SCHEMBL7067142

SCHEMBL7067142

Nc1cc2oc(=O)[nH]c2cc1F

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMO O15229 1/20 0.52
NOS1 P29475 4/20 0.44
NOS3 P29474 3/20 0.44
NOS2 P35228 3/20 0.44
LMNA P02545 1/20 0.44
CYP1A2 P05177 1/20 0.44
ADRA2A P08913 1/20 0.44
TSHR P16473 1/20 0.44
THPO P40225 1/20 0.44
BLM P54132 1/20 0.44
NPSR1 Q6W5P4 1/20 0.44
OGT O15294 1/20 0.41
ACLY P53396 1/20 0.40
PDE3B Q13370 2/20 0.39
PDE3A Q14432 2/20 0.39
CREBBP Q92793 1/20 0.37
KDM4E B2RXH2 1/20 0.37
ALDH1A1 P00352 1/20 0.37
PPM1D O15297 1/20 0.36
POLB P06746 2/20 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
SCHEMBL9874657 0.93 KMO (0.52) KMONOS1NOS3NOS2LMNA
SCHEMBL9680309 0.84 KMO (0.59) KMONOS1NOS3NOS2LMNA
SCHEMBL2549381 0.84 KMO (0.59) KMONOS1NOS3NOS2LMNA
SCHEMBL522196 0.78 NOS1 (0.53) KMONOS1NOS3NOS2LMNA
SCHEMBL12420056 0.78 KMO (0.72) KMONOS1NOS3NOS2LMNA
SCHEMBL24981075 0.78 KMO (0.52) KMONOS1NOS3NOS2LMNA
SCHEMBL4297310 0.78 KMO (0.52) KMONOS1NOS3NOS2LMNA
SCHEMBL29455648 0.78 KMO (0.52) KMONOS1NOS3NOS2LMNA
SCHEMBL1115840 0.78 KMO (0.72) KMONOS1NOS3NOS2LMNA
SCHEMBL5539443 0.78 KMO (0.52) KMONOS1NOS3NOS2LMNA

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-1316550-A1 6-Acylamino-5-substituted-benzoxazol-2-one compounds and method for using them EASTMAN KODAK COMPANY (US) 2003-06-04 EP disclosed
US-6515176-B1 Disclosed is a 6-acylamino-5-substituted-benzoxazol-2-one compound having the structural formula I: Also disclosed is a method for forming a cyan dye-forming coupler from the above compound. The method and intermediate with a simplified EASTMAN KODAK COMPANY 2003-02-04 US disclosed
EP-0385664-B1 Antiinflammatory benzoxazolones PFIZER (US) 1994-01-12 EP disclosed
US-5149821-A Process and intermediates for optically active 3-formyltetrahydropyrans PFIZER INC (US) 1992-09-22 US disclosed
US-5086062-A Inhibitors of lipoxygenase and-or cyclooxygenase enzymes PFIZER INC. (US) 1992-02-04 US disclosed
EP-0385664-A2 Antiinflammatory benzoxazolones PFIZER INC. (US) 1990-09-05 EP disclosed