Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1098138

CCCN=C(N)N.Cl

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
SCHEMBL1626211 0.97
Bromide SCHEMBL9335511 0.94
Methylamine SCHEMBL27336591 0.94 MEN1 (0.59)
Trimethylammonium SCHEMBL27330103 0.88 MEN1 (0.54)
SCHEMBL27759182 0.86 MEN1 (0.52)
Sulfuric Acid SCHEMBL10930722 0.84 NPSR1 (0.57)
Hydrochloric Acid SCHEMBL4604366 0.82
Hydrochloric Acid SCHEMBL28349745 0.80 MEN1 (0.90)
SCHEMBL10769165 0.79
SCHEMBL10769161 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 26 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3161102-B1 PHOTOCHROMIC ARTICLES CONTAINING POLYOXOMETALATE DERIVATIVES AND METHODS OF MAKING SAME 3M INNOVATIVE PROPERTIES CO (US) 2019-01-16 EP claimed
US-9976077-B2 Photochromic articles containing polyoxometalate derivatives and methods of making same 3M INNOVATIVE PROPERTIES COMPANY (US) 2018-05-22 US claimed
US-20170198215-A1 PHOTOCHROMIC ARTICLES CONTAINING POLYOXOMETALATE DERIVATIVES AND METHODS OF MAKING SAME 3M INNOVATIVE PROPERTIES COMPANY 2017-07-13 US claimed
EP-3161102-A1 PHOTOCHROMIC ARTICLES CONTAINING POLYOXOMETALATE DERIVATIVES AND METHODS OF MAKING SAME 3M Innovative Properties Company (US) 2017-05-03 EP claimed
WO-2016003683-A1 PHOTOCHROMIC ARTICLES CONTAINING POLYOXOMETALATE DERIVATIVES AND METHODS OF MAKING SAME 3M INNOVATIVE PROPERTIES COMPANY (US) 2016-01-07 WO claimed
US-10711182-B2 Photochromic articles containing a polyoxometalate and methods of making and using same 3M INNOVATIVE PROPERTIES COMPANY (US) 2020-07-14 US disclosed
CN-107849437-B Photochromic articles comprising polyoxometallates and methods of making and using the same 3M创新有限公司 2020-06-05 CN disclosed
EP-3161102-B1 PHOTOCHROMIC ARTICLES CONTAINING POLYOXOMETALATE DERIVATIVES AND METHODS OF MAKING SAME 3M INNOVATIVE PROPERTIES CO (US) 2019-01-16 EP disclosed
US-20180194994-A1 PHOTOCHROMIC ARTICLES CONTAINING A POLYOXOMETALATE AND METHODS OF MAKING AND USING SAME 3M INNOVATIVE PROPERTIES COMPANY 2018-07-12 US disclosed
US-9976077-B2 Photochromic articles containing polyoxometalate derivatives and methods of making same 3M INNOVATIVE PROPERTIES COMPANY (US) 2018-05-22 US disclosed
US-20170198215-A1 PHOTOCHROMIC ARTICLES CONTAINING POLYOXOMETALATE DERIVATIVES AND METHODS OF MAKING SAME 3M INNOVATIVE PROPERTIES COMPANY 2017-07-13 US disclosed
EP-3161102-A1 PHOTOCHROMIC ARTICLES CONTAINING POLYOXOMETALATE DERIVATIVES AND METHODS OF MAKING SAME 3M Innovative Properties Company (US) 2017-05-03 EP disclosed
WO-2007144769-A2 ARYL- AND HETEROARYL-ETHYL-ACYLGUANIDINE DERIVATIVES, THEIR PREPARATION AND THEIR APPLICATION IN THERAPEUTICS SANOFI-AVENTIS (FR) 2007-12-21 WO disclosed
EP-1248812-A1 METHOD FOR PREPARING POLYETHER COPOLYMERS WITH POLYCARBONATES AND POLYARYLATES GENERAL ELECTRIC COMPANY (US) 2002-10-16 EP disclosed
WO-2001042337-A1 METHOD FOR PREPARING POLYETHER COPOLYMERS WITH POLYCARBONATES AND POLYARYLATES GENERAL ELECTRIC COMPANY (US) 2001-06-14 WO disclosed
EP-0846108-A1 AMINO-SUBSTITUTED THIADIAZOLES, PYRIMIDINES, TRIAZINES OR TRIAZOLES USEFUL AS CTF RECEPTOR ANTAGONISTS NEUROCRINE BIOSCIENCES, INC. (US) 1998-06-10 EP disclosed
WO-1996039400-A1 AMINO-SUBSTITUTED THIADIAZOLES, PYRIMIDINES, TRIAZINES OR TRIAZOLES USEFUL AS CTF RECEPTOR ANTAGONISTS NEUROCRINE BIOSCIENCES, INC. (US) 1996-12-12 WO disclosed
EP-0593438-A1 FUNGICIDAL COMPOSITIONS, FUNGICIDAL COMPOUNDS, THEIR PRODUCTION AND USE DOWELANCO (US) 1994-04-27 EP disclosed
US-5292743-A Substituted guanidines; low phytotoxicity; agricultural use DOWELANCO (US) 1994-03-08 US disclosed
WO-1991005473-A1 FUNGICIDAL COMPOSITIONS, FUNGICIDAL COMPOUNDS, THEIR PRODUCTION AND USE DOW CHEMICAL COMPANY LIMITED (GB) 1991-05-02 WO disclosed