SCHEMBL8024010

SCHEMBL8024010

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

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TDP1 Q9NUW8 2/20 0.50
CHRM1 P11229 1/20 0.50
AKR1A1 P14550 1/20 0.50
CHRM3 P20309 1/20 0.50
HTR2A P28223 1/20 0.50
HTR2C P28335 1/20 0.50
ADRA1A P35348 1/20 0.50
HRH1 P35367 1/20 0.50
DRD3 P35462 1/20 0.50
SLC6A3 Q01959 1/20 0.50
HDAC1 Q13547 1/20 0.50
HDAC2 Q92769 1/20 0.50
GPR84 Q9NQS5 3/20 0.41
FFAR1 O14842 1/20 0.41
TP53 P04637 1/20 0.41
SLC1A3 P43003 2/20 0.39
SLC1A2 P43004 2/20 0.39
SLC1A1 P43005 2/20 0.39
GRIK1 P39086 1/20 0.39
GRIK2 Q13002 1/20 0.39

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
SCHEMBL599200 1.00 TDP1 (0.50) TDP1CHRM1AKR1A1CHRM3HTR2A
SCHEMBL2932676 1.00 TDP1 (0.50) TDP1CHRM1AKR1A1CHRM3HTR2A
SCHEMBL8024004 1.00 TDP1 (0.50) TDP1CHRM1AKR1A1CHRM3HTR2A
SCHEMBL9059526 0.87 TP53 (0.47) TDP1CHRM1AKR1A1CHRM3HTR2A
SCHEMBL5250951 0.86 CA2 (0.50) TDP1CHRM1AKR1A1CHRM3HTR2A
SCHEMBL5907622 0.84 GPR84 (0.57) GPR84FFAR1SLC1A2SLC1A1GRIK1
SCHEMBL5031485 0.84 TDP1 (0.60) TDP1CHRM1AKR1A1CHRM3HTR2A
SCHEMBL14110749 0.84 TDP1 (0.60) TDP1CHRM1AKR1A1CHRM3HTR2A
SCHEMBL9431401 0.82 GPR84 (0.61) GPR84FFAR1GRIK1GRIK2ACE2
Undecane SCHEMBL20589952 0.82 GPR84 (0.55) GPR84FFAR1CA2MAPK1ACE2

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