SCHEMBL8017237

SCHEMBL8017237

C=CCC(C(=O)O)[C@@H](C)O

nearest known ligand 0.39

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
GRIK1 P39086 2/20 0.39
GRIK2 Q13002 2/20 0.39
CYP2C19 P33261 1/20 0.38
CPA1 P15085 1/20 0.38
TP53 P04637 1/20 0.38
ALDH1A1 P00352 1/20 0.35
SLC1A3 P43003 1/20 0.34
SLC1A2 P43004 1/20 0.34
SLC1A1 P43005 1/20 0.34
TDP1 Q9NUW8 1/20 0.33
MMP2 P08253 2/20 0.32
MMP3 P08254 2/20 0.32
MMP7 P09237 2/20 0.32
MMP1 P03956 1/20 0.32
ABCC4 O15439 1/20 0.31
MAPT P10636 1/20 0.31
PTGS2 P35354 1/20 0.31

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
SCHEMBL6530502 1.00 GRIK1 (0.39) GRIK1GRIK2CYP2C19CPA1TP53
SCHEMBL23688391 1.00 GRIK1 (0.39) GRIK1GRIK2CYP2C19CPA1TP53
SCHEMBL6530499 1.00 GRIK1 (0.39) GRIK1GRIK2CYP2C19CPA1TP53
SCHEMBL8020514 1.00 GRIK1 (0.39) GRIK1GRIK2CYP2C19CPA1TP53
SCHEMBL2987273 0.84 SLC1A3 (0.45) GRIK1GRIK2CYP2C19CPA1TP53
SCHEMBL4798136 0.84 SLC1A3 (0.45) GRIK1GRIK2CYP2C19CPA1TP53
SCHEMBL2987274 0.84 SLC1A3 (0.45) GRIK1GRIK2CYP2C19CPA1TP53
SCHEMBL1133379 0.83 GRIK1 (0.46) GRIK1GRIK2CYP2C19CPA1ALDH1A1
SCHEMBL17213409 0.83 GRIK1 (0.37) GRIK1GRIK2CYP2C19CPA1TP53
SCHEMBL11199369 0.82 GRIK1 (0.39) GRIK1GRIK2CYP2C19CPA1TP53

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 7 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0774452-B1 Optically active compounds having plural chiral centers and the production thereof CHISSO CORP (JP) 2000-01-26 EP disclosed
EP-0428392-B1 Processes for the preparation of optically active compounds having plural chiral centers CHISSO CORP (JP) 1998-05-27 EP disclosed
EP-0774452-A1 Optically active compounds having plural chiral centers and the production thereof Chisso Corporation (JP) 1997-05-21 EP disclosed
US-5574182-A HYDROLYSING 3-HYDROXYCARBOXYLIC ACID, CYCLIZING ESTER TO FORM 1,3-DIOXAN-4-ONE, DECYCLIZATION AND ESTERIFICATION CHISSO CORPORATION (JP) 1996-11-12 US disclosed
US-5411877-A Esterification CHISSO CORPORATION (JP) 1995-05-02 US disclosed
US-5348870-A Using hydrolase to effect ester interchange and resolution, then alcoholysis or hydrolysis and dehydration with cyclization and crystallization CHISSO CORPORATION (JP) 1994-09-20 US disclosed
EP-0428392-A2 Optically active compounds having plural chiral centers and the production thereof Chisso Corporation (JP) 1991-05-22 EP disclosed