Hydrochloric Acid

Hydrochloric Acid

SCHEMBL186835

CCCCCCCCCCN(C)C.Cl

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

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 13)

geneUniProtsupporting neighboursconfidence
CA2 known ✓ P00918 1/20 0.42
S1PR2 known ✓ O95136 1/20 0.41
S1PR1 known ✓ P21453 1/20 0.41
S1PR3 known ✓ Q99500 1/20 0.41
S1PR5 known ✓ Q9H228 1/20 0.41
DNM1 Q05193 10/20 1.00
TSHR P16473 2/20 0.69
ALDH1A1 P00352 1/20 0.69
THRB P10828 1/20 0.50
GBA1 P04062 1/20 0.44
CA12 O43570 1/20 0.42
CA1 P00915 1/20 0.42
CA9 Q16790 1/20 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 SCHEMBL20142868 1.00 DNM1 (1.00) DNM1TSHRALDH1A1THRBGBA1
Hydrochloric Acid SCHEMBL173970 1.00 DNM1 (1.00) DNM1TSHRALDH1A1THRBGBA1
Hydrochloric Acid SCHEMBL4581667 1.00 DNM1 (1.00) DNM1TSHRALDH1A1THRBGBA1
Hydrochloric Acid SCHEMBL25273059 1.00 DNM1 (1.00) DNM1TSHRALDH1A1THRBGBA1
Hydrochloric Acid SCHEMBL19327730 1.00 DNM1 (1.00) DNM1TSHRALDH1A1THRBGBA1
Hydrochloric Acid SCHEMBL25273058 1.00 DNM1 (1.00) DNM1TSHRALDH1A1THRBGBA1
Hydrochloric Acid SCHEMBL11211039 1.00 DNM1 (1.00) DNM1TSHRALDH1A1THRBGBA1
Hydrochloric Acid SCHEMBL564629 1.00 DNM1 (1.00) DNM1TSHRALDH1A1THRBGBA1
Hydrochloric Acid SCHEMBL237081 1.00 DNM1 (1.00) DNM1TSHRALDH1A1THRBGBA1
Hydrochloric Acid SCHEMBL8369176 1.00 DNM1 (1.00) DNM1TSHRALDH1A1THRBGBA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119978729-A Mildew-proof polyester composite material 山西机电职业技术学院 2025-05-13 CN claimed
EP-4384156-A1 HIGH MOLECULAR IODINE CONCENTRATION COMPOSITIONS, PHARMACEUTICAL FORMULATIONS, PREPARATION AND USES I2Pure Corp. (US) 2024-06-19 EP claimed
CN-118103037-A High concentration molecular iodine composition, pharmaceutical preparation, preparation and use I2普乐公司 2024-05-28 CN claimed
CN-116832388-B Foaming agent for water film-forming foam extinguishing agent and preparation method thereof 成都科宏达化学有限责任公司 2024-04-12 CN claimed
CN-117769588-A Methods and reagents for enhancing chemiluminescent signals 欧蒙医学实验诊断股份公司 2024-03-26 CN claimed
WO-2023225254-A1 LAUNDRY DETERGENT FORMULATIONS THE PROCTER & GAMBLE COMPANY (US) 2023-11-23 WO claimed
CN-116832388-A Foaming agent for water film-forming foam extinguishing agent and preparation method thereof 四川科宏达集团有限责任公司 2023-10-03 CN claimed
WO-2023019033-A1 HIGH MOLECULAR IODINE CONCENTRATION COMPOSITIONS, PHARMACEUTICAL FORMULATIONS, PREPARATION AND USES I2PURE CORP. (US) 2023-02-16 WO claimed
US-20230019880-A1 COMPOSITIONS JVS Products Ltd. (GB) 2023-01-19 US claimed
CN-115420698-A Method for detecting hyaluronic acid content in textile 江苏金太阳纺织科技股份有限公司 2022-12-02 CN claimed
US-7244418-B2 Antimicrobial artificial nail composition and methods for preparing and using same WOODWARD LABORATORIES, INC. (US) 2007-07-17 US claimed
WO-2006136397-A1 METHOD FOR ANTIMOCROBIAL FINISHING OF POLYMERS Süd-Chemie AG (DE) 2006-12-28 WO claimed
US-20050112022-A1 Room sanitizing method and apparatus MORGAN DAVID M (US) 2005-05-26 US claimed
US-20030086880-A1 Antimicrobial artificial nail composition and methods for preparing and using same BROWN RUDNICK LLP 2003-05-08 US claimed
US-6479039-B1 Antimicrobial artificial nail composition and methods for preparing and using same WOODWARD LABORATORIES, INC. 2002-11-12 US claimed
WO-2001003656-A1 ANTIMICROBIAL ARTIFICIAL NAIL COMPOSITION AND METHODS FOR PREPARING AND USING SAME WOODWARD LABORATORIES, INC. (US) 2001-01-18 WO claimed
EP-0978574-A1 Compositions of cationic surfactants and their use as antifouling agents for induced draft fans (IDF) NALCO CHEMICAL COMPANY (US) 2000-02-09 EP claimed
EP-0587757-A1 THERMOSETTING POWDER COATING COMPOSITIONS PPG INDUSTRIES, INC. (US) 1994-03-23 EP claimed
WO-1992022405-A1 ONE STEP PROCESS FOR IMPARTING DECAY RESISTANCE AND FIRE RETARDANCY TO WOOD PRODUCTS THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, U.S. DEPARTMENT OF COMMERCE (US) 1992-12-23 WO claimed
WO-1992021727-A1 THERMOSETTING POWDER COATING COMPOSITIONS EASTMAN KODAK COMPANY (US) 1992-12-10 WO claimed

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-20030086880-A1 Antimicrobial artificial nail composition and methods for preparing and using same POLR1C, NACA, PIK3C3 CA2 4619/4885S1PR2 4654/4885S1PR1 4434/4885

“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.