SCHEMBL5743430

SCHEMBL5743430

CCN(CCCO)Cc1ccccc1.CS(=O)(=O)O

nearest known ligand 0.55

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
MAOB known ✓ P27338 4/20 0.51
HTR1A known ✓ P08908 1/20 0.47
ADRA2A known ✓ P08913 1/20 0.47
CHRM1 known ✓ P11229 1/20 0.47
DRD1 known ✓ P21728 1/20 0.47
SLC6A2 known ✓ P23975 1/20 0.47
SLC6A4 known ✓ P31645 1/20 0.47
ADRA1A known ✓ P35348 1/20 0.47
DRD3 known ✓ P35462 1/20 0.47
SLC6A3 known ✓ Q01959 1/20 0.47
APP P05067 3/20 0.55
BCHE P06276 3/20 0.53
ACHE P22303 3/20 0.53
ACKR3 P25106 1/20 0.50
GAA P10253 1/20 0.48
CHRM2 P08172 1/20 0.47
OPRM1 P35372 1/20 0.47
KCNH2 Q12809 1/20 0.47
HDAC3 O15379 1/20 0.46
HDAC1 Q13547 1/20 0.46

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
SCHEMBL5745444 0.91 APP (0.51) APPBCHEACHEMAOBACKR3
SCHEMBL5744289 0.91 BCHE (0.57) APPBCHEACHEMAOBACKR3
SCHEMBL5745728 0.85 MCHR1 (0.52) APPBCHEACHEMAOBOPRM1
SCHEMBL20754749 0.83 BCHE (0.55) APPBCHEACHEMAOBACKR3
SCHEMBL5672853 0.82 HTT (0.55) BCHEACHEHDAC3HDAC1HDAC2
SCHEMBL5867108 0.81 SIGMAR1 (0.56) APPACKR3
SCHEMBL1302287 0.80 HTT (0.56) APPBCHEACHEMAOBCHRM2
SCHEMBL465332 0.80 ACKR3 (0.52) ACKR3OPRM1HDAC3HDAC1HDAC2
SCHEMBL140525 0.80 HDAC3 (0.54) BCHEACHEACKR3CHRM2HTR1A
SCHEMBL5743428 0.79 MAOB (0.51) APPBCHEACHEMAOBCHRM2

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 MAOB 3129/4885HTR1A 4585/4885ADRA2A 3351/4885
US-20030176711-A1 Process for the production of sulfonic esters TST, STS, SELENOI MAOB 3129/4885HTR1A 4585/4885ADRA2A 3351/4885
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 MAOB 3182/4885HTR1A 4490/4885ADRA2A 2878/4885

“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.