SCHEMBL6135511

SCHEMBL6135511

C[C@@]1(c2ccc(Br)cc2)NC(=O)N(CC(=O)O)C1=O

nearest known ligand 0.64

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 4/20 0.64
L3MBTL1 Q9Y468 1/20 0.53
HTT P42858 1/20 0.52
POLB P06746 1/20 0.50
FPR2 P25090 1/20 0.50
MEN1 O00255 1/20 0.49

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
SCHEMBL6270655 1.00 KMT2A (0.64) KMT2AL3MBTL1HTTPOLBFPR2
SCHEMBL8054430 1.00 KMT2A (0.64) KMT2AL3MBTL1HTTPOLBFPR2
SCHEMBL17622984 0.87 KMT2A (0.73) KMT2AHTTPOLBMEN1
SCHEMBL7982747 0.86 KMT2A (0.64) KMT2AL3MBTL1HTTPOLBMEN1
SCHEMBL7982744 0.86 KMT2A (0.64) KMT2AL3MBTL1HTTPOLBMEN1
SCHEMBL7982748 0.86 KMT2A (0.64) KMT2AL3MBTL1HTTPOLBMEN1
SCHEMBL7031885 0.83 KMT2A (0.62) KMT2AL3MBTL1HTTMEN1
SCHEMBL8476428 0.83 KMT2A (0.62) KMT2AL3MBTL1HTTMEN1
SCHEMBL7034455 0.83 KMT2A (0.62) KMT2AL3MBTL1HTTMEN1
SCHEMBL3896913 0.82 KCNH2 (0.64) KMT2A

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
US-6018053-A Process for the preparation of chiral, nonracemic (4-aryl-2,5-dioxoimidazolidin-1-yl) acetic acids HOECHST AKTIENGESELLSCHAFT (DE) 2000-01-25 US claimed
WO-2015037243-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE HYDANTOIN COMPOUND 興和株式会社 (JP) 2015-03-19 WO disclosed
EP-0816343-B1 Process for the preparation of chiral, non-racemic (4-aryl-2,5-dioxoimidazolidin-1-yl)-acetic acids SANOFI AVENTIS DEUTSCHLAND (DE) 2005-12-14 EP disclosed
EP-0811616-B1 Salts of 3-(2-(4-(4-(Amino-imino-methyl)-phenyl)-4-methyl-2,5-dioxo-imidazolidin-1-yl)-acetylamino)-3-phenyl-propionic acid ethylester AVENTIS PHARMA GMBH (DE) 2005-05-04 EP disclosed
EP-0823898-B1 HYDANTOINE DERIVATIVES AS INTERMEDIATE PRODUCTS FOR ACTIVE PHARMACEUTICAL AGENTS HOECHST AG (DE) 2003-02-26 EP disclosed
US-6294562-B1 AMIDINO COMPOUNDS WITH AMIDO ESTERS CARDIOVASCULAR SYSTEM, DISEASES OF THE CORONARY VASCULAR SYSTEM OR THE CEREBROVASCULAR SYSTEM, OR PERIPHERAL ARTERIAL VASCULAR DISEASE HOECHST AKTIENGESELLSCHAFT (DE) 2001-09-25 US disclosed
US-6018053-A Process for the preparation of chiral, nonracemic (4-aryl-2,5-dioxoimidazolidin-1-yl) acetic acids HOECHST AKTIENGESELLSCHAFT (DE) 2000-01-25 US disclosed
US-5939556-A Hydantoin compounds, salts thereof, processes for their preparation, and processes for preparing pharmaceutically active compounds comprising them HOECHST AKTIENGESELLSCHAFT (DE) 1999-08-17 US disclosed
EP-0823898-A1 HYDANTOINE DERIVATIVES AS INTERMEDIATE PRODUCTS FOR ACTIVE PHARMACEUTICAL AGENTS HOECHST AKTIENGESELLSCHAFT (DE) 1998-02-18 EP disclosed
EP-0816343-A1 Process for the preparation of chiral, non-racemic (4-aryl-2,5-dioxoimidazolin-1-yl)-acetic acids HOECHST AKTIENGESELLSCHAFT (DE) 1998-01-07 EP disclosed
EP-0811616-A1 Salts of 3-(2-(4-(4-(Amino-imino-methyl)-phenyl)-4-methyl-2,5-dioxo-imidazolidin-1-yl)-acetylamino)-3-phenyl-propionic acid ethylester HOECHST AKTIENGESELLSCHAFT (DE) 1997-12-10 EP disclosed
WO-1996033976-A1 HYDANTOINE DERIVATIVES AS INTERMEDIATE PRODUCTS FOR ACTIVE PHARMACEUTICAL AGENTS HOECHST AKTIENGESELLSCHAFT (DE) 1996-10-31 WO disclosed