SCHEMBL5453660

SCHEMBL5453660

O=S(=O)(O)N(O)S(=O)(=O)O.[Na]

nearest known ligand 0.39

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
CA5A P35218 2/20 0.39
CA5B Q9Y2D0 2/20 0.39
TSHR P16473 3/20 0.33
CA1 P00915 1/20 0.33
CA2 P00918 1/20 0.33
NT5E P21589 1/20 0.33
CA4 P22748 1/20 0.33
CA6 P23280 1/20 0.33
CA7 P43166 1/20 0.33
CA9 Q16790 1/20 0.33
TDP1 Q9NUW8 1/20 0.33
MEN1 O00255 1/20 0.31
ALDH1A1 P00352 1/20 0.31
KMT2A Q03164 1/20 0.31

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
SCHEMBL2896087 0.96 CA5A (0.42) CA5ACA5BTSHRCA1CA2
Ammonia Solution, Strong SCHEMBL11225196 0.92 CA5A (0.39) CA5ACA5BTSHRCA1CA2
SCHEMBL28486849 0.92 CA5A (0.39) CA5ACA5BTSHRCA1CA2
SCHEMBL7787751 0.92 CA5A (0.39) CA5ACA5BTSHRCA1CA2
Ammonia Solution, Strong SCHEMBL7567432 0.92 CA5A (0.39) CA5ACA5BTSHRCA1CA2
Water SCHEMBL11797712 0.88 CA5A (0.36) CA5ACA5BTSHRCA1CA2
SCHEMBL29079969 0.73
Sulfuric Acid SCHEMBL9933397 0.66 CA5A (0.86) CA5ACA5BTSHRCA1CA2
Sulfuric Acid SCHEMBL517258 0.66 CA5A (0.86) CA5ACA5BTSHRCA1CA2
Sulfuric Acid SCHEMBL1420916 0.66 CA5A (0.86) CA5ACA5BTSHRCA1CA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114181107-A Synthesis method of benzyloxy amine hydrochloride 宁波睿田科技有限公司 2022-03-15 CN disclosed
CN-112479166-A Method for preparing hydroxylamine hydrochloride by utilizing waste incineration fly ash 常熟理工学院 2021-03-12 CN disclosed
CN-100364963-C Preparation of O-substituted hydroxylamines BASF AG (DE) 2008-01-30 CN disclosed
US-20070179293-A1 Method for the production of o-substituted hydroxylamine compounds BASF AKTIENGESELLSCHAFT (DE) 2007-08-02 US disclosed
CN-1819991-A Preparation of O-substituted hydroxylamines BASF AG (DE) 2006-08-16 CN disclosed
EP-1661884-A1 PROCESS FOR PRODUCTION OF O-SUBSTITUTED HYDROXYLAMINES BASF AKTIENGESELLSCHAFT (DE) 2006-05-31 EP disclosed
US-6485700-B1 Process for producing free hydroxylamine aqueous solution TORAY FINE CHEMICALS CO., LTD. (JP) 2002-11-26 US disclosed
US-4591598-A Derivatives of 2-azabicyclo[3.1.0]hexane-3-carboxylic acid, and hypotensive use thereof HOECHST AKTIENGESELLSCHAFT (DE) 1986-05-27 US disclosed