Hydrochloric Acid

Hydrochloric Acid

SCHEMBL5688552

Cl.ONCCc1ccc(O)c(O)c1

nearest known ligand 0.69

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
DRD1 known ✓ P21728 3/20 0.59
SLC6A2 known ✓ P23975 3/20 0.59
DRD3 known ✓ P35462 3/20 0.59
SLC6A3 known ✓ Q01959 3/20 0.59
GAA known ✓ P10253 2/20 0.59
ADRA2A known ✓ P08913 2/20 0.59
DRD2 known ✓ P14416 2/20 0.59
DRD4 known ✓ P21917 2/20 0.59
PTGS1 known ✓ P23219 2/20 0.58
ADRB2 known ✓ P07550 2/20 0.55
ADRA1A known ✓ P35348 2/20 0.55
HTR1A known ✓ P08908 1/20 0.55
ADRA1D known ✓ P25100 1/20 0.55
ADRA1B known ✓ P35368 1/20 0.55
CHRM1 known ✓ P11229 1/20 0.53
ADRA2B known ✓ P18089 1/20 0.53
ADRA2C known ✓ P18825 1/20 0.53
SLC6A4 known ✓ P31645 1/20 0.53
PTGS2 known ✓ P35354 1/20 0.53
HRH1 known ✓ P35367 1/20 0.53

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
SCHEMBL30637623 0.98 MAPT (0.68) MAPTKDM4EALDH1A1LMNABLM
SCHEMBL735617 0.98 MAPT (0.68) MAPTKDM4EALDH1A1LMNABLM
Bromide SCHEMBL8585786 0.96 MAPT (0.66) MAPTKDM4EALDH1A1LMNABLM
Phosphoric Acid SCHEMBL15103074 0.89 MAPT (0.58) MAPTKDM4EALDH1A1LMNABLM
Dopamine SCHEMBL1809112 0.85 KDM4E (0.67) MAPTKDM4EALDH1A1LMNABLM
SCHEMBL11806768 0.83 DRD1 (0.71) MAPTKDM4EALDH1A1LMNABLM
SCHEMBL30082728 0.83 MAPT (0.70) MAPTKDM4EALDH1A1LMNABLM
SCHEMBL30088530 0.83 DRD1 (0.71) MAPTKDM4EALDH1A1LMNABLM
Deoxiepinephrine SCHEMBL31364234 0.82 MAPT (1.00) MAPTKDM4EALDH1A1LMNABLM
Deoxiepinephrine SCHEMBL1320882 0.82 MAPT (1.00) MAPTKDM4EALDH1A1LMNABLM

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 15 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110903658-B Preparation method of low-temperature flexible modified asphalt rubber material 湖北工业大学 2021-11-12 CN claimed
CN-110903658-A Preparation method of low-temperature flexible modified asphalt rubber material 湖北工业大学 2020-03-24 CN claimed
CN-118703012-B Composite membrane suitable for Prussian blue positive electrode material, and preparation method and application thereof 太仓中科赛诺新能源科技有限公司 2024-11-15 CN disclosed
CN-118703012-A Composite membrane suitable for Prussian blue positive electrode material, and preparation method and application thereof 太仓中科赛诺新能源科技有限公司 2024-09-27 CN disclosed
CN-110903658-B Preparation method of low-temperature flexible modified asphalt rubber material 湖北工业大学 2021-11-12 CN disclosed
CN-110903658-A Preparation method of low-temperature flexible modified asphalt rubber material 湖北工业大学 2020-03-24 CN disclosed
CN-105017528-B A kind of preparation method and applications of the polymer containing catechol 中山大学 2018-01-23 CN disclosed
EP-1265483-B1 USE OF PHENYLETHYLAMINE DERIVATIVES FOR THE ANITMICROBIAL TREATMENT OF SURFACES CIBA SC HOLDING AG (CH) 2006-03-29 EP disclosed
US-6846492-B2 Use of phenylethylamine derivatives for the antimicrobial treatment of surfaces CIBA SPECIALTY CHEMICALS CORPORATION (US) 2005-01-25 US disclosed
US-20030207884-A1 Use of phenylethylamine derivatives for the antimicrobial treatment of surfaces CIBA SPECIALTY CHEMICALS CORP. 2003-11-06 US disclosed
US-5759701-A INK JET PRINTING XEROX CORPORATION (US) 1998-06-02 US disclosed
US-5635322-A Process for developing and overcoating migration imaging members XEROX CORPORTION (US) 1997-06-03 US disclosed
US-5580689-A SOLFTENABLE LAYER OF SOFTENABLE MATERIAL, PIGMENT SENSITIVE TO INFRARED OR RED LIGHT ILLUMINATION, AND MIGRATION MARKING MATERIAL XEROX CORPORATION (US) 1996-12-03 US disclosed
US-5534374-A Migration imaging members XEROX CORPORATION (US) 1996-07-09 US disclosed
EP-0673781-A1 Recording sheets containing amine salts and quaternary choline halides XEROX CORPORATION (US) 1995-09-27 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 (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-20030207884-A1 Use of phenylethylamine derivatives for the antimicrobial treatment of surfaces CLTC, TUBA3C, AOC1 DRD1 2392/4885SLC6A2 4468/4885DRD3 1117/4885

“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.