Perchlorate

Perchlorate

SCHEMBL1826508

O.O.O.O.O.O.[Fe+3].[O-][Cl+3]([O-])([O-])[O-].[O-][Cl+3]([O-])([O-])[O-].[O-][Cl+3]([O-])([O-])[O-]

nearest known ligand 0.00

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Known targets — ChEMBL curated mechanism

ABCC9ABL1ACEACHEACVR1ADORA1ADORA2AADORA2BADORA3ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALOX5ATP4AATP4BBCRBTKCACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGCRBNCUL4ACXCR1CXCR2DDB1DDCDHFRDPP4DRD2DRD3DRD4EGFRERBB2ERBB4ESR1ESR2FDPSFKBP1AFLT1FLT3FLT4GARTGHSRGRIA1GRIA2GRIA3GRIA4GRIK1GRIK2GRIK3GRIK4GRIK5GRIN2AGSK3AGSK3BHDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IDH1IDH2IMPA1ITGA2BITGB3JAK1JAK2JAK3KCNJ11KCNK3KCNK9KDRKITMEN1METMMP1MMP13MMP7MMP8NANOD2NS5bODC1OPG057OPRD1OPRK1OPRM1PPARP1PARP2PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PKLRPPARDPPATPTGS1PTGS2RBX1ROCK1ROCK2RRM1RRM2RRM2BSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC10A2SLC5A2SLC6A2SLC6A3SLC6A4SLC9A3SYKTACR1THRATHRBTOP1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYK2TYMSVDRampCblablaT-3blaT-4blaT-5blaT-6blaUOE-1dacAdacBdacCfolAfolPftsIgyrAgyrBileSmecAmrcAmrcBmrdAparCparEpbp2pbp4pbpApbpFrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUthyAykgMykgO

The experimentally established mechanism targets of Perchlorate. 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
Perchlorate SCHEMBL5025959 1.00
Perchlorate SCHEMBL1141945 1.00
Perchlorate SCHEMBL31325319 1.00
Perchlorate SCHEMBL30389139 0.91
Perchlorate SCHEMBL269886 0.91
Perchlorate SCHEMBL246911 0.83
Perchlorate SCHEMBL1824678 0.83
Perchlorate SCHEMBL892566 0.83
Perchlorate SCHEMBL1701054 0.83
Perchlorate SCHEMBL2685167 0.83

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108070092-B Supermolecular gel based on functionalized column [5] arene and application thereof in identifying iron ions and L-Cys 西北师范大学 2020-10-23 CN claimed
EP-1218322-B1 PROCESS FOR MAKING A CATALYST COMPOSITION CONOCOPHILLIPS CO (US) 2011-05-04 EP claimed
WO-2006137855-A2 METHOD FOR THE PRODUCTION OF POLYMERIZED NANOPARTICLES AND MICROPARTICLES BY TERNARY AGENT CONCENTRATION AND TEMPERATURE ALTERATION INDUCED IMMISCIBILITY BAUSCH & LOMB INCORPORATED (US) 2006-12-28 WO claimed
WO-2006137856-A2 METHOD FOR THE PRODUCTION OF NANOPARTICLES AND MICROPARTICLES BY TERNARY AGENT CONCENTRATION AND TEMPERATURE ALTERATION INDUCED IMMISCIBILITY BAUSCH & LOMB INCORPORATED (US) 2006-12-28 WO claimed
EP-1218322-A4 CATALYST COMPOSITION AND PROCESS FOR MAKING THE COMPOSITION CONOCOPHILLIPS CO (US) 2006-07-12 EP claimed
US-20060057222-A1 Method for the production of polymerized nanoparticles and microparticles by ternary agent concentration and temperature alteration induced immiscibility BAUSCH & LOMB INCORPORATED 2006-03-16 US claimed
US-20060057215-A1 Method for the production of nanoparticles and microparticles by ternary agent concentration and temperature alteration induced immiscibility BAUSCH & LOMB INCORPORATED 2006-03-16 US claimed
EP-1230025-A1 PROCESS FOR PRODUCING A METAL ALUMINATE CATALYST SUPPORT Philips Petroleum Company (US) 2002-08-14 EP claimed
US-20020107424-A1 Hydrocarbon hydrogenation catalyst and process CHEUNG TIN-TACK PETER (US) 2002-08-08 US claimed
US-6417136-B2 METAL ALUMINATE SUPPORT WITH PALLADIUM AND A SILVER OR ALKALI METAL CATALYST COMPONENT; SUPPORT IS PREPARED BY CALCINING A MIXTURE OF ALUMINA AND A MELTED METAL COMPONENT PHILLIPS PETROLEUM COMPANY 2002-07-09 US claimed
EP-1218322-A1 CATALYST COMPOSITION AND PROCESS FOR MAKING THE COMPOSITION Phillips Petroleum Company (US) 2002-07-03 EP claimed
US-6369000-B1 IMPREGNATING ALUMINA WITH A MELTED METAL COMPOUND, CALCINING, DOES NOT INVOLVE PHYSICAL MIXING OR COPRECIPITATION PHILLIPS PETROLEUM COMPANY 2002-04-09 US claimed
US-20010046943-A1 HYDROCARBON HYDROGENATION CATALYST AND PROCESS CHEVRON PHILLIPS CHEMICAL COMPANY LP 2001-11-29 US claimed
WO-2001019763-A1 CATALYST COMPOSITION AND PROCESS FOR MAKING THE COMPOSITION PHILLIPS PETROLEUM COMPANY (US) 2001-03-22 WO claimed
WO-2001019514-A1 PROCESS FOR PRODUCING A METAL ALUMINATE CATALYST SUPPORT PHILIPS PETROLEUM COMPANY (US) 2001-03-22 WO claimed
CN-118594551-A Solid solution catalyst and preparation method and application thereof 华南师范大学 2024-09-06 CN disclosed
CN-108772027-B Preparation and application of supramolecular organogel and metal gel thereof 西北师范大学 2021-01-19 CN disclosed
EP-0594890-A1 Polycyclic compounds, their preparation and their use as phosphodiesterases inhibitors TSUMURA &amp; CO. (JP) 1994-05-04 EP disclosed
EP-0511666-A1 Process for the preparation of polycyclic compounds TSUMURA &amp; CO. (JP) 1992-11-04 EP disclosed
EP-0486807-A1 Process for preparing 5-aroyl-2,3-dihydro-1H-pyrrolizine-1,1-dicarboxylates SYNTEX (U.S.A.) INC. (US) 1992-05-27 EP disclosed