SCHEMBL9203441

SCHEMBL9203441

CCOC(=O)[C@@H](Br)[C@@H](CC)C(=O)OCC

nearest known ligand 0.40

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.40
TRPA1 O75762 1/20 0.39
LMNA P02545 2/20 0.39
HSD17B10 Q99714 1/20 0.39
ALOX15 P16050 1/20 0.37
MGAM O43451 1/20 0.37
GAA P10253 1/20 0.37
SI P14410 1/20 0.37
MGAM2 Q2M2H8 1/20 0.37
SOAT1 P35610 1/20 0.37
PIN1 Q13526 1/20 0.32
KMT2A Q03164 2/20 0.32
L3MBTL1 Q9Y468 2/20 0.32
MEN1 O00255 1/20 0.32
NPC1 O15118 1/20 0.32
CAD P27708 1/20 0.32
HCAR2 Q8TDS4 1/20 0.31
CPB2 Q96IY4 1/20 0.31
MAPT P10636 1/20 0.31
HPGD P15428 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
SCHEMBL9213373 0.87 CYP2C19 (0.40) ALDH1A1TRPA1LMNAHSD17B10ALOX15
SCHEMBL1415615 0.83 ALDH1A1 (0.50) ALDH1A1TRPA1LMNAHSD17B10ALOX15
SCHEMBL22144315 0.83 ALDH1A1 (0.50) ALDH1A1TRPA1LMNAHSD17B10ALOX15
SCHEMBL235849 0.83 ALDH1A1 (0.50) ALDH1A1TRPA1LMNAHSD17B10ALOX15
SCHEMBL10867163 0.81 ALDH1A1 (0.43) ALDH1A1TRPA1LMNAHSD17B10ALOX15
SCHEMBL11302245 0.79 ALDH1A1 (0.42) ALDH1A1TRPA1LMNAHSD17B10ALOX15
SCHEMBL3464999 0.78 ALDH1A1 (0.37) ALDH1A1TRPA1LMNAHSD17B10ALOX15
SCHEMBL30438662 0.77 ZDHHC7 (0.42) ALDH1A1TRPA1MGAMGAASI
SCHEMBL9205071 0.77 ZDHHC7 (0.42) ALDH1A1TRPA1MGAMGAASI
SCHEMBL23255902 0.77 ALDH1A1 (0.40) ALDH1A1TRPA1LMNAHSD17B10ALOX15

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0643710-A1 SYNTHESIS OF OPTICALLY ACTIVE LACTONES FROM L-ASPARTIC ACID AND INTERMEDIATES THEREOF THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 1995-03-22 EP disclosed
US-5322942-A Deprotecting and hydrolyzing protected aspartic acid diester, reacting with nitrosylating agent in presence of hydrogen halide, esterifying, reacting with acyl aryl derivative REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 1994-06-21 US disclosed
WO-1992021675-A1 SYNTHESIS OF OPTICALLY ACTIVE LACTONES FROM L-ASPARTIC ACID AND INTERMEDIATES THEREOF THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 1992-12-10 WO disclosed