Hydrochloric Acid

Hydrochloric Acid

SCHEMBL158567

Cl.Nc1c(Br)cc(Br)cc1CNC1CCCCC1

nearest known ligand 0.74

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
▸ SLC6A4 known ✓ P31645 2/20 0.72
▸ KCNH2 known ✓ Q12809 2/20 0.72
▸ HRH2 known ✓ P25021 1/20 0.72
▸ SLC6A2 known ✓ P23975 1/20 0.52
▸ PDE4A known ✓ P27815 1/20 0.52
▸ SLC6A3 known ✓ Q01959 1/20 0.52
▸ SIGMAR1 known ✓ Q99720 1/20 0.52
▸ GAA known ✓ P10253 1/20 0.43
▸ ADRB2 known ✓ P07550 3/20 0.40
▸ HRH3 known ✓ Q9Y5N1 1/20 0.39
▸ CYP3A4 P08684 2/20 0.74
▸ TDP1 Q9NUW8 2/20 0.74
▸ ALOX15 P16050 1/20 0.74
▸ TSHR P16473 1/20 0.74
▸ CYP2D6 P10635 3/20 0.72
▸ LMNA P02545 2/20 0.72
▸ CYP1A2 P05177 2/20 0.72
▸ GBA1 P04062 1/20 0.72
▸ CNR1 P21554 1/20 0.72
▸ TBXA2R P21731 1/20 0.72

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 SCHEMBL29729337 1.00 CYP3A4 (0.74) CYP3A4TDP1ALOX15TSHRCYP2D6
SCHEMBL24446594 0.98 CYP2D6 (0.74) CYP3A4TDP1ALOX15TSHRCYP2D6
SCHEMBL30080216 0.98 CYP2D6 (0.74) CYP3A4TDP1ALOX15TSHRCYP2D6
SCHEMBL2342350 0.98 CYP2D6 (0.74) CYP3A4TDP1ALOX15TSHRCYP2D6
SCHEMBL24446500 0.89 CYP2D6 (0.65) CYP3A4TDP1ALOX15TSHRCYP2D6
SCHEMBL22927420 0.89 CYP2D6 (0.65) CYP3A4TDP1ALOX15TSHRCYP2D6
SCHEMBL24446428 0.88 CYP2D6 (0.67) CYP3A4TDP1ALOX15TSHRCYP2D6
SCHEMBL22927156 0.87 CYP2D6 (0.67) CYP3A4TDP1ALOX15TSHRCYP2D6
Hydrochloric Acid SCHEMBL10808670 0.87 CYP3A4 (0.77) CYP3A4TDP1ALOX15TSHRCYP2D6
Hydrochloric Acid SCHEMBL10808667 0.87 CYP3A4 (0.77) CYP3A4TDP1ALOX15TSHRCYP2D6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2875359-A2 COMPOSITIONS AND METHODS FOR TREATING OR PREVENTING METABOLIC SYNDROME DISORDERS Charles R Drew University of Medicine and Science (US) 2015-05-27 — — EP claimed
CN-104356002-A Preparation process of impurities contained in expectorant drug bromhexine hydrochloride UNIV HEBEI MEDICAL 2015-02-18 — — CN claimed
EP-2670404-A1 SIRTUIN MODULATORS AS VIRUS PRODUCTION MODULATORS The Trustees of Princeton University (US) 2013-12-11 — — EP claimed
WO-2013149258-A2 COMPOSITIONS AND METHODS FOR TREATING OR PREVENTING METABOLIC SYNDROME DISORDERS Charles Drew University of Medicine and Science (US) 2013-10-03 — — WO claimed
WO-2012106509-A1 SIRTUIN MODULATORS AS VIRUS PRODUCTION MODULATORS THE TRUSTEES OF PRINCETON UNIVERSITY (US) 2012-08-09 — — WO claimed
US-12533425-B2 Methods and systems using peptides for targeting and mapping human nerves in image guided surgery, diagnostics and therapeutic delivery ALUME BIOSCIENCES, INC. (US) 2026-01-27 — — US disclosed
EP-4484952-A2 OPTIMIZED PEPTIDES FOR TARGETING HUMAN NERVES AND THEIR USE IN IMAGE GUIDED SURGERY, DIAGNOSTICS AND THERAPEUTIC DELIVERY The Regents of the University of California (US) 2025-01-01 — — EP disclosed
US-20240358634-A1 AURIS FORMULATIONS FOR TREATING OTIC DISEASES AND CONDITIONS DOMPÉ FARMACEUTICI S.P.A. (IT) 2024-10-31 — — US disclosed
EP-3661539-B1 OPTIMIZED PEPTIDES FOR TARGETING HUMAN NERVES AND THEIR USE IN IMAGE GUIDED SURGERY, DIAGNOSTICS AND THERAPEUTIC DELIVERY UNIV CALIFORNIA (US) 2024-10-09 — — EP disclosed
US-20240207421-A1 NERVE TARGETING PEPTIDES AND METHODS OF USE ALUME BIOSCIENCES INC (US) 2024-06-27 — — US disclosed
US-20240207422-A1 NERVE TARGETING PEPTIDE CONJUGATES AND METHODS OF USE ALUME BIOSCIENCES INC (US) 2024-06-27 — — US disclosed
US-11969501-B2 Auris formulations for treating otic diseases and conditions DOMPÉ FARMACEUTICI S.P.A. (IT) 2024-04-30 — — US disclosed
US-20060111435-A1 Contacting cells with sirtuin activator or inhibitor; increasing or decreasing fat accumulation PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2006-05-25 — — US disclosed
US-20060084085-A1 Methods and compositions for modulating Bax-mediated apoptosis PRESIDENT AND FELLOWS OF HARVARD COLLEGE 2006-04-20 — — US disclosed
WO-2006007411-A2 METHODS AND COMPOSITIONS FOR MODULATING BAX-MEDIATED APOPTOSIS PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2006-01-19 — — WO disclosed
WO-2005065667-A2 COMPOSITIONS FOR TREATING OR PREVENTING OBESITY AND INSULIN RESISTANCE DISORDERS PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 2005-07-21 — — WO disclosed
US-20040219207-A1 Drug preparation comprising alpha-lipoic acid, ambroxol and/or inhibitors of the angiotensin-converting enzyme (ACE) and its use for the treatment of neurodegenerative diseases KEYNEUROTEK PHARMACEUTICALS AG (DE) 2004-11-04 — — US disclosed
EP-1442743-A1 Medicament comprising alpha-lipoic acid, ambroxol and/or inhibitors of the angiotensin converting enzyme (ACE) for use in the treatment of neurodegenerative diseases KeyNeurotek AG (DE) 2004-08-04 — — EP disclosed
US-20040138311-A1 Medicament containing an effector of the glutathione metabolism together with $g(a)-lipoic acid for treating diabetes mellitus ESPARMA GMBH (DE) 2004-07-15 — — US disclosed
US-20040127550-A1 Medicament containing an effector of the glutathione metabolism together with alpha-lipoic acid for use in kidney replacement therapy SERUMWERK BERNBURG AG (DE) 2004-07-01 — — 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 (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-20060111435-A1 Contacting cells with sirtuin activator or inhibitor; increasing or decreasing fat accumulation FABP4, PLIN1, SIRT1 SLC6A4 4637/4885KCNH2 4828/4885HRH2 4813/4885
US-20040219207-A1 Drug preparation comprising alpha-lipoic acid, ambroxol and/or inhibitors of the angiotensin-converting enzyme (ACE) and its use for the treatment of neurodegenerative diseases ACE, LCT, CTSA SLC6A4 3525/4885KCNH2 4446/4885HRH2 164/4885
US-12533425-B2 Methods and systems using peptides for targeting and mapping human nerves in image guided surgery, diagnostics and therapeutic delivery NGLY1, VGF, GAP43 SLC6A4 3444/4885KCNH2 2148/4885HRH2 1524/4885
US-20240358634-A1 AURIS FORMULATIONS FOR TREATING OTIC DISEASES AND CONDITIONS OTC, AQP4, SLC26A4 SLC6A4 867/4885KCNH2 2334/4885HRH2 269/4885
US-20060084085-A1 Methods and compositions for modulating Bax-mediated apoptosis BAX, BCL2, CASP3 SLC6A4 4844/4885KCNH2 4677/4885HRH2 4689/4885
US-20040138311-A1 Medicament containing an effector of the glutathione metabolism together with $g(a)-lipoic acid for treating diabetes mellitus GSR, GLS, MGST3 SLC6A4 1732/4885KCNH2 4861/4885HRH2 2795/4885
US-11969501-B2 Auris formulations for treating otic diseases and conditions OTC, AQP4, SLC26A4 SLC6A4 867/4885KCNH2 2334/4885HRH2 269/4885
US-20040127550-A1 Medicament containing an effector of the glutathione metabolism together with alpha-lipoic acid for use in kidney replacement therapy GLS, GSTA1, GSTK1 SLC6A4 2878/4885KCNH2 4702/4885HRH2 2254/4885

“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.

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