SCHEMBL8017449

SCHEMBL8017449

CCCC(C(=O)OC(C)(C)C)C(C)O

nearest known ligand 0.36

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA1 P00915 4/20 0.36
CA2 P00918 3/20 0.36
CA7 P43166 2/20 0.36
CTSK P43235 8/20 0.36
CTSS P25774 2/20 0.36
NOS1 P29475 2/20 0.35
NOS3 P29474 1/20 0.35
NOS2 P35228 1/20 0.35
CYP2D6 P10635 1/20 0.33
MEN1 O00255 1/20 0.32
GAA P10253 1/20 0.32
KMT2A Q03164 1/20 0.32
CHRM1 P11229 1/20 0.31
AKR1A1 P14550 1/20 0.31
CHRM3 P20309 1/20 0.31
HTR2A P28223 1/20 0.31
HTR2C P28335 1/20 0.31
ADRA1A P35348 1/20 0.31
HRH1 P35367 1/20 0.31
DRD3 P35462 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
SCHEMBL12321026 0.85 CTSK (0.36) CA1CA2CA7CTSKCTSS
SCHEMBL8007209 0.84 CA1 (0.34) CA1CA2CA7CTSKCTSS
SCHEMBL12098467 0.81 CHRM1 (0.38) CA1CA2CA7CTSKCTSS
SCHEMBL15015760 0.81 CHRM1 (0.40) CA1CA2CA7CTSKCTSS
SCHEMBL28732870 0.80 CA1 (0.41) CA1CA2CA7CTSKCTSS
SCHEMBL23151921 0.78 NOS1 (0.39) CA1CA2CA7CTSKCTSS
SCHEMBL30571827 0.78 CHRM1 (0.38) CA1CA2CA7CTSKCTSS
SCHEMBL17449756 0.78 CTSK (0.38) CA1CA2CA7CTSKCTSS
SCHEMBL5216229 0.78 CTSK (0.38) CA1CA2CA7CTSKCTSS
SCHEMBL12236056 0.78 CTSK (0.38) CA1CA2CA7CTSKCTSS

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