Known targets — ChEMBL curated mechanism
ABCC9ABL1ACEACHEACVR1ADORA1ADORA2AADORA2BADORA3ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALOX5ATP4AATP4BBCRBTKCACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGCRBNCUL4ACXCR1CXCR2DDB1DDCDHFRDPP4DRD2DRD3DRD4EGFRERBB2ERBB4ESR1ESR2FDPSFKBP1AFLT1FLT3FLT4GARTGHSRGRIA1GRIA2GRIA3GRIA4GRIK1GRIK2GRIK3GRIK4GRIK5GRIN2AGSK3AGSK3BHDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IDH1IDH2IMPA1ITGA2BITGB3JAK1JAK2JAK3KCNJ11KCNK3KCNK9KDRKITMEN1METMMP1MMP13MMP7MMP8NANOD2NS5bODC1OPG057OPRD1OPRK1OPRM1PPARP1PARP2PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PKLRPPARDPPATPTGS1PTGS2RBX1ROCK1ROCK2RRM1RRM2RRM2BSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC10A2SLC5A2SLC6A2SLC6A3SLC6A4SLC9A3SYKTACR1THRATHRBTOP1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYK2TYMSVDRampCblablaT-3blaT-4blaT-5blaT-6blaUOE-1dacAdacBdacCfolAfolPftsIgyrAgyrBileSmecAmrcAmrcBmrdAparCparEpbp2pbp4pbpApbpFrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUthyAykgMykgO
The experimentally established mechanism targets of Sulfurous Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| Sulfurous Acid SCHEMBL5833535 | 1.00 | — | — | |
| Sulfurous Acid SCHEMBL28289603 | 0.94 | CA4 (0.31) | — | |
| Sulfurous Acid SCHEMBL6419307 | 0.94 | — | — | |
| Sulfurous Acid SCHEMBL42806 | 0.94 | — | — | |
| Sulfurous Acid SCHEMBL12273732 | 0.94 | CA1 (0.30) | — | |
| Sulfurous Acid SCHEMBL8003772 | 0.88 | — | — | |
| Sulfurous Acid SCHEMBL11138663 | 0.88 | — | — | |
| Sulfurous Acid SCHEMBL8003768 | 0.88 | — | — | |
| Sulfurous Acid SCHEMBL11014695 | 0.88 | — | — | |
| Sulfurous Acid SCHEMBL916642 | 0.88 | — | — |
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 158 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20250269427-A1 | GOLD POWDER AND METHOD OF PRODUCING THE SAME | SUMITOMO METAL MINING CO., LTD. (JP) | 2025-08-28 | — | — | US | disclosed |
| EP-2614048-B1 | PURIFICATION OF FLUOROALKANESULFONATE SALTS | CHEMOURS CO FC LLC (US) | 2018-06-13 | — | — | EP | disclosed |
| CN-103097349-B | The purification of fluorine-containing paraffin sulfonate | 纳幕尔杜邦公司 | 2016-08-17 | — | — | CN | disclosed |
| EP-2118194-B1 | FLAME RETARDANT POLYCARBONATE COMPOSITIONS | DU PONT (US) | 2014-12-03 | — | — | EP | disclosed |
| US-8715521-B2 | Absorption cycle utilizing ionic liquid as working fluid | E I DU PONT DE NEMOURS AND COMPANY (US) | 2014-05-06 | — | — | US | disclosed |
| US-8707720-B2 | Hybrid vapor compression-absorption cycle | E I DU PONT DE NEMOURS AND COMPANY (US) | 2014-04-29 | — | — | US | disclosed |
| US-8628644-B2 | Utilizing ionic liquids for hydrofluorocarbon separation | E I DU PONT NEMOURS AND COMPANY (US) | 2014-01-14 | — | — | US | disclosed |
| US-8568608-B2 | Vapor compression cycle utilizing ionic liquid as compressor lubricant | E I DU PONT DE NEMOURS AND COMPANY (US) | 2013-10-29 | — | — | US | disclosed |
| EP-2614048-A1 | PURIFICATION OF FLUOROALKANESULFONATE SALTS | E.I. Du Pont De Nemours And Company (US) | 2013-07-17 | — | — | EP | disclosed |
| US-8461378-B2 | Purification of fluoroalkanesulfonate salts | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2013-06-11 | — | — | US | disclosed |
| US-20070066854-A1 | Preparation of polytrimethylene ether glycol and copolymers thereof | THE CHEMOURS COMPANY FC, LLC | 2007-03-22 | — | — | US | disclosed |
| US-20070066852-A1 | Preparation of poly(tetramethylene) glycol | THE CHEMOURS COMPANY FC, LLC | 2007-03-22 | — | — | US | disclosed |
| US-20070019708-A1 | Hybrid vapor compression-absorption cycle | E. I. DU PONT DE NEMOURS AND COMPANY | 2007-01-25 | — | — | US | disclosed |
| WO-2006133330-A1 | HYDROFLUOROALKANESULFONIC ACIDS AND SALTS FROM FLUOROVINYL ETHERS | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2006-12-14 | — | — | WO | disclosed |
| WO-2006133331-A1 | MANUFACTURE OF HYDROFLUOROALKANESULFONIC ACIDS | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 2006-12-14 | — | — | WO | disclosed |
| US-20060276670-A1 | Hydrofluoroalkanesulfonic acids from fluorovinyl ethers | THE CHEMOURS COMPANY FC, LLC | 2006-12-07 | — | — | US | disclosed |
| US-20060276671-A1 | Manufacture of hydrofluoroalkanesulfonic acids | THE CHEMOURS COMPANY FC, LLC | 2006-12-07 | — | — | US | disclosed |
| WO-2006124776-A2 | HYBRID VAPOR COMPRESSION-ABSORPTION CYCLE | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2006-11-23 | — | — | WO | disclosed |
| US-20060197053-A1 | Absorption cycle utilizing ionic liquid as working fluid | E. I. DU PONT DE NEMOURS AND COMPANY | 2006-09-07 | — | — | US | disclosed |
| WO-2006084262-A1 | ABSORPTION CYCLE UTILIZING IONIC LIQUID AS WORKING FLUID | E.I. DUPONT DE NEMOURS AND COMPANY (US) | 2006-08-10 | — | — | WO | disclosed |