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 SCHEMBL5353098 | 1.00 | — | — | |
| Water SCHEMBL8911037 | 1.00 | — | — | |
| Water SCHEMBL8063198 | 1.00 | — | — | |
| Water SCHEMBL16443 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL106286 | 0.82 | — | — | |
| Water SCHEMBL23461833 | 0.67 | — | — | |
| Water SCHEMBL23631871 | 0.67 | — | — | |
| Water SCHEMBL20562889 | 0.67 | — | — | |
| Water SCHEMBL25334174 | 0.67 | — | — | |
| Water SCHEMBL21379772 | 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 1894 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-122059785-A | Method for preparing 1, 1-disubstituted alkene by rhodium-catalyzed decarboxylation cracking | 华南理工大学 | 2026-05-19 | — | — | CN | claimed |
| CN-122032634-A | Composite molecular sieve and preparation method and application thereof | 中国石油化工股份有限公司 | 2026-05-15 | — | — | CN | claimed |
| CN-122032631-A | Catalyst for catalytic cracking of alkane and method for catalytic cracking of alkane | 中国石油化工股份有限公司 | 2026-05-15 | — | — | CN | 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 |
| CN-120115163-A | Three-functional amorphous/crystalline Rh (OH)3/NiMoO4Preparation method and application of heterojunction electrolyzed water catalyst | 昆明理工大学 | 2025-06-10 | — | — | CN | claimed |
| CN-120115192-A | Rhodium-tungsten opposite site MOF-based catalyst, preparation and application | 南京工业大学 | 2025-06-10 | — | — | CN | claimed |
| CN-116606197-B | Method and product for preparing aldehyde by Fischer-Tropsch oil hydroformylation reaction | 国家能源集团宁夏煤业有限责任公司 | 2025-05-06 | — | — | CN | claimed |
| CN-119571376-A | Preparation method for preparing single-atom electrocatalyst on surface of current collector in situ | 苏州行则兴氢能源科技有限公司 | 2025-03-07 | — | — | CN | claimed |
| CN-116556044-B | High-entropy hydrotalcite modified carbon fiber photo-thermal conversion material and preparation method thereof | 武汉科技大学 | 2025-02-28 | — | — | CN | claimed |
| CN-119456022-A | Carbide-promoted noble metal-based catalyst and preparation method and application thereof | 大连理工大学 | 2025-02-18 | — | — | CN | claimed |
| EP-0262310-A1 | Process for the isomerization of unbranched functionalised compounds with terminal double bonds | HÜLS AKTIENGESELLSCHAFT (DE) | 1988-04-06 | — | — | EP | claimed |
| EP-0114612-B1 | RACEMIC AND OPTICALLY ACTIF 3-HYDROXY-ALPHA-CYCLOCITRAL, THEIR ACETALS AND OPTICALLY ACTIF 3-OXO-ALPHA-CYCLOCITRALACETALS, AND ALSO THE PREPARATION AND USE OF THESE COMPOUNDS | BASF Aktiengesellschaft (DE) | 1988-03-23 | — | — | EP | claimed |
| US-4728630-A | Rhodium on carbon catalyst | AMOCO CORPORATION (US) | 1988-03-01 | — | — | US | claimed |
| EP-0219288-A1 | Rhodium on carbon catalyst | AMOCO CORPORATION (US) | 1987-04-22 | — | — | EP | claimed |
| CN-86106590-A | Be stated from the rhodium catalyst on the carbon | — | 1987-04-22 | — | — | CN | claimed |
| US-4636333-A | PERFUMES | INTERNATIONAL FLAVORS & FRAGRANCES INC. (US) | 1987-01-13 | — | — | US | claimed |
| US-4581343-A | IMPREGNATING SUPPORT WITH PLATINUM AND CERIUM GROUP METAL COMPOUNDS; REDUCING AND CALCING | PRO-CATALYSE (FR) | 1986-04-08 | — | — | US | claimed |
| EP-0114612-A2 | Racemic and optically actif 3-hydroxy-alpha-cyclocitral, their acetals and optically actif 3-oxo-alpha-cyclocitralacetals, and also the preparation and use of these compounds | BASF Aktiengesellschaft (DE) | 1984-08-01 | — | — | EP | claimed |
| US-4115417-A | ENANTIOSELECTIVITY | HOFFMANN-LA ROCHE INC. (US) | 1978-09-19 | — | — | US | claimed |
| US-4085145-A | Process for manufacturing carbonyl compounds by oxidation with molecular oxygen of olefinic compounds in liquid phase in the presence of soluble bimetallic catalysts | INSTITUT FRANCAIS DU PETROLE (FR) | 1978-04-18 | — | — | US | claimed |