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 SCHEMBL933615 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL2599287 | 1.00 | — | — | |
| SCHEMBL18973928 | 0.97 | — | — | |
| SCHEMBL1603964 | 0.97 | — | — | |
| SCHEMBL5217527 | 0.97 | — | — | |
| Alcohol SCHEMBL28644071 | 0.89 | CA1 (0.38) | — | |
| Trimethylammonium SCHEMBL27707662 | 0.89 | CA1 (0.38) | — | |
| SCHEMBL1400213 | 0.87 | TSHR (0.48) | — | |
| Trimethylammonium SCHEMBL27455354 | 0.85 | CA1 (0.39) | — | |
| Phosphoric Acid SCHEMBL28639835 | 0.83 | GABRR1 (0.50) | — |
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 329 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-120987546-B | Efficient sludge dehydrating agent and preparation method thereof | 东莞市凯威尔环保材料有限公司 | 2026-05-22 | — | — | CN | claimed |
| WO-2026097978-A1 | LIGNIN-MODIFIED WATERBORNE POLYURETHANE STRIPPABLE COATING AND PREPARATION METHOD THEREFOR | 中海油常州涂料化工研究院有限公司 | 2026-05-15 | — | — | WO | claimed |
| CN-119140074-B | Humidity response type CO2Separating material, preparation and application thereof | 深碳科技(深圳)有限公司 | 2025-02-25 | — | — | CN | claimed |
| CN-119331505-A | Lignin modified waterborne polyurethane strippable coating and preparation method thereof | 中海油常州涂料化工研究院有限公司 | 2025-01-21 | — | — | CN | claimed |
| CN-119140074-A | Humidity response type CO2Separating material, preparation and application thereof | 深碳科技(深圳)有限公司 | 2024-12-17 | — | — | CN | claimed |
| CN-118791030-A | Separation process of insoluble matters in polyaluminum chloride preparation process | 太仓市业洪净水新材料有限公司 | 2024-10-18 | — | — | CN | claimed |
| CN-118459796-A | Method for preparing polymer microsphere by using modified lignin as Pickering emulsion stable particle, product and application | 中国石油化工股份有限公司 | 2024-08-09 | — | — | CN | claimed |
| CN-115219632-B | HPLC-ELSD detection method for (S) -1-amino-3-chloro-2-propanol hydrochloride | 山东达因海洋生物制药股份有限公司 | 2024-04-05 | — | — | CN | claimed |
| CN-116789557-A | Synthesis method of (S) -1-amino-3-chloro-2-propanol hydrochloride | 迪嘉药业集团股份有限公司 | 2023-09-22 | — | — | CN | claimed |
| CN-114287421-B | Ultraviolet-resistant biological pesticide composite microcapsule and preparation method thereof | 上海师范大学 | 2023-07-18 | — | — | CN | claimed |
| EP-1028940-B1 | PROCESS TO PRODUCE OXAZOLIDINONES | PHARMACIA & UPJOHN CO LLC (US) | 2007-04-18 | — | — | EP | claimed |
| CN-1673166-A | Heat insulating mortar powder and its prepn process | YUQIAO BUILDING MATERIAL SCI T (CN) | 2005-09-28 | — | — | CN | claimed |
| US-20040006238-A1 | Process to produce oxazolidinones | PHARMACIA & UPJOHN COMPANY | 2004-01-08 | — | — | US | claimed |
| US-20030216572-A1 | PROCESS TO PRODUCE OXAZOLIDINONES | PHARMACIA & UPJOHN COMPANY | 2003-11-20 | — | — | US | claimed |
| US-6613944-B2 | Reacting phthalimide with an epoxide in the presence of potassium phthalimide in DMF or DMAC to give a phthalimide alkylalcohol, deacylation with aqueous acid | PHARMACIA & UPJOHN COMPANY | 2003-09-02 | — | — | US | claimed |
| US-20030130509-A1 | PROCESS TO PRODUCE 3-CARBON AMINO ALCOHOL SALTS | PHARMACIA & UPJOHN COMPANY | 2003-07-10 | — | — | US | claimed |
| US-6563003-B2 | The present invention includes a number of novel intermediates such as the (S)-secondary alcohol of formula (VIIIA) X2-CH2-C*H(OH)-CH2-NH-CO-RN (VIIIA) and processes for production of pharmacologically useful oxazolidinones. | PHARMACIA & UPJOHN COMPANY | 2003-05-13 | — | — | US | claimed |
| US-20030065219-A1 | PROCESS TO PRODUCE OXAZOLIDINONES | PHARMACIA & UPJOHN COMPANY | 2003-04-03 | — | — | US | claimed |
| US-20020095054-A1 | Process to produce oxazolidinones | PHARMACIA & UPJOHN COMPANY | 2002-07-18 | — | — | US | claimed |
| US-20020032348-A1 | Process to produce oxazolidinones | PEARLMAN BRUCE ALLEN (US) | 2002-03-14 | — | — | US | claimed |