Ammonia Solution, Strong

Ammonia Solution, Strong

SCHEMBL718320

CC(O)C(C)(C)Cl.N

nearest known ligand 0.00

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⚠ 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
SCHEMBL10544027 0.96
Phosphine SCHEMBL11450724 0.92
SCHEMBL4601424 0.80
Ammonia Solution, Strong SCHEMBL11313397 0.77 LMNA (0.38)
Ammonia Solution, Strong SCHEMBL5088015 0.75
Trichloroethane SCHEMBL9551993 0.75
SCHEMBL20544013 0.75
SCHEMBL306919 0.75
SCHEMBL4407513 0.72
SCHEMBL7904519 0.72

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10184058-B2 Ink composition for detecting plasma treatment and indicator for detecting plasma treatment SAKURA COLOR PRODUCTS CORPORATION (JP) 2019-01-22 US disclosed
US-10181414-B2 Indicator used in electronic device manufacturing apparatus and method for designing and/or managing the apparatus SAKURA COLOR PRODUCTS CORPORATION (JP) 2019-01-15 US disclosed
US-10153186-B2 2018-12-11 US disclosed
US-10068784-B2 2018-09-04 US disclosed
US-20170044389-A1 INK COMPOSITION FOR DETECTING PLASMA TREATMENT AND INDICATOR FOR DETECTING PLASMA TREATMENT SAKURA COLOR PRODUCTS CORPORATION (JP) 2017-02-16 US disclosed
US-20160141192-A1 INDICATOR USED IN ELECTRONIC DEVICE MANUFACTURING APPARATUS AND METHOD FOR DESIGNING AND/OR MANAGING THE APPARATUS SAKURA COLOR PRODUCTS CORPORATION (JP) 2016-05-19 US disclosed
US-9029603-B2 Process for preparing alkylated p-phenylenediamines JIANGSU SINORGCHEM TECHNOLOGY CO., LTD. (CN) 2015-05-12 US disclosed
US-20130066113-A1 PROCESS FOR PREPARING ALKYLATED P-PHENYLENEDIAMINES JIANGSU SINORGCHEM TECHNOLOGY CO., LTD. (CN) 2013-03-14 US disclosed
US-8293673-B2 Process for preparing 4-aminodiphenylamine JIANGSU SINORGCHEM TECHNOLOGY CO., LTD. (CN) 2012-10-23 US disclosed
US-20120053367-A1 PROCESS FOR PREPARING 4-AMINODIPHENYLAMINE JIANGSU SINORGCHEM TECHNOLOGY CO., LTD. (CN) 2012-03-01 US disclosed
US-20090048465-A1 PROCESS FOR PREPARING 4-AMINODIPHENYLAMINE JIANGSU SINORGCHEM TECHNOLOGY CO., LTD. (CN) 2009-02-19 US disclosed
US-20080039657-A1 PROCESS FOR PREPARING 4-AMINODIPHENYLAMINE JIANGSU SINORGCHEM TECHNOLOGY CO., LTD. (CN) 2008-02-14 US disclosed
EP-1591438-B1 A PROCESS FOR PREPARING 4-AMINODIPHENYLAMINE SINORGCHEM CO SHANDONG (CN) 2007-11-21 EP disclosed
US-20070232832-A1 PROCESS FOR PREPARING 4-AMINODIPHENYLAMINE SINORGCHEM CO. 2007-10-04 US disclosed
US-20070227675-A1 PROCESS FOR PREPARING 4-AMINODIPHENYLAMINE SINORGCHEM CO. 2007-10-04 US disclosed
US-7235694-B2 Reacting nitrobenzene and aniline in presence of a powdery complex base catalyst to perform condensation, hydrogenation, separation and refining; reuse the catalyst; tetraalkyl ammonium hydroxide and a tetraalkyl ammonium salt SINORGCHEM CO., SHANDONG (CN) 2007-06-26 US disclosed
US-20060247473-A1 Reacting nitrobenzene and aniline in presence of a powdery complex base catalyst to perform condensation, hydrogenation, separation and refining; reuse the catalyst; tetraalkyl ammonium hydroxide and a tetraalkyl ammonium salt SINORGCHEM CO. (CN) 2006-11-02 US disclosed
US-7084302-B2 reacting nitrobenzene and aniline in presence of condensation basic catalyst to form mixtures of 4-nitrodiphenylamine and 4-nitrosodiphenylamine, then reacting with hydrogen in the presence of hydrogenation catalysts, separation and refining SINORGCHEM SHANDONG CO., LTD. (CN) 2006-08-01 US disclosed
EP-1591438-A1 A PROCESS FOR PREPARING 4-AMINODIPHENYLAMINE Wang, Nongyue (CN) 2005-11-02 EP disclosed
US-20050240058-A1 reacting nitrobenzene and aniline in presence of condensation basic catalyst to form mixtures of 4-nitrodiphenylamine and 4-nitrosodiphenylamine, then reacting with hydrogen in the presence of hydrogenation catalysts, separation and refining NONGYUE WANG AND GUANGQIANG SHI (CN) 2005-10-27 US disclosed