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 SCHEMBL27488879 | 1.00 | HTT (0.38) | — | |
| Hydrochloric Acid SCHEMBL28540815 | 0.96 | HTT (0.36) | — | |
| SCHEMBL35686 | 0.95 | — | — | |
| SCHEMBL5579990 | 0.95 | — | — | |
| Bromide SCHEMBL29550005 | 0.91 | — | — | |
| Iodide SCHEMBL3681300 | 0.91 | — | — | |
| SCHEMBL6731744 | 0.91 | — | — | |
| SCHEMBL29475435 | 0.91 | — | — | |
| SCHEMBL4070674 | 0.84 | LMNA (0.30) | — | |
| Guanidine SCHEMBL28319252 | 0.84 | LMNA (0.43) | — |
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 211 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-122025855-A | Ionic liquid-based high-pressure quick-charging electrolyte and preparation method thereof | 南京大学 | 2026-05-12 | — | — | CN | claimed |
| US-20250313801-A1 | SPECIFIC T CELL FOR PREVENTING OR TREATING CANCER, AND PREPARATION METHOD THEREOF | SUZHOU ERSHENG BIOPHARMACEUTICAL CO., LTD. (CN) | 2025-10-09 | — | — | US | claimed |
| EP-4534652-A1 | SPECIFIC T CELL FOR PREVENTING OR TREATING CANCER, AND PREPARATION METHOD THEREFOR | Suzhou Ersheng Biopharmaceutical Co., Ltd. (CN) | 2025-04-09 | — | — | EP | claimed |
| CN-116062730-B | Preparation method of pre-lithiated silicon-based composite material, pre-lithiated silicon-based composite material and application thereof | 胜华新材料科技(眉山)有限公司 | 2025-03-11 | — | — | CN | claimed |
| CN-119097135-A | Green ecological antibacterial composite protective mask | 多明氧科技(广东)有限公司 | 2024-12-10 | — | — | CN | claimed |
| CN-117865367-A | Method for mixed treatment of organophosphorus wastewater and ammonia nitrogen wastewater and preparation of struvite | 中国石油化工股份有限公司 | 2024-04-12 | — | — | CN | claimed |
| CN-112635835-B | High-low temperature compatible non-aqueous electrolyte and lithium ion battery | 远景动力技术(江苏)有限公司 | 2024-03-29 | — | — | CN | claimed |
| WO-2023227085-A1 | SPECIFIC T CELL FOR PREVENTING OR TREATING CANCER, AND PREPARATION METHOD THEREFOR | 苏州尔生生物医药有限公司 | 2023-11-30 | — | — | WO | claimed |
| CN-112670581-B | Nonaqueous electrolyte suitable for temperature of minus 20 ℃ to 60 ℃ and lithium ion battery based on nonaqueous electrolyte | 远景动力技术(江苏)有限公司 | 2023-11-17 | — | — | CN | claimed |
| CN-114958314-B | Composite base liquid and preparation method and application thereof | 中海石油(中国)有限公司湛江分公司 | 2023-11-10 | — | — | CN | claimed |
| US-20100284954-A1 | PROCESS FOR RELAXING KERATIN FIBRES | L'OREAL (FR) | 2010-11-11 | — | — | US | claimed |
| CN-1304368-C | Improved technique for producing tetramethyl guanidine | XINHUAWANBO CHEMICAL CO LTD SH (CN) | 2007-03-14 | — | — | CN | claimed |
| US-20060127337-A1 | Process for relaxing keratin fibres | L'OREAL (FR) | 2006-06-15 | — | — | US | claimed |
| CN-1760177-A | Improved technique for producing tetramethyl guanidine | XINHUAWANBO CHEMICAL CO LTD SH (CN) | 2006-04-19 | — | — | CN | claimed |
| CN-1193984-C | Process for the preparation of intermediate-1,1,3,3,-tetramethyl carbamidine hydrochloride of 1,1,3,3-tetramethyl carbamidine | SIPING CITY FINE CHEMICALS CO (CN) | 2005-03-23 | — | — | CN | claimed |
| CN-1485317-A | Process for the preparation of intermediate-1,1,3,3,-tetramethyl carbamidine hydrochloride of 1,1,3,3-tetramethyl carbamidine | 四平市精细化学品有限公司 | 2004-03-31 | — | — | CN | claimed |
| EP-1363345-A2 | Guanidine derivatives as cations for ambient temperature molten salts in electrochemical power sources | Wilson Greatbatch Technologies, Inc. (US) | 2003-11-19 | — | — | EP | claimed |
| US-20030211389-A1 | Guanidine derivatives as cations for ambient temperature molten salts in electrochemical power sources | GREATBATCH LTD. | 2003-11-13 | — | — | US | claimed |
| CN-1100037-C | Process for preparing tetramethyl guanidine | XINHUA INDUSTRY AND TRADE CO L (CN) | 2003-01-29 | — | — | CN | claimed |
| CN-1262271-A | Process for preparing tetramethyl guanidine | XINHUA INDUSTRY AND TRADE CO L (CN) | 2000-08-09 | — | — | CN | claimed |