SCHEMBL8334285

SCHEMBL8334285

COC(=O)C(O)C(Cc1ccccc1)N1C(=O)c2ccccc2C1=O

nearest known ligand 0.54

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
▸ ALDH1A1 P00352 4/20 0.54
▸ GAA P10253 2/20 0.54
▸ TDP1 Q9NUW8 1/20 0.52
▸ POLB P06746 3/20 0.51
▸ L3MBTL1 Q9Y468 2/20 0.51
▸ HSD11B1 P28845 1/20 0.50
▸ KMT2A Q03164 3/20 0.46
▸ MEN1 O00255 2/20 0.46
▸ LTA4H P09960 1/20 0.46
▸ PKM P14618 1/20 0.45
▸ SMN1; SMN2 Q16637 1/20 0.45
▸ MAPT P10636 1/20 0.43

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
SCHEMBL8474228 0.88 ALDH1A1 (0.52) ALDH1A1GAATDP1POLBL3MBTL1
SCHEMBL8475112 0.87 TDP1 (0.54) ALDH1A1GAATDP1POLBL3MBTL1
SCHEMBL8474009 0.87 TDP1 (0.54) ALDH1A1GAATDP1POLBL3MBTL1
SCHEMBL8475810 0.84 ALDH1A1 (0.65) ALDH1A1GAATDP1POLBL3MBTL1
SCHEMBL8471464 0.84 ALDH1A1 (0.65) ALDH1A1GAATDP1POLBL3MBTL1
SCHEMBL8799115 0.82 TDP1 (0.54) ALDH1A1GAATDP1POLBL3MBTL1
SCHEMBL8799111 0.82 TDP1 (0.54) ALDH1A1GAATDP1POLBL3MBTL1
SCHEMBL19597540 0.82 ALDH1A1 (0.70) ALDH1A1GAATDP1POLBL3MBTL1
SCHEMBL19597541 0.82 ALDH1A1 (0.70) ALDH1A1GAATDP1POLBL3MBTL1
SCHEMBL14866021 0.77 TDP1 (0.58) ALDH1A1GAATDP1POLBL3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5994555-A (4S,5S)-4-BENZYL-2-OXO-OXAZOLIDINE-5-CARBOXYLIC ACID FROM PHENYLALANINE AND PHTHALIC ANHYDRIDE F. HOFFMAN-LAROCHE AG (CH) 1999-11-30 — — US disclosed
US-5919949-A α-hydroxy acid esters useful as intermediates in the production of β-amino alcohols HOFFMANN-LA ROCHE INC. (US) 1999-07-06 — — US disclosed
US-5859248-A Process for the production of a β-amino alcohol F. HOFFMAN-LA ROCHE AG (CH) 1999-01-12 — — US disclosed
US-5578730-A Process for producing β-aminoalcohols compounds HOFFMANN-LA ROCHE INC. (US) 1996-11-26 — — US disclosed
US-5516930-A Intermediates in the production beta aminoalcohols HOFFMANN-LA ROCHE INC. (US) 1996-05-14 — — US disclosed
US-5512682-A Nitrile compounds useful as intermediates in the production of beta amino alcohols HOFFMANN-LA ROCHE INC. (US) 1996-04-30 — — US disclosed
US-5512688-A METHANESULFONIC ACID(4S,-5S)-4-BENZYL-2-OXO-OXAZOLIDINE -5YLMETHYL ESTER; CHEMICAL INTERMEDIATE FOR FORMING CERTAIN AMINO ACID DERIVATIVES USEFUL AS PHROPHYLAXIS OR TRETAMENT OF RITRO-VIRAL INFECTIONS HOFFMANN-LA ROCHE INC. (US) 1996-04-30 — — US disclosed
US-5495025-A Isoindole compounds which are useful as intermediates HOFFMANN-LA ROCHE INC. (US) 1996-02-27 — — US disclosed
US-5455353-A 4-(benzyl-2-oxo-oxazolidin-5 ylmethyl)N tertbutyl-decahydroisoquinoline-3-carboxamides HOFFMANN-LA ROCHE INC. (US) 1995-10-03 — — US disclosed
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