Hydrochloric Acid

Hydrochloric Acid

SCHEMBL354780

Cl.NCCN1C(=O)C=CC1=O

nearest known ligand 0.59

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
HSP90AA1 known ✓ P07900 1/20 0.56
PTGS1 known ✓ P23219 7/20 0.46
PTGS2 known ✓ P35354 7/20 0.46
CA2 known ✓ P00918 1/20 0.41
MGLL Q99685 9/20 0.59
FAAH O00519 5/20 0.59
ALDH1A1 P00352 2/20 0.56
LMNA P02545 2/20 0.56
MAPT P10636 2/20 0.56
NPSR1 Q6W5P4 2/20 0.56
TLR9 Q9NR96 1/20 0.56
TP53 P04637 1/20 0.56
PKM P14618 1/20 0.56
HPGD P15428 1/20 0.56
XBP1 P17861 1/20 0.56
MAPK1 P28482 1/20 0.56
HTT P42858 1/20 0.56
RECQL P46063 1/20 0.56
RAB9A P51151 1/20 0.56
SMN1; SMN2 Q16637 1/20 0.56

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
SCHEMBL304989 0.97 MGLL (0.62) MGLLFAAHALDH1A1LMNAMAPT
SCHEMBL18045365 0.97 MGLL (0.62) MGLLFAAHALDH1A1LMNAMAPT
Hydrochloric Acid SCHEMBL16876819 0.85 MGLL (0.68) MGLLFAAHALDH1A1LMNAMAPT
Hydrochloric Acid SCHEMBL1726633 0.83 MGLL (0.73) MGLLFAAHALDH1A1LMNAMAPT
SCHEMBL1047471 0.82 MGLL (0.71) MGLLFAAHALDH1A1LMNAMAPT
Hydrochloric Acid SCHEMBL3402339 0.81 MGLL (0.74) MGLLFAAHALDH1A1LMNAMAPT
SCHEMBL17920257 0.81 MGLL (0.44) MGLLFAAHALDH1A1LMNAMAPT
Hydrochloric Acid SCHEMBL7515365 0.81 MGLL (0.74) MGLLFAAHALDH1A1LMNAMAPT
SCHEMBL2919549 0.80 MGLL (0.76) MGLLFAAHALDH1A1LMNAMAPT
SCHEMBL14678413 0.80 MGLL (0.77) MGLLFAAHALDH1A1LMNAMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119971033-A Metal polyphenol nano material with photo-thermal effect and tumor microenvironment immunoregulation function, and preparation method and application thereof 海南大学 2025-05-13 CN claimed
CN-119894224-A Perovskite solar cell and preparation method thereof 中国华能集团清洁能源技术研究院有限公司 2025-04-25 CN claimed
CN-119823163-A Small molecular boron-10 carrying agent, preparation method and application 东莞市人民医院 2025-04-15 CN claimed
CN-119744101-A Perovskite solar cell preparation method based on passivation additive and perovskite solar cell 中国华能集团清洁能源技术研究院有限公司 2025-04-01 CN claimed
CN-119405830-A Nanometer antibody conjugate and preparation method and application thereof 北京大学 2025-02-11 CN claimed
CN-115887685-B Antibody macromolecule conjugate and preparation method and application thereof 国家纳米科学中心 2024-02-09 CN claimed
CN-116535686-A Dual-functional hydrogel and preparation method and application thereof 中国科学院苏州纳米技术与纳米仿生研究所 2023-08-04 CN claimed
CN-115887685-A Antibody polymer conjugate and preparation method and application thereof 国家纳米科学中心 2023-04-04 CN claimed
CN-115337268-A Matrix metalloproteinase 2 sensitive nano system and preparation method and application thereof 四川大学华西医院 2022-11-15 CN claimed
CN-112933293-B Injectable hydrogel for treating central nerve injury and preparation method thereof 浙江大学 2022-06-10 CN claimed
US-10466234-B2 Method of producing labeled antibody FURUKAWA ELECTRIC CO., LTD. (JP) 2019-11-05 US claimed
CN-110201189-A Albumin mating type near infrared fluorescent dye-maleimide conjugate 沈阳药科大学 2019-09-06 CN claimed
CN-105349403-B A kind of preparation of electrically charged nanostructure cell chip and application process 北京科技大学 2018-11-06 CN claimed
WO-2026100725-A1 ANTI-CCR8 ANTIBODY AND ANTIBODY-DRUG CONJUGATE THEREOF 住友ファーマ株式会社 2026-05-15 WO disclosed
US-12625134-B2 Complex liquid crystal droplets MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 2026-05-12 US disclosed
WO-2026089784-A2 COMPOUNDS AND COMPOSITIONS FOR CONJUGATION TO BIOLIGANDS FOR IMAGING AND RADIOPHARMACEUTICAL APPLICATIONS THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL (US) 2026-04-30 WO disclosed
EP-0830370-A4 1998-03-25 EP disclosed
WO-1997019100-A1 N-1-CARBOXYALKYL DERIVATIVES OF LSD BOEHRINGER MANNHEIM CORPORATION (US) 1997-05-29 WO disclosed
US-5595741-A Aminoalkylmaleimides and hapten and antigen derivatives derived therefrom as well as conjugates with peptides or proteins BOEHRINGER MANNHEIM GMBH (DE) 1997-01-21 US disclosed
US-5525474-A IMMUNOASSAY; LINKING THE HAPTENIC DRUG VIA ITS MALEIMIDE MOIETY AND A SULFHYDRYL BRIDGE TO AN IMMUNOGENIC CARRIER TO STIMULATE ANTIBODIES BOEHRINGER MANNHEIM CORPORATION (US) 1996-06-11 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-12625134-B2 Complex liquid crystal droplets MAFG, SFN, FLNB HSP90AA1 3947/4885PTGS1 4000/4885PTGS2 2856/4885

“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.