SCHEMBL7465166

SCHEMBL7465166

Cc1ccc(S(=O)(=O)O)cc1.Clc1ccc(OC[C@@H]2CCNC2)cn1

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 16)

geneUniProtsupporting neighboursconfidence
CHRNB2 known ✓ P17787 3/20 0.46
CHRNA4 known ✓ P43681 3/20 0.46
KDM1A O60341 7/20 0.46
KCNH2 Q12809 2/20 0.46
RCOR1 Q9UKL0 1/20 0.46
CHRNA3 P32297 5/20 0.46
CHRNB4 P30926 2/20 0.46
CHRNA7 P36544 1/20 0.46
CHRNB1 P11230 1/20 0.42
CHRNB3 Q05901 1/20 0.42
SLC6A2 P23975 3/20 0.41
SLC6A4 P31645 3/20 0.41
SLC6A3 Q01959 1/20 0.41
EP300 Q09472 1/20 0.41
MAOB P27338 1/20 0.39
AKT1 P31749 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
SCHEMBL7462728 1.00 KDM1A (0.46) KDM1AKCNH2RCOR1CHRNA3CHRNB2
SCHEMBL7466362 0.88 KDM1A (0.46) KDM1AKCNH2RCOR1CHRNB2CHRNA4
SCHEMBL7468111 0.88 KDM1A (0.46) KDM1AKCNH2RCOR1CHRNB2CHRNA4
SCHEMBL7460130 0.87 KDM1A (0.50) KDM1AKCNH2RCOR1CHRNA3CHRNB2
SCHEMBL7456585 0.84 KDM1A (0.48) KDM1AKCNH2RCOR1SLC6A2SLC6A4
SCHEMBL7470528 0.84 KDM1A (0.48) KDM1AKCNH2RCOR1SLC6A2SLC6A4
SCHEMBL7461389 0.84 KDM1A (0.48) KDM1AKCNH2RCOR1SLC6A2SLC6A4
Tebanicline SCHEMBL29373633 0.84 CHRNA3 (0.67) CHRNA3CHRNB2CHRNA4CHRNB4CHRNA7
Tebanicline SCHEMBL7417623 0.84 CHRNA3 (0.67) CHRNA3CHRNB2CHRNA4CHRNB4CHRNA7
SCHEMBL7463964 0.83 CHRNB2 (0.62) CHRNA3CHRNB2CHRNA4CHRNB4CHRNA7

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20020151712-A1 3-pyrrolidinyloxy-3'-pyridyl ether compounds useful for controlling chemical synaptic transmission LIN NAN-HORNG (US) 2002-10-17 US disclosed
EP-1212319-A2 3-PYRROLIDINYLOXY-3'-PYRIDYL ETHER COMPOUNDS USEFUL FOR CONTROLLING CHEMICAL SYNAPTIC TRANSMISSION Abbott Laboratories (US) 2002-06-12 EP disclosed
WO-2001019817-A2 3-PYRROLIDINYLOXY-3'-PYRIDYL ETHER COMPOUNDS USEFUL FOR CONTROLLING CHEMICAL SYNAPTIC TRANSMISSION ABBOTT LABORATORIES (US) 2001-03-22 WO 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 (1 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-20020151712-A1 3-pyrrolidinyloxy-3'-pyridyl ether compounds useful for controlling chemical synaptic transmission GAP43, SLC18A2, GABRE CHRNB2 16/4885CHRNA4 12/4885KDM1A 2535/4885

“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.