SCHEMBL8473232

SCHEMBL8473232

CC(=O)O[C@@H](C#N)[C@H](Cc1ccccc1)N1C(=O)c2ccccc2C1=O

nearest known ligand 0.51

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
▸ TDP1 Q9NUW8 1/20 0.51
▸ ALDH1A1 P00352 5/20 0.49
▸ GAA P10253 2/20 0.49
▸ POLB P06746 3/20 0.48
▸ KMT2A Q03164 2/20 0.48
▸ L3MBTL1 Q9Y468 2/20 0.47
▸ HSD11B1 P28845 1/20 0.44
▸ SMN1; SMN2 Q16637 2/20 0.42
▸ PKM P14618 1/20 0.42
▸ MAPT P10636 2/20 0.40
▸ MEN1 O00255 1/20 0.40
▸ LMNA P02545 1/20 0.40
▸ AADAT Q8N5Z0 1/20 0.40
▸ TSHR P16473 1/20 0.39

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
SCHEMBL9089272 1.00 TDP1 (0.51) TDP1ALDH1A1GAAPOLBKMT2A
SCHEMBL9088479 0.85 ALDH1A1 (0.46) TDP1ALDH1A1GAAPOLBKMT2A
SCHEMBL7841102 0.85 ALDH1A1 (0.46) TDP1ALDH1A1GAAPOLBKMT2A
SCHEMBL8860083 0.79 ALDH1A1 (0.51) TDP1ALDH1A1GAAPOLBKMT2A
SCHEMBL8860080 0.79 ALDH1A1 (0.51) TDP1ALDH1A1GAAPOLBKMT2A
SCHEMBL7837330 0.79 TDP1 (0.58) TDP1ALDH1A1GAAPOLBKMT2A
SCHEMBL8556604 0.79 TDP1 (0.58) TDP1ALDH1A1GAAPOLBKMT2A
SCHEMBL7837333 0.79 TDP1 (0.58) TDP1ALDH1A1GAAPOLBKMT2A
SCHEMBL7848776 0.79 TDP1 (0.58) TDP1ALDH1A1GAAPOLBKMT2A
SCHEMBL9011551 0.78 MEN1 (0.46) POLBKMT2ASMN1; SMN2MAPTMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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-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
EP-0635493-A2 Process for the preparationof a beta-aminoalcohol F. HOFFMANN-LA ROCHE AG (CH) 1995-01-25 — — EP disclosed
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