SCHEMBL8668203

SCHEMBL8668203

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

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 2/20 0.60
HDAC1 Q13547 3/20 0.50
LMNA P02545 3/20 0.50
MAPT P10636 3/20 0.50
HDAC3 O15379 2/20 0.50
HDAC4 P56524 2/20 0.50
HDAC2 Q92769 2/20 0.50
HDAC8 Q9BY41 2/20 0.50
HDAC6 Q9UBN7 2/20 0.50
PLIN1 O60240 2/20 0.50
RECQL P46063 2/20 0.50
PLIN5 Q00G26 2/20 0.50
ABHD5 Q8WTS1 2/20 0.50
CYP2D6 P10635 2/20 0.50
ALDH1A1 P00352 2/20 0.50
TNKS O95271 1/20 0.50
HCAR2 Q8TDS4 1/20 0.50
HDAC7 Q8WUI4 1/20 0.50
HDAC10 Q969S8 1/20 0.50
HDAC11 Q96DB2 1/20 0.50

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
SCHEMBL3452258 1.00 CYP1A2 (0.60) CYP1A2HDAC1LMNAMAPTHDAC3
SCHEMBL3452259 1.00 CYP1A2 (0.60) CYP1A2HDAC1LMNAMAPTHDAC3
SCHEMBL2910722 1.00 CYP1A2 (0.60) CYP1A2HDAC1LMNAMAPTHDAC3
SCHEMBL1618939 1.00 CYP1A2 (0.60) CYP1A2HDAC1LMNAMAPTHDAC3
SCHEMBL8060342 1.00 CYP1A2 (0.60) CYP1A2HDAC1LMNAMAPTHDAC3
SCHEMBL11337304 1.00 CYP1A2 (0.60) CYP1A2HDAC1LMNAMAPTHDAC3
SCHEMBL10337684 0.80 CYP1A2 (0.57) CYP1A2HDAC1LMNAMAPTHDAC3
SCHEMBL2636177 0.80 CYP1A2 (0.62) CYP1A2HDAC1LMNAMAPTHDAC3
SCHEMBL5311482 0.80 NFE2L2 (0.55) MAOB
SCHEMBL5311487 0.80 NFE2L2 (0.55) MAOB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0380689-B1 PROCESS FOR PREPARING OPTICALLY ACTIVE 2-HYDROXY-4-PHENYL-3-BUTENOIC ACID DAICEL CHEM (JP) 1995-10-04 EP claimed
US-5429935-A Reduction of the corresponding ketone with microorganisms DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1995-07-04 US claimed
US-5194380-A Treatment with a microorganism DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1993-03-16 US claimed
EP-0380689-A1 PROCESS FOR PREPARING OPTICALLY ACTIVE 2-HYDROXY-4-PHENYL-3-BUTENOIC ACID DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1990-08-08 EP claimed
JP-10075797-A None JP disclosed
JP-10075798-A None JP disclosed
JP-4018050-A None JP disclosed
JP-2100688-A None JP disclosed
JP-6197774-A None JP disclosed
CN-109234325-A A kind of application of lactic dehydrogenase in asymmetric syntheses chiral hydroxyl group compound 上海弈柯莱生物医药科技有限公司 2019-01-18 CN disclosed
JP-H1075797-A PRODUCTION OF (R)-2-HYDROXY-4-PHENYL-3-BUTENOIC ACID BY ENZYMATIC METHOD DAICEL CHEM IND LTD 1998-03-24 JP disclosed
JP-H1075798-A PRODUCTION OF (R)-2-HYDROXY-4-PHENYL-3-BUTENOIC ACID DAICEL CHEM IND LTD 1998-03-24 JP disclosed
US-5288620-A Reducing 2-oxo-4-phenyl-3-butenoic acid with enzyme preparation derived from microorganisms DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1994-02-22 US disclosed
US-5194380-A Treatment with a microorganism DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1993-03-16 US disclosed
US-5194380-A Treatment with a microorganism DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1993-03-16 US disclosed
JP-H0418050-A PRODUCTION OF (R)-2-HYDROXY-4-PHENYL-3-BUTENOIC ACID YOSHITOMI PHARMACEUT IND LTD 1992-01-22 JP disclosed
EP-0380689-A1 PROCESS FOR PREPARING OPTICALLY ACTIVE 2-HYDROXY-4-PHENYL-3-BUTENOIC ACID DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1990-08-08 EP disclosed
EP-0380689-A1 PROCESS FOR PREPARING OPTICALLY ACTIVE 2-HYDROXY-4-PHENYL-3-BUTENOIC ACID DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1990-08-08 EP disclosed
JP-H02100688-A PRODUCTION OF (R)-2-HYDROXY-4-PHENYL-3-BUTENOIC ACID DAICEL CHEM IND LTD 1990-04-12 JP disclosed
WO-1990000613-A1 PROCESS FOR PREPARING OPTICALLY ACTIVE 2-HYDROXY-4-PHENYL-3-BUTENOIC ACID DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1990-01-25 WO disclosed