SCHEMBL5746256

SCHEMBL5746256

CC1CCN(C(c2ccccc2)c2ccccc2)CC1O.CS(=O)(=O)O

nearest known ligand 0.51

Known targets — ChEMBL curated mechanism

ABL1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB2AGTR1BCL2BCL2A1BCL2L1BCL2L10BCL2L2BCRBRAFCHRM1CHRNA10CHRNA9DRD1DRD2DRD3DRD4DRD5EGFRF2FLT1FLT4GCKGHSRGNRHRGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHTR1AHTR1BHTR1DHTR2AHTR2CHTR3AIDH2KDRKITMAOBMCL1MTTPPP4HBPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PIKFYVEROCK1ROCK2SLC18A2SLC6A2SLC6A3SLC6A4TACR1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8gyrAgyrBparCparEpol

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 18)

geneUniProtsupporting neighboursconfidence
SLC6A2 known ✓ P23975 1/20 0.40
SLC6A9 P48067 7/20 0.47
OPRL1 P41146 2/20 0.45
OPRM1 P35372 1/20 0.45
CYP2D6 P10635 3/20 0.43
CYP3A4 P08684 2/20 0.43
ALOX15 P16050 1/20 0.42
ALDH1A1 P00352 1/20 0.42
DPP4 P27487 1/20 0.41
KMT2A Q03164 3/20 0.41
L3MBTL3 Q96JM7 1/20 0.41
L3MBTL1 Q9Y468 1/20 0.41
MEN1 O00255 2/20 0.41
LMNA P02545 2/20 0.41
GAA P10253 1/20 0.41
NPSR1 Q6W5P4 1/20 0.41
TSHR P16473 1/20 0.40
PMP22 Q01453 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
SCHEMBL5746042 0.92 OPRL1 (0.51) SLC6A9OPRL1OPRM1CYP2D6ALDH1A1
SCHEMBL5768221 0.89 SLC6A9 (0.47) SLC6A9OPRL1OPRM1CYP2D6CYP3A4
SCHEMBL5744745 0.88 SLC6A9 (0.46) SLC6A9OPRL1OPRM1CYP2D6ALDH1A1
SCHEMBL5745466 0.87 SLC6A9 (0.47) SLC6A9OPRL1OPRM1CYP2D6CYP3A4
SCHEMBL5744952 0.87 SLC6A9 (0.44) SLC6A9OPRL1OPRM1CYP2D6CYP3A4
SCHEMBL5745487 0.84 CYP2D6 (0.51) OPRL1OPRM1CYP2D6CYP3A4ALOX15
SCHEMBL5745187 0.82 KDM4E (0.47) SLC6A9OPRL1OPRM1CYP2D6CYP3A4
SCHEMBL5745379 0.81 CYP2D6 (0.47) SLC6A9OPRL1OPRM1CYP2D6CYP3A4
SCHEMBL5745248 0.80 OPRL1 (0.51) SLC6A9OPRL1OPRM1CYP2D6ALDH1A1
SCHEMBL5745110 0.78 CYP2D6 (0.47) SLC6A9OPRL1OPRM1CYP2D6ALDH1A1

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-20030176711-A1 Process for the production of sulfonic esters KANEKA CORPORATION (JP) 2003-09-18 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-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 SLC6A2 2246/4885SLC6A9 200/4885OPRL1 3971/4885
US-20030176711-A1 Process for the production of sulfonic esters TST, STS, SELENOI SLC6A2 2246/4885SLC6A9 200/4885OPRL1 3971/4885
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 SLC6A2 1200/4885SLC6A9 111/4885OPRL1 2795/4885

“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.