Hydrochloric Acid

Hydrochloric Acid

SCHEMBL460378

Cl.O=C1PC(=O)C(O)C1O

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
SCHEMBL264289 0.96
SCHEMBL6243027 0.96
Hydrochloric Acid SCHEMBL7931820 0.94
Bromide SCHEMBL7877090 0.93
Water SCHEMBL274857 0.93
SCHEMBL7929182 0.93
Iodide SCHEMBL7058984 0.93
Bicarbonate SCHEMBL9960105 0.87 CA1 (0.31)
Cyanide SCHEMBL7573657 0.87
Boric Acid SCHEMBL7999344 0.87

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 38 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2528864-B1 METHOD OF PRODUCING CYCLOHEXASILANE COMPOUNDS Ndsu res found (US) 2017-03-29 EP claimed
US-8975429-B2 Method of producing cyclohexasilane compounds NDSU RESEARCH FOUNDATION (US) 2015-03-10 US claimed
EP-2528864-A1 METHOD OF PRODUCING CYCLOHEXASILANE COMPOUNDS Ndsu Research Foundation (US) 2012-12-05 EP claimed
US-20120294791-A1 METHOD OF PRODUCING CYCLOHEXASILANE COMPOUNDS NDSU RESEARCH FOUNDATION 2012-11-22 US claimed
WO-2011094191-A1 METHOD OF PRODUCING CYCLOHEXASILANE COMPOUNDS NDSU RESEARCH FOUNDATION (US) 2011-08-04 WO claimed
US-6169209-B1 BRINGING AN ORGANIC PHOSPHONIUM BROMIDE INTO CONTACT WITH A CHLORIDE ION IN A HETEROGENEOUS MIXTURE SOLUTION COMPRISING WATER AND AN ORGANIC SOLVENT TO FORM ORGANIC PHOSPHONIUM CHLORIDE UBE INDUSTRIES, LTD. (JP) 2001-01-02 US claimed
WO-2024141311-A1 SILYLATED POLYMER AND MIXTURES COMPRISING SAID POLYMER EVONIK OPERATIONS GMBH (DE) 2024-07-04 WO disclosed
EP-2528864-B1 METHOD OF PRODUCING CYCLOHEXASILANE COMPOUNDS Ndsu res found (US) 2017-03-29 EP disclosed
US-9174918-B2 Process for preparing diaryl oxalate UBE INDUSTRIES, LTD. (JP) 2015-11-03 US disclosed
US-8975429-B2 Method of producing cyclohexasilane compounds NDSU RESEARCH FOUNDATION (US) 2015-03-10 US disclosed
EP-2456747-B1 Method for preparing alkoxyenones and enaminoketones BAYER CROPSCIENCE AG (DE) 2014-06-25 EP disclosed
EP-2528864-A1 METHOD OF PRODUCING CYCLOHEXASILANE COMPOUNDS Ndsu Research Foundation (US) 2012-12-05 EP disclosed
US-20120296063-A1 PROCESS FOR PREPARING DIARYL OXALATE UBE CORPORATION (JP) 2012-11-22 US disclosed
EP-0834496-A1 Preparation of diaryl carbonate UBE INDUSTRIES, LTD. (JP) 1998-04-08 EP disclosed
US-5731453-A Process for producing a diaryl carbonate UBE INDUSTRIES, LTD. (JP) 1998-03-24 US disclosed
EP-0826658-A1 Catalyst for decarbonylation reaction UBE INDUSTRIES, LTD. (JP) 1998-03-04 EP disclosed
EP-0795539-A1 Process for producing a diaryl carbonate UBE INDUSTRIES LIMITED (JP) 1997-09-17 EP disclosed
US-5648510-A DECARBONYLATION OF OXALATE UBE INDUSTRIES, LTD. (JP) 1997-07-15 US disclosed
EP-0737665-A1 Process for preparation of diaryl carbonate UBE INDUSTRIES, LTD. (JP) 1996-10-16 EP disclosed
US-5565573-A Synthesis of epibatidine and analogs thereof IOWA STATE UNIVERSITY RESEARCH FOUNDATION, INC. (US) 1996-10-15 US disclosed