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 SCHEMBL7690033 | 1.00 | — | — | |
| SCHEMBL371051 | 0.91 | — | — | |
| Hydrochloric Acid SCHEMBL27547868 | 0.83 | — | — | |
| SCHEMBL27854925 | 0.83 | — | — | |
| Water SCHEMBL4029249 | 0.73 | — | — | |
| Water SCHEMBL28212635 | 0.73 | — | — | |
| Hydrochloric Acid SCHEMBL27614972 | 0.67 | — | — | |
| Ammonia Solution, Strong SCHEMBL11413422 | 0.67 | — | — | |
| Water SCHEMBL598083 | 0.62 | — | — | |
| Water SCHEMBL11403741 | 0.62 | — | — |
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 75 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-10308997-B2 | Method for producing elemental rhodium | Heraeus Deutschland GmbH & Co. KG (DE) | 2019-06-04 | — | — | US | claimed |
| CN-102585003-B | The preparation method and applications of tumor-targeted photosensitive immunoconjugate | 中国科学院福建物质结构研究所 | 2017-10-31 | — | — | CN | claimed |
| WO-2005107742-A1 | NOVEL ANTIVIRAL HELIOXANTHIN ANALOGS | YALE UNIVERSITY (US) | 2005-11-17 | — | — | WO | claimed |
| JP-9052913-A | — | — | None | — | — | JP | disclosed |
| WO-2024129632-A1 | PROCESS FOR PRODUCING LOW GLOSS COATING SURFACE BY RADIATION CURING | COVESTRO LLC (US) | 2024-06-20 | — | — | WO | disclosed |
| WO-2024042082-A1 | PROCESS FOR PROVIDING LOW GLOSS COATINGS | COVESTRO (NETHERLANDS) B.V. (NL) | 2024-02-29 | — | — | WO | disclosed |
| WO-2023227683-A1 | PROCESS FOR PROVIDING LOW GLOSS COATINGS | COVESTRO (NETHERLANDS) B.V. (NL) | 2023-11-30 | — | — | WO | disclosed |
| WO-2023227680-A1 | PROCESS FOR PROVIDING LOW GLOSS COATINGS | COVESTRO (NETHERLANDS) B.V. (NL) | 2023-11-30 | — | — | WO | disclosed |
| CN-109988072-B | Synthetic method of 2' -oxydiethylamine and product thereof | 安徽工业大学科技园有限公司 | 2022-04-12 | — | — | CN | disclosed |
| WO-2020253872-A1 | 2-BENZYLIDENE HYDRAZINOADENOSINE COMPOUNDS HAVING A2A ADENOSINE RECEPTOR AGNOSTIC ACTIVITY | 中国人民解放军军事科学院军事医学研究院 | 2020-12-24 | — | — | WO | disclosed |
| CN-107980105-B | Resist stripping liquid | 松下知识产权经营株式会社 | 2019-10-18 | — | — | CN | disclosed |
| EP-1761578-A1 | LOW NMP AQUEOUS POLYURETHANE COMPOSITION WITH A DILUENT | DSMIP Assets B.V. (NL) | 2007-03-14 | — | — | EP | disclosed |
| WO-2006002865-A1 | LOW NMP AQUEOUS POLYURETHANE COMPOSITION WITH A DILUENT | DSM IP ASSETS BV (NL) | 2006-01-12 | — | — | WO | disclosed |
| WO-2006002864-A1 | LOW NMP AQUEOUS POLYURETHANE COMPOSITION WITH A REACTIVE DILUENT | DSM IP ASSETS BV (NL) | 2006-01-12 | — | — | WO | disclosed |
| WO-2006002866-A1 | LOW NWP AQUEOUS POLYURETHANE COMPOSITION | DSM IP ASSETS BV (NL) | 2006-01-12 | — | — | WO | disclosed |
| CN-1621522-A | Method for stabilizing cholesterol dehydrogenase, composition containing cholesterol dehydrogenase, and cholesterol detection reagent | SYSMEX CORP (JP) | 2005-06-01 | — | — | CN | disclosed |
| US-6479660-B1 | Process for the preparation of anti-malarial drugs | SMITHKLINE BEECHAM P.L.C. (GB) | 2002-11-12 | — | — | US | disclosed |
| EP-0871616-A1 | PROCESS FOR THE PREPARATION OF ANTI-MALARIAL DRUGS | SMITHKLINE BEECHAM PLC (GB) | 1998-10-21 | — | — | EP | disclosed |
| WO-1997013753-A1 | PROCESS FOR THE PREPARATION OF ANTI-MALARIAL DRUGS | SMITHKLINE BEECHAM P.L.C. (GB) | 1997-04-17 | — | — | WO | disclosed |
| JP-H0952913-A | ACID/ALDEHYDE ABSORBING POLYMER AND ITS PRODUCTION | JAPAN EXLAN CO LTD | 1997-02-25 | — | — | JP | disclosed |