SCHEMBL7906110

SCHEMBL7906110

NC(=O)C(CCO)c1ccccc1

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
EPHX1 P07099 1/20 0.61
CYP2C19 P33261 3/20 0.43
CYP2D6 P10635 2/20 0.43
SMN1; SMN2 Q16637 2/20 0.43
CYP1A2 P05177 1/20 0.43
PKM P14618 1/20 0.43
NPSR1 Q6W5P4 1/20 0.43
TRPA1 O75762 1/20 0.43
ALOX5 P09917 1/20 0.43
SLC6A3 Q01959 3/20 0.42
DRD3 P35462 2/20 0.42
LMNA P02545 1/20 0.42
ADORA3 P0DMS8 1/20 0.42
EDNRB P24530 1/20 0.42
MAPK1 P28482 1/20 0.42
MC4R P32245 1/20 0.42
MC3R P41968 1/20 0.42
DRD2 P14416 1/20 0.42
BCAT2 O15382 1/20 0.42
GABBR2 O75899 1/20 0.40

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
SCHEMBL7906106 1.00 EPHX1 (0.61) EPHX1CYP2C19CYP2D6SMN1; SMN2CYP1A2
SCHEMBL7909103 1.00 EPHX1 (0.61) EPHX1CYP2C19CYP2D6SMN1; SMN2CYP1A2
SCHEMBL19205724 0.89 EPHX1 (0.58) EPHX1CYP2C19CYP2D6SMN1; SMN2CYP1A2
SCHEMBL27691659 0.84 EPHX1 (0.61) EPHX1CYP2C19CYP2D6SMN1; SMN2CYP1A2
SCHEMBL819393 0.83 CYP2C19 (0.55) EPHX1CYP2C19CYP2D6SMN1; SMN2TRPA1
SCHEMBL6359024 0.83 EPHX1 (0.66) EPHX1CYP2C19CYP2D6SMN1; SMN2CYP1A2
SCHEMBL23977 0.83 EPHX1 (0.66) EPHX1CYP2C19CYP2D6SMN1; SMN2CYP1A2
SCHEMBL16881947 0.83 EPHX1 (0.66) EPHX1CYP2C19CYP2D6SMN1; SMN2CYP1A2
SCHEMBL7899585 0.83 CYP2C19 (0.55) EPHX1CYP2C19CYP2D6SMN1; SMN2TRPA1
SCHEMBL27689551 0.83 EPHX1 (0.66) EPHX1CYP2C19CYP2D6SMN1; SMN2CYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118240193-A Preparation method of recyclable N-acylated polyaminoester 苏州大学 2024-06-25 CN claimed
CN-118240193-A Preparation method of recyclable N-acylated polyaminoester 苏州大学 2024-06-25 CN disclosed
US-6207862-B1 PRECURSORS ARE CHIRAL 4-HYDROXYCARBOXAMIDES, 4-HYDROXYHYDROXAMIC ACIDS, OR 4-HYDROXYHYDRAZIDES PRODUCED FROM GAMMA-LACTONES, WHICH IN TURN ARE DERIVED FROM 1,4-DIOLS BY STEREOSELECTIVE OXIDATION, BIOCATALYTICS, INC. 2001-03-27 US disclosed
WO-1999032649-A1 METHODS AND PRECURSORS FOR THE PRODUCTION OF CHIRAL 1,3-AMINOALCOHOLS BIOCATALYTICS, INC. (US) 1999-07-01 WO disclosed
US-5916786-A Method for the production of chiral 1,3-aminoalcohols BIOCATALYTICS, INC. (US) 1999-06-29 US disclosed
CN-88102419-A ASSAY FOR ANTI-PRE-S ANTIBODY 1988-11-09 CN disclosed