Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2385698

Cl.OCCNS

nearest known ligand 0.00

Full drug profile on Sugi Atlas →

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.

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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.

Compoundsimilaritytop predictedshared targets
Hydrochloric Acid SCHEMBL27874762 1.00
SCHEMBL2783999 0.96
Diethanolamine SCHEMBL1886510 0.70
Diethanolamine SCHEMBL1011320 0.70
SCHEMBL25924148 0.67
Hydrochloric Acid SCHEMBL650652 0.67 SMN1; SMN2 (0.43)
Hydrochloric Acid SCHEMBL5552704 0.67
Diethanolamine SCHEMBL5391215 0.67
SCHEMBL9664789 0.66
Diethanolamine SCHEMBL1539154 0.64

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 16 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117168937-A Sealing tablet composition for delaying fluorescence quenching, sealing tablet and application thereof 河南赛诺特生物技术有限公司 2023-12-05 CN disclosed
EP-2370401-B1 AMIDE-LINKED PERFLUOROPOLYETHER THIOL COMPOUNDS AND PROCESSES FOR THEIR PREPARATION AND USE 3M INNOVATIVE PROPERTIES CO (US) 2018-01-24 EP disclosed
US-20170253570-A1 AMIDE-LINKED PERFLUOROPOLYETHER THIOL COMPOUNDS AND PROCESSES FOR THEIR PREPARATION AND USE 3M INNOVATIVE PROPERTIES COMPANY 2017-09-07 US disclosed
US-9688649-B2 Amide-linked perfluoropolyether thiol compounds and processes for their preparation and use 3M INNOVATIVE PROPERTIES COMPANY (US) 2017-06-27 US disclosed
EP-2370269-B1 PATTERNING PROCESS 3M INNOVATIVE PROPERTIES CO (US) 2015-08-05 EP disclosed
US-20150051362-A1 AMIDE-LINKED PERFLUOROPOLYETHER THIOL COMPOUNDS AND PROCESSES FOR THEIR PREPARATION AND USE 3M INNOVATIVE PROPERTIES CO (US) 2015-02-19 US disclosed
US-8901263-B2 Amide-linked perfluoropolyether thiol compounds and processes for their preparation and use 3M INNOVATIVE PROPERTIES COMPANY (US) 2014-12-02 US disclosed
US-8858813-B2 Patterning process 3M INNOVATIVE PROPERTIES COMPANY (US) 2014-10-14 US disclosed
EP-2370269-A1 PATTERNING PROCESS 3M Innovative Properties Company (US) 2011-10-05 EP disclosed
EP-2370401-A1 AMIDE-LINKED PERFLUOROPOLYETHER THIOL COMPOUNDS AND PROCESSES FOR THEIR PREPARATION AND USE 3M Innovative Properties Company (US) 2011-10-05 EP disclosed
US-20110237765-A1 Amide-linked Perfluoropolyether Thiol Compounds and Processes for their Preparation and Use 3M INNOVATIVE PROPERTIES COMPANY 2011-09-29 US disclosed
US-20110226733-A1 PATTERNING PROCESS 3M INNOVATIVE PROPERTIES COMPANY 2011-09-22 US disclosed
WO-2010068535-A1 PATTERNING PROCESS 3M INNOVATIVE PROPERTIES COMPANY (US) 2010-06-17 WO disclosed
WO-2010068531-A1 AMIDE-LINKED PERFLUOROPOLYETHER THIOL COMPOUNDS AND PROCESSES FOR THEIR PREPARATION AND USE 3M INNOVATIVE PROPERTIES COMPANY (US) 2010-06-17 WO disclosed
EP-1214428-A1 METHOD FOR PRODUCING ACTIVE SERINE PROTEASES AND INACTIVE VARIANTS Max-Planck-Gesellschaft E.V. (DE) 2002-06-19 EP disclosed
WO-2001018215-A1 METHOD FOR PRODUCING ACTIVE SERINE PROTEASES AND INACTIVE VARIANTS MAX-PLANCK-GESELLSCHAFT E.V. (DE) 2001-03-15 WO disclosed