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 SCHEMBL4456796 | 1.00 | — | — | |
| Water SCHEMBL17460462 | 1.00 | — | — | |
| Water SCHEMBL28283070 | 1.00 | — | — | |
| Ammonia Solution, Strong SCHEMBL28220936 | 0.97 | — | — | |
| Hydrochloric Acid SCHEMBL6288509 | 0.97 | — | — | |
| Hydrochloric Acid SCHEMBL28859819 | 0.97 | — | — | |
| Water SCHEMBL5815301 | 0.97 | — | — | |
| Water SCHEMBL5310125 | 0.97 | — | — | |
| SCHEMBL30349526 | 0.96 | — | — | |
| SCHEMBL15545054 | 0.96 | — | — |
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 147 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-106620825-B | A kind of bi-component quick-acting haemostatic powder gel and its application | 浙江大学 | 2019-11-12 | — | — | CN | claimed |
| CN-110251457-A | A kind of antitumor sustained-release implant and preparation method thereof with strong adherency and hemostatic function | 合肥工业大学 | 2019-09-20 | — | — | CN | claimed |
| CN-109252165-A | A kind of preparation method for subtracting copper liquid subtracting copper composition and include the composition | 苏州纳勒电子科技有限公司 | 2019-01-22 | — | — | CN | claimed |
| CN-107149700-A | A kind of three component biological glues and its preparation and application | 浙江大学 | 2017-09-12 | — | — | CN | claimed |
| CN-100475791-C | Method for preparing 6-hydroxyl-3-cyanogen pyridine | SHANDONG INST LIGHT INDUSTRY (CN) | 2009-04-08 | — | — | CN | claimed |
| CN-101270082-A | Method for preparing 6-hydroxyl-3-cyanogen pyridine | SHANDONG INST LIGHT INDUSTRY (CN) | 2008-09-24 | — | — | CN | claimed |
| CN-1064359-C | Diindole heterocyclic compounds, preparing method and use thereof | SHANGHAI INST ORGANIC CHEM (CN) | 2001-04-11 | — | — | CN | claimed |
| CN-1224015-A | Diindole heterocyclic compounds, preparing method and use thereof | SHANGHAI INST ORGANIC CHEM (CN) | 1999-07-28 | — | — | CN | claimed |
| US-20250206764-A1 | TRIAZOLE COMPOUND, METHOD FOR SYNTHESIZING SAID TRIAZOLE COMPOUND, COUPLING AGENT AND USES THEREOF | SHIKOKU CHEMICALS CORPORATION (JP) | 2025-06-26 | — | — | US | disclosed |
| CN-119823001-A | Urea compounds antagonizing LPA1 receptor | 大正制药株式会社 | 2025-04-15 | — | — | CN | disclosed |
| CN-114206832-B | Urea compounds antagonizing LPA1 receptor | 大正制药株式会社 | 2025-04-04 | — | — | CN | disclosed |
| EP-4501937-A1 | TRIAZOLE COMPOUND, METHOD FOR SYNTHESIZING SAID TRIAZOLE COMPOUND, COUPLING AGENT AND USES THEREOF | Shikoku Chemicals Corporation (JP) | 2025-02-05 | — | — | EP | disclosed |
| CN-118922427-A | Triazole compound, synthesis method of triazole compound, coupling agent and application thereof | 四国化成工业株式会社 | 2024-11-08 | — | — | CN | disclosed |
| CN-108383858-B | Derivatives of imidazothiadiazoles and imidazopyrazines for the treatment of platelet aggregation | 百时美施贵宝公司 | 2024-09-20 | — | — | CN | disclosed |
| CN-1042356-A | 1, 4-diaza * derivatives and their pharmaceutical use | EISAI CO LTD (JP) | 1990-05-23 | — | — | CN | disclosed |
| CN-1040582-A | New peptidase inhibitors | MERRELL DOW PHARMA (US) | 1990-03-21 | — | — | CN | disclosed |
| CN-1037704-A | The glutaramide diuretic agents of enantiomorph | PFIZER (US) | 1989-12-06 | — | — | CN | disclosed |
| EP-0140731-A2 | Natriuretic factors | INSTITUT DE RECHERCHES CLINIQUES DE MONTREAL (CA) | 1985-05-08 | — | — | EP | disclosed |
| EP-0000017-B1 | 1-(2-PHENYLETHYL)-TRIAZOLIUM SALTS, THEIR PREPARATION AND THEIR USE AS FUNGICIDES | BAYER AG (DE) | 1981-09-30 | — | — | EP | disclosed |
| EP-0000017-A1 | 1-(2-Phenylethyl)-triazolium salts, their preparation and their use as fungicides | BAYER AG (DE) | 1978-12-20 | — | — | EP | disclosed |