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 | |
|---|---|---|---|---|
| SCHEMBL22489 | 0.95 | — | — | |
| SCHEMBL10713958 | 0.95 | TSHR (0.46) | — | |
| SCHEMBL18918455 | 0.95 | — | — | |
| SCHEMBL4873099 | 0.95 | TSHR (0.46) | — | |
| SCHEMBL4438485 | 0.95 | — | — | |
| Bromide SCHEMBL1786729 | 0.91 | TSHR (0.42) | — | |
| SCHEMBL1789456 | 0.91 | — | — | |
| Cyclohexane SCHEMBL7515073 | 0.91 | TSHR (0.42) | — | |
| SCHEMBL28908204 | 0.91 | — | — | |
| Methane SCHEMBL29241723 | 0.91 | — | — |
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 6 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-114796745-A | Atomization treatment device for preparing mixed ozone and liquid and using method | 广东怡康生物科技有限公司 | 2022-07-29 | — | — | CN | claimed |
| CN-218565869-U | Xenon excimer light source active oxygen cluster circulating thickening disinfection refrigeration freezer | 郑州圣华药物食品技术开发有限公司 | 2023-03-03 | — | — | CN | disclosed |
| CN-115591003-A | Combined application design scheme of xenon excimer light source and active oxygen cluster digestion filter disc | 郑州圣华药物食品技术开发有限公司（CN） | 2023-01-13 | — | — | CN | disclosed |
| CN-115569227-A | Xenon excimer light source and krypton chloride excimer light source combined killing design method | 郑州圣华药物食品技术开发有限公司 | 2023-01-06 | — | — | CN | disclosed |
| CN-114796745-A | Atomization treatment device for preparing mixed ozone and liquid and using method | 广东怡康生物科技有限公司 | 2022-07-29 | — | — | CN | disclosed |
| CN-113307326-A | Preparation of tungsten-based oxide/carbon-based nano composite hydrosol and application of tungsten-based oxide/carbon-based nano composite hydrosol in wastewater treatment | 江西善拓环境科技有限公司 | 2021-08-27 | — | — | CN | disclosed |