Hydrochloric Acid

Hydrochloric Acid

SCHEMBL558002

CCCCN1C=CN(CCCC)C1.Cl

nearest known ligand 0.37

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.

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
GAA known ✓ P10253 4/20 0.33
SIGMAR1 known ✓ Q99720 1/20 0.30
GLB1 P16278 1/20 0.37
MEN1 O00255 1/20 0.33
LMNA P02545 1/20 0.33
MAPK1 P28482 1/20 0.33
KMT2A Q03164 1/20 0.33
GBA1 P04062 3/20 0.32
TP53 P04637 1/20 0.32
DNM1 Q05193 4/20 0.32
GNAI3 P08754 1/20 0.31
GNAO1 P09471 1/20 0.31
GNAI1 P63096 1/20 0.31
GBA2 Q9HCG7 6/20 0.31
UGCG Q16739 3/20 0.31
MGAM O43451 2/20 0.31
SI P14410 2/20 0.31
AGL P35573 2/20 0.31
EBP Q15125 1/20 0.30

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

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
SCHEMBL329125 0.97 GLB1 (0.38) GLB1GAALMNAKMT2AGBA1
Hydrochloric Acid SCHEMBL960559 0.95 GLB1 (0.34) GLB1GAAMEN1LMNAMAPK1
Hydrochloric Acid SCHEMBL962418 0.95 GNAI3 (0.38) GLB1DNM1GNAI3GNAO1GNAI1
Iodide SCHEMBL31332603 0.95 GLB1 (0.37) GLB1GAALMNAKMT2AGBA1
Bromide SCHEMBL556686 0.95 GLB1 (0.37) GLB1GAAKMT2AGBA1TP53
Bromide SCHEMBL23071102 0.95 GLB1 (0.37) GLB1GAAKMT2AGBA1TP53
Hydrochloric Acid SCHEMBL958641 0.93 GNAI3 (0.41) DNM1GNAI3GNAO1GNAI1EBP
Hydrochloric Acid SCHEMBL961164 0.93 GLB1 (0.33) GLB1GAAMEN1LMNAMAPK1
SCHEMBL899123 0.92 GLB1 (0.35) GLB1GAAGBA1TP53
Hydrochloric Acid SCHEMBL29290774 0.92 GLB1 (0.35) GLB1GAAMEN1KMT2AGBA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119660720-A Corrosion inhibitor based on N, S, P co-doped carbon quantum dots, and preparation method and application thereof 盐城工学院 2025-03-21 CN claimed
CN-111836849-B Process for producing fibers, films and moldings of polybenzazole polymer (P) 巴斯夫欧洲公司 2023-04-07 CN claimed
CN-115466735-A Method for extracting lysozyme from eggs by using ionic liquid 河南工学院 2022-12-13 CN claimed
EP-3512905-B1 METHOD FOR PRODUCING A POLYBENZAZOL POLYMER (P) BASF SE (DE) 2022-08-24 EP claimed
CN-109790292-B Process for preparing polybenzazole polymer (P) 巴斯夫欧洲公司 2022-05-31 CN claimed
EP-3762447-A1 METHOD FOR PRODUCING FIBRES, FILMS AND MOULDED BODIES OF A POLYBENZAZOLE POLYMER (P) BASF SE (DE) 2021-01-13 EP claimed
US-20200407508-A1 METHOD FOR PRODUCING FIBERS, FILMS AND MOLDINGS OF A POLYBENZAZOLE POLYMER (P) BASF SE (DE) 2020-12-31 US claimed
CN-111836849-A Process for producing fibers, films and moldings of polybenzazole polymer (P) 巴斯夫欧洲公司 2020-10-27 CN claimed
CN-107413379-B Catalyst for alkyl carbonate and aryl alcohol ester exchange reaction and preparation method thereof 濮阳市宏源石油化工有限公司 2020-08-25 CN claimed
WO-2019170529-A1 METHOD FOR PRODUCING FIBRES, FILMS AND MOULDED BODIES OF A POLYBENZAZOLE POLYMER (P) BASF SE (DE) 2019-09-12 WO claimed
CN-107413379-A For alkyl carbonate and the catalyst and preparation method of aryl alcohol transesterification reaction 濮阳市宏源石油化工有限公司 2017-12-01 CN claimed
US-9267214-B2 Aluminum recovery process BOARD OF TRUSTEES OF THE UNIVERSITY OF ALABAMA (US) 2016-02-23 US claimed
US-20110000782-A1 ALUMINUM RECOVERY PROCESS THE UNIVERSITY OF ALABAMA (US) 2011-01-06 US claimed
WO-2009102419-A2 ALUMINUM RECOVERY PROCESS THE UNIVERSITY OF ALABAMA (US) 2009-08-20 WO claimed
US-12291506-B2 Method for producing amidate compound, and amidate compound KOEI CHEMICAL COMPANY, LIMITED (JP) 2025-05-06 US disclosed
CN-119925380-A N-heterocyclic carbene-gold (I) -benzyne complex and antibacterial application thereof 中山大学 2025-05-06 CN disclosed
CN-119660720-A Corrosion inhibitor based on N, S, P co-doped carbon quantum dots, and preparation method and application thereof 盐城工学院 2025-03-21 CN disclosed
US-6712950-B2 PROVIDING LIQUID ELECTROLYTE WHICH IS NOT AQUEOUS SOLUTION, PROVIDING HYDROGEN GAS TO ANODE, ELECTROCHEMICALLY OXIDIZING NEGATIVELY CHARGED NITROGEN CONTAINING SPECIES IN ELECTROLYTE AT ANODE TO ATOMIC NITROGEN SPECIES, REACTING WITH HYDROGEN LYNNTECH, INC. 2004-03-30 US disclosed
US-6426161-B1 LIGHTWEIGHT BIPOLAR PLATE COMPRISING GAS FLOW CHANNELS AND CONTACT SURFACES, CHARACTERIZED IN THAT PLATE COMPRISES LIGHT METAL SELECTED FROM ALUMINUM, MAGNESIUM AND MIXTURES THEREOF AND SURFACES OF GAS FLOW CHANNELS ARE HYDROPHOBIC LYNNTECH, INC. 2002-07-30 US disclosed
US-6203936-B1 BIPOLAR PLATES WITH SUBSTRATES OF METALS OR ALLOYS OF MAGNESIUM, ALUMINUM AND NICKEL WITH ELECTROLESS METAL LAYER LYNNTECH INC. 2001-03-20 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-12291506-B2 Method for producing amidate compound, and amidate compound NAAA, NIT2, PAM GAA 1679/4885SIGMAR1 2319/4885GLB1 1443/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.