SCHEMBL529800

SCHEMBL529800

CN(S(C)(=O)=O)S(=O)(=O)N=C=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
SCHEMBL25512909 0.79
SCHEMBL25513162 0.77 F2 (0.31)
SCHEMBL11873327 0.75
SCHEMBL11870347 0.73 CHRM2 (0.30)
SCHEMBL11870391 0.72
SCHEMBL9364361 0.72
SCHEMBL875900 0.69 KDM4E (0.42)
SCHEMBL11871908 0.69 CA1 (0.33)
SCHEMBL11876997 0.69
SCHEMBL11873287 0.68 NPC1 (0.32)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4648133-A1 FLUORINATED SALT AS COMPONENT OF ELECTROLYTES FOR IMPROVING PERFORMANCE OF CELLS AND BATTERIES Fundación Centro de Investigación Cooperativa de Energías Alternativas, CIC Energigune Fundazioa (ES) 2025-11-12 EP disclosed
WO-2023092884-A1 ISOCYANATE ELECTROLYTE ADDITIVE CONTAINING SULFONAMIDE STRUCTURE GROUP, AND USE THEREOF 中节能万润股份有限公司 2023-06-01 WO disclosed
WO-2014157591-A1 NONAQUEOUS ELECTROLYTE SOLUTION AND NONAQUEOUS ELECTROLYTE BATTERY USING SAME 三菱化学株式会社 (JP) 2014-10-02 WO disclosed
EP-2598556-B1 PROCESS FOR PRODUCING SILOXANE COPOLYMERS WITH URETHANE-SULPHONAMIDO LINKING GROUPS WACKER CHEMIE AG (DE) 2014-09-03 EP disclosed
US-8741979-B2 Process for producing siloxane copolymers with urethane-sulphonamido linking groups WACKER CHEMIE AG (DE) 2014-06-03 US disclosed
EP-2598556-A1 PROCESS FOR PRODUCING SILOXANE COPOLYMERS WITH URETHANE-SULPHONAMIDO LINKING GROUPS Wacker Chemie AG (DE) 2013-06-05 EP disclosed
US-20130123376-A1 PROCESS FOR PRODUCING SILOXANE COPOLYMERS WITH URETHANE-SULPHONAMIDO LINKING GROUPS WACKER CHEMIE AG (DE) 2013-05-16 US disclosed
CN-103025799-A Process for producing siloxane copolymers with urethane-sulphonamido linking groups WACKER CHEMIE AG 2013-04-03 CN disclosed
WO-2012013558-A1 PROCESS FOR PRODUCING SILOXANE COPOLYMERS WITH URETHANE-SULPHONAMIDO LINKING GROUPS WACKER CHEMIE AG (DE) 2012-02-02 WO disclosed
US-5569761-A REACTING SULFONAMIDO DERIVATIVES WITH AMINE SUBSTITUTED TRIAZINE OR PYRIMIDINE DERIVATIVES HOECHST AKTIENGESELLSCHAFT (DE) 1996-10-29 US disclosed
US-5414084-A Reaction 2-aminopyrimidine or amino-1,3,5-triazine derivative; purity; by-product inhibition HOECHST AKTIENGESELLSCHAFT (DE) 1995-05-09 US disclosed
US-5294741-A Continuous process for the preparation of sulfonylisocyanates HOECHST AKTIENGESELLSCHAFT (DE) 1994-03-15 US disclosed
US-5189217-A Process for the production of 1-(N-Methanesulfonyl-N-methylaminosulfonyl)-3-(2-pyrimidyl)urea derivatives LONZA, LTD. (CH) 1993-02-23 US disclosed
US-5180826-A Multistage reaction of chlorosulfonylisocyanate and methane sulfonylethylamine and reacting with aminopyrimidine LONZA LTD. (CH) 1993-01-19 US disclosed
EP-0507093-A2 Process for the preparation of sulfonylureas Hoechst Schering AgrEvo GmbH (DE) 1992-10-07 EP disclosed
EP-0504817-A1 Process for the preparation of 1-(N-methylsulfonyl-N-methylaminosulfonyl)-3-(2-pyrimidyl)-urea derivatives LONZA AG (CH) 1992-09-23 EP disclosed
EP-0131258-B1 N-ALKOXY- AND N-ALKYLSULFONYLAMINOSULFONYL UREAS, AND PYRIMIDO- OR TRIAZINO-THIATRIAZINE OXIDES AS INTERMEDIATES HOECHST AKTIENGESELLSCHAFT (DE) 1989-08-30 EP disclosed
US-3931277-A SULFONYLAMINO-SULFONYL, FUNGICIDE AND ANTHELMINTIC INTERMEDIATES HOECHST AKTIENGESELLSCHAFT (DT) 1976-01-06 US disclosed