SCHEMBL4597353

SCHEMBL4597353

O=C(O)[C@H](CC1CC1)N1C(=O)NC2(CCCCC2)C1=O

nearest known ligand 0.46

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 2/20 0.41
ALDH1A1 P00352 2/20 0.41
LMNA P02545 1/20 0.41
KMT2A Q03164 2/20 0.41
RAB9A P51151 3/20 0.39
MAPT P10636 1/20 0.39
L3MBTL1 Q9Y468 1/20 0.38
FPR2 P25090 2/20 0.38
NPC1 O15118 1/20 0.38
AKR1B1 P15121 1/20 0.38
POLB P06746 1/20 0.38

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
SCHEMBL4597158 1.00 SMN1; SMN2 (0.41) SMN1; SMN2ALDH1A1LMNAKMT2ARAB9A
SCHEMBL4597700 0.99 SMN1; SMN2 (0.40) SMN1; SMN2ALDH1A1LMNAKMT2ARAB9A
SCHEMBL4595627 0.99 SMN1; SMN2 (0.40) SMN1; SMN2ALDH1A1LMNAKMT2ARAB9A
SCHEMBL1107305 0.82 L3MBTL1 (0.40) SMN1; SMN2ALDH1A1LMNAKMT2ARAB9A
SCHEMBL4595755 0.82 KMT2A (0.41) LMNAKMT2AL3MBTL1POLB
SCHEMBL4595752 0.82 KMT2A (0.41) LMNAKMT2AL3MBTL1POLB
SCHEMBL4596828 0.82 KMT2A (0.41) LMNAKMT2AL3MBTL1POLB
SCHEMBL4595759 0.80 L3MBTL1 (0.44) SMN1; SMN2KMT2ARAB9AMAPTL3MBTL1
SCHEMBL4595768 0.80 L3MBTL1 (0.44) SMN1; SMN2KMT2ARAB9AMAPTL3MBTL1
SCHEMBL4597654 0.78 SMN1; SMN2 (0.43) SMN1; SMN2KMT2ARAB9AMAPTL3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1506177-B1 PROCESS FOR THE PREPARATION OF THE ENANTIOMERIC FORMS OF 2-SUBSTITUTED 2-(2,5-DIOXOIMIDAZOLIDIN-1-YL)-ACETIC ACID DERIVATIVES SANOFI AVENTIS DEUTSCHLAND (DE) 2008-01-16 EP disclosed
US-6908752-B2 Process for the preparation of the enant iomeric forms of 2-substituted 2- (2, 5-dioxoimidazolidin-1yl) -acetic acid derivatives AVENTIS PHARMA DEUTSCHLAND GMBH (DE) 2005-06-21 US disclosed
EP-1183241-B1 SPIROIMIDAZOLIDINE DERIVATIVES, THEIR PREPARATION, THEIR USE AND PHARMACEUTICAL PREPARATIONS COMPRISING THEM AVENTIS PHARMA GMBH (DE) 2003-09-17 EP disclosed
US-20030054507-A1 Process for the preparation of the enant iomeric forms of 2-substituted 2- (2, 5-dioxoimidazolidin-1-yl) -acetic acid derivatives SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2003-03-20 US disclosed
US-6399643-B1 ANTIINFLAMMATORY AGENTS; ANTIARTHRITIC AGENTS AVENTIS PHARMA DEUTSCHLAND GMBH (DE) 2002-06-04 US disclosed
EP-1183241-A1 SPIROIMIDAZOLIDINE DERIVATIVES, THEIR PREPARATION, THEIR USE AND PHARMACEUTICAL PREPARATIONS COMPRISING THEM Aventis Pharma Deutschland GmbH (DE) 2002-03-06 EP disclosed
WO-2000069831-A1 SPIROIMIDAZOLIDINE DERIVATIVES, THEIR PREPARATION, THEIR USE AND PHARMACEUTICAL PREPARATIONS COMPRISING THEM AVENTIS PHARMA DEUTSCHLAND GMBH (DE) 2000-11-23 WO disclosed