SCHEMBL8396789

SCHEMBL8396789

O=C(O)NCCNC(=O)c1ccc(Cl)cn1

nearest known ligand 0.76

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
▸ MAOB P27338 2/20 0.71
▸ EGLN1 Q9GZT9 2/20 0.54
▸ NPC1 O15118 1/20 0.52
▸ RAB9A P51151 1/20 0.52
▸ MAOA P21397 1/20 0.52
▸ DGAT1 O75907 1/20 0.52
▸ HIF1A Q16665 3/20 0.48
▸ KMT2A Q03164 1/20 0.46

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
SCHEMBL8973342 0.93 MAOB (0.81) MAOBEGLN1NPC1RAB9AMAOA
SCHEMBL19835607 0.86 MAOB (0.76) MAOBEGLN1NPC1RAB9AMAOA
SCHEMBL16887934 0.85 MAOB (0.69) MAOBEGLN1NPC1RAB9AMAOA
SCHEMBL29262574 0.83 MAOB (0.71) MAOBEGLN1NPC1RAB9AMAOA
Lazabemide SCHEMBL20769840 0.83 MAOB (1.00) MAOBEGLN1NPC1RAB9AMAOA
Lazabemide SCHEMBL29710899 0.83 MAOB (1.00) MAOBEGLN1NPC1RAB9AMAOA
SCHEMBL14329887 0.83 MAOB (0.71) MAOBEGLN1NPC1RAB9AMAOA
Lazabemide SCHEMBL121998 0.83 MAOB (1.00) MAOBEGLN1NPC1RAB9AMAOA
SCHEMBL29459609 0.83 MAOB (0.71) MAOBEGLN1NPC1RAB9AMAOA
Lazabemide SCHEMBL1230476 0.82 MAOB (0.97) MAOBEGLN1NPC1RAB9AMAOA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2012079583-A1 SYSTEM PROVIDING CONTROLLED DELIVERY OF GASEOUS CO FOR CARBONYLATION REACTIONS AARHUS UNIVERSITET (DK) 2012-06-21 — — WO disclosed
EP-0611774-B1 Production of amides and peptides without racemization in the presence of catalytic amounts of a N-hydroxy-compound HOFFMANN LA ROCHE (CH) 1999-05-26 — — EP disclosed
EP-0582825-B1 Amidation of pyridines HOFFMANN LA ROCHE (CH) 1999-04-21 — — EP disclosed
CN-1035873-C Preparation of amides and peptides HOFFMANN LA ROCHE (CH) 1997-09-17 — — CN disclosed
US-5536816-A Process for producing amides using catalytic amounts of an N-hydroxy compound HOFFMANN-LA ROCHE INC. (US) 1996-07-16 — — US disclosed
US-5534635-A Process for preparing pyridine-2-carboxamides HOFFMANN-LA ROCHE INC. (US) 1996-07-09 — — US disclosed
CN-1111237-A Preparation of amides and peptides HOFFMANN LA ROCHE (CH) 1995-11-08 — — CN disclosed
US-5380861-A Process for preparing pyridine 2-carboxamides HOFFMANN-LA ROCHE INC. (US) 1995-01-10 — — US disclosed
EP-0611774-A1 Production of amides and peptides without racemization in the presence of catalytic amounts of a N-hydroxy-compound F. HOFFMANN-LA ROCHE AG (CH) 1994-08-24 — — EP disclosed
EP-0582825-A1 Amidation of pyridines F. HOFFMANN-LA ROCHE AG (CH) 1994-02-16 — — EP disclosed
EP-0385210-A2 Amidation of pyridines F. HOFFMANN-LA ROCHE AG (CH) 1990-09-05 — — EP disclosed
US-4764522-A ANTIDEPRESSANT, ANTIPARKINSON DISEASE HOFFMANN-LA ROCHE INC. (US) 1988-08-16 — — US disclosed
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