Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2570665

COc1ccc(C(=N)N)cc1.Cl

nearest known ligand 0.95

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 15)

geneUniProtsupporting neighboursconfidence
CA2 known ✓ P00918 1/20 0.59
PARP1 known ✓ P09874 1/20 0.59
PRSS1 P07477 10/20 0.95
PRSS2 P07478 3/20 0.95
PRSS3 P35030 3/20 0.95
PTGIR P43119 1/20 0.75
NQO2 P16083 2/20 0.68
ST14 Q9Y5Y6 2/20 0.64
F2 P00734 2/20 0.64
PLAU P00749 1/20 0.64
CA1 P00915 1/20 0.59
PARP10 Q53GL7 1/20 0.59
PARP2 Q9UGN5 1/20 0.59
PARP4 Q9UKK3 1/20 0.59
TMPRSS2 O15393 1/20 0.55

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
SCHEMBL428892 0.98 PRSS1 (1.00) PRSS1PRSS2PRSS3PTGIRNQO2
SCHEMBL9852190 0.92 PRSS1 (0.81) PRSS1PRSS2PRSS3PTGIRNQO2
SCHEMBL15293729 0.91 PRSS1 (0.88) PRSS1PRSS2PRSS3PTGIRNQO2
SCHEMBL9852193 0.90 PRSS1 (0.84) PRSS1PRSS2PRSS3PTGIRNQO2
SCHEMBL5788625 0.86 PTGIR (1.00) PRSS1PRSS2PRSS3PTGIRNQO2
Hydrochloric Acid SCHEMBL30859643 0.84 ALDH1A1 (0.74) PRSS1PRSS2PRSS3PTGIRNQO2
SCHEMBL10890871 0.83 PRSS1 (0.72) PRSS1PRSS2PRSS3PTGIRNQO2
Hydrochloric Acid SCHEMBL31546705 0.82 PRSS1 (0.66) PRSS1PRSS2PRSS3PTGIRNQO2
SCHEMBL14599566 0.82 NQO2 (1.00) PRSS1PRSS2PRSS3PTGIRNQO2
Hydrochloric Acid SCHEMBL30999366 0.80 PRSS1 (0.78) PRSS1PRSS2PRSS3ST14F2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120166906-A Two-dimensional/three-dimensional perovskite heterojunction based on amidino cation and application of perovskite heterojunction in solar cell 西安交通大学 2025-06-17 CN claimed
CN-118086928-A Method for electrochemical synthesis of pyrimidoindole derivative under mild condition 湘潭大学 2024-05-28 CN claimed
CN-117926289-A Method for electrochemically synthesizing N-sulfoamidine derivatives under mild condition 湘潭大学 2024-04-26 CN claimed
CN-117003738-A Imidazole spiro compound and synthesis method thereof 湘潭大学 2023-11-07 CN claimed
CN-116947854-A Preparation method of imidazo [2,1-a ] isoquinoline compound 赣南师范大学 2023-10-27 CN claimed
CN-114853681-A Preparation method of pyrimidine heterocyclic guanyl formate compound 南京工业大学 2022-08-05 CN claimed
CN-113024470-B 4-perfluoroalkyl substituted pyrimidine compound and preparation method and application thereof 南京工业大学 2022-05-24 CN claimed
CN-113024470-A 4-perfluoroalkyl substituted pyrimidine compound and preparation method and application thereof 南京工业大学 2021-06-25 CN claimed
CN-112159411-A Trifluoromethyl substituted pyrimido [1,3] diaza compound and preparation method thereof 南京工业大学 2021-01-01 CN claimed
JP-7233154-A None JP disclosed
JP-1319465-A None JP disclosed
CN-120166906-A Two-dimensional/three-dimensional perovskite heterojunction based on amidino cation and application of perovskite heterojunction in solar cell 西安交通大学 2025-06-17 CN disclosed
CN-118086928-A Method for electrochemical synthesis of pyrimidoindole derivative under mild condition 湘潭大学 2024-05-28 CN disclosed
CN-117926289-A Method for electrochemically synthesizing N-sulfoamidine derivatives under mild condition 湘潭大学 2024-04-26 CN disclosed
US-4113868-A 5,6-DIHYDROPYRIMIDIN-4(3H)ONE DERIVATIVES, AND ANTIEDEMA COMPOSITIONS AND METHODS EMPLOYING THEM CHINOIN GYOGYSZER ES VEGYESZETI TERMEKEK GYARA R.T. (HU) 1978-09-12 US disclosed
US-4093811-A 2-Aryl-4-cyanomethyl-5-methylimidazoles MCNEIL LABORATORIES, INCORPORATED (US) 1978-06-06 US disclosed
US-4026891-A HYPOTENSIVE AGENTS, ANTITHROMBOTICS, AND CARDIOTONICS BOEHRINGER INGELHEIM GMBH (DT) 1977-05-31 US disclosed
US-3968213-A 4-HYDROXY-5-CARBOXY PYRIMIDINES PFIZER INC. (US) 1976-07-06 US disclosed
US-3957784-A ANTIALLERGY AGENTS PFIZER INC. (US) 1976-05-18 US disclosed
US-3940395-A CNS DEPRESSANT AMERICAN HOME PRODUCTS CORPORATION (US) 1976-02-24 US disclosed