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 SCHEMBL1237503 | 1.00 | — | — | |
| Water SCHEMBL1316344 | 1.00 | — | — | |
| Water SCHEMBL1251114 | 1.00 | — | — | |
| Water SCHEMBL4653984 | 1.00 | — | — | |
| Water SCHEMBL187338 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL52396 | 0.82 | — | — | |
| Water SCHEMBL28232325 | 0.82 | — | — | |
| Water SCHEMBL9700718 | 0.82 | — | — | |
| Water SCHEMBL27538871 | 0.82 | — | — | |
| Water SCHEMBL25188536 | 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
Appears in 3797 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-121892226-B | Catalytic material for capturing and methanolizing carbon dioxide in flue gas, preparation method and application | 西南石油大学 | 2026-05-19 | — | — | CN | claimed |
| CN-122059870-A | Synthesis method of N-Boc-4-oxo-3-piperidinecarboxylic acid ethyl ester | 苏州敬业医药化工有限公司 | 2026-05-19 | — | — | CN | claimed |
| CN-122032542-A | Catalyst for preparing cinnamyl alcohol by cinnamyl aldehyde hydrogenation, preparation and application thereof | 山西科技学院 | 2026-05-15 | — | — | CN | claimed |
| CN-122013241-A | Doping regulation type ruthenium iridium-based electrocatalytic oxygen evolution catalyst and preparation method thereof | 北京化工大学 | 2026-05-12 | — | — | CN | claimed |
| CN-118513075-B | Benzylamine lead-iodine/molybdenum disulfide photocatalyst, preparation method and application thereof, and photocatalytic total water splitting method | 山东大学 | 2026-02-27 | — | — | CN | claimed |
| US-12529154-B2 | Electrode for electrolysis | LG CHEM, LTD. (KR) | 2026-01-20 | — | — | US | claimed |
| US-12515964-B2 | Tin oxide forming composition | LG CHEM, LTD. (KR) | 2026-01-06 | — | — | US | claimed |
| EP-4635623-A1 | AMMONIA DECOMPOSITION CATALYST AND METHOD FOR PRODUCING SAME | POSCO Holdings Inc. (KR) | 2025-10-22 | — | — | EP | claimed |
| US-12428742-B2 | Electrode for electrolysis | LG CHEM, LTD. (KR) | 2025-09-30 | — | — | US | claimed |
| US-20250198996-A1 | EXTENDED LIVE CELL BARCODING APPROACH FOR MULTIPLEXED MASS CYTOMETRY | BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) | 2025-06-19 | — | — | US | claimed |
| US-4614822-A | Catalytic oxidation of 3,3-dimethyl-2-hydroxybutyric acid to 2-oxo acid and preparation of 4-amino-6-tert.-butyl-3-thio-1,2,4-triazine-5(4-H)-one | MOBAY CHEMICAL CORPORATION (US) | 1986-09-30 | — | — | US | claimed |
| EP-0146508-A2 | Promoted nickel and/or cobalt catalyst, its use and process performed in its presence | BEROL NOBEL AB (SE) | 1985-06-26 | — | — | EP | claimed |
| EP-0048373-B1 | PROCESS FOR PREPARING PYRAZOLE | BAYER AG (DE) | 1984-05-09 | — | — | EP | claimed |
| EP-0048373-A2 | Process for preparing pyrazole | BAYER AG (DE) | 1982-03-31 | — | — | EP | claimed |
| EP-0011207-B1 | PROCESS FOR THE PREPARATION OF 3,3-DIMETHYL-2-OXO-BUTANOIC ACID | Mobay Chemical Corporation (US) | 1981-11-25 | — | — | EP | claimed |
| US-4269784-A | WAXES, OILS, AND THEIR DEUTERATED OR TRITERATED DERIVATIVES; HOMOGENEITY AQUEOUS SOLUTION OF A RUTHENIUM HALIDE, -ACETYLACETONATE, OR COMPLEX SALT | EXXON RESEARCH & ENGINEERING COMPANY (US) | 1981-05-26 | — | — | US | claimed |
| US-4260820-A | HOMOLOGATION WITH SYNTHESIS GAS USING IODIDE OR BROMIDE PROMOTER WITH RUTHENIUM COMPOUND CATALYST | TEXACO DEVELOPMENT CORP. (US) | 1981-04-07 | — | — | US | claimed |
| US-4223160-A | NIOBIUM AND RUTHENIUM SALTS AS CATALYSTS | UNION CARBIDE CORPORATION (US) | 1980-09-16 | — | — | US | claimed |
| EP-0011207-A1 | Process for the preparation of 3,3-dimethyl-2-oxo-butanoic acid | Mobay Chemical Corporation (US) | 1980-05-28 | — | — | EP | claimed |
| US-4107079-A | NOBLE METAL COORDINATION COMPLEX | RHONE-POULENC INDUSTRIES (FR) | 1978-08-15 | — | — | US | claimed |