SCHEMBL6359897

SCHEMBL6359897

CCCC(=O)OC(C)C1CO1

nearest known ligand 0.42

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 2/20 0.40
LMNA P02545 4/20 0.39
NLRP3 Q96P20 1/20 0.35
PRKCA P17252 4/20 0.34
FFAR3 O14843 1/20 0.33
HDAC3 O15379 1/20 0.33
HDAC1 Q13547 1/20 0.33
HDAC2 Q92769 1/20 0.33
HDAC8 Q9BY41 1/20 0.33
MAPT P10636 1/20 0.33
MAPK1 P28482 1/20 0.33
FAAH O00519 1/20 0.33
MGLL Q99685 1/20 0.33

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
SCHEMBL6350436 0.86 MEN1 (0.33) ALDH1A1LMNA
SCHEMBL11465302 0.86 LMNA (0.59) ALDH1A1LMNAPRKCAMAPTMAPK1
SCHEMBL11455752 0.86 LMNA (0.59) ALDH1A1LMNAPRKCAMAPTMAPK1
SCHEMBL11457947 0.86 LMNA (0.59) ALDH1A1LMNAPRKCAMAPTMAPK1
SCHEMBL11474946 0.86 LMNA (0.59) ALDH1A1LMNAPRKCAMAPTMAPK1
SCHEMBL11457565 0.86 LMNA (0.59) ALDH1A1LMNAPRKCAMAPTMAPK1
SCHEMBL11455540 0.86 LMNA (0.59) ALDH1A1LMNAPRKCAMAPTMAPK1
SCHEMBL11468104 0.79 PRKCA (0.52) ALDH1A1LMNAPRKCAMAPTFAAH
SCHEMBL1903350 0.76
SCHEMBL941154 0.74 LMNA (0.43) ALDH1A1LMNA

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
US-20050165201-A1 Epoxidizing an alpha-halohydrin intermediate from a halide substitution-deesterification of an alpha -hydroxy ester derivative obtained by the coupling reaction of a phenol and a glycidyl ester BORIACK CLINTON J (US) 2005-07-28 US disclosed
US-20030149219-A1 Process for manufacturing a hydroxyester derivative intermediate and epoxy resins prepared therefrom BORIACK CLINTON J (US) 2003-08-07 US disclosed
US-6534621-B2 Epoxidizing an alpha-halohydrin intermediate produced from an in situ halide substitution-deesterification of an alpha-hydroxy ester derivative DOW GLOBAL TECHNOLOGIES INC. 2003-03-18 US disclosed
EP-1290058-A2 PROCESS FOR MANUFACTURING A HYDROXYESTER DERIVATIVE INTERMEDIATE AND EPOXY RESINS PREPARED THEREFROM DOW GLOBAL TECHNOLOGIES INC. (US) 2003-03-12 EP disclosed
US-20020045707-A1 Process for manufacturing a hydroxyester derivative intermediate and epoxy resins prepared therefrom DOW GLOBAL TECHNOLOGIES INC. 2002-04-18 US disclosed
WO-2001088013-A2 PROCESS FOR MANUFACTURING A HYDROXYESTER DERIVATIVE INTERMEDIATE AND EPOXY RESINS PREPARED THEREFROM DOW GLOBAL TECHNOLOGIES INC (US) 2001-11-22 WO disclosed