SCHEMBL5091012

SCHEMBL5091012

CCc1nccn1C.Cc1ccc(S(=O)(=O)O)cc1

nearest known ligand 0.54

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 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 3/20 0.54
ALDH1A1 P00352 4/20 0.48
KDM4E B2RXH2 3/20 0.47
MAPT P10636 2/20 0.47
TDP1 Q9NUW8 2/20 0.47
LMNA P02545 1/20 0.47
HTT P42858 1/20 0.47
SMN1; SMN2 Q16637 1/20 0.47
L3MBTL1 Q9Y468 1/20 0.47
KCNA5 P22460 2/20 0.43
MAPK1 P28482 1/20 0.40
CYP2D6 P10635 3/20 0.40
FDPS P14324 1/20 0.38
RAPGEF4 Q8WZA2 1/20 0.38
KMT2A Q03164 3/20 0.38
MEN1 O00255 2/20 0.38
CYP1A2 P05177 2/20 0.38
CYP3A4 P08684 1/20 0.38
CYP2C9 P11712 1/20 0.38
HPGD P15428 1/20 0.38

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 0.90 TSHR (0.53) TSHRALDH1A1KDM4EMAPTTDP1
SCHEMBL2396708 0.87 TSHR (0.50) TSHRALDH1A1KDM4EMAPTTDP1
SCHEMBL30564825 0.84 ALDH1A1 (0.47) TSHRALDH1A1KDM4EMAPTTDP1
Sulfuric Acid SCHEMBL2857065 0.83 FDPS (0.47) TSHRALDH1A1HTTMAPK1FDPS
Sulfuric Acid SCHEMBL28074354 0.83 FDPS (0.47) TSHRALDH1A1HTTMAPK1FDPS
Sulfuric Acid SCHEMBL28845974 0.83 FDPS (0.47) TSHRALDH1A1HTTMAPK1FDPS
SCHEMBL29036131 0.83 TSHR (0.49) TSHRALDH1A1KDM4EMAPTTDP1
SCHEMBL29859863 0.83 ALDH1A1 (0.46) TSHRALDH1A1KDM4EMAPTTDP1
SCHEMBL2998201 0.82 KDM4E (0.51) TSHRALDH1A1KDM4EMAPTTDP1
SCHEMBL28879101 0.82 TSHR (0.48) TSHRALDH1A1KDM4EMAPTTDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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-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
US-20230279560-A1 CYCLIC COMPOUNDS AS AROMA CHEMICALS BASF SE (DE) 2023-09-07 US disclosed
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
EP-4189141-A1 CYCLIC COMPOUNDS AS AROMA CHEMICALS BASF SE (DE) 2023-06-07 EP 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-20080139710-A1 Conductive Composition, Conductive Molded Body and Conductive Gel Composition, and Method for Producing the Same KANEKA CORPORATION (JP) 2008-06-12 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-20230279560-A1 CYCLIC COMPOUNDS AS AROMA CHEMICALS C1S, VDAC2, VDAC3 TSHR 4215/4885ALDH1A1 1019/4885KDM4E 3321/4885

“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.