Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2680168

Cl.N#CC(N)Cc1ccccc1

nearest known ligand 0.54

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 20)

geneUniProtsupporting neighboursconfidence
SLC6A2 known ✓ P23975 2/20 0.50
MAOA known ✓ P21397 1/20 0.50
SLC6A4 known ✓ P31645 1/20 0.50
SLC6A3 known ✓ Q01959 1/20 0.50
SIGMAR1 known ✓ Q99720 1/20 0.50
PTGS1 known ✓ P23219 1/20 0.45
MAOB known ✓ P27338 1/20 0.42
EPHX1 P07099 1/20 0.54
TAAR1 Q96RJ0 2/20 0.50
CYP2A6 P11509 1/20 0.50
ADORA2A P29274 1/20 0.50
ADORA1 P30542 1/20 0.50
CTSC P53634 4/20 0.47
ANPEP P15144 2/20 0.47
CYP2D6 P10635 1/20 0.47
ALPI P09923 1/20 0.45
PKM P14618 1/20 0.45
XIAP P98170 1/20 0.45
SLC7A5 Q01650 1/20 0.45
LAP3 P28838 3/20 0.42

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
Hydrochloric Acid SCHEMBL5562831 1.00 EPHX1 (0.54) EPHX1SLC6A2TAAR1MAOASLC6A4
SCHEMBL2921309 0.98 EPHX1 (0.56) EPHX1SLC6A2TAAR1MAOASLC6A4
SCHEMBL1598678 0.98 EPHX1 (0.56) EPHX1SLC6A2TAAR1MAOASLC6A4
SCHEMBL5186213 0.98 EPHX1 (0.56) EPHX1SLC6A2TAAR1MAOASLC6A4
SCHEMBL2074585 0.86 CTSC (0.50) EPHX1SLC6A2TAAR1MAOASLC6A4
SCHEMBL2074587 0.86 CTSC (0.50) EPHX1SLC6A2TAAR1MAOASLC6A4
SCHEMBL4426620 0.84 CTSC (0.50) EPHX1SLC6A2TAAR1MAOASLC6A4
SCHEMBL23340080 0.81 LTA4H (0.61) SLC6A2MAOASLC6A3PTGS1LAP3
SCHEMBL19982072 0.81 LTA4H (0.61) SLC6A2MAOASLC6A3PTGS1LAP3
SCHEMBL16553364 0.80 CTSC (0.41) EPHX1SLC6A2TAAR1SLC6A4SLC6A3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4760089-A Benzonitrile derivative; enzyme inhibitor SMITHKLINE BECKMAN CORPORATION (US) 1988-07-26 US claimed
US-20260028662-A1 OPLOPHORUS-DERIVED LUCIFERASES, NOVEL COELENTERAZINE SUBSTRATES, AND METHODS OF USE PROMEGA CORP (US) 2026-01-29 US disclosed
US-12435354-B2 Oplophorus-derived luciferases, novel coelenterazine substrates, and methods of use PROMEGA CORPORATION (US) 2025-10-07 US disclosed
US-12215375-B2 Oplophorus-derived luciferases, novel coelenterazine substrates, and methods of use PROMEGA CORPORATION (US) 2025-02-04 US disclosed
US-20240158831-A1 OPLOPHORUS-DERIVED LUCIFERASES, NOVEL COELENTERAZINE SUBSTRATES, AND METHODS OF USE PROMEGA CORPORATION 2024-05-16 US disclosed
US-11661623-B2 Oplophorus-derived luciferases, novel coelenterazine substrates, and methods of use PROMEGA CORPORATION (US) 2023-05-30 US disclosed
US-20220348983-A1 OPLOPHORUS-DERIVED LUCIFERASES, NOVEL COELENTERAZINE SUBSTRATES, AND METHODS OF USE PROMEGA CORPORATION 2022-11-03 US disclosed
CN-106148362-B Novel coelenterazine substrates and methods of use thereof 普罗梅加公司 2021-04-30 CN disclosed
US-20200399676-A1 OPLOPHORUS-DERIVED LUCIFERASES, NOVEL COELENTERAZINE SUBSTRATES, AND METHODS OF USE PROMEGA CORPORATION 2020-12-24 US disclosed
US-10774364-B2 Oplophorus-derived luciferases, novel coelenterazine substrates, and methods of use PROMEGA CORPORATION (US) 2020-09-15 US disclosed
EP-0313091-B1 AMIDE DERIVATIVES, PROCESSES FOR PRODUCTION THEREOF, AND AGRICULTURAL-HORTICULTURAL FUNGICIDE CONTAINING THEM MITSUI TOATSU CHEMICALS, Inc. (JP) 1993-09-01 EP disclosed
CN-1066363-A MICROBICIDES COMPOSITION FOR AGRICULTURE-HORTICULTURE MITSUI TOATSU CHEMICALS (JP) 1992-11-25 CN disclosed
CN-1018828-B Process for preparing thiazole or isothiazole amide derivatives MITSUI TOATSU CHEMICALS (JP) 1992-10-28 CN disclosed
US-5104886-A Syntergistic mixtures of amide substituted thiazoles and other fungicides MITSUI TOATSU CHEMICALS, INC. (JP) 1992-04-14 US disclosed
US-4980363-A CONTROLLING PLANT DISEASES MITSUI TOATSU CHEMICALS, INC. (JP) 1990-12-25 US disclosed
CN-1035826-A Novel amide derivative and agricultural-horticultural fungicide containing the same MITSUI TOATSU CHEMICALS (JP) 1989-09-27 CN disclosed
EP-0313091-A2 Amide derivatives, processes for production thereof, and agricultural-horticultural fungicide containing them MITSUI TOATSU CHEMICALS, Inc. (JP) 1989-04-26 EP disclosed
EP-0219961-B1 IRREVERSIBLE DOPAMINE-B-HYDROXYLASE INHIBITORS SMITHKLINE BECKMAN CORPORATION (US) 1989-03-08 EP disclosed
US-4760089-A Benzonitrile derivative; enzyme inhibitor SMITHKLINE BECKMAN CORPORATION (US) 1988-07-26 US disclosed
EP-0219961-A1 Irreversible dopamine-B-hydroxylase inhibitors SMITHKLINE BECKMAN CORPORATION (US) 1987-04-29 EP 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 (8 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-12435354-B2 Oplophorus-derived luciferases, novel coelenterazine substrates, and methods of use RNGTT, UPF1, LUC7L2 SLC6A2 3141/4885MAOA 3476/4885SLC6A4 3746/4885
US-10774364-B2 Oplophorus-derived luciferases, novel coelenterazine substrates, and methods of use RNGTT, UPF1, LUC7L2 SLC6A2 3141/4885MAOA 3476/4885SLC6A4 3746/4885
US-20220348983-A1 OPLOPHORUS-DERIVED LUCIFERASES, NOVEL COELENTERAZINE SUBSTRATES, AND METHODS OF USE RNGTT, UPF1, LUC7L2 SLC6A2 3141/4885MAOA 3476/4885SLC6A4 3746/4885
US-20240158831-A1 OPLOPHORUS-DERIVED LUCIFERASES, NOVEL COELENTERAZINE SUBSTRATES, AND METHODS OF USE RNGTT, UPF1, LUC7L2 SLC6A2 3141/4885MAOA 3476/4885SLC6A4 3746/4885
US-11661623-B2 Oplophorus-derived luciferases, novel coelenterazine substrates, and methods of use RNGTT, UPF1, LUC7L2 SLC6A2 3141/4885MAOA 3476/4885SLC6A4 3746/4885
US-12215375-B2 Oplophorus-derived luciferases, novel coelenterazine substrates, and methods of use RNGTT, UPF1, LUC7L2 SLC6A2 3141/4885MAOA 3476/4885SLC6A4 3746/4885
US-20260028662-A1 OPLOPHORUS-DERIVED LUCIFERASES, NOVEL COELENTERAZINE SUBSTRATES, AND METHODS OF USE RNGTT, VIP, PREP SLC6A2 3036/4885MAOA 2307/4885SLC6A4 3154/4885
US-20200399676-A1 OPLOPHORUS-DERIVED LUCIFERASES, NOVEL COELENTERAZINE SUBSTRATES, AND METHODS OF USE RNGTT, UPF1, LUC7L2 SLC6A2 3141/4885MAOA 3476/4885SLC6A4 3746/4885

“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.