Hydrochloric Acid

Hydrochloric Acid

SCHEMBL3665643

CCCCCCCCCCCCCCCCCCNCc1ccc(C)cc1.Cl

nearest known ligand 0.79

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
CHRM2 known ✓ P08172 4/20 0.79
HRH3 known ✓ Q9Y5N1 1/20 0.70
S1PR1 known ✓ P21453 5/20 0.54
S1PR3 known ✓ Q99500 5/20 0.54
S1PR2 known ✓ O95136 4/20 0.54
S1PR4 known ✓ O95977 2/20 0.54
HDAC3 known ✓ O15379 1/20 0.52
HDAC4 known ✓ P56524 1/20 0.52
HDAC1 known ✓ Q13547 1/20 0.52
HDAC7 known ✓ Q8WUI4 1/20 0.52
HDAC2 known ✓ Q92769 1/20 0.52
HDAC10 known ✓ Q969S8 1/20 0.52
HDAC11 known ✓ Q96DB2 1/20 0.52
HDAC8 known ✓ Q9BY41 1/20 0.52
HDAC6 known ✓ Q9UBN7 1/20 0.52
HDAC9 known ✓ Q9UKV0 1/20 0.52
HDAC5 known ✓ Q9UQL6 1/20 0.52
MAOA known ✓ P21397 1/20 0.52
S1PR5 known ✓ Q9H228 1/20 0.51
LMNA P02545 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 SCHEMBL5713118 1.00 CHRM2 (0.79) CHRM2LMNAHRH4HRH3CYP1A2
Hydrochloric Acid SCHEMBL5713126 1.00 CHRM2 (0.79) CHRM2LMNAHRH4HRH3CYP1A2
SCHEMBL14288543 0.98 CHRM2 (0.81) CHRM2LMNAHRH4HRH3CYP1A2
SCHEMBL18485193 0.98 CHRM2 (0.81) CHRM2LMNAHRH4HRH3CYP1A2
Hydrochloric Acid SCHEMBL27688883 0.92 CHRM2 (0.71) CHRM2LMNAHRH4HRH3CYP1A2
P-Xylene SCHEMBL27855318 0.91 MAOA (0.67) CHRM2LMNAHRH4HRH3CYP1A2
SCHEMBL11922802 0.90 CHRM2 (0.74) CHRM2LMNAHRH4HRH3CYP1A2
SCHEMBL9637156 0.90 HRH4 (0.84) CHRM2LMNAHRH4HRH3CYP1A2
SCHEMBL10747074 0.90 HRH4 (0.84) CHRM2LMNAHRH4HRH3CYP1A2
SCHEMBL9259496 0.90 HRH4 (0.84) CHRM2LMNAHRH4HRH3CYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12370352-B2 Nasal and ophthalmic delivery of aqueous corticosteroid solutions CYDEX PHARMACEUTICALS, INC. (US) 2025-07-29 US disclosed
US-20220339414-A1 NASAL AND OPHTHALMIC DELIVERY OF AQUEOUS CORTICOSTEROID SOLUTIONS CITIBANK, N.A., AS ADMINISTRATIVE AGENT 2022-10-27 US disclosed
CN-106038481-A Nasal and ocular administration of aqueous corticosteroid solutions 锡德克斯药物公司 2016-10-26 CN disclosed
EP-2173169-B1 NASAL DELIVERY OF AQUEOUS CORTICOSTEROID SOLUTIONS CYDEX PHARMACEUTICALS INC (US) 2014-05-21 EP disclosed
EP-2173169-A1 NASAL AND OPHTHALMIC DELIVERY OF AQUEOUS CORTICOSTEROID SOLUTIONS CyDex Pharmaceuticals, Inc. (US) 2010-04-14 EP disclosed
US-20090312724-A1 Nasal and Ophthalmic Delivery of Aqueous Corticosteroid Solutions CYDEX PHARMACEUTICALS, INC. (US) 2009-12-17 US disclosed
WO-2009003199-A1 NASAL AND OPHTHALMIC DELIVERY OF AQUEOUS CORTICOSTEROID SOLUTIONS CYDEX PHARMACEUTICALS, INC. (US) 2008-12-31 WO disclosed
US-7344783-B2 Durable hydrophobic surface coatings using silicone resins SHELL OIL COMPANY (US) 2008-03-18 US disclosed
EP-1215226-B1 Diene-based rubber/inorganic compound complexes, methods for producing the same and rubber compositions containing the same JSR CORP (JP) 2006-06-07 EP disclosed
EP-1660601-A1 DURABLE HYDROPHOBIC SURFACE COATINGS USING SILICONE RESINS SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) 2006-05-31 EP disclosed
US-6969706-B1 Preserved pharmaceutical compositions comprising cyclodextrins ALLERGAN, INC. (US) 2005-11-29 US disclosed
US-20050256083-A1 Ophthalmic liquid containing a cyclodextrin, a guanidine-based cationic compound, and sorbic acid ALLERGAN, INC. (US) 2005-11-17 US disclosed
WO-2005007764-A1 DURABLE HYDROPHOBIC SURFACE COATINGS USING SILICONE RESINS SHELL INTERNATIONALE RESEARCH MAATSCHAPPIJ B.V. (NL) 2005-01-27 WO disclosed
US-20050009953-A1 Durable hydrophobic surface coatings using silicone resins PENNZOIL-QUAKER STATE COMPANY 2005-01-13 US disclosed
US-20040214797-A1 Preserved pharmaceutical compositions comprising cyclodextrins ALLERGAN, INC. 2004-10-28 US disclosed
US-6740704-B2 UNIFORM DISPERSION JSR CORPORATION (JP) 2004-05-25 US disclosed
US-20020111418-A1 Methods for producing diene-based rubber/inorganic compound complexes and rubber compositions containing the same JSR CORPORATION (JP) 2002-08-15 US disclosed
EP-1215226-A2 Diene-based rubber/inorganic compound complexes, methods for producing the same and rubber compositions containing the same JSR Corporation (JP) 2002-06-19 EP disclosed
US-5998488-A PREVENT ADSORPTION OF MICROBIOCIDES BY CONTACT LENSES; MIXTURE CONTAINING BORIC ACID, ETHYLENEDIAMINE AND A CYCLODEXTRIN LION CORPORATION (JP) 1999-12-07 US disclosed
US-5425804-A Modified organic silicone oil; polishing agent for the coated surfaces of automobiles and for plastics, rubbers and glass TAIHO INDUSTRIES CO., LTD. (JP) 1995-06-20 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 (5 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-20040214797-A1 Preserved pharmaceutical compositions comprising cyclodextrins DDOST, RPN1, GANC CHRM2 2987/4885HRH3 4303/4885S1PR1 2135/4885
US-20090312724-A1 Nasal and Ophthalmic Delivery of Aqueous Corticosteroid Solutions CRH, HRH1, IL5 CHRM2 607/4885HRH3 10/4885S1PR1 141/4885
US-20050256083-A1 Ophthalmic liquid containing a cyclodextrin, a guanidine-based cationic compound, and sorbic acid SORBS1, GANC, UACA CHRM2 1215/4885HRH3 2523/4885S1PR1 1762/4885
US-12370352-B2 Nasal and ophthalmic delivery of aqueous corticosteroid solutions CRH, HRH1, IL5 CHRM2 607/4885HRH3 10/4885S1PR1 141/4885
US-20220339414-A1 NASAL AND OPHTHALMIC DELIVERY OF AQUEOUS CORTICOSTEROID SOLUTIONS CRH, HRH1, IL5 CHRM2 607/4885HRH3 10/4885S1PR1 141/4885

“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.