Known targets — ChEMBL curated mechanism
ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Hydrochloric Acid. 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 | |
|---|---|---|---|---|
| Hydrochloric Acid SCHEMBL3677634 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL29050865 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL6031805 | 1.00 | CA4 (0.33) | — | |
| Nitrogen SCHEMBL11433330 | 0.87 | — | — | |
| Hydrochloric Acid SCHEMBL11003423 | 0.82 | CA4 (0.50) | — | |
| Hydrochloric Acid SCHEMBL8378160 | 0.82 | — | — | |
| Hydrochloric Acid SCHEMBL2382161 | 0.82 | — | — | |
| Hydrochloric Acid SCHEMBL9373462 | 0.82 | CA4 (0.50) | — | |
| Hydrochloric Acid SCHEMBL377646 | 0.82 | — | — | |
| Hydrochloric Acid SCHEMBL249006 | 0.82 | — | — |
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 137 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-119978276-A | Ratio-type rare earth functionalized covalent organic framework fluorescent probe and preparation method and application thereof | 中国科学院赣江创新研究院 | 2025-05-13 | — | — | CN | claimed |
| CN-116789163-B | Bimetallic oxide and preparation method thereof and application of bimetallic oxide in signal flip detection of antibiotics | 郑州大学 | 2025-02-18 | — | — | CN | claimed |
| CN-119349528-A | Preparation method of optical scandium metaphosphate | 磁县鑫钰光电科技有限公司 | 2025-01-24 | — | — | CN | claimed |
| CN-118955933-A | Metal organic framework material, preparation method and application thereof in photodynamic sterilization | 四川大学 | 2024-11-15 | — | — | CN | claimed |
| CN-118961666-A | Fluorescent detection method and device for fluoride ions | 四川大学 | 2024-11-15 | — | — | CN | claimed |
| CN-114920278-A | Anhydrous scandium trichloride, and preparation method and application thereof | 苏州欣诺科生物科技有限公司 | 2022-08-19 | — | — | CN | claimed |
| CN-114609198-B | Rare earth element doping and precious metal modification-based tin oxide-based hydrogen sensing material and preparation method and application thereof | 兰州大学 | 2022-08-19 | — | — | CN | claimed |
| CN-114682786-A | Preparation method of micro-nano metal powder | 合肥学院 | 2022-07-01 | — | — | CN | claimed |
| CN-114609198-A | Tin oxide-based hydrogen sensing material based on rare earth element doping and precious metal modification as well as preparation method and application thereof | 兰州大学 | 2022-06-10 | — | — | CN | claimed |
| CN-112851513-A | Synthetic method of 3-carbonyl 5-hydroxy ester compound | 温州大学新材料与产业技术研究院 | 2021-05-28 | — | — | CN | claimed |
| CN-110773192-A | Preparation method of carbon-supported high-entropy monatomic catalyst | 天津理工大学 | 2020-02-11 | — | — | CN | claimed |
| CN-118955933-B | Metal organic framework material, preparation method and application thereof in photodynamic sterilization | 四川大学 | 2026-01-27 | — | — | CN | disclosed |
| US-12440584-B2 | Macrocyclic ligands with pendant chelating moieties and complexes thereof | LUMIPHORE, INC. (US) | 2025-10-14 | — | — | US | disclosed |
| CN-120026273-A | High-performance ScYSZ thermal barrier coating for continuously preparing double gradual change structure and preparation method thereof | 西安交通大学 | 2025-05-23 | — | — | CN | disclosed |
| CN-119978276-A | Ratio-type rare earth functionalized covalent organic framework fluorescent probe and preparation method and application thereof | 中国科学院赣江创新研究院 | 2025-05-13 | — | — | CN | disclosed |
| US-5610113-A | REACTION OF TRIMETHYLHYDROQUINONE AND ISOPHYTOL, CONDENSATION AND CYCLIZATION, SCANDIUM SAPONITE CATALYST | EISAI CO., LTD. (JP) | 1997-03-11 | — | — | US | disclosed |
| EP-0752629-A1 | Fixing member and fixing apparatus including same | CANON KABUSHIKI KAISHA (JP) | 1997-01-08 | — | — | EP | disclosed |
| US-5536852-A | ETHERIFICATION, CYCLIZATION | EISAI CO., LTD. (JP) | 1996-07-16 | — | — | US | disclosed |
| EP-0677520-A1 | Process for the preparation of alpha-tocopherol derivatives, and catalyst | Eisai Co., Ltd. (JP) | 1995-10-18 | — | — | EP | disclosed |
| CN-1015552-B | Dehydrogenation method of rare earth alloy | MENG XIANZONG (CN) | 1992-02-19 | — | — | CN | disclosed |