SCHEMBL1820544

SCHEMBL1820544

C[C@H](O)C(=O)c1ccccc1

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 4/20 0.58
CES2 O00748 4/20 0.58
CES1 P23141 4/20 0.58
TDP1 Q9NUW8 2/20 0.54
L3MBTL1 Q9Y468 2/20 0.54
PGR P06401 1/20 0.53
ADRA2A P08913 1/20 0.53
ADRA2B P18089 1/20 0.53
HTR2A P28223 1/20 0.53
HRH1 P35367 1/20 0.53
KCNH2 Q12809 1/20 0.53
ALKBH5 Q6P6C2 1/20 0.48
MAPT P10636 3/20 0.48
SMN1; SMN2 Q16637 2/20 0.48
NPSR1 Q6W5P4 2/20 0.48
ATM Q13315 2/20 0.48
MDM2 Q00987 1/20 0.48
XBP1 P17861 1/20 0.48
ALDH1A1 P00352 4/20 0.48
TSHR P16473 3/20 0.48

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
SCHEMBL1093883 1.00 LMNA (0.58) LMNACES2CES1TDP1L3MBTL1
SCHEMBL27003 1.00 LMNA (0.58) LMNACES2CES1TDP1L3MBTL1
Methane SCHEMBL9356267 0.98 LMNA (0.56) LMNACES2CES1TDP1L3MBTL1
SCHEMBL27719890 0.98 LMNA (0.56) LMNACES2CES1TDP1L3MBTL1
SCHEMBL10944827 0.91 ALDH1A1 (0.58) LMNACES2CES1TDP1L3MBTL1
Acrylic Acid SCHEMBL28676895 0.88 AKT1 (0.50) LMNACES2CES1TDP1L3MBTL1
SCHEMBL21456599 0.87 KDM4E (0.43) LMNACES2CES1PGRADRA2A
SCHEMBL29234971 0.84 LMNA (0.44) LMNACES2CES1TDP1L3MBTL1
Phenylglycine SCHEMBL28088318 0.83 LMNA (0.52) LMNACES2CES1TDP1L3MBTL1
Piperidine SCHEMBL6693285 0.83 LMNA (0.43) LMNACES2CES1TDP1L3MBTL1

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 27 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2316926-B1 Enantioselective production of alpha-hydroxy carbonyl compounds UNIV BONN (DE) 2016-04-13 EP claimed
EP-2316926-A1 Enantioselective production of alpha-hydroxy carbonyl compounds Rheinische Friedrich-Wilhelms-Universität Bonn (DE) 2011-05-04 EP claimed
EP-0643781-B1 ELECTROCATALYTIC ASYMMETRIC DIHYDROXYLATION OF OLEFINIC COMPOUNDS SEPRACOR INC (US) 1998-06-24 EP claimed
EP-0643781-A1 ELECTROCATALYTIC ASYMMETRIC DIHYDROXYLATION OF OLEFINIC COMPOUNDS SEPRACOR, INC. (US) 1995-03-22 EP claimed
WO-1993017150-A1 ELECTROCATALYTIC ASYMMETRIC DIHYDROXYLATION OF OLEFINIC COMPOUNDS SEPRACOR, INC. (US) 1993-09-02 WO claimed
CN-116731985-A Cytochrome P450 monooxygenase P450PL2 mutant and application thereof 中国科学院新疆理化技术研究所 2023-09-12 CN disclosed
EP-2316926-B1 Enantioselective production of alpha-hydroxy carbonyl compounds UNIV BONN (DE) 2016-04-13 EP disclosed
EP-2316926-A1 Enantioselective production of alpha-hydroxy carbonyl compounds Rheinische Friedrich-Wilhelms-Universität Bonn (DE) 2011-05-04 EP disclosed
EP-1048737-B1 Stereoselective synthesis of 2-hydroxycétones FORSCHUNGSZENTRUM JUELICH GMBH (DE) 2007-06-06 EP disclosed
US-7166749-B2 Process for preparing chiral aromatic α-hydroxy ketones using 2-hydroxy-3-oxoacid synthase BEN-GURION UNIVERSITY OF THE NEGEV (IL) 2007-01-23 US disclosed
US-7166749-B2 Process for preparing chiral aromatic α-hydroxy ketones using 2-hydroxy-3-oxoacid synthase BEN-GURION UNIVERSITY OF THE NEGEV (IL) 2007-01-23 US disclosed
US-7045334-B2 Nucleotide sequence encoding a benzaldehyde lyase, and process for stereoselectively synthesizing 2-hydroxyketones Forschungszentrum Jülich GmbH (DE) 2006-05-16 US disclosed
EP-0643781-A4 ELECTROCATALYTIC ASYMMETRIC DIHYDROXYLATION OF OLEFINIC COMPOUNDS. 1995-04-26 EP disclosed
EP-0643781-A1 ELECTROCATALYTIC ASYMMETRIC DIHYDROXYLATION OF OLEFINIC COMPOUNDS SEPRACOR, INC. (US) 1995-03-22 EP disclosed
US-5302257-A Preparing optically active glycols using catalyst complex of osmium tetroxide and chiral oxidation resistant tertiary amine, employing secondary oxidant to generate osmium tetroxide, electrolytically regenerating secondary oxidant SEPRACOR, INC. (US) 1994-04-12 US disclosed
WO-1993017150-A1 ELECTROCATALYTIC ASYMMETRIC DIHYDROXYLATION OF OLEFINIC COMPOUNDS SEPRACOR, INC. (US) 1993-09-02 WO disclosed
WO-1992017433-A1 PREPARATION OF CHIRAL HYDROXYKETONES SCHERING CORPORATION (US) 1992-10-15 WO disclosed
EP-0506341-A1 Preparation of chiral hydroxyketones SCHERING CORPORATION (US) 1992-09-30 EP disclosed
EP-0400239-A1 Process for asymmetric reduction of ketones with baker's yeast Daito Corporation (JP) 1990-12-05 EP disclosed
EP-0051061-A2 Novel intermediates and process for their preparation THE WELLCOME FOUNDATION LIMITED (GB) 1982-05-05 EP disclosed