SCHEMBL7840770

SCHEMBL7840770

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

nearest known ligand 0.77

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ALDH1A1 P00352 5/20 0.77
▸ GAA P10253 1/20 0.77
▸ POLB P06746 4/20 0.72
▸ L3MBTL1 Q9Y468 2/20 0.72
▸ AADAT Q8N5Z0 1/20 0.64
▸ SMN1; SMN2 Q16637 2/20 0.62
▸ PKM P14618 1/20 0.62
▸ TSHR P16473 1/20 0.58
▸ KMT2A Q03164 4/20 0.58
▸ MEN1 O00255 2/20 0.58
▸ LMNA P02545 1/20 0.58
▸ MAPT P10636 1/20 0.58
▸ TDP1 Q9NUW8 1/20 0.57
▸ HSD11B1 P28845 1/20 0.56
▸ HTT P42858 1/20 0.55
▸ RECQL P46063 1/20 0.55
▸ NPSR1 Q6W5P4 1/20 0.55
▸ KDM4E B2RXH2 1/20 0.53
▸ TP53 P04637 1/20 0.53
▸ GLA P06280 1/20 0.53

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
SCHEMBL29459253 1.00 ALDH1A1 (0.77) ALDH1A1GAAPOLBL3MBTL1AADAT
SCHEMBL7270563 1.00 ALDH1A1 (0.77) ALDH1A1GAAPOLBL3MBTL1AADAT
SCHEMBL29459410 1.00 ALDH1A1 (0.77) ALDH1A1GAAPOLBL3MBTL1AADAT
SCHEMBL28661085 1.00 ALDH1A1 (0.77) ALDH1A1GAAPOLBL3MBTL1AADAT
SCHEMBL4861809 0.87 ALDH1A1 (1.00) ALDH1A1GAAPOLBL3MBTL1AADAT
SCHEMBL392680 0.87 ALDH1A1 (1.00) ALDH1A1GAAPOLBL3MBTL1AADAT
SCHEMBL30216480 0.87 ALDH1A1 (1.00) ALDH1A1GAAPOLBL3MBTL1AADAT
SCHEMBL478614 0.87 ALDH1A1 (1.00) ALDH1A1GAAPOLBL3MBTL1AADAT
SCHEMBL30632385 0.86 AADAT (0.60) ALDH1A1GAAPOLBL3MBTL1AADAT
Hydrochloric Acid SCHEMBL7840775 0.85 ALDH1A1 (0.97) ALDH1A1GAAPOLBL3MBTL1AADAT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0778827-B1 PROCESS FOR PRODUCING A BETA-AMINO ALCOHOL DEGUSSA (DE) 2001-12-12 — — EP claimed
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 claimed
US-5859248-A Process for the production of a β-amino alcohol F. HOFFMAN-LA ROCHE AG (CH) 1999-01-12 — — US claimed
US-5321166-A Method for the production of aldehydes HOFFMANN-LA ROCHE INC. (US) 1994-06-14 — — US claimed
EP-3924349-A2 AMINO ACID DERIVATIVES FOR THE TREATMENT OF INFLAMMATORY DISEASES The Roskamp Institute (US) 2021-12-22 — — EP disclosed
CN-113614074-A Amino acid derivatives for the treatment of inflammatory diseases 罗斯坎普研究所 2021-11-05 — — CN disclosed
WO-2020053373-A1 NOVEL TRF1 MODULATORS AND ANALOGUES THEREOF Fundación Del Sector Público Estatal Centro Nacional De Investigaciones Oncológicas Carlos III (F.S.P. CNIO) (ES) 2020-03-19 — — WO disclosed
WO-2013006792-A1 ANTIVIRAL COMPOUNDS PHARMARESOURCES (SHANGHAI) CO., LTD. (CN) 2013-01-10 — — WO disclosed
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-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-5495025-A Isoindole compounds which are useful as intermediates HOFFMANN-LA ROCHE INC. (US) 1996-02-27 — — US disclosed
US-5488115-A Alcohols HOFFMANN-LA ROCHE INC. (US) 1996-01-30 — — 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
US-5451678-A Intermediates for viricides HOFFMANN-LA ROCHE INC. (US) 1995-09-19 — — US disclosed
CN-1104641-A Process for preparing N-tert-butylamides HOFFMANN LA ROCHE (CH) 1995-07-05 — — CN disclosed
US-5321166-A Method for the production of aldehydes HOFFMANN-LA ROCHE INC. (US) 1994-06-14 — — US disclosed
US-4147700-A HYDRAZINOLYZING A PHTHALYL DERIVATIVE SHIONOGI & CO., LTD. (JP) 1979-04-03 — — US disclosed
US-4141901-A REDUCING AN AZIDO DERIVATIVE SHIONOGI & CO., LTD. (JP) 1979-02-27 — — US disclosed
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