SCHEMBL5745487

SCHEMBL5745487

CS(=O)(=O)O.OC1CCN(C(c2ccccc2)c2ccccc2)CC1

nearest known ligand 0.54

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 20)

geneUniProtsupporting neighboursconfidence
ADRA2A known ✓ P08913 1/20 0.49
CHRM1 known ✓ P11229 1/20 0.49
DRD1 known ✓ P21728 1/20 0.49
ADRA1D known ✓ P25100 1/20 0.49
HTR2A known ✓ P28223 1/20 0.49
HTR2C known ✓ P28335 1/20 0.49
DRD3 known ✓ P35462 1/20 0.49
SLC6A3 known ✓ Q01959 1/20 0.49
MAOB known ✓ P27338 1/20 0.45
CYP2D6 P10635 3/20 0.51
CYP3A4 P08684 2/20 0.51
KMT2A Q03164 3/20 0.50
ALDH1A1 P00352 2/20 0.50
L3MBTL3 Q96JM7 1/20 0.50
L3MBTL1 Q9Y468 1/20 0.50
OPRM1 P35372 3/20 0.49
CHRM2 P08172 1/20 0.49
CHRM4 P08173 1/20 0.49
CHRM5 P08912 1/20 0.49
ADORA3 P0DMS8 1/20 0.49

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
SCHEMBL5745466 0.91 SLC6A9 (0.47) CYP2D6CYP3A4KMT2AALDH1A1L3MBTL3
SCHEMBL5745201 0.88 L3MBTL3 (0.61) CYP2D6KMT2AALDH1A1L3MBTL3L3MBTL1
Hydrochloric Acid SCHEMBL10797918 0.87 L3MBTL3 (0.59) CYP2D6KMT2AALDH1A1L3MBTL3L3MBTL1
SCHEMBL5743946 0.86 CYP2D6 (0.49) CYP2D6CYP3A4KMT2AALDH1A1L3MBTL3
SCHEMBL5746256 0.84 SLC6A9 (0.47) CYP2D6CYP3A4KMT2AALDH1A1L3MBTL3
SCHEMBL5745379 0.84 CYP2D6 (0.47) CYP2D6CYP3A4KMT2AALDH1A1OPRM1
SCHEMBL18555997 0.83 CYP2D6 (0.56) CYP2D6CYP3A4KMT2AALDH1A1OPRM1
SCHEMBL5745187 0.82 KDM4E (0.47) CYP2D6CYP3A4KMT2AALDH1A1L3MBTL3
SCHEMBL5768221 0.81 SLC6A9 (0.47) CYP2D6CYP3A4KMT2AALDH1A1L3MBTL3
SCHEMBL5745490 0.80 CYP2D6 (0.50) CYP2D6CYP3A4KMT2AALDH1A1L3MBTL3

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 ADRA2A 3351/4885CHRM1 2782/4885DRD1 1309/4885
US-20030176711-A1 Process for the production of sulfonic esters TST, STS, SELENOI ADRA2A 3351/4885CHRM1 2782/4885DRD1 1309/4885
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 ADRA2A 2878/4885CHRM1 2011/4885DRD1 538/4885

“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.