Known targets — ChEMBL curated mechanism
ABCC9ABL1ACEACHEACVR1ADORA1ADORA2AADORA2BADORA3ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALOX5ATP4AATP4BBCRBTKCACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGCRBNCUL4ACXCR1CXCR2DDB1DDCDHFRDPP4DRD2DRD3DRD4EGFRERBB2ERBB4ESR1ESR2FDPSFKBP1AFLT1FLT3FLT4GARTGHSRGRIA1GRIA2GRIA3GRIA4GRIK1GRIK2GRIK3GRIK4GRIK5GRIN2AGSK3AGSK3BHDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IDH1IDH2IMPA1ITGA2BITGB3JAK1JAK2JAK3KCNJ11KCNK3KCNK9KDRKITMEN1METMMP1MMP13MMP7MMP8NANOD2NS5bODC1OPG057OPRD1OPRK1OPRM1PPARP1PARP2PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PKLRPPARDPPATPTGS1PTGS2RBX1ROCK1ROCK2RRM1RRM2RRM2BSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC10A2SLC5A2SLC6A2SLC6A3SLC6A4SLC9A3SYKTACR1THRATHRBTOP1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYK2TYMSVDRampCblablaT-3blaT-4blaT-5blaT-6blaUOE-1dacAdacBdacCfolAfolPftsIgyrAgyrBileSmecAmrcAmrcBmrdAparCparEpbp2pbp4pbpApbpFrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUthyAykgMykgO
The experimentally established mechanism targets of Water. 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 | |
|---|---|---|---|---|
| Water SCHEMBL845276 | 1.00 | — | — | |
| Water SCHEMBL10451236 | 1.00 | — | — | |
| Fluoride Ion SCHEMBL50564 | 0.82 | — | — | |
| Water SCHEMBL31001052 | 0.82 | — | — | |
| Water SCHEMBL23631871 | 0.67 | — | — | |
| Water SCHEMBL25293610 | 0.67 | — | — | |
| Water SCHEMBL11364888 | 0.67 | — | — | |
| Water SCHEMBL25293755 | 0.67 | — | — | |
| Water SCHEMBL38219 | 0.67 | — | — | |
| Water SCHEMBL7594200 | 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 115 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-112321388-A | Preparation method of deuterated methanol with high conversion rate | 徐州亚兴医疗科技有限公司 | 2021-02-05 | — | — | CN | claimed |
| US-9809515-B2 | Dehydrofluorination of pentafluoroalkanes to form tetrafluoroolefins | ARKEMA INC. (US) | 2017-11-07 | — | — | US | claimed |
| US-20170022128-A1 | DEHYDROFLUORINATION OF PENTAFLUOROALKANES TO FORM TETRAFLUOROOLEFINS | ARKEMA INC (US) | 2017-01-26 | — | — | US | claimed |
| US-9492816-B2 | Dehydrofluorination of pentafluoroalkanes to form tetrafluoroolefins | ARKEMA INC. (US) | 2016-11-15 | — | — | US | claimed |
| EP-2569269-A1 | DEHYDROFLUORINATION OF PENTAFLUOROALKANES TO FORM TETRAFLUOROOLEFINS | ARKEMA INC. (US) | 2013-03-20 | — | — | EP | claimed |
| US-20130060069-A1 | DEHYDROFLUORINATION OF PENTAFLUOROALKANES TO FORM TETRAFLUOROOLEFINS | ARKEMA INC. (US) | 2013-03-07 | — | — | US | claimed |
| WO-2011140013-A1 | DEHYDROFLUORINATION OF PENTAFLUOROALKANES TO FORM TETRAFLUOROOLEFINS | ARKEMA INC. (US) | 2011-11-10 | — | — | WO | claimed |
| US-7211607-B2 | Method for producing high surface area chromia materials for catalysis | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) | 2007-05-01 | — | — | US | claimed |
| US-20030202933-A1 | Method for producing high surface area chromia materials for catalysis | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA | 2003-10-30 | — | — | US | claimed |
| US-20260137621-A1 | ORALLY BIOAVAILABLE LIPID-BASED CONSTRUCTS | DIASOME PHARMACEUTICALS INC (US) | 2026-05-21 | — | — | US | disclosed |
| US-20260124139-A1 | LIPID CONSTRUCT FOR DELIVERY OF INSULIN TO A MAMMAL | DIASOME PHARMACEUTICALS INC (US) | 2026-05-07 | — | — | US | disclosed |
| US-20250288521-A1 | ORALLY BIOAVAILABLE LIPID-BASED CONSTRUCTS | DIASOME PHARMACEUTICALS INC (US) | 2025-09-18 | — | — | US | disclosed |
| US-RE50296-E1 | Electron beam resist composition | THE UNIVERSITY OF MANCHESTER (GB) | 2025-02-11 | — | — | US | disclosed |
| CN-119082627-A | Aluminum alloy for automobile main structural beam and preparation method thereof | 哈尔滨宏源铝业有限责任公司 | 2024-12-06 | — | — | CN | disclosed |
| EP-1087753-A1 | TARGETED LIPOSOMAL DRUG DELIVERY SYSTEM | SDG, Inc. (US) | 2001-04-04 | — | — | EP | disclosed |
| WO-1999059545-A9 | TARGETED LIPOSOMAL DRUG DELIVERY SYSTEM | SDG INC (US) | 2000-04-27 | — | — | WO | disclosed |
| EP-0747510-B1 | Deposition of chromium oxides from a trivalent chromium solution | ATOTECH USA INC (US) | 2000-04-19 | — | — | EP | disclosed |
| US-6004448-A | APPLYING A COATING OF CHROMIUM OXIDE ON A ELECTROCONDUCTIVE METAL SUBSTRATE FROM CHROMIUM BATH WITH BUFFERS | ATOTECH USA, INC. (US) | 1999-12-21 | — | — | US | disclosed |
| WO-1999059545-A1 | TARGETED LIPOSOMAL DRUG DELIVERY SYSTEM | SDG, INC. (US) | 1999-11-25 | — | — | WO | disclosed |
| EP-0747510-A1 | Deposition of chromium oxides from a trivalent chromium solution | ATOTECH USA, INC. (US) | 1996-12-11 | — | — | EP | disclosed |