SCHEMBL7303570

SCHEMBL7303570

O=S(=O)([O-])NO.[Na+]

nearest known ligand 0.00

Known targets — ChEMBL curated mechanism

ABCC8ACEADORA1ADORA2AADORA2BADORA3ALDH5A1ALOX5ALOX5APATP4AATP4BBRAFCA1CA12CA2CA4CYSLTR1DHFRDPEP1EDNRAEDNRBESR2F10FDPSFGF1GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTGNRHRGSC1HMGCRIMPDH1IMPDH2KCNJ11LY96NOD2NR3C1NS3NS4ANS5bP2RY1P2RY12P2RY2P2RY4P2RY6PBP2XPDE3APDE3BPDE4APDE4BPDE4CPDE4DPDK1PDK2PDK3PDK4PPARGPPATPTGIRPTGS1PTGS2RAF1RYR1RYR3SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASERPINC1SLC12A1SLC12A3SYKTHRATHRBTLR3TLR4TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYMSVKORC1XDHblablaIMP-1blaOXA-33blaOXA-58blaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAfolPfolP1ftsIfusAgaggyrAgyrBmecAmrcAmrcBmrdApbp1apbp1bpbp2pbp2apbp2bpbp3pbp4pbpApbpBpbpCpbpFpolponBrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpoArpoBrpoCrpoZrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

⚠ 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
Potassium Ion SCHEMBL11396402 0.92
SCHEMBL11835162 0.89 CA2 (0.44)
Sodium Iminodisulfonate SCHEMBL6282225 0.70 MEN1 (0.43)
SCHEMBL5093119 0.67
Sulfuric Acid SCHEMBL27312 0.67
Sulfuric Acid SCHEMBL27823566 0.67 TSHR (1.00)
Sulfuric Acid SCHEMBL2381067 0.67 TSHR (1.00)
Sulfuric Acid SCHEMBL4653387 0.67
SCHEMBL16516368 0.67 TSHR (0.61)
SCHEMBL10445874 0.67

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0271142-B1 Improved modacrylic fibre, endowed with characteristics of reduced flammability and process for its preparation ENICHEM FIBRE SPA (IT) 1994-09-07 EP claimed
EP-0271142-A2 Improved modacrylic fibre, endowed with characteristics of reduced flammability and process for its preparation ENICHEM FIBRE S.p.A. (IT) 1988-06-15 EP claimed
CN-117946306-B Diketoxime resin, preparation method thereof and nickel removal method of lithium battery recovery liquid 江苏海普功能材料有限公司 2024-06-07 CN disclosed
CN-117946306-A Diketoxime resin, preparation method thereof and nickel removal method of lithium battery recovery liquid 江苏海普功能材料有限公司 2024-04-30 CN disclosed
CN-114824398-B Polyacrylic acid grafted polymer flow battery system 中盐金坛盐化有限责任公司 2023-07-25 CN disclosed
CN-114824398-A Polyacrylic acid grafted polymer flow battery system 中盐金坛盐化有限责任公司 2022-07-29 CN disclosed
US-20010034312-A1 Aqueous hydroxylamine solution BASF AKTIENGESELLSCHAFT (DE) 2001-10-25 US disclosed
US-6300518-B1 CONCENTRATED AQUEOUS SOLUTION OF HYDROXYLAMINE WHICH CONTAINS ALMOST NO METAL IMPURITIES, STABILIZED WITH TRANS-1,2-DIAMINOCYCLOHEXANE-N,N,N',N'-TETRAACETIC ACID NISSIN CHEMICAL CO., LTD. (JP) 2001-10-09 US disclosed
US-5874432-A Saccharin derivatives useful as proteolytic enzyme inhibitors and compositions and method of use thereof SANOFI (FR) 1999-02-23 US disclosed
EP-0471756-B1 SACCHARIN DERIVATIVES USEFUL AS PROTEOLYTIC ENZYME INHIBITORS AND PREPARATION THEREOF SANOFI SA (FR) 1997-10-29 EP disclosed
US-5650422-A TREATMENT OF EMPHYSEMA, ARTHRITIS OR PANCREATITIS SANOFI (FR) 1997-07-22 US disclosed
WO-1990013549-A1 SACCHARIN DERIVATIVES USEFUL AS PROTEOLYTIC ENZYME INHIBITORS AND PREPARATION THEREOF STERLING WINTHROP INC. (US) 1990-11-15 WO disclosed
US-4960909-A ANTICOAGULANTS; VASODILATORS; BRONCHODILATOR AGENTS SHIONOGI & CO., LTD. (JP) 1990-10-02 US disclosed
US-4861913-A Bicyclic sulfonamide derivatives SHIONOGI & CO., LTD. (JP) 1989-08-29 US disclosed
EP-0271142-A2 Improved modacrylic fibre, endowed with characteristics of reduced flammability and process for its preparation ENICHEM FIBRE S.p.A. (IT) 1988-06-15 EP disclosed
EP-0247975-A2 A polymer support for topo-chemical reactions; a process for its preparation, the support produced and its application Ente per le nuove tecnologie, l'energia e l'ambiente (ENEA) (IT) 1987-12-02 EP disclosed
EP-0226346-A1 Bicyclic sulfonamide derivatives SHIONOGI & CO., LTD. (JP) 1987-06-24 EP disclosed
US-4064351-A PROSTAGLANDIN SANKYO COMPANY LIMITED (JA) 1977-12-20 US disclosed
US-4004072-A Process for producing acrylonitrile polymers MITSUBISHI RAYON CO., LTD. (JA) 1977-01-18 US disclosed
US-3931120-A BIS(2-CHLOROETHYL) VINYL PHOSPHONATE ASAHI KASEI KOGYO KABUSHIKI KAISHA (JA) 1976-01-06 US disclosed