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 SCHEMBL101772 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL9699743 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL6840677 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL30887880 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL104802 | 1.00 | — | — | |
| SCHEMBL72838 | 0.97 | — | — | |
| SCHEMBL41892 | 0.97 | — | — | |
| SCHEMBL104803 | 0.97 | — | — | |
| SCHEMBL30039818 | 0.97 | — | — | |
| SCHEMBL25301326 | 0.94 | — | — |
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 1407 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-119874660-A | Amino acid derivative-rhodamine B conjugate, preparation method thereof and application thereof as fluorescent tracer | 内蒙古农业大学 | 2025-04-25 | — | — | CN | claimed |
| CN-119776326-A | Aminopeptidase and preparation method and application thereof | 浙江震元生物科技有限公司 | 2025-04-08 | — | — | CN | claimed |
| CN-119735558-A | Preparation method and intermediate of aza-quinolinone derivative | 成都苑东生物制药股份有限公司 | 2025-04-01 | — | — | CN | claimed |
| EP-4506356-A1 | METHANOL-INDUCIBLE PROMOTER AND USE THEREOF IN PREPARATION OF L-ALANYL-L-GLUTAMINE | Wuhan Grand Hoyo Co., Ltd. (CN) | 2025-02-12 | — | — | EP | claimed |
| CN-119409588-A | Caffeoyl amino acid methyl ester derivative and preparation method and application thereof | 西北大学 | 2025-02-11 | — | — | CN | claimed |
| CN-118546847-B | Recombinant escherichia coli for producing alpha-amino acid ester acyltransferase as well as construction method and application thereof | 合肥工业大学 | 2025-01-10 | — | — | CN | claimed |
| CN-118910104-A | Codon-optimized non-glycosylated coding Aet gene, recombinant and application thereof | 大连医诺生物股份有限公司 | 2024-11-08 | — | — | CN | claimed |
| CN-118879657-A | Beta-amino acid ester acyltransferase mutant, application to L-carnosine and preparation method thereof | 合肥工业大学 | 2024-11-01 | — | — | CN | claimed |
| CN-116064606-B | Codon-optimized non-glycosylated coding Aet gene, recombinant and application thereof | 大连医诺生物股份有限公司 | 2024-09-27 | — | — | CN | claimed |
| CN-118546847-A | Recombinant escherichia coli for producing alpha-amino acid ester acyltransferase as well as construction method and application thereof | 合肥工业大学 | 2024-08-27 | — | — | CN | claimed |
| CN-104480075-A | Bio-enzyme for synthesis of N(2)-L-alanyl-L-glutamine by catalysis as well as preparation method and application thereof | Jiangsu chengxin pharmaceutical co ltd | 2015-04-01 | — | — | CN | claimed |
| CN-104480172-A | Method of producing L-alanyl-L-glutamine from recombinant escherichia coli | UNIV JIANGNAN | 2015-04-01 | — | — | CN | claimed |
| CN-103073618-A | Preparation method for benzyloxycarbonyl alanyl alanine | GL BIOCHEM SHANGHAI LTD | 2013-05-01 | — | — | CN | claimed |
| CN-101724017-B | 4-nitro-L-phenylalanine dipeptide derivatives as well as preparation method and applications thereof | UNIV SOUTHWEST | 2012-07-25 | — | — | CN | claimed |
| CN-102329245-A | Adamantine derivative with anti-avian influenza virus activity and preparation method for adamantine derivative | UNIV WUHAN | 2012-01-25 | — | — | CN | claimed |
| CN-101245096-B | Liquid phase synthesizing method for N-benzyl oxylcarbonyl isoleucyl -beta-tert-butyl glutamyl-alanyl-amino aldehyde | SHANGHAI INST ORGANIC CHEM | 2010-12-15 | — | — | CN | claimed |
| CN-101724017-A | 4-nitro-L-phenylalanine dipeptide derivatives as well as preparation method and applications thereof | CHENGDU DIAO PHARMACEUTICAL GR | 2010-06-09 | — | — | CN | claimed |
| CN-101560184-A | N-chiral quaternary ammonium salt derived from amino acid and preparation method thereof | CHENGDU INST BIOLOGY CAS (CN) | 2009-10-21 | — | — | CN | claimed |
| CN-101245096-A | Liquid phase synthesizing method for N-benzyl oxylcarbonyl isoleucyl -beta-tert-butyl glutamyl-alanyl-amino aldehyde | SHANGHAI INST ORGANIC CHEM (CN) | 2008-08-20 | — | — | CN | claimed |
| CN-1609097-A | Serine synthesizing process | CAI YAN (CN) | 2005-04-27 | — | — | CN | claimed |