SCHEMBL8745903

SCHEMBL8745903

NC(O)(CCC(=O)O)C1CCCCC1

nearest known ligand 0.39

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.39
MEN1 O00255 1/20 0.37
CYP1A2 P05177 1/20 0.37
THRB P10828 1/20 0.37
KMT2A Q03164 1/20 0.37
LMNA P02545 1/20 0.37
KDM5A P29375 3/20 0.34
PHF8 Q9UPP1 3/20 0.34
KDM2A Q9Y2K7 3/20 0.34
KDM4C Q9H3R0 2/20 0.34
EPHX2 P34913 1/20 0.34
KDM4A O75164 1/20 0.34
KEAP1 Q14145 1/20 0.33
NFE2L2 Q16236 1/20 0.33
GRM2 Q14416 1/20 0.33
GRM3 Q14832 1/20 0.33
EPHX1 P07099 1/20 0.33
FOLH1 Q04609 1/20 0.32
KIF11 P52732 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
Hydrochloric Acid SCHEMBL8745885 0.98 ALDH1A1 (0.38) ALDH1A1MEN1CYP1A2THRBKMT2A
SCHEMBL9225076 0.89 ALDH1A1 (0.41) ALDH1A1MEN1CYP1A2THRBKMT2A
SCHEMBL6282896 0.80 ALDH1A1 (0.36) ALDH1A1LMNAEPHX2KEAP1NFE2L2
SCHEMBL8745889 0.77 ALDH1A1 (0.39) ALDH1A1THRBLMNAKDM5APHF8
SCHEMBL10355082 0.77 KEAP1 (0.38) KEAP1NFE2L2GRM2GRM3KIF11
SCHEMBL9225516 0.76 ALDH1A1 (0.42) ALDH1A1MEN1CYP1A2THRBKMT2A
SCHEMBL16670669 0.75 ALDH1A1 (0.35) ALDH1A1MEN1CYP1A2THRBKMT2A
SCHEMBL7297962 0.75 LMNA (0.37) ALDH1A1MEN1KMT2ALMNAEPHX2
SCHEMBL19150278 0.74 ALDH1A1 (0.40) ALDH1A1MEN1CYP1A2THRBKMT2A
SCHEMBL19148259 0.74 ALDH1A1 (0.40) ALDH1A1MEN1CYP1A2THRBKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0519763-B1 Cyclohexylbutyric acid derivatives and their use in the production of optically active cyclohexylnorstatine TAKASAGO PERFUMERY CO LTD (JP) 1997-02-05 EP disclosed
US-5502221-A HYPOTENSIVE INTERMEDIATE TAKASAGO INTERNATIONAL CORPORATION (JP) 1996-03-26 US disclosed
US-5442105-A Catalytic hydrogenation, epoxidation, reacting product with trialkylsilyl azide in the presence of a Lewis acid, hydrogenolysis TAKASAGO INTERNATIONAL CORPORATION (JP) 1995-08-15 US disclosed
EP-0519763-A2 Cyclohexylbutyric acid derivatives and their use in the production of optically active cyclohexylnorstatine TAKASAGO INTERNATIONAL CORPORATION (JP) 1992-12-23 EP disclosed
US-5166400-A Intermediates for isopropyl 3S-amino-2R-hydroxy-alkanoates PFIZER INC. (US) 1992-11-24 US disclosed
US-5036155-A Process for isopropyl 3S-amino-2R-hydroxy-alkanoates PFIZER INC. (US) 1991-07-30 US disclosed
US-4965372-A Process and intermediates for isopropyl 3S-amino-2R-hydroxy-alkanoates PFIZER INC. (US) 1990-10-23 US disclosed
EP-0379288-A1 Process and intermediates for isopropyl 3S-amino-2R-hydroxyalkanoates PFIZER INC. (US) 1990-07-25 EP disclosed