Hydrochloric Acid

Hydrochloric Acid

SCHEMBL3247161

COc1c(C)cnc(CO)c1C.Cl

nearest known ligand 0.64

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 7/20 0.44
HSP90AB1 known ✓ P08238 2/20 0.44
CHRM2 known ✓ P08172 1/20 0.40
CHRM1 known ✓ P11229 1/20 0.40
PTGS1 known ✓ P23219 1/20 0.40
OPRM1 known ✓ P35372 1/20 0.40
DRD3 known ✓ P35462 1/20 0.40
KCNH2 known ✓ Q12809 1/20 0.40
AGXT P21549 1/20 0.64
PDE10A Q9Y233 1/20 0.43
KMT2A Q03164 4/20 0.42
WDR5 P61964 3/20 0.42
ATP4A P20648 3/20 0.42
ATP4B P51164 3/20 0.42
TRAP1 Q12931 2/20 0.42
SHMT2 P34897 1/20 0.42
HSP90B1 P14625 1/20 0.42
BRS3 P32247 2/20 0.41
DDAH1 O94760 2/20 0.41
ENGASE Q8NFI3 2/20 0.41

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
SCHEMBL29382857 0.98 AGXT (0.66) AGXTHSP90AA1HSP90AB1PDE10AKMT2A
SCHEMBL1060082 0.98 AGXT (0.66) AGXTHSP90AA1HSP90AB1PDE10AKMT2A
Hydrochloric Acid SCHEMBL8063817 0.92 AGXT (0.55) AGXTHSP90AA1HSP90AB1PDE10AKMT2A
SCHEMBL3802902 0.87 AGXT (0.54) AGXTHSP90AA1HSP90AB1PDE10AKMT2A
Hydrochloric Acid SCHEMBL29385728 0.83 AGXT (0.62) AGXTHSP90AA1HSP90AB1PDE10AKMT2A
Hydrochloric Acid SCHEMBL28313021 0.83 AGXT (0.62) AGXTHSP90AA1HSP90AB1PDE10AKMT2A
Hydrochloric Acid SCHEMBL1061557 0.83 AGXT (0.67) AGXTHSP90AA1HSP90AB1PDE10AKMT2A
Hydrochloric Acid SCHEMBL311423 0.83 AGXT (0.62) AGXTHSP90AA1HSP90AB1PDE10AKMT2A
SCHEMBL8910240 0.83 AGXT (0.49) AGXTHSP90AA1HSP90AB1PDE10AKMT2A
SCHEMBL154027 0.82 AGXT (0.66) AGXTHSP90AA1HSP90AB1PDE10AKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2842953-A1 Process for the preparation of esomeprazole magnesium dihydrate Cipla Limited (IN) 2015-03-04 EP claimed
US-20130150587-A1 Process for the Preparation of Esomeprazole Magnesium Dihydrate CIPLA LIMITED (IN) 2013-06-13 US claimed
US-20100113526-A1 Process for the Preparation of Esomeprazole Magnesium Dihydrate CIPLA LIMITED (IN) 2010-05-06 US claimed
EP-2125783-A2 PROCESS FOR THE PREPARATION OF ESOMEPRAZOLE MAGNESIUM DIHYDRATE Cipla Limited (IN) 2009-12-02 EP claimed
WO-2008102145-A2 PROCESS FOR THE PREPARATION OF ESOMEPRAZOLE MAGNESIUM DIHYDRATE CIPLA LIMITED (IN) 2008-08-28 WO claimed
CN-116410179-B Preparation method of proton pump inhibitor thioether intermediate compound 山东新时代药业有限公司 2025-10-28 CN disclosed
CN-115227656-B Preparation method of omeprazole sodium for injection 海南锦瑞制药有限公司 2023-07-25 CN disclosed
CN-116410179-A Preparation method of proton pump inhibitor thioether intermediate compound 山东新时代药业有限公司 2023-07-11 CN disclosed
EP-2842953-A1 Process for the preparation of esomeprazole magnesium dihydrate Cipla Limited (IN) 2015-03-04 EP disclosed
EP-2186807-B1 Process for the preparation of esomeprazole magnesium dihydrate CIPLA LTD (IN) 2015-01-07 EP disclosed
US-20130150587-A1 Process for the Preparation of Esomeprazole Magnesium Dihydrate CIPLA LIMITED (IN) 2013-06-13 US disclosed
US-8394963-B2 Process for the preparation of esomeprazole magnesium dihydrate CIPLA LIMITED (IN) 2013-03-12 US disclosed
EP-0134400-B1 FLUOROALKOXYSUBSTITUTED PYRIDYLMETHYLTHIO-(OR SULFINYL-)BENZIMIDAZOLES HAVING A SECRETOLYTIC ACTIVITY Byk Gulden Lomberg Chemische Fabrik GmbH (DE) 1993-03-24 EP disclosed
EP-0127763-B1 TRICYCLIC ETHERS, PROCESS FOR THEIR PREPARATION, THEIR USE AND MEDICAMENTS CONTAINING THEM Byk Gulden Lomberg Chemische Fabrik GmbH (DE) 1990-01-24 EP disclosed
US-4560693-A ANTISECRETORY, ANTIULCER AGENTS BYK GULDEN LOMBERG CHEMISCHE FABRIK GMBH (DE) 1985-12-24 US disclosed
US-4555518-A ANTIULCER AGENTS BYK GULDEN LOMBERG CHEMISCHE FABRIK GMBH (DE) 1985-11-26 US disclosed
EP-0134400-A2 Fluoroalkoxysubstituted pyridylmethylthio-(or sulfinyl-)benzimidazoles having a secretolytic activity Byk Gulden Lomberg Chemische Fabrik GmbH (DE) 1985-03-20 EP disclosed
EP-0127763-A1 Tricyclic ethers, process for their preparation, their use and medicaments containing them Byk Gulden Lomberg Chemische Fabrik GmbH (DE) 1984-12-12 EP disclosed
US-4472409-A ANTIULCER AGENTS BYK GULDEN LOMBERG CHEMISCHE FABRIK GESELLSCHAFT MIT BESCHRANKTER HAFTUNG (DE) 1984-09-18 US disclosed
EP-0080602-A1 Substituted benzimidazoles, process for their preparation, their use and medicaments containing them Byk Gulden Lomberg Chemische Fabrik GmbH (DE) 1983-06-08 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 (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-20100113526-A1 Process for the Preparation of Esomeprazole Magnesium Dihydrate CYP2D6, TPMT, CYP3A4 HSP90AA1 1849/4885HSP90AB1 1754/4885CHRM2 2024/4885
US-20130150587-A1 Process for the Preparation of Esomeprazole Magnesium Dihydrate CYP2D6, TPMT, CYP3A4 HSP90AA1 1849/4885HSP90AB1 1754/4885CHRM2 2024/4885

“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.