Water

Water

SCHEMBL408582

O.O.O.[Na+].[Na+].[S-2]

nearest known ligand 0.00

Full drug profile on Sugi Atlas →

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.

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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.

Compoundsimilaritytop predictedshared targets
Water SCHEMBL8745624 1.00
Water SCHEMBL261167 1.00
Water SCHEMBL2166807 1.00
Water SCHEMBL1960739 1.00
Water SCHEMBL5359540 1.00
Water SCHEMBL2569158 1.00
Water SCHEMBL10748032 1.00
Water SCHEMBL392487 1.00
Water SCHEMBL6690795 1.00
Water SCHEMBL16539020 1.00

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 150 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116496192-B Preparation method of 4-phenylthio-1, 2-phenylenediamine 山东国邦药业有限公司 2023-09-19 CN claimed
CN-116496192-A Preparation method of 4-phenylthio-1, 2-phenylenediamine 山东国邦药业有限公司 2023-07-28 CN claimed
CN-111171320-B Production method of catalyst-removed polyphenylene sulfide resin 四川明道和化学新材料有限公司 2022-05-06 CN claimed
CN-109232893-B High-efficiency synthesis method of polyphenylene sulfide resin 宜宾学院 2021-02-19 CN claimed
US-20200164341-A1 METHOD OF MAKING A MERCURY SORBENT AMCOL INTERNATIONAL CORP (US) 2020-05-28 US claimed
CN-111171320-A Production method of catalyst-removed polyphenylene sulfide resin 四川明道和化学新材料有限公司 2020-05-19 CN claimed
US-20180304229-A1 IMPROVED METHOD OF MAKING A MERCURY SORBENT AMCOL INTERNATIONAL CORPORATION (US) 2018-10-25 US claimed
EP-3368210-A1 IMPROVED METHOD OF MAKING A MERCURY SORBENT Amcol International Corporation (US) 2018-09-05 EP claimed
CN-108484911-A A kind of polyphenylene sulfide dewatering 内蒙古聚贤化工材料科技有限公司 2018-09-04 CN claimed
US-7109362-B2 Process for the preparation of lipoic acid and dihydrolipoic acid BASF AKTIENGESELLSCHAFT (DE) 2006-09-19 US claimed
EP-1339705-B1 METHOD FOR PRODUCING LIPOIC ACID AND DIHYDROLIPOIC ACID BASF AG (DE) 2006-06-07 EP claimed
US-20050101669-A1 Process for the preparation of lipoic acid and dihydrolipoic acid BASF AKTIENGESELLSCHAFT (DE) 2005-05-12 US claimed
JP-2045531-A None JP disclosed
US-20250228242-A1 PROTEIN AGGREGATION INHIBITING COMPOUNDS FOR PLANT DISEASE CONTROL MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2025-07-17 US disclosed
EP-3634403-B1 PHENYL-HETEROCYCLE-PHENYL DERIVATIVES FOR USE IN THE TREATMENT OR PREVENTION OF MELANOMA MAX PLANCK GESELLSCHAFT (DE) 2025-06-25 EP disclosed
CN-118265453-A Protein aggregation inhibiting compounds for plant disease control 马克斯·普朗克科学促进学会 2024-06-28 CN disclosed
US-4362864-A Process for the preparation of polyarylene sulphides BAYER AKTIENGESELLSCHAFT (DE) 1982-12-07 US disclosed
US-4255157-A A MIXTURE OF AN ALKALI METAL SULFIDE OR POLYSULFIDE OR ITS HYDRATE, A CARBONACEOUS MATERIAL, AND A POWDER OF IRON, MAGNESIUM, OR ALUMINUM OR ITS ALLOY; SPONTANEOUS COMBUSTION TOYO INK MANUFACTURING CO., LTD. (JP) 1981-03-10 US disclosed
US-4181671-A POLYVINYL CHLORIDE, HEAT RESISTANCE AKZO N.V. (NL) 1980-01-01 US disclosed
US-4134878-A SYNERGISTIC, VINYL HALIDE POLYMER AKZO N.V. (NL) 1979-01-16 US disclosed