SCHEMBL233440

SCHEMBL233440

O=C(O)[C@H](O)CCc1ccccc1

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CNR2 P34972 1/20 0.50
TSHR P16473 1/20 0.50
KEAP1 Q14145 1/20 0.50
DPP4 P27487 1/20 0.49
MMP2 P08253 1/20 0.49
MMP9 P14780 1/20 0.49
MMP12 P39900 1/20 0.49
MMP13 P45452 1/20 0.49
MMP14 P50281 1/20 0.49
ANPEP P15144 2/20 0.48
ERAP1 Q9NZ08 2/20 0.48
ERAP2 Q6P179 1/20 0.48
CYP1A2 P05177 1/20 0.48
MME P08473 1/20 0.47
PPARG P37231 1/20 0.47
PPARA Q07869 1/20 0.47
MEN1 O00255 1/20 0.47
HTT P42858 1/20 0.47
KMT2A Q03164 1/20 0.47
SMN1; SMN2 Q16637 1/20 0.47

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
SCHEMBL360781 1.00 CNR2 (0.50) CNR2TSHRKEAP1DPP4MMP2
SCHEMBL233441 1.00 CNR2 (0.50) CNR2TSHRKEAP1DPP4MMP2
Ammonia Solution, Strong SCHEMBL28234808 0.98 CNR2 (0.49) CNR2TSHRKEAP1DPP4MMP2
SCHEMBL27859676 0.98 CNR2 (0.49) CNR2TSHRKEAP1DPP4MMP2
SCHEMBL27859674 0.98 CNR2 (0.49) CNR2TSHRKEAP1DPP4MMP2
Nitrous Acid SCHEMBL27625772 0.92 MME (0.46) CNR2TSHRKEAP1DPP4MMP2
SCHEMBL5962191 0.89 S1PR2 (0.54) CNR2TSHRMMEMEN1HTT
Trifluoroacetic Acid SCHEMBL8142317 0.89 CPA1 (0.49) CNR2TSHRKEAP1CYP1A2MME
SCHEMBL7761730 0.89 S1PR2 (0.54) CNR2TSHRMMEMEN1HTT
SCHEMBL8688130 0.89 S1PR2 (0.54) CNR2TSHRMMEMEN1HTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4661890-A1 PTP1B/TC-PTP DUAL INHIBITORS AND PROTEIN DEGRADERS Purdue Research Foundation (US) 2025-12-17 EP claimed
CN-119177259-B Method for synthesizing optically active (R) -2-hydroxy-4-phenylbutyric acid by utilizing multienzyme catalysis in micro-flow field 南京工业大学 2025-03-14 CN claimed
CN-119177259-A Method for synthesizing optically active (R) -2-hydroxy-4-phenylbutyric acid by utilizing multienzyme catalysis in micro-flow field 南京工业大学 2024-12-24 CN claimed
WO-2024167565-A1 PTP1B/TC-PTP DUAL INHIBITORS AND PROTEIN DEGRADERS PURDUE RESEARCH FOUNDATION (US) 2024-08-15 WO claimed
CN-115851641-A Fusion enzyme for efficiently producing (R) -2-hydroxy-4-phenylbutyric ethyl butyrate and application thereof 浙江工业大学 2023-03-28 CN claimed
CN-115820622-A Double-enzyme self-assembly compound and application of compound in synthesizing (R) -2-hydroxy-4-phenylbutyrate 浙江工业大学 2023-03-21 CN claimed
EP-3543225-B1 METHOD FOR PREPARING LISINOPRIL INTERMEDIATE ZHEJIANG HUAHAI PHARM CO LTD (CN) 2023-01-04 EP claimed
CN-110903177-B Method for preparing levo muscone 万华化学集团股份有限公司 2022-07-12 CN claimed
CN-111218441-B Magnetic immobilized yeast cell and application thereof in preparation of (R) -2-hydroxy-4-phenylbutyrate ethyl ester 浙江工业大学 2022-03-18 CN claimed
CN-106866402-B Preparation method of (R) -2-hydroxy-4-phenylbutyric acid 泰州市产品质量监督检验所 2021-08-31 CN claimed
EP-0394448-B1 PROCESS FOR PREPARING OPTICALLY ACTIVE 2-HYDROXY-4-PHENYLBUTYRIC ACIDS DAICEL CHEM (JP) 1996-05-01 EP claimed
EP-0371408-B1 Biocatalysts and process for their preparation CIBA GEIGY AG (CH) 1994-06-22 EP claimed
EP-0379288-B1 Process and intermediates for isopropyl 3S-amino-2R-hydroxyalkanoates PFIZER (US) 1993-12-22 EP claimed
EP-0347374-B1 Process for the preparation of hydroxy acids CIBA GEIGY AG (CH) 1993-12-15 EP claimed
US-5256552-A Reduction of 2-oxo-4-phenylbutyric acid with microorganism DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1993-10-26 US claimed
EP-0280285-B1 PROCESS FOR MAKING AND ISOLATING (R)-2-HYDROXY 4-PHENYLBUTYRIC ACID AND ESTERS MERRELL DOW PHARMACEUTICALS INC. (US) 1992-09-02 EP claimed
US-5098841-A Reduction of 2-oxo-4-phenylbutyric acid with the enzyme D lactate dehydrogenase from staphylococcus or from bovine heart CIBA-GEIGY CORPORATION (US) 1992-03-24 US claimed
EP-0394448-A1 PROCESS FOR PREPARING OPTICALLY ACTIVE 2-HYDROXY-4-PHENYLBUTYRIC ACIDS DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 1990-10-31 EP claimed
US-4837354-A Process for making and isolating (R)-2-hydroxy-4-phenylbutyric acid and esters MERRELL DOW PHARMACEUTICALS INC. (US) 1989-06-06 US claimed
EP-0280285-A2 Process for making and isolating (R)-2-hydroxy 4-phenylbutyric acid and esters MERRELL DOW PHARMACEUTICALS INC. (US) 1988-08-31 EP claimed