SCHEMBL7680574

SCHEMBL7680574

CC(C)(C)[C@@H]1OC(=O)[C@](c2ccccc2)(C2(O)CCCCC2)O1

nearest known ligand 0.36

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPK1 P28482 1/20 0.33
SMN1; SMN2 Q16637 1/20 0.33
CHRM3 P20309 1/20 0.33
AKR1C1 Q04828 1/20 0.33
APOBEC3A P31941 1/20 0.32
HTT P42858 1/20 0.32
APOBEC3G Q9HC16 1/20 0.32
HDAC4 P56524 1/20 0.32
POLB P06746 1/20 0.32
GPR55 Q9Y2T6 1/20 0.32
SSTR4 P31391 1/20 0.32
GRIN1 Q05586 2/20 0.32
GRIN2A Q12879 2/20 0.32
ALDH1A1 P00352 1/20 0.31
GRIN2D O15399 1/20 0.31
GRIN3B O60391 1/20 0.31
CYP2B6 P20813 1/20 0.31
SLC6A2 P23975 1/20 0.31
SLC6A4 P31645 1/20 0.31
PRCP P42785 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
SCHEMBL2795267 1.00 MAPK1 (0.33) MAPK1SMN1; SMN2CHRM3AKR1C1APOBEC3A
SCHEMBL1993661 0.99 MAPK1 (0.34) MAPK1SMN1; SMN2CHRM3AKR1C1APOBEC3A
SCHEMBL6589887 0.99 MAPK1 (0.34) MAPK1SMN1; SMN2CHRM3AKR1C1APOBEC3A
SCHEMBL21028879 0.75 POLB (0.38) MAPK1SMN1; SMN2HTTPOLBGPR55
SCHEMBL7681801 0.71 L3MBTL1 (0.44) CHRM3
SCHEMBL10029146 0.70 HCAR3 (0.37) MAPK1SMN1; SMN2HTTPOLBGPR55
SCHEMBL19850785 0.70 HCAR3 (0.37) MAPK1SMN1; SMN2HTTPOLBGPR55
SCHEMBL7559609 0.70 AKR1C1 (0.38) SMN1; SMN2AKR1C1HDAC4GRIN1GRIN2A
SCHEMBL13715499 0.69 L3MBTL1 (0.43) MAPK1SMN1; SMN2CHRM3SLC6A2SLC6A4
SCHEMBL19839514 0.69 L3MBTL1 (0.43) MAPK1SMN1; SMN2CHRM3SLC6A2SLC6A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6376684-B1 CHEMICAL INTERMEDIATE FOR OXYBUTYNIN-TYPE COMPOUNDS SEPRACOR INC. 2002-04-23 US disclosed
EP-1127043-A1 STEREOSELECTIVE PROCESS FOR PREPARING (CYCLO)ALKYL PHENYLGLYCOLIC ACIDS Sepracor Inc. (US) 2001-08-29 EP disclosed
US-6180823-B1 CONDENSING SUBSTITUTED ACETALDEHYDE WITH ENANTIOMER OF MANDELIC ACID TO PROVIDE 5-PHENYL-1,3-DIOXOLAN-4-ONE, CONDENSING WITH CYCLOHEXANONE, DEHYDRATING PRODUCT, HYDROLYZING, REDUCING TO ALPHA-CYCLOHEXYLPHENYLGLYCOLIC ACID SEPRACOR INC. 2001-01-30 US disclosed
WO-2000027786-A1 STEREOSELECTIVE PROCESS FOR PREPARING (CYCLO)ALKYL PHENYLGLYCOLIC ACIDS SEPRACOR INC. (US) 2000-05-18 WO disclosed