Bms-223131

Bms-223131

SCHEMBL3269828

O=c1[nH]c2ccc(C(F)(F)F)cc2c(-c2cc(Cl)ccc2O)c1CCO

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

KCNMA1

The experimentally established mechanism targets of Bms-223131. 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
CYP2C9 P11712 10/20 1.00
CYP3A4 P08684 4/20 1.00
CYP2C19 P33261 4/20 1.00
CYP2D6 P10635 2/20 1.00
CYP1A2 P05177 1/20 1.00
BIRC5 O15392 1/20 0.44
EEF2K O00418 1/20 0.43
PLK4 O00444 1/20 0.43
IKBKB O14920 1/20 0.43
DYRK3 O43781 1/20 0.43
PIM1 P11309 1/20 0.43
CDK2 P24941 1/20 0.43
AKT1 P31749 1/20 0.43
AKT2 P31751 1/20 0.43
CLK2 P49760 1/20 0.43
GSK3B P49841 1/20 0.43
IRAK1 P51617 1/20 0.43
RPS6KA3 P51812 1/20 0.43
NEK4 P51957 1/20 0.43
PLK1 P53350 1/20 0.43

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
Bms-223131 SCHEMBL30627537 1.00 CYP2C9 (1.00) CYP2C9CYP3A4CYP2C19CYP2D6CYP1A2
Bms-223131 SCHEMBL27618716 1.00 CYP2C9 (1.00) CYP2C9CYP3A4CYP2C19CYP2D6CYP1A2
SCHEMBL5159321 0.94 CYP2C9 (0.88) CYP2C9CYP3A4CYP2C19CYP2D6CYP1A2
SCHEMBL5163058 0.94 CYP2C9 (0.88) CYP2C9CYP3A4CYP2C19CYP2D6CYP1A2
SCHEMBL3275049 0.93 CYP2C9 (0.86) CYP2C9CYP3A4CYP2C19CYP2D6CYP1A2
SCHEMBL5158929 0.92 CYP2C9 (0.86) CYP2C9CYP3A4CYP2C19CYP2D6CYP1A2
SCHEMBL5159796 0.89 CYP2C9 (0.80) CYP2C9CYP3A4CYP2C19CYP2D6CYP1A2
SCHEMBL5160635 0.88 CYP2C9 (0.78) CYP2C9CYP3A4CYP2C19CYP2D6CYP1A2
SCHEMBL5159637 0.86 CYP2C9 (0.76) CYP2C9CYP3A4CYP2C19CYP2D6CYP1A2
SCHEMBL5161367 0.86 CYP2C9 (1.00) CYP2C9CYP3A4CYP2C19CYP2D6CYP1A2

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 29 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1575589-A4 ATROPISOMERS OF 3-SUBSTITUTED-4-ARYLQUINOLIN-2-ONE DERIVATIVES BRISTOL MYERS SQUIBB CO (US) 2008-05-21 EP claimed
EP-1133474-B1 3-SUBSTITUTED-4-ARYLQUINOLIN-2-ONE DERIVATIVES AS POTASSIUM CHANNEL MODULATORS BRISTOL MYERS SQUIBB CO (US) 2007-02-21 EP claimed
EP-1575589-A1 ATROPISOMERS OF 3-SUBSTITUTED-4-ARYLQUINOLIN-2-ONE DERIVATIVES Bristol-Myers Squibb Company (US) 2005-09-21 EP claimed
EP-1133474-A4 3-SUBSTITUTED-4-ARYLQUINOLIN-2-ONE DERIVATIVES AS POTASSIUM CHANNEL MODULATORS BRISTOL MYERS SQUIBB CO (US) 2005-02-16 EP claimed
US-20040147749-A1 Atropisomers of 3-substituted-4-arylquinolin-2-one derivatives BRISTOL-MYERS SQUIBB COMPANY 2004-07-29 US claimed
WO-2004058260-A1 ATROPISOMERS OF 3-SUBSTITUTED-4-ARYLQUINOLIN-2-ONE DERIVATIVES BRISTOL-MYERS SQUIBB COMPANY (US) 2004-07-15 WO claimed
CN-1129582-C 3-substituted-4-arylquinolin-2-one derivatives as potassium channel modulators BRISTOL MYERS SQUIBB CO (US) 2003-12-03 CN claimed
CN-1329599-A 3-substituted-4-arylquinolin-2-one derivatives as potassium channel modulators BRISTOL MYERS SQUIBB CO (US) 2002-01-02 CN claimed
EP-1133474-A1 3-SUBSTITUTED-4-ARYLQUINOLIN-2-ONE DERIVATIVES AS POTASSIUM CHANNEL MODULATORS BRISTOL-MYERS SQUIBB COMPANY (US) 2001-09-19 EP claimed
US-6184231-B1 NEUROPROTECTANTS; TREATMENT OF CENTRAL NERVOUS SYSTEM DISORDERS, TRAUMATIC BRAIN INJURY, SEXUAL DYSFUNCTION BRISTOL-MYERS SQUIBB 2001-02-06 US claimed
WO-2000034244-A1 3-SUBSTITUTED-4-ARYLQUINOLIN-2-ONE DERIVATIVES AS POTASSIUM CHANNEL MODULATORS BRISTOL-MYERS SQUIBB COMPANY (US) 2000-06-15 WO claimed
EP-1575589-B1 ATROPISOMERS OF 3-SUBSTITUTED-4-ARYLQUINOLIN-2-ONE DERIVATIVES BRISTOL MYERS SQUIBB CO (US) 2010-06-30 EP disclosed
EP-1575589-A4 ATROPISOMERS OF 3-SUBSTITUTED-4-ARYLQUINOLIN-2-ONE DERIVATIVES BRISTOL MYERS SQUIBB CO (US) 2008-05-21 EP disclosed
EP-1133474-B1 3-SUBSTITUTED-4-ARYLQUINOLIN-2-ONE DERIVATIVES AS POTASSIUM CHANNEL MODULATORS BRISTOL MYERS SQUIBB CO (US) 2007-02-21 EP disclosed
EP-1575589-A1 ATROPISOMERS OF 3-SUBSTITUTED-4-ARYLQUINOLIN-2-ONE DERIVATIVES Bristol-Myers Squibb Company (US) 2005-09-21 EP disclosed
US-6353119-B1 FROM A SUBSTITUTED COUMARIN AND USING A PHOTOCHEMICAL CYCLIZATION METHOD ON A DIHYDROFURAN INTERMEDIATE BRISTOL-MYERS SQUIBB COMPANY 2002-03-05 US disclosed
CN-1329599-A 3-substituted-4-arylquinolin-2-one derivatives as potassium channel modulators BRISTOL MYERS SQUIBB CO (US) 2002-01-02 CN disclosed
EP-1133474-A1 3-SUBSTITUTED-4-ARYLQUINOLIN-2-ONE DERIVATIVES AS POTASSIUM CHANNEL MODULATORS BRISTOL-MYERS SQUIBB COMPANY (US) 2001-09-19 EP disclosed
US-6184231-B1 NEUROPROTECTANTS; TREATMENT OF CENTRAL NERVOUS SYSTEM DISORDERS, TRAUMATIC BRAIN INJURY, SEXUAL DYSFUNCTION BRISTOL-MYERS SQUIBB 2001-02-06 US disclosed
WO-2000034244-A1 3-SUBSTITUTED-4-ARYLQUINOLIN-2-ONE DERIVATIVES AS POTASSIUM CHANNEL MODULATORS BRISTOL-MYERS SQUIBB COMPANY (US) 2000-06-15 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-20040147749-A1 Atropisomers of 3-substituted-4-arylquinolin-2-one derivatives KCNN3, KCNN1, KCNN2 CYP2C9 475/4885CYP3A4 178/4885CYP2C19 584/4885

“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.