Hydrochloric Acid

Hydrochloric Acid

SCHEMBL3665862

Cl.NCc1cccc2ccccc12

nearest known ligand 0.95

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 18)

geneUniProtsupporting neighboursconfidence
CA2 known ✓ P00918 1/20 0.48
HTR2A known ✓ P28223 1/20 0.46
CYP1A2 P05177 2/20 0.56
CYP2C19 P33261 2/20 0.56
CYP2C9 P11712 1/20 0.56
HPGD P15428 2/20 0.53
HTT P42858 1/20 0.53
CYP2D6 P10635 2/20 0.52
TDP1 Q9NUW8 1/20 0.50
ACP3 P15309 1/20 0.48
ALDH1A1 P00352 2/20 0.47
TSHR P16473 2/20 0.47
HSD17B10 Q99714 2/20 0.47
RECQL P46063 1/20 0.47
LOXL2 Q9Y4K0 1/20 0.47
CYP3A4 P08684 1/20 0.46
KEAP1 Q14145 1/20 0.46
MTNR1A P48039 1/20 0.46

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 SCHEMBL1922860 1.00 CYP1A2 (0.56) CYP1A2CYP2C19CYP2C9HPGDHTT
Hydrochloric Acid SCHEMBL11771194 0.98 CYP1A2 (0.54) CYP1A2CYP2C19CYP2C9HPGDHTT
SCHEMBL110689 0.98 CYP1A2 (0.58) CYP1A2CYP2C19CYP2C9HPGDHTT
SCHEMBL29484446 0.98 CYP1A2 (0.58) CYP1A2CYP2C19CYP2C9HPGDHTT
Iodide SCHEMBL19990736 0.95 CYP1A2 (0.56) CYP1A2CYP2C19CYP2C9HPGDHTT
Ammonia Solution, Strong SCHEMBL9173309 0.95 CYP1A2 (0.56) CYP1A2CYP2C19CYP2C9HPGDHTT
SCHEMBL20593911 0.95 CYP1A2 (0.56) CYP1A2CYP2C19CYP2C9HPGDHTT
Bromide SCHEMBL22401521 0.95 CYP1A2 (0.56) CYP1A2CYP2C19CYP2C9HPGDHTT
Iodide SCHEMBL28994517 0.93 CYP1A2 (0.54) CYP1A2CYP2C19CYP2C9HPGDHTT
Dimethylamine SCHEMBL28254662 0.89 CYP1A2 (0.52) CYP1A2CYP2C19CYP2C9HPGDHTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2848336-A1 METHOD FOR MANUFACTURING HOLLOW METAL NANOPARTICLES, AND HOLLOW METAL NANOPARTICLES MANUFACTURED THEREBY LG Chem, Ltd. (KR) 2015-03-18 EP claimed
WO-2009114695-A1 NANOPARTICULATE COMPOSITIONS OF ANGIOGENESIS INHIBITORS ELAN PHARMA INTERNATIONAL LTD. (IE) 2009-09-17 WO claimed
EP-1915139-A1 NANOPARTICULATE AND CONTROLLED RELEASE COMPOSITIONS COMPRISING A CEPHALOSPORIN Elan Pharma International Limited (IE) 2008-04-30 EP claimed
WO-2008010784-A1 NANOPARTICULATE AND CONTROLLED RELEASE COMPOSITIONS COMPRISING A CEPHALOSPORIN ELAN PHARMA INTERNATIONAL LIMITED (IE) 2008-01-24 WO claimed
US-20070264348-A1 Nanoparticulate fibrate formulations ELAN PHARMA INTERNATIONAL, LTD. 2007-11-15 US claimed
US-6976647-B2 System and method for milling materials ELAN PHARMA INTERNATIONAL, LIMITED (IE) 2005-12-20 US claimed
US-20050107366-A1 Spin trapping pharmaceutical compositions and methods for use thereof CARNEY JOHN M (US) 2005-05-19 US claimed
US-20050019412-A1 Novel glipizide compositions ELAN PHARMA INTERNATIONAL LIMITED 2005-01-27 US claimed
US-20040164194-A1 System and method for milling materials ELAN PHARMA INTERNATIONAL LIMITED 2004-08-26 US claimed
EP-0223157-B1 IMPROVED AUTOFLUOROGRAM COMPOSITION E.I. DU PONT DE NEMOURS AND COMPANY (US) 1990-01-31 EP claimed
EP-0223157-A1 Improved autofluorogram composition E.I. DU PONT DE NEMOURS AND COMPANY (US) 1987-05-27 EP claimed
CN-112055581-B Ultrasound-induced drug delivery system using drug carrier comprising nanobubbles and drug 三育大学校产学协力团 2023-04-07 CN disclosed
CN-115802770-A Method for efficiently passivating lead iodide-rich wide-band-gap perovskite by using pure-chlorine two-dimensional perovskite and solar cell thereof 华侨大学 2023-03-14 CN disclosed
WO-2023013834-A1 HEAT SINK PAINT COMPOSITION, PREPARATION METHOD THEREFOR, HEAT SINK COATING FILM FORMED THEREFROM, AND HEAT SINK COMPRISING SAME 퓨어만 주식회사 2023-02-09 WO disclosed
CN-110636837-B Pharmaceutical composition of CYP17 inhibitor and preparation method thereof 江苏恒瑞医药股份有限公司 2022-05-24 CN disclosed
EP-0409617-A2 Thiolactams, process for their preparation and use as biocides ZENECA LIMITED (GB) 1991-01-23 EP disclosed
EP-0223157-B1 IMPROVED AUTOFLUOROGRAM COMPOSITION E.I. DU PONT DE NEMOURS AND COMPANY (US) 1990-01-31 EP disclosed
US-4710319-A Autofluorogram composition E. I. DU PONT DE NEMOURS AND COMPANY (US) 1987-12-01 US disclosed
EP-0223157-A1 Improved autofluorogram composition E.I. DU PONT DE NEMOURS AND COMPANY (US) 1987-05-27 EP disclosed
US-4202882-A TETRAAZO FUSED HETEROCYCLE AND QUATERNARY AMMONIUM COMPOUND POLYCRAFT LABORATORIES, INC., A CORP. OF NJ. 1980-05-13 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 (2 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-20050107366-A1 Spin trapping pharmaceutical compositions and methods for use thereof PPOX, TXN2, TXN CA2 4846/4885HTR2A 2374/4885CYP1A2 1203/4885
US-20050019412-A1 Novel glipizide compositions DPP4, GID4, SLC5A2 CA2 514/4885HTR2A 845/4885CYP1A2 2122/4885

“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.