SCHEMBL8552133

SCHEMBL8552133

O=C1c2ccccc2C(=O)N1[C@@H](Cc1ccccc1)[C@H](O)CO

nearest known ligand 0.56

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
▸ ALDH1A1 P00352 4/20 0.56
▸ GAA P10253 1/20 0.56
▸ TDP1 Q9NUW8 1/20 0.55
▸ POLB P06746 3/20 0.54
▸ L3MBTL1 Q9Y468 2/20 0.54
▸ SMN1; SMN2 Q16637 2/20 0.47
▸ PKM P14618 1/20 0.47
▸ AADAT Q8N5Z0 1/20 0.44
▸ KMT2A Q03164 3/20 0.44
▸ MEN1 O00255 2/20 0.44
▸ LMNA P02545 1/20 0.44
▸ MAPT P10636 1/20 0.44
▸ TSHR P16473 1/20 0.44
▸ HSD11B1 P28845 1/20 0.43
▸ HTT P42858 1/20 0.42
▸ RECQL P46063 1/20 0.42
▸ NPSR1 Q6W5P4 1/20 0.42

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
SCHEMBL8552131 1.00 ALDH1A1 (0.56) ALDH1A1GAATDP1POLBL3MBTL1
SCHEMBL8554995 0.86 ALDH1A1 (0.56) ALDH1A1GAATDP1POLBL3MBTL1
SCHEMBL12646714 0.86 ALDH1A1 (0.55) ALDH1A1GAATDP1POLBL3MBTL1
SCHEMBL8554996 0.86 ALDH1A1 (0.56) ALDH1A1GAATDP1POLBL3MBTL1
SCHEMBL14866021 0.86 TDP1 (0.58) ALDH1A1GAATDP1POLBL3MBTL1
SCHEMBL10431147 0.82 TDP1 (0.54) ALDH1A1GAATDP1POLBL3MBTL1
SCHEMBL10554493 0.82 TDP1 (0.54) ALDH1A1GAATDP1POLBL3MBTL1
SCHEMBL10431148 0.82 TDP1 (0.54) ALDH1A1GAATDP1POLBL3MBTL1
SCHEMBL8798595 0.81 ALDH1A1 (0.50) ALDH1A1GAATDP1POLBL3MBTL1
Acetic Acid SCHEMBL8860077 0.81 ALDH1A1 (0.55) 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 10 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0738724-A2 Process for the preparation of an N-terbutylamide derivative F. HOFFMANN-LA ROCHE AG (CH) 1996-10-23 — — EP claimed
US-5502210-A 1H-isoindole-1,3-dione compounds HOFFMANN-LA ROCHE INC. (US) 1996-03-26 — — US claimed
EP-0634410-A1 Process for the preparation of a N-tert.butylisoquinolin-3-carboxamide derivative and intermediate compounds of these process F. HOFFMANN-LA ROCHE AG (CH) 1995-01-18 — — EP claimed
EP-0738724-B1 Process for the preparation of an N-terbutylamide derivative HOFFMANN LA ROCHE (CH) 1998-11-04 — — EP disclosed
US-5698698-A Process for preparation of N-tert.butyl-decahydro-2- 2(R)-hydroxy-4-phenyl-3(S)-phthalimidobutyl!-(4aS,8aS)-isoquinoline-3(S)-carboxamide HOFFMANN-LA ROCHE INC. (US) 1997-12-16 — — US disclosed
US-5641886-A Process for preparation of N-tert.butyl-decahydro-2-[2(R)-hydroxy-4-phenyl-3(S)-phthalimidobutyl]-(4AS,8AS)-isoquinoline-3(S)-carboxamide HOFFMANN-LA ROCHE INC. (US) 1997-06-24 — — US disclosed
EP-0634410-B1 Process for the preparation of a N-tert.butylisoquinolin-3-carboxamide derivative and intermediate compounds of these process HOFFMANN LA ROCHE (CH) 1997-02-26 — — EP disclosed
EP-0738724-A2 Process for the preparation of an N-terbutylamide derivative F. HOFFMANN-LA ROCHE AG (CH) 1996-10-23 — — EP disclosed
US-5502210-A 1H-isoindole-1,3-dione compounds HOFFMANN-LA ROCHE INC. (US) 1996-03-26 — — US disclosed
EP-0634410-A1 Process for the preparation of a N-tert.butylisoquinolin-3-carboxamide derivative and intermediate compounds of these process F. HOFFMANN-LA ROCHE AG (CH) 1995-01-18 — — EP disclosed
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