Hydrochloric Acid

Hydrochloric Acid

SCHEMBL5000725

C=CC(=O)OC(C)C(c1ccccc1)N(C)C.Cl

nearest known ligand 0.42

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
CHRNB4 known ✓ P30926 1/20 0.35
CHRNA3 known ✓ P32297 1/20 0.35
HCAR2 Q8TDS4 1/20 0.42
LMNA P02545 1/20 0.41
ALDH1A1 P00352 3/20 0.38
KDM4E B2RXH2 1/20 0.38
KMT2A Q03164 2/20 0.36
MEN1 O00255 1/20 0.36
MAPT P10636 1/20 0.36
CYP2C9 P11712 1/20 0.36
HSD17B10 Q99714 1/20 0.36
AOC3 Q16853 4/20 0.36
THRB P10828 1/20 0.36
CHRNB2 P17787 1/20 0.35
CHRNA4 P43681 1/20 0.35
ALOX5 P09917 1/20 0.35
CYP2C19 P33261 1/20 0.35
MTOR P42345 1/20 0.35
LTB4R Q15722 1/20 0.34
LTB4R2 Q9NPC1 1/20 0.34

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
SCHEMBL5664548 0.98 HCAR2 (0.43) HCAR2LMNAALDH1A1KDM4EKMT2A
Fluoride SCHEMBL28527584 0.97 HCAR2 (0.42) HCAR2LMNAALDH1A1KDM4EKMT2A
Iodide SCHEMBL22042239 0.97 HCAR2 (0.42) HCAR2LMNAALDH1A1KDM4EKMT2A
Bromide SCHEMBL28534138 0.97 HCAR2 (0.42) HCAR2LMNAALDH1A1KDM4EKMT2A
Ethyl Chloride SCHEMBL5032981 0.92 HCAR2 (0.38) HCAR2LMNAALDH1A1KDM4EHSD17B10
Hydrochloric Acid SCHEMBL21693858 0.86 HCAR2 (0.41) HCAR2LMNAALDH1A1KDM4EKMT2A
Bromide SCHEMBL21693860 0.83 HCAR2 (0.41) HCAR2LMNAALDH1A1KDM4EKMT2A
Iodide SCHEMBL21693887 0.83 HCAR2 (0.41) HCAR2LMNAALDH1A1KDM4EKMT2A
Fluoride SCHEMBL28507999 0.83 HCAR2 (0.41) HCAR2LMNAALDH1A1KDM4EKMT2A
Hydrochloric Acid SCHEMBL28537615 0.83 LMNA (0.38) HCAR2LMNAALDH1A1KDM4EKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115322386-A Amphoteric polyacrylamide, and preparation method and application thereof 浙江传化华洋化工有限公司 2022-11-11 CN claimed
CN-110407974-B Preparation method of crosslinkable amphoteric polyacrylamide polymer 浙江传化华洋化工有限公司 2021-09-21 CN claimed
CN-103509180-B Polymeric dispersions and the method preparing polymeric dispersions AKZO NOBEL N. V. (NL) 2015-12-09 CN claimed
US-20040024242-A1 Method for making aqueous solutions of (meth)acryloyloxyethylbenzyldimethylammonium chlorides ATOFINA (FR) 2004-02-05 US claimed
EP-4508160-A1 COMPOSITIONS COMPRISING POLYMER, SCALE INHIBITOR AND QUATERNARY AMMONIUM COMPOUND, METHOD AND USES Independence Oilfield Chemicals, LLC (US) 2025-02-19 EP disclosed
CN-113631682-B Polymer dispersions for wax inhibition during stimulation 能源解决方案(美国)有限责任公司 2024-01-26 CN disclosed
WO-2023210593-A1 METHOD FOR TREATING ORGANIC WASTEWATER CONTAINING AMIDE COMPOUNDS KJ CHEMICALS CORPORATION (JP) 2023-11-02 WO disclosed
WO-2023199013-A1 COMPOSITIONS COMPRISING POLYMER, SCALE INHIBITOR AND QUATERNARY AMMONIUM COMPOUND, METHOD AND USES. INDEPENDENCE OILFIELD CHEMICALS LLC (US) 2023-10-19 WO disclosed
US-20230322977-A1 AQUEOUS FORMULATIONS INDEPENDENCE OILFIELD CHEMICALS LLC 2023-10-12 US disclosed
CN-113166050-B Method for producing organotellurium compound and method for producing vinyl polymer 大塚化学株式会社 2023-04-18 CN disclosed
CN-110709052-B Hair composition in foam form providing improved moisturized feel in application 宝洁公司 2023-04-04 CN disclosed
CN-110709057-B Hair care compositions providing improved in-use moisturized feel 宝洁公司 2023-04-04 CN disclosed
EP-1511776-A1 A WATER-SOLUBLE POLYMER DISPERSION AND A METHOD OF PRODUCING A WATER-SOLUBLE POLYMER DISPERSION AKZO Nobel N.V. (NL) 2005-03-09 EP disclosed
US-20050034829-A1 Sheet surface treating and ink-jet printing paper HYMO CORPORATION 2005-02-17 US disclosed
US-20040024242-A1 Method for making aqueous solutions of (meth)acryloyloxyethylbenzyldimethylammonium chlorides ATOFINA (FR) 2004-02-05 US disclosed
US-6669815-B1 Cationic graft copolymer comprising vinyl alcohol and di(meth)allylamine-based or N-vinylcarboxylic acid amide comonomers HYMO CORPORATION (JP) 2003-12-30 US disclosed
WO-2003097703-A1 A WATER-SOLUBLE POLYMER DISPERSION AND A METHOD OF PRODUCING A WATER-SOLUBLE POLYMER DISPERSION AKZO NOBEL N.V. (NL) 2003-11-27 WO disclosed
EP-1022383-B1 SHEET SURFACE TREATING AGENT AND INK-JET PRINTING PAPER HYMO CORP (JP) 2003-11-26 EP disclosed
EP-1022383-A1 SHEET SURFACE TREATING AGENT AND INK-JET PRINTING PAPER HYMO CORPORATION (JP) 2000-07-26 EP disclosed
US-5260480-A Quaternization process NORSOLOR (FR) 1993-11-09 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 (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-20040024242-A1 Method for making aqueous solutions of (meth)acryloyloxyethylbenzyldimethylammonium chlorides DDT, BCHE, ACMSD CHRNB4 1849/4885CHRNA3 726/4885HCAR2 3886/4885

“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.