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SCHEMBL2937219

SCHEMBL2937219

N#CCOS(=O)(=O)[O-].N#CCOS(=O)(=O)[O-].N#CCOS(=O)(=O)[O-].N#CCOS(=O)(=O)[O-].N#CCOS(=O)(=O)[O-].N#CCOS(=O)(=O)[O-].N#CCOS(=O)(=O)[O-].N#CCOS(=O)(=O)[O-].N#CCOS(=O)(=O)[O-].N#CCOS(=O)(=O)[O-].N#CCOS(=O)(=O)[O-].N#CCOS(=O)(=O)[O-].N#CCOS(=O)(=O)[O-].N#CCOS(=O)(=O)[O-].N#CCOS(=O)(=O)[O-].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[Cu+2]

nearest known ligand 0.32

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
▸ RECQL P46063 2/20 0.32
▸ GLA P06280 1/20 0.32
▸ HPGD P15428 1/20 0.32
▸ TSHR P16473 1/20 0.32
▸ MAPK1 P28482 1/20 0.32
▸ EPHX2 P34913 1/20 0.32
▸ BLM P54132 1/20 0.32

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
SCHEMBL2769491 1.00 RECQL (0.32) RECQLGLAHPGDTSHRMAPK1
Tetrabuthylammonium SCHEMBL7880331 0.77 RECQL (0.46) RECQLGLAHPGDTSHRMAPK1
Tetrabuthylammonium SCHEMBL3255325 0.75 RECQL (0.44) RECQLGLAHPGDTSHRMAPK1
Lithium Ion SCHEMBL17456575 0.72 RECQL (0.34) RECQLGLAHPGDTSHRMAPK1
Lithium Ion SCHEMBL17456510 0.70 RECQL (0.39) RECQLGLAHPGDTSHRMAPK1
SCHEMBL17456476 0.68 CA2 (0.35) RECQLGLAHPGDTSHRMAPK1
Lithium Ion SCHEMBL17456420 0.68 — —
SCHEMBL17456413 0.68 — —
Ammonia Solution, Strong SCHEMBL5462398 0.68 — —
Lithium Ion SCHEMBL22189212 0.65 ADAM17 (0.36) RECQLGLAHPGDTSHRMAPK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1712627-B1 POLYPEPTIDE HAVING AMIDASE ACTIVITY AND GENE THEREOF KANEKA CORP (JP) 2010-09-22 — — EP disclosed
US-7655450-B2 Polypeptide having amidase activity and gene thereof KANEKA CORPORATION (JP) 2010-02-02 — — US disclosed
US-20090136994-A1 Polypeptide having amidase activity and gene thereof KANEKA CORPORATION (JP) 2009-05-28 — — US disclosed
EP-1712627-A1 POLYPEPTIDE HAVING AMIDASE ACTIVITY AND GENE THEREOF KANEKA CORPORATION (JP) 2006-10-18 — — EP disclosed
US-20060172393-A1 Process for producing optically active alpha -methylcysteine derivative KANEKA CORPORATION 2006-08-03 — — US disclosed
EP-1584690-A1 PROCESS FOR PRODUCING OPTICALLY ACTIVE a-METHYLCYSTEINE DERIVATIVE KANEKA CORPORATION (JP) 2005-10-12 — — EP disclosed