic acid in acidic media EOS Holding SA (CH) 2014-08-20 EP disclosed
US-8027150-B2 Conductive polymer solid electrolytic capacitor KANEKA CORPORATION (JP) 2011-09-27 US disclosed
US-20080218942-A1 Conductive polymer solid electrolytic capacitor KANEKA CORPORATION (JP) 2008-09-11 US disclosed