SCHEMBL5396117

SCHEMBL5396117

O=c1[nH]c2ccccc2c(-c2ccccc2)c1O

nearest known ligand 0.75

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 2/20 0.75
KDM4E B2RXH2 4/20 0.65
ALDH1A1 P00352 3/20 0.65
IDE P14735 1/20 0.65
MPI P34949 1/20 0.65
CACNA1B Q00975 1/20 0.65
APBA1 Q02410 1/20 0.65
PDE9A O76083 1/20 0.59
DAO P14920 1/20 0.59
DDO Q99489 1/20 0.59
HPGD P15428 1/20 0.57
ESR1 P03372 3/20 0.56
ESR2 Q92731 3/20 0.56
MAP2 P11137 1/20 0.54
PADI4 Q9UM07 1/20 0.52
EGFR P00533 1/20 0.51
SERPINE1 P05121 1/20 0.51
GRIN2D O15399 1/20 0.51
GRIN3B O60391 1/20 0.51
GRIN1 Q05586 1/20 0.51

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
SCHEMBL29709937 1.00 MAPT (0.75) MAPTKDM4EALDH1A1IDEMPI
SCHEMBL15713617 0.87 MAPK14 (0.63) MAPTKDM4EALDH1A1IDEMPI
SCHEMBL4455323 0.86 MAPT (1.00) MAPTKDM4EALDH1A1IDEMPI
SCHEMBL28132803 0.83 MAPT (0.71) MAPTKDM4EALDH1A1IDEMPI
SCHEMBL24095581 0.81 KDM4E (0.79) MAPTKDM4EALDH1A1MAP2
SCHEMBL25849861 0.81 PIM1 (0.66) MAPTKDM4EALDH1A1HPGDPADI4
SCHEMBL7811680 0.79 KDM4E (0.70) MAPTKDM4EALDH1A1PDE9AHPGD
SCHEMBL1884123 0.79 KDM4E (1.00) MAPTKDM4EALDH1A1IDEMPI
SCHEMBL8987076 0.79 MAPT (0.60) MAPTKDM4EALDH1A1PDE9ADAO
SCHEMBL31179077 0.79 MAPK1 (0.68) MAPTKDM4EALDH1A1PDE9AHPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240315965-A1 COMPOSITIONS AND METHODS RELATED TO PHARMACEUTICAL EXCIPIENTS Natural Extraction Systems, LLC (US) 2024-09-26 US claimed
WO-2022182527-A1 COMPOSITIONS AND METHODS RELATED TO PHARMACEUTICAL EXCIPIENTS Natural Extraction Systems, LLC (US) 2022-09-01 WO claimed
US-6126924-A Light responsive self-tanning products and methods for use SCALES-MEDEIROS VIRGINIA A (US) 2000-10-03 US claimed
US-20260048025-A1 COMPOSITIONS AND METHODS RELATED TO DISSOLVED OXIDES NATURAL EXTRACTION SYS LLC (US) 2026-02-19 US disclosed
US-12409152-B2 Compositions and methods related to dissolved oxides Natural Extraction Systems, LLC (US) 2025-09-09 US disclosed
US-20250161394-A1 Compositions Comprising Kavalactones NATURAL EXTRACTION SYS LLC (US) 2025-05-22 US disclosed
US-20240315965-A1 COMPOSITIONS AND METHODS RELATED TO PHARMACEUTICAL EXCIPIENTS Natural Extraction Systems, LLC (US) 2024-09-26 US disclosed
US-20220362169-A1 COMPOSITIONS AND METHODS RELATED TO DISSOLVED OXIDES Natural Extraction Systems, LLC 2022-11-17 US disclosed
WO-2022182527-A1 COMPOSITIONS AND METHODS RELATED TO PHARMACEUTICAL EXCIPIENTS Natural Extraction Systems, LLC (US) 2022-09-01 WO disclosed
WO-2021042001-A1 COMPOSITIONS AND METHODS RELATED TO DISSOLVED OXIDES Natural Extraction Systems, LLC (US) 2021-03-04 WO disclosed
US-10568877-B2 Preparation and anti-HSV-1 application of quinolinone derivatives OCEAN UNIVERSITY OF CHINA (CN) 2020-02-25 US disclosed
EP-1011677-A1 4-ARYL-3-AMINOQUINOLINE-2-ONE DERIVATIVES AS POTASSIUM CHANNEL MODULATORS Bristol-Myers Squibb Company (US) 2000-06-28 EP disclosed
US-5972961-A ANTIISCHEMIC AGENTS; ANTICONVULSANTS; HEADACHES; SEXUAL DISORDERS BRISTOL-MYERS SQUIBB COMPANY (US) 1999-10-26 US disclosed
EP-0942723-A1 4-ARYL-3-HYDROXYQUINOLIN-2-ONE DERIVATIVES AS ION CHANNEL MODULATORS Bristol-Myers Squibb Company (US) 1999-09-22 EP disclosed
US-5922735-A CALCIUM-ACTIVATED POTASSIUM CHANNELS AND ARE USEFUL TREATING THE DISORDER RESPONSIVE TO THE OPENING OF THE POTASSIUM CHANNELS SUCH AS ISCHEMIA, CONVULSIONS, ASTHMA, IRRITABLE BOWEL SYNDROME, MIGRAINE, TRAUMATIC BRAIN INJURY BRISTOL-MYERS SQUIBB COMPANY (US) 1999-07-13 US disclosed
US-5892045-A 4-aryl-3-hydroxyquinolin-2-one derivatives as ion channel modulators BRISTOL-MYERS SQUIBB COMPANY (US) 1999-04-06 US disclosed
WO-1999009983-A1 4-ARYL-3-AMINOQUINOLINE-2-ONE DERIVATIVES AS POTASSIUM CHANNEL MODULATORS BRISTOL-MYERS SQUIBB COMPANY (US) 1999-03-04 WO disclosed
WO-1998023273-A1 4-ARYL-3-HYDROXYQUINOLIN-2-ONE DERIVATIVES AS ION CHANNEL MODULATORS BRISTOL-MYERS SQUIBB COMPANY (US) 1998-06-04 WO disclosed
US-4668627-A 3-16-ISOCYANO-3,7-DIOXATRICYCLO/4.1.0.0.2,4/HEPT-4-YL/ PROPENOIC ACID KUREHA KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1987-05-26 US disclosed
US-4542154-A 2188,3-(6-ISOCYANO-3,7-DIOXATRICYCLOE4.1.0.0.2.4)HEPT-4-YL) PROPENOIC ACID KUREHA KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1985-09-17 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-12409152-B2 Compositions and methods related to dissolved oxides PRKG2, PRKG1, CIT MAPT 2118/4885KDM4E 4365/4885ALDH1A1 4556/4885
US-20260048025-A1 COMPOSITIONS AND METHODS RELATED TO DISSOLVED OXIDES SCO2, CNR2, CNR1 MAPT 3552/4885KDM4E 3795/4885ALDH1A1 1371/4885
US-10568877-B2 Preparation and anti-HSV-1 application of quinolinone derivatives RPL5, TOP1, TOP2A MAPT 442/4885KDM4E 948/4885ALDH1A1 1996/4885
US-20220362169-A1 COMPOSITIONS AND METHODS RELATED TO DISSOLVED OXIDES PRKG2, PRKG1, CIT MAPT 2118/4885KDM4E 4365/4885ALDH1A1 4556/4885

“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.