SCHEMBL5744644

SCHEMBL5744644

Cc1ccc(S(=O)(=O)O)cc1.OC1CN1C(c1ccccc1)c1ccccc1

nearest known ligand 0.51

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
OPRM1 known ✓ P35372 3/20 0.46
CYP2D6 P10635 2/20 0.51
MAPK1 P28482 1/20 0.51
OPRD1 P41143 3/20 0.46
OPRK1 P41145 3/20 0.46
OPRL1 P41146 3/20 0.46
PKM P14618 1/20 0.44
ALDH1A1 P00352 3/20 0.43
NPSR1 Q6W5P4 1/20 0.43
GAA P10253 1/20 0.42
SLC6A9 P48067 1/20 0.41
SMN1; SMN2 Q16637 2/20 0.41
TSHR P16473 1/20 0.41
CACNA2D1 P54289 1/20 0.40
CACNA1B Q00975 1/20 0.40
CACNB1 Q02641 1/20 0.40
CACNA1C Q13936 1/20 0.40
MEN1 O00255 1/20 0.40
KMT2A Q03164 1/20 0.40
KDM4E B2RXH2 1/20 0.40

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
SCHEMBL5742740 0.87 CYP2D6 (0.47) CYP2D6MAPK1OPRM1OPRD1OPRK1
SCHEMBL5745148 0.85 CYP2D6 (0.50) CYP2D6MAPK1OPRM1OPRD1OPRK1
SCHEMBL5744335 0.84 CYP2D6 (0.44) CYP2D6OPRM1OPRD1OPRK1OPRL1
SCHEMBL5745456 0.82 CYP2D6 (0.47) CYP2D6MAPK1OPRM1OPRD1OPRK1
SCHEMBL5743946 0.81 CYP2D6 (0.49) CYP2D6MAPK1OPRM1OPRD1OPRK1
SCHEMBL8534954 0.81 OPRM1 (0.47) CYP2D6MAPK1OPRM1OPRD1OPRK1
SCHEMBL5744690 0.81 CYP2D6 (0.46) CYP2D6MAPK1OPRM1OPRD1OPRK1
SCHEMBL5745798 0.81 CYP2D6 (0.51) CYP2D6MAPK1OPRM1OPRD1OPRK1
SCHEMBL5746014 0.80 ALDH1A1 (0.46) CYP2D6MAPK1OPRM1OPRD1OPRK1
SCHEMBL5745110 0.79 CYP2D6 (0.47) CYP2D6MAPK1OPRM1OPRD1OPRK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1288198-B1 PROCESS FOR THE PRODUCTION OF SULFONIC ESTERS KANEKA CORP (JP) 2006-12-20 EP disclosed
US-6992205-B2 Process for the production of sulfonic esters KANEKA CORPORATION (JP) 2006-01-31 US disclosed
US-6864372-B2 Process for the production of sulfonic esters KANEKA CORPORATION (JP) 2005-03-08 US disclosed
US-6794519-B2 Process for the production of sulfonic esters KANEKA CORPORATION (JP) 2004-09-21 US disclosed
US-20030176713-A1 Reacting an amino alcohol derivative with organic sulfonyl halide in a mixed solvent composed of an aprotic organic solvent and water in presence of a non-water prohibiting inorganic base KANEKA CORPORATION (JP) 2003-09-18 US disclosed
US-20030176711-A1 Process for the production of sulfonic esters KANEKA CORPORATION (JP) 2003-09-18 US disclosed
US-20030162966-A1 PROCESS FOR THE PRODUCTION OF SULFONIC ESTERS KANEKA CORPORATION (JP) 2003-08-28 US disclosed
EP-1288198-A1 PROCESS FOR THE PRODUCTION OF SULFONIC ESTERS KANEKA CORPORATION (JP) 2003-03-05 EP 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 (3 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-20030162966-A1 PROCESS FOR THE PRODUCTION OF SULFONIC ESTERS TST, STS, SELENOI OPRM1 2799/4885CYP2D6 675/4885MAPK1 816/4885
US-20030176711-A1 Process for the production of sulfonic esters TST, STS, SELENOI OPRM1 2799/4885CYP2D6 675/4885MAPK1 816/4885
US-20030176713-A1 Reacting an amino alcohol derivative with organic sulfonyl halide in a mixed solvent composed of an aprotic organic solvent and water in presence of a non-water prohibiting inorganic base BRAF, ADH1C, TST OPRM1 1372/4885CYP2D6 1620/4885MAPK1 1036/4885

“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.