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 | |
|---|---|---|---|---|
| Methane SCHEMBL27558325 | 0.96 | — | — | |
| SCHEMBL1980 | 0.96 | — | — | |
| Methane SCHEMBL28271988 | 0.92 | — | — | |
| Fluoride SCHEMBL1025919 | 0.92 | — | — | |
| SCHEMBL27764889 | 0.92 | — | — | |
| Fluoride SCHEMBL73857 | 0.92 | — | — | |
| Chloromethane SCHEMBL29210875 | 0.92 | — | — | |
| Ammonia Solution, Strong SCHEMBL4950713 | 0.92 | — | — | |
| Iodide SCHEMBL115030 | 0.92 | — | — | |
| SCHEMBL28154308 | 0.92 | — | — |
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 253 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-115260092-B | Synthesis method of 2-chloronicotinamide and N-substituted derivative thereof | 山东京博生物科技有限公司 | 2023-08-25 | — | — | CN | claimed |
| CN-115260092-A | Synthesis method of 2-chloronicotinamide and N-substituted derivative thereof | 山东京博生物科技有限公司 | 2022-11-01 | — | — | CN | claimed |
| CN-108101799-A | A kind of high-efficient production technology of glycine | 严世佳 | 2018-06-01 | — | — | CN | claimed |
| US-9777022-B2 | Process for the preparation of macrocyclic polyazacarboxylate ligands and chelates | GUERBET (FR) | 2017-10-03 | — | — | US | claimed |
| EP-2920156-B9 | PROCESS FOR THE PREPARATION OF MACROCYCLIC POLYAZACARBOXYLATE LIGANDS AND CHELATES | GUERBET SA (FR) | 2017-04-19 | — | — | EP | claimed |
| EP-2920156-B1 | PROCESS FOR THE PREPARATION OF MACROCYCLIC POLYAZACARBOXYLATE LIGANDS AND CHELATES | GUERBET SA (FR) | 2016-12-07 | — | — | EP | claimed |
| US-20160185803-A1 | PROCESS FOR THE PREPARATION OF MACROCYCLIC POLYAZACARBOXYLATE LIGANDS AND CHELATES | MALLINCKRODT LLC | 2016-06-30 | — | — | US | claimed |
| US-9315474-B2 | Process for the preparation of macrocyclic polyazacarboxylate ligands and chelates | LIEBEL-FLARSHEIM COMPANY LLC (US) | 2016-04-19 | — | — | US | claimed |
| EP-2920156-A1 | PROCESS FOR THE PREPARATION OF MACROCYCLIC POLYAZACARBOXYLATE LIGANDS AND CHELATES | Mallinckrodt LLC (US) | 2015-09-23 | — | — | EP | claimed |
| US-20150259304-A1 | PROCESS FOR THE PREPARATION OF MACROCYCLIC POLYAZACARBOXYLATE LIGANDS AND CHELATES | GUERBET (FR) | 2015-09-17 | — | — | US | claimed |
| CN-103204824-B | 2-aminothiazole-4-amide derivative, its preparation method and application | UNIV TSINGHUA GRADUATE SCHOOL | 2015-04-08 | — | — | CN | claimed |
| CN-103204862-B | 6-phenylimidazol[2, 1-b]thiazole-3-amide derivative, its preparation method and application | UNIV TSINGHUA GRADUATE SCHOOL | 2014-12-17 | — | — | CN | claimed |
| WO-2014192030-A2 | AN IMPROVED PROCESS FOR PREPARATION OF DABIGATRAN ETEXILATE AND PHARMACEUTICALLY ACCEPTABLE ACID ADDITION SALTS THEREOF | LAURUS LABS PRIVATE LIMITED (IN) | 2014-12-04 | — | — | WO | claimed |
| WO-2014055504-A1 | PROCESS FOR THE PREPARATION OF MACROCYCLIC POLYAZACARBOXYLATE LIGANDS AND CHELATES | MALLINCKRODT LLC (US) | 2014-04-10 | — | — | WO | claimed |
| CN-103204824-A | 2-aminothiazole-4-amide derivative, its preparation method and application | UNIV TSINGHUA GRADUATE SCHOOL | 2013-07-17 | — | — | CN | claimed |
| CN-103204862-A | 6-phenylimidazol[2, 1-b]thiazole-3-amide derivative, its preparation method and application | UNIV TSINGHUA GRADUATE SCHOOL | 2013-07-17 | — | — | CN | claimed |
| CN-1196684-C | Process for producing N.N'-carbonyl dilactan | SNPC (FR) | 2005-04-13 | — | — | CN | claimed |
| US-6699988-B2 | BY REACTING PHOSGENE AND LACTAM IN THE PRESENCE OF A NON-NUCLEOPHILIC ALIPHATIC TERTIARY AMINE, SUCH AS N,N-DIISOPROPYLETHYLAMINE; HIGH PURITY, GOOD YIELDS | SNPE (FR) | 2004-03-02 | — | — | US | claimed |
| US-20010044532-A1 | Process for the preparation of N,N' -carbonylbislactams | ISOCHEM (FR) | 2001-11-22 | — | — | US | claimed |
| CN-1322718-A | Preparation method of N, N' -carbonyl dilactan | SNPC (FR) | 2001-11-21 | — | — | CN | claimed |