SCHEMBL5744690

SCHEMBL5744690

CC1CN(C(c2ccccc2)c2ccccc2)CC1O.Cc1ccc(S(=O)(=O)O)cc1

nearest known ligand 0.46

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 0.42
CYP2D6 P10635 1/20 0.46
MAPK1 P28482 1/20 0.46
SLC6A9 P48067 3/20 0.45
OPRL1 P41146 4/20 0.42
OPRD1 P41143 2/20 0.42
OPRK1 P41145 2/20 0.42
ALDH1A1 P00352 1/20 0.42
CACNA2D1 P54289 1/20 0.42
CACNA1B Q00975 1/20 0.42
CACNB1 Q02641 1/20 0.42
CACNA1C Q13936 1/20 0.42
PKM P14618 1/20 0.40
MAOA P21397 1/20 0.39
CA12 O43570 1/20 0.39
CA1 P00915 1/20 0.39
CA2 P00918 1/20 0.39
CA7 P43166 1/20 0.39
CA9 Q16790 1/20 0.39
CA14 Q9ULX7 1/20 0.39

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
SCHEMBL5745110 0.91 CYP2D6 (0.47) CYP2D6MAPK1SLC6A9OPRL1OPRM1
SCHEMBL5744745 0.91 SLC6A9 (0.46) CYP2D6MAPK1SLC6A9OPRL1OPRM1
SCHEMBL5745148 0.87 CYP2D6 (0.50) CYP2D6MAPK1SLC6A9OPRL1OPRM1
SCHEMBL5744952 0.86 SLC6A9 (0.44) CYP2D6MAPK1SLC6A9OPRL1OPRM1
SCHEMBL5743681 0.83 OPRL1 (0.48) CYP2D6SLC6A9OPRL1OPRM1OPRD1
SCHEMBL5745456 0.81 CYP2D6 (0.47) CYP2D6MAPK1SLC6A9OPRL1OPRM1
SCHEMBL5742740 0.81 CYP2D6 (0.47) CYP2D6MAPK1SLC6A9OPRL1OPRM1
SCHEMBL5743946 0.81 CYP2D6 (0.49) CYP2D6MAPK1SLC6A9OPRL1OPRM1
SCHEMBL5744644 0.81 CYP2D6 (0.51) CYP2D6MAPK1SLC6A9OPRL1OPRM1
SCHEMBL7468276 0.80 CYP2D6 (0.44) CYP2D6MAPK1SLC6A9OPRL1OPRM1

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.