SCHEMBL5174348

SCHEMBL5174348

CN(C)[C@H](COc1cnc(Cl)c(Br)c1)Cc1ccccc1.Cc1ccc(S(=O)(=O)O)cc1

nearest known ligand 0.74

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 3)

geneUniProtsupporting neighboursconfidence
OPRM1 known ✓ P35372 1/20 0.35
CYP1A2 P05177 1/20 0.36
CYP2C19 P33261 1/20 0.36

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
SCHEMBL5173028 0.87 SCN4A (0.41)
SCHEMBL5174166 0.86
SCHEMBL7596570 0.86
SCHEMBL5175322 0.84
SCHEMBL5174765 0.84
SCHEMBL5200173 0.81 CYP1A2 (0.33) CYP1A2CYP2C19OPRM1
SCHEMBL5174496 0.80 AKT1 (0.43) CYP1A2CYP2C19
SCHEMBL5172997 0.80 AKT1 (0.43) CYP1A2CYP2C19
SCHEMBL5174551 0.78 CYP1A2 (0.36) CYP1A2CYP2C19
SCHEMBL5174053 0.78 CYP1A2 (0.41) CYP1A2CYP2C19

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1257535-B1 SUBSTITUTED PYRIDINE COMPOUNDS USEFUL FOR CONTROLLING CHEMICAL SYNAPTIC TRANSMISSION ABBOTT LAB (US) 2007-05-23 EP disclosed
US-6656958-B2 Preferred compounds are 3'-(5'- and/or 6'-substituted) pyridyl ethers; selectively controlling neurotransmitter release in mammals using these compounds ABBOTT LABORATORIES 2003-12-02 US disclosed
EP-1257535-A1 SUBSTITUTED PYRIDINE COMPOUNDS USEFUL FOR CONTROLLING CHEMICAL SYNAPTIC TRANSMISSION ABBOTT LABORATORIES (US) 2002-11-20 EP disclosed
US-20020058646-A1 Substituted pyridine compounds useful for controlling chemical synaptic transmission ABBVIE INC. 2002-05-16 US disclosed
US-20010034357-A1 Substituted pyridine compounds useful for controlling chemical synaptic transmission ABBOTT LABORATORIES 2001-10-25 US disclosed
WO-2001056991-A1 SUBSTITUTED PYRIDINE COMPOUNDS USEFUL FOR CONTROLLING CHEMICAL SYNAPTIC TRANSMISSION ABBOTT LABORATORIES (US) 2001-08-09 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 (2 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-20020058646-A1 Substituted pyridine compounds useful for controlling chemical synaptic transmission SLC18A2, SLC18A3, CHRNA4 OPRM1 304/4885CYP1A2 1893/4885CYP2C19 1658/4885
US-20010034357-A1 Substituted pyridine compounds useful for controlling chemical synaptic transmission SLC18A2, SLC18A3, CHRNA4 OPRM1 304/4885CYP1A2 1893/4885CYP2C19 1658/4885

“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.