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 SCHEMBL11274092 | 1.00 | — | — | |
| SCHEMBL50123 | 0.93 | — | — | |
| SCHEMBL17004026 | 0.93 | — | — | |
| SCHEMBL3359476 | 0.86 | — | — | |
| Ammonia Solution, Strong SCHEMBL29017501 | 0.86 | — | — | |
| Ammonia Solution, Strong SCHEMBL11409106 | 0.86 | — | — | |
| SCHEMBL29110032 | 0.86 | — | — | |
| SCHEMBL31239165 | 0.86 | — | — | |
| Fluoride SCHEMBL34460639 | 0.86 | — | — | |
| Methane SCHEMBL28819313 | 0.86 | — | — |
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 28 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-117924364-A | Chiral agent for preparing homogeneous oligomer | 卫材 R&D 管理有限公司 | 2024-04-26 | — | — | CN | claimed |
| CN-108350005-B | Chiral agent for preparing homogeneous oligomer | 卫材R&D管理有限公司 | 2024-02-06 | — | — | CN | claimed |
| CN-113461733-A | Chiral reagents for the preparation of homogeneous oligomers | 卫材R&D管理有限公司 | 2021-10-01 | — | — | CN | claimed |
| CN-100360545-C | Organic phosphoramide hydrochloride | WUHAN COLLEGE OF CHEMICAL TECH (CN) | 2008-01-09 | — | — | CN | claimed |
| JP-60045586-A | — | — | None | — | — | JP | disclosed |
| US-20250282727-A1 | Method for Preparing 2-chloro-5-methylpyridine by Continuous Flow | JIANGSU YANGNONG CHEMICAL GROUP CO., LTD. (CN) | 2025-09-11 | — | — | US | disclosed |
| US-20240238323-A1 | MODIFIED NUCLEOSIDES AND NUCLEOTIDES ANALOGS AS ANTIVIRAL AGENTS FOR CORONA AND OTHER VIRUSES | EMORY UNIVERSITY | 2024-07-18 | — | — | US | disclosed |
| CN-117924364-A | Chiral agent for preparing homogeneous oligomer | 卫材 R&D 管理有限公司 | 2024-04-26 | — | — | CN | disclosed |
| CN-117769427-A | Modified nucleosides and nucleotide analogues as antiviral agents for coronaviruses and other viruses | 埃默里大学 | 2024-03-26 | — | — | CN | disclosed |
| EP-4319763-A2 | MODIFIED NUCLEOSIDES AND NUCLEOTIDES ANALOGS AS ANTIVIRAL AGENTS FOR CORONA AND OTHER VIRUSES | Emory University (US) | 2024-02-14 | — | — | EP | disclosed |
| CN-108350005-B | Chiral agent for preparing homogeneous oligomer | 卫材R&D管理有限公司 | 2024-02-06 | — | — | CN | disclosed |
| WO-2024016618-A1 | METHOD FOR PREPARING 2-CHLORO-5-METHYLPYRIDINE THROUGH CONTINUOUS FLOW | 江苏瑞祥化工有限公司 | 2024-01-25 | — | — | WO | disclosed |
| CN-1465581-A | Organic phosphoramide hydrochloride | 武汉化工学院 | 2004-01-07 | — | — | CN | disclosed |
| CN-1465581-A | Organic phosphoramide hydrochloride | 武汉化工学院 | 2004-01-07 | — | — | CN | disclosed |
| EP-0127541-B1 | SALTS OF AMINO-BETA-LACTAMIC ACIDS AND PROCESS FOR THE PREPARATION THEREOF | GEMA S.A. (ES) | 1990-08-01 | — | — | EP | disclosed |
| US-4908356-A | Substituted perhydro-1,3-oxazine containing phosphamide | RESEARCH CORPORATION TECHNOLOGIES, INC. (US) | 1990-03-13 | — | — | US | disclosed |
| WO-1989011283-A1 | ALDOPHOSPHAMIDE DERIVATIVES USEFUL AS ANTITUMOR AGENTS | RESEARCH CORPORATION TECHNOLOGIES, INC. (US) | 1989-11-30 | — | — | WO | disclosed |
| US-4659814-A | Salts of amino-beta-lactamic acids and process for the preparation thereof | GEMA, S.A. (ES) | 1987-04-21 | — | — | US | disclosed |
| JP-S6045586-A | THIONOPHOSPHORIC ACID AMIDE DERIVATIVE, ITS PREPARATION AND PLANT BLIGHT CONTROLLING AGENT CONTAINING SAID DERIVATIVE AS ACTIVE COMPONENT | SUMITOMO CHEM CO LTD | 1985-03-12 | — | — | JP | disclosed |
| EP-0127541-A2 | Salts of amino-beta-lactamic acids and process for the preparation thereof | GEMA S.A. (ES) | 1984-12-05 | — | — | EP | disclosed |