Known targets — ChEMBL curated mechanism
ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Aluminum Chloride Anhydrous. 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 | |
|---|---|---|---|---|
| Aluminum Chloride Anhydrous SCHEMBL28547138 | 0.91 | — | — | |
| Aluminum Chloride Anhydrous SCHEMBL11658277 | 0.91 | — | — | |
| Aluminum Chloride Anhydrous SCHEMBL27717642 | 0.91 | — | — | |
| Aluminum Chloride Anhydrous SCHEMBL1565 | 0.89 | — | — | |
| Aluminum Chloride Anhydrous SCHEMBL29104163 | 0.89 | — | — | |
| Aluminum Chloride Anhydrous SCHEMBL27401552 | 0.89 | — | — | |
| Aluminum Chloride Anhydrous SCHEMBL28381460 | 0.89 | — | — | |
| Aluminum Chloride Anhydrous SCHEMBL20137344 | 0.80 | — | — | |
| Aluminum Chloride Anhydrous SCHEMBL20915013 | 0.80 | — | — | |
| Aluminum Chloride Anhydrous SCHEMBL22228666 | 0.80 | — | — |
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 82 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-114410320-A | Retired photovoltaic module pyrolysis treatment cooperative full-component recovery method and system | 中国科学院广州能源研究所 | 2022-04-29 | — | — | CN | claimed |
| CN-113942994-A | Method for separating electrolyte from waste cathode carbon block of electrolytic aluminum | 阿坝铝厂 | 2022-01-18 | — | — | CN | claimed |
| EP-3299369-B1 | PYRIDO-AZAHETERECYDIC COMPOUND AND PREPARATION METHOD AND USE THEREOF | SHANGHAI INST MATERIA MEDICA CAS (CN) | 2020-11-11 | — | — | EP | claimed |
| CN-107709320-B | Pyrido-nitrogen heterocyclic compound and preparation method and application thereof | 中国科学院上海药物研究所 | 2020-11-06 | — | — | CN | claimed |
| US-20180244667-A1 | PYRIDO-AZAHETERECYDIC COMPOUND AND PREPARATION METHOD AND USE THEREOF | SHANGHAI INSTITUTE OF MATERIA MEDICA, CHINESE ACADEMY OF SCIENCES (CN) | 2018-08-30 | — | — | US | claimed |
| EP-3299369-A1 | PYRIDO-AZAHETERECYDIC COMPOUND AND PREPARATION METHOD AND USE THEREOF | Shanghai Institute of Materia Medica, Chinese Academy of Sciences (CN) | 2018-03-28 | — | — | EP | claimed |
| CN-106279147-A | A kind of pyrido nitrogen heterocyclic and its production and use | 中国科学院上海药物研究所 | 2017-01-04 | — | — | CN | claimed |
| EP-0425359-B1 | Process for the preparation of 3-benzoyl-benzofuran derivatives | SANOFI SA (FR) | 1995-10-11 | — | — | EP | claimed |
| CN-223556031-U | Poly chlorine aluminium chloride PAC production reaction mixing arrangement | 水清华(天津)生态科技有限公司 | 2025-11-18 | — | — | CN | disclosed |
| US-20250171764-A1 | PURIFICATION OF NUCLEIC ACIDS USING COPPER-TITANIUM OXIDES | ABBOTT MOLECULAR INC. | 2025-05-29 | — | — | US | disclosed |
| US-12234448-B2 | Purification of nucleic acids using titanium oxides | ABBOTT MOLECULAR INC. | 2025-02-25 | — | — | US | disclosed |
| US-11840494-B2 | Process for treating polyalkylaromatic hydrocarbons | VERSALIS S.P.A. (IT) | 2023-12-12 | — | — | US | disclosed |
| CN-117209343-A | Continuous synthesis method of 2-naphthol compound | 菏泽学院 | 2023-12-12 | — | — | CN | disclosed |
| US-20230279194-A1 | PROCESS FOR CATALYTIC UPCYCLING OF HYDROCARBON POLYMERS TO ALKYLAROMATIC COMPOUNDS | UNITED STATES DEPARTMENT OF ENERGY | 2023-09-07 | — | — | US | disclosed |
| CN-1254280-A | A regioselective alkylation process for preparing substituted benzo [b] thiophenes | LILLY CO ELI (US) | 2000-05-24 | — | — | CN | disclosed |
| CN-1252717-A | Intermediate and method for preparing benzo [ b ] thiophene | LILLY CO ELI (US) | 2000-05-10 | — | — | CN | disclosed |
| US-5266711-A | Process for the preparation of 3-benzoyl benzofuran derivatives | SANOFI (FR) | 1993-11-30 | — | — | US | disclosed |
| CN-1038310-A | Little chromium passivating technology of no nitrate radical and sulfate radical | STATE OPERATED NO 812 FACTORY (CN) | 1989-12-27 | — | — | CN | disclosed |
| US-4873019-A | LIQUID CRYSTALS | MERCK PATENT GESELLSCHAFT MIT BESCHRANKTER HAFTUNG (DE) | 1989-10-10 | — | — | US | disclosed |
| US-4400541-A | Process for preparing bis-(diphenylsulfoniophenyl)-sulfide bis-chloride | THE SOUTHLAND CORPORATION (US) | 1983-08-23 | — | — | US | disclosed |