SCHEMBL5857447

SCHEMBL5857447

O=C1Cc2c(ccc3ccccc23)N1c1cc(Cl)ccc1O

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
OPRK1 P41145 1/20 0.41
PDE4D Q08499 1/20 0.41
CYP1A2 P05177 1/20 0.38
CYP3A4 P08684 1/20 0.38
CYP2D6 P10635 1/20 0.38
CYP2C19 P33261 1/20 0.38
HTT P42858 2/20 0.37
KMT2A Q03164 3/20 0.37
MEN1 O00255 2/20 0.36
MAPT P10636 2/20 0.36
ALOX12 P18054 1/20 0.36
DHFR P00374 1/20 0.36
TYMS P04818 1/20 0.36
GAA P10253 1/20 0.35
MAPK1 P28482 1/20 0.35
APAF1 O14727 1/20 0.35
IDO1 P14902 1/20 0.35
TDO2 P48775 1/20 0.35
IDO2 Q6ZQW0 1/20 0.35
KCNMA1 Q12791 1/20 0.34

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
SCHEMBL11809930 0.70 OPRK1 (0.67) OPRK1PDE4DHTTKMT2AMEN1
SCHEMBL30917263 0.68 CRHR1 (0.43) CYP1A2CYP3A4CYP2C19HTTKMT2A
SCHEMBL9765524 0.61 KDM4E (0.55) CYP1A2ALDH1A1KDM4E
SCHEMBL1552234 0.61 MAPT (0.60) OPRK1CYP1A2CYP2C19HTTKMT2A
SCHEMBL31065536 0.61 MAPT (0.60) OPRK1CYP1A2CYP2C19HTTKMT2A
SCHEMBL6762628 0.61 MAPT (0.60) OPRK1CYP1A2CYP2C19HTTKMT2A
SCHEMBL29366223 0.61 MAPT (0.60) OPRK1CYP1A2CYP2C19HTTKMT2A
SCHEMBL1758306 0.60 ALDH1A1 (0.64) CYP1A2CYP3A4MAPTMAPK1ALDH1A1
SCHEMBL9212130 0.60 CYP2A6 (0.56) CYP1A2MAPTALDH1A1KDM4E
SCHEMBL16110543 0.60 OPRK1 (0.65) OPRK1PDE4DCYP1A2CYP3A4CYP2D6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7015242-B2 Methods for treating hyperactive gastrointestinal motility WYETH (US) 2006-03-21 US claimed
EP-1634594-A1 Use of 3-substituted oxindole derivatives as KCNQ potassium channel modulators NeuroSearch A/S (DK) 2006-03-15 EP claimed
EP-1303269-B1 USE OF 3-SUBSTITUTED OXINDOLE DERIVATIVES AS KCNQ POTASSIUM CHANNEL MODULATORS NEUROSEARCH AS (DK) 2005-12-07 EP claimed
US-20040029949-A1 Methods for treating hyperactive gastric motility WYETH (US) 2004-02-12 US claimed
US-20030181507-A1 Use of 3-substituted oxindole derivatives as kcnq potassium channel modulators NEUROSEARCH A/S (DK) 2003-09-25 US claimed
EP-1326597-A2 METHODS FOR MODULATING BLADDER FUNCTION AMERICAN HOME PRODUCTS CORPORATION (US) 2003-07-16 EP claimed
US-20020183395-A1 Methods for treating hyperactive gastric motility WYETH 2002-12-05 US claimed
WO-2002080898-A2 METHODS FOR TREATING HYPERACTIVE GASTRIC MOTILITY WYETH (US) 2002-10-17 WO claimed
WO-2002032419-A2 METHODS FOR MODULATING BLADDER FUNCTION WYETH (US) 2002-04-25 WO claimed
US-6348486-B1 TREATMENT OF INCONTINENCE AMERICAN HOME PRODUCTS CORPORATION 2002-02-19 US claimed
EP-0747354-B1 3-Substituted oxindole derivatives as potassium channel modulators BRISTOL MYERS SQUIBB CO (US) 2000-08-16 EP claimed
EP-0747354-A1 3-Substituted oxindole derivatives as potassium channel modulators BRISTOL-MYERS SQUIBB COMPANY (US) 1996-12-11 EP claimed
US-5565483-A ADMINISTERING AS THERAPY FOR ISCHEMIA, CONVULSIONS OR ASTHMA BRISTOL-MYERS SQUIBB COMPANY (US) 1996-10-15 US claimed
WO-2024054807-A1 COMBINATION THERAPIES INCLUDING METAL CHANNEL ACTIVATORS AND TDP-43 MODULATORS BIOHAVEN THERAPEUTICS LTD. (VG) 2024-03-14 WO disclosed
WO-2024050389-A1 COMBINATION THERAPIES INCLUDING METAL CHANNEL ACTIVATORS AND NMDA RECEPTOR ANTAGONISTS BIOHAVEN THERAPEUTICS LTD. (VG) 2024-03-07 WO disclosed
US-20060160892-A1 Methods for treating hyperactive gastric motility WYETH (US) 2006-07-20 US disclosed
WO-2002000217-A1 USE OF 3-SUBSTITUTED OXINDOLE DERIVATIVES AS KCNQ POTASSIUM CHANNEL MODULATORS NEUROSEARCH A/S (DK) 2002-01-03 WO disclosed
EP-0747354-B1 3-Substituted oxindole derivatives as potassium channel modulators BRISTOL MYERS SQUIBB CO (US) 2000-08-16 EP disclosed
US-5602169-A USEFUL IN REDUCING NEURONAL DAMAGE DURING ISCHEMIC STROKE BRISTOL-MYERS SQUIBB COMPANY (US) 1997-02-11 US disclosed
US-5565483-A ADMINISTERING AS THERAPY FOR ISCHEMIA, CONVULSIONS OR ASTHMA BRISTOL-MYERS SQUIBB COMPANY (US) 1996-10-15 US 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 (4 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-20040029949-A1 Methods for treating hyperactive gastric motility KCNQ5, KCNQ3, KCNQ4 OPRK1 97/4885PDE4D 339/4885CYP1A2 647/4885
US-20020183395-A1 Methods for treating hyperactive gastric motility KCNQ5, KCNQ3, KCNQ4 OPRK1 109/4885PDE4D 280/4885CYP1A2 724/4885
US-20030181507-A1 Use of 3-substituted oxindole derivatives as kcnq potassium channel modulators KCNQ1, KCNQ2, KCNQ3 OPRK1 53/4885PDE4D 1090/4885CYP1A2 1886/4885
US-20060160892-A1 Methods for treating hyperactive gastric motility KCNQ5, KCNQ3, KCNQ4 OPRK1 117/4885PDE4D 271/4885CYP1A2 817/4885

“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.