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 SCHEMBL6096305 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL9731799 | 1.00 | — | — | |
| SCHEMBL6096493 | 0.98 | — | — | |
| SCHEMBL6950087 | 0.98 | — | — | |
| SCHEMBL6096311 | 0.98 | — | — | |
| Hydrochloric Acid SCHEMBL29060562 | 0.82 | LTA4H (0.36) | — | |
| Methylene Chloride SCHEMBL29028670 | 0.82 | KIF11 (0.35) | — | |
| Hydrochloric Acid SCHEMBL2386334 | 0.82 | LTA4H (0.36) | — | |
| SCHEMBL26269818 | 0.79 | — | — | |
| SCHEMBL2385218 | 0.79 | — | — |
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 35 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-110642736-A | Synthesis method of acetamido-3-methyl chloropropionate | 湖北宇阳药业有限公司 | 2020-01-03 | — | — | CN | claimed |
| CN-110590587-A | Synthetic method of 3-chloro-L-alanine methyl ester hydrochloride | 湖北宇阳药业有限公司 | 2019-12-20 | — | — | CN | claimed |
| CN-120329231-B | L-selenium-methyl selenocysteine synthesis method | 江西川奇药业有限公司 | 2025-11-18 | — | — | CN | disclosed |
| CN-120329231-A | L-selenium-methyl selenocysteine synthesis method | 江西川奇药业有限公司 | 2025-07-18 | — | — | CN | disclosed |
| CN-116332780-B | Synthesis method of S-3-chloro-D-alanine methyl ester hydrochloride | 河北国龙制药有限公司 | 2025-03-18 | — | — | CN | disclosed |
| CN-116332780-A | Synthesis method of S-3-chloro-D-alanine methyl ester hydrochloride | 河北国龙制药有限公司 | 2023-06-27 | — | — | CN | disclosed |
| WO-2020134137-A1 | METHOD FOR SYNTHESIZING R-3-CHLOROALANINE METHYL ESTER HYDROCHLORIDE | 北京富盛嘉华医药科技有限公司 | 2020-07-02 | — | — | WO | disclosed |
| CN-110642736-A | Synthesis method of acetamido-3-methyl chloropropionate | 湖北宇阳药业有限公司 | 2020-01-03 | — | — | CN | disclosed |
| CN-110642736-A | Synthesis method of acetamido-3-methyl chloropropionate | 湖北宇阳药业有限公司 | 2020-01-03 | — | — | CN | disclosed |
| CN-110590587-A | Synthetic method of 3-chloro-L-alanine methyl ester hydrochloride | 湖北宇阳药业有限公司 | 2019-12-20 | — | — | CN | disclosed |
| CN-110590587-A | Synthetic method of 3-chloro-L-alanine methyl ester hydrochloride | 湖北宇阳药业有限公司 | 2019-12-20 | — | — | CN | disclosed |
| EP-0219344-B1 | VINYL MONOMERS AND DERIVED LIQUID CRYSTALLINE POLYMERS | The University of Southern Mississippi (US) | 1991-04-17 | — | — | EP | disclosed |
| US-4985522-A | Polymers containing pendant urea groups | THE UNIVERSITY OF SOUTHERN MISSISSIPPI (US) | 1991-01-15 | — | — | US | disclosed |
| US-4970210-A | ENZYME INHIBITORS | ABBOTT LABORATORIES (US) | 1990-11-13 | — | — | US | disclosed |
| US-4906767-A | Monomers with urea groups | THE UNIVERSITY OF SOUTHERN MISSISSIPPI (US) | 1990-03-06 | — | — | US | disclosed |
| EP-0299449-A2 | Pyridazinone, triazinone and oxapyridazinone lipoxygenase inhibiting compounds | ABBOTT LABORATORIES (US) | 1989-01-18 | — | — | EP | disclosed |
| US-4793949-A | New vinyl monomers capable of forming side-chain liquid crystalline polymers and the resulting polymers | UNIVERSITY OF SOUTHERN MISSISSIPPI (US) | 1988-12-27 | — | — | US | disclosed |
| EP-0219344-A1 | Vinyl monomers and derived liquid crystalline polymers | The University of Southern Mississippi (US) | 1987-04-22 | — | — | EP | disclosed |
| CN-86102923-A | The method for preparing antibiotic derivatives | — | 1986-11-12 | — | — | CN | disclosed |
| US-4613658-A | Vinyl monomers capable of forming side-chain liquid crystalline polymers and the resulting polymers | UNIVERSITY OF SOUTHERN MISSISSIPPI (US) | 1986-09-23 | — | — | US | disclosed |