SCHEMBL2238464

SCHEMBL2238464

CN1CC(=O)N(O)C1=O

nearest known ligand 0.00

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
SCHEMBL2235528 0.75 BRD4 (0.41)
SCHEMBL2238580 0.75 BRD4 (0.31)
SCHEMBL2240832 0.72
SCHEMBL27030667 0.72 PLA2G7 (0.36)
SCHEMBL2239140 0.72 KMT2A (0.32)
SCHEMBL22070 0.72
Hydrochloric Acid SCHEMBL28447867 0.70 PLA2G7 (0.35)
SCHEMBL1685396 0.70 PLA2G7 (0.35)
Bromide SCHEMBL28907673 0.70 PLA2G7 (0.35)
SCHEMBL11930000 0.70 PLA2G7 (0.33)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3324185-B1 IMMUNOASSAY AND IMMUNOCHROMATOGRAPHIC KIT TANAKA PRECIOUS METAL IND (JP) 2020-11-18 EP disclosed
US-10591469-B2 Immunoassay method and immunochromatographic kit TANAKA KIKINZOKU KOGYO K.K. (JP) 2020-03-17 US disclosed
US-20180209970-A1 IMMUNOASSAY METHOD AND IMMUNOCHROMATOGRAPHIC KIT TANAKA KIKINZOKU KOGYO K.K. (JP) 2018-07-26 US disclosed
EP-3324185-A1 IMMUNOASSAY AND IMMUNOCHROMATOGRAPHIC KIT Tanaka Kikinzoku Kogyo K.K. (JP) 2018-05-23 EP disclosed
CN-107850593-A Method of immunity, immune chromatography reagent kit 田中贵金属工业株式会社 2018-03-27 CN disclosed
US-9522889-B2 ATX modulating agents BIOGEN MA INC. (US) 2016-12-20 US disclosed
US-20150210647-A1 ATX MODULATING AGENTS BIOGEN MA, INC. 2015-07-30 US disclosed
CN-104434912-A Application of 5-hydroxy-1-methyl hydantoin JILIN PROVINCE CHUANGZHI PHARMACEUTICAL DEV CO LTD 2015-03-25 CN disclosed
US-7994330-B2 Oxidizing p-xylene to terephthalic acid using a catalyst having a dicarboximide skeleton; hydrothermally treating the product with hot water, decomposing and removing catalyst impurities DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 2011-08-09 US disclosed
CN-100537031-C Processes for production of organic compounds DAICEL CHEM (JP) 2009-09-09 CN disclosed
CN-1964934-A Process for producing aromatic carboxylic acid DAICEL CHEM (JP) 2007-05-16 CN disclosed
EP-1734029-A1 PROCESS FOR PRODUCING AROMATIC CARBOXYLIC ACID Daicel Chemical Industries, Ltd. (JP) 2006-12-20 EP disclosed
EP-1342715-B1 Process for producing oximes using nitirites DAICEL CHEM (JP) 2006-09-13 EP disclosed
US-7091342-B2 Catalyst comprising cyclic acylurea compounds and processes for production organic compounds with the same DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 2006-08-15 US disclosed
US-20060030716-A1 Catalyst comprising cyclic acylurea compound and process for producing organic compounds using the catalyst ISHII YASUTAKA 2006-02-09 US disclosed
US-20050020439-A1 Catalyst comprising cyclic acylurea compounds and processes for production organic compounds with the same DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 2005-01-27 US disclosed
EP-1459804-A1 CATALYSTS COMPRISING CYCLIC ACYLUREA COMPOUNDS AND PROCESSES FOR PRODUCTION OF ORGANIC COMPOUNDS WITH THE SAME Daicel Chemical Industries, Ltd. (JP) 2004-09-22 EP disclosed
US-6768023-B2 REACTING AN ESTER OR SALT OF NITROUS ACID WITH A COMPOUND THAT GENERATES A FREE RADICAL IN THE PRESENCE OF A NITROGEN CONTAINING CYCLIC COMPOUND CONTAINING AN N-OXY OR -HYDROXY IMIDE GROUP; FORMING OXIMES, NITRO COMPOUNDS, AND KETONES DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 2004-07-27 US disclosed
US-20030171618-A1 Process for producing organic compounds using nitrites DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 2003-09-11 US disclosed
EP-1342715-A2 Process for producing oximes using nitirites Daicel Chemical Industries, Ltd. (JP) 2003-09-10 EP disclosed