SCHEMBL9025433

SCHEMBL9025433

COC1(OC)C[C@H](C(=O)O)C1C(=O)O

nearest known ligand 0.35

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
GRM4 Q14833 4/20 0.35
CYP2C19 P33261 3/20 0.35
MEN1 O00255 1/20 0.35
ALDH1A1 P00352 1/20 0.35
CYP1A2 P05177 1/20 0.35
KMT2A Q03164 1/20 0.35
TDP1 Q9NUW8 1/20 0.35
GRM8 O00222 1/20 0.35
GRM6 O15303 1/20 0.35
CYP2D6 P10635 1/20 0.35
CYP2C9 P11712 1/20 0.35
APLNR P35414 1/20 0.33
SLC6A12 P48065 1/20 0.31
SLC6A11 P48066 1/20 0.31
GABRR1 P24046 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
SCHEMBL8019500 1.00 GRM4 (0.35) GRM4CYP2C19MEN1ALDH1A1CYP1A2
SCHEMBL8018708 0.78 GRM4 (0.32) GRM4CYP2C19MEN1ALDH1A1CYP1A2
SCHEMBL8015707 0.78 GRM4 (0.32) GRM4CYP2C19MEN1ALDH1A1CYP1A2
SCHEMBL8018705 0.78 GRM4 (0.32) GRM4CYP2C19MEN1ALDH1A1CYP1A2
SCHEMBL9565510 0.74 GRM4 (0.32) GRM4CYP2C19MEN1ALDH1A1CYP1A2
SCHEMBL9565506 0.74 GRM4 (0.32) GRM4CYP2C19MEN1ALDH1A1CYP1A2
SCHEMBL9096914 0.71 MAPT (0.35) GRM4CYP2C19MEN1ALDH1A1CYP1A2
SCHEMBL31104772 0.67 APLNR (0.34) CYP2C19APLNR
SCHEMBL4335552 0.65 GRM4 (0.44) GRM4CYP2C19MEN1ALDH1A1CYP1A2
SCHEMBL9094264 0.65 GRM4 (0.50) GRM4CYP2C19MEN1ALDH1A1CYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0458643-B1 Process for preparing an optically active cyclobutanone, an intermediate in the synthesis of an optically active cyclobutane nucleoside SQUIBB & SONS INC (US) 1995-11-29 EP claimed
US-5344962-A Intermediates in the synthesis of an optically active cyclobutane nucleoside E. R. SQUIBB & SONS, INC. (US) 1994-09-06 US claimed
EP-0458643-A2 Process for preparing an optically active cyclobutanone, an intermediate in the synthesis of an optically active cyclobutane nucleoside E.R. SQUIBB & SONS, INC. (US) 1991-11-27 EP claimed
EP-0458363-B1 Fluorinated bis(hydroxymethyl) cyclobutyl purines and pyrimidines SQUIBB & SONS INC (US) 1996-02-07 EP disclosed
EP-0458643-B1 Process for preparing an optically active cyclobutanone, an intermediate in the synthesis of an optically active cyclobutane nucleoside SQUIBB & SONS INC (US) 1995-11-29 EP disclosed
US-5344962-A Intermediates in the synthesis of an optically active cyclobutane nucleoside E. R. SQUIBB & SONS, INC. (US) 1994-09-06 US disclosed
EP-0554025-A2 Fluorinated cyclobutyl purines and pyrimidines E.R. SQUIBB & SONS, INC. (US) 1993-08-04 EP disclosed
US-5233076-A Process for preparing an optically active cyclobutanone, an intermediate in the synthesis of an optically active cyclobutane nucleoside E. R. SQUIBB & SONS, INC. (US) 1993-08-03 US disclosed
WO-1991018969-A1 FLUORINATED BIS(HYDROXYMETHYL)CYCLOBUTYL PURINES AND PYRIMIDINES E.R. SQUIBB & SONS, INC. (US) 1991-12-12 WO disclosed
EP-0458363-A1 Fluorinated bis(hydroxymethyl) cyclobutyl purines and pyrimidines E.R. SQUIBB & SONS, INC. (US) 1991-11-27 EP disclosed
EP-0458643-A2 Process for preparing an optically active cyclobutanone, an intermediate in the synthesis of an optically active cyclobutane nucleoside E.R. SQUIBB & SONS, INC. (US) 1991-11-27 EP disclosed