Hydrochloric Acid

Hydrochloric Acid

SCHEMBL375108

COC(=O)C1(N)CCC1.Cl

nearest known ligand 0.43

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 13)

geneUniProtsupporting neighboursconfidence
NPSR1 Q6W5P4 1/20 0.43
CYP4F2 P78329 1/20 0.36
CYP4A11 Q02928 1/20 0.36
LMNA P02545 1/20 0.34
MAPT P10636 1/20 0.33
MEN1 O00255 1/20 0.33
CYP3A4 P08684 1/20 0.33
KMT2A Q03164 1/20 0.33
ALDH1A1 P00352 1/20 0.32
L3MBTL1 Q9Y468 1/20 0.32
SOD1 P00441 1/20 0.31
TSHR P16473 1/20 0.30
CYP2C19 P33261 1/20 0.30

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
SCHEMBL1433032 0.98
Hydrochloric Acid SCHEMBL485571 0.95 NPSR1 (0.48) NPSR1CYP4F2CYP4A11LMNAMAPT
Hydrochloric Acid SCHEMBL644319 0.93 NPSR1 (0.47) NPSR1CYP4F2CYP4A11LMNAMAPT
Hydrochloric Acid SCHEMBL1809798 0.93 NPSR1 (0.47) NPSR1CYP4F2CYP4A11LMNAMAPT
Hydrochloric Acid SCHEMBL5196791 0.93 NPSR1 (0.47) NPSR1CYP4F2CYP4A11LMNAMAPT
Hydrochloric Acid SCHEMBL1115400 0.93 NPSR1 (0.47) NPSR1CYP4F2CYP4A11LMNAMAPT
SCHEMBL331908 0.93 NPSR1 (0.50) NPSR1CYP4F2CYP4A11LMNAMAPT
SCHEMBL1809800 0.91 NPSR1 (0.48) NPSR1CYP4F2CYP4A11LMNAMAPT
SCHEMBL28766822 0.91 NPSR1 (0.48) NPSR1CYP4F2CYP4A11LMNAMAPT
SCHEMBL1772581 0.91 NPSR1 (0.48) NPSR1CYP4F2CYP4A11LMNAMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12209081-B2 Heterocycle derivatives for treating TRPM3 mediated disorders KATHOLIEKE UNIVERSITEIT LEUVEN (BE) 2025-01-28 US disclosed
CN-119372649-A Compatible display panel aluminum etching solution, and preparation method and application thereof 浙江奥首材料科技有限公司 2025-01-28 CN disclosed
CN-115232125-B Polysubstituted benzene immunomodulatory compounds, composition and application thereof 杭州和正医药有限公司 2024-06-18 CN disclosed
WO-2024067566-A1 SATURATED RING DERIVATIVE, PHARMACEUTICAL COMPOSITION COMPRISING SAME, AND PHARMACEUTICAL USE THEREOF 苏州阿尔脉生物科技有限公司 2024-04-04 WO disclosed
CN-117800894-A Saturated cyclic derivative, pharmaceutical composition containing same and medical application of saturated cyclic derivative 苏州阿尔脉生物科技有限公司 2024-04-02 CN disclosed
CN-116761796-A Aryl derivatives for the treatment of TRPM3 mediated disorders 勒芬天主教大学 2023-09-15 CN disclosed
EP-4196466-A1 PHD INHIBITOR COMPOUNDS, COMPOSITIONS, AND METHODS OF USE Akebia Therapeutics Inc. (US) 2023-06-21 EP disclosed
CN-115232125-A Multi-substituted benzene immunomodulatory compounds, compositions and uses thereof 杭州和正医药有限公司 2022-10-25 CN disclosed
CN-112812113-B Immunomodulatory compounds, compositions and uses thereof 杭州和正医药有限公司 2022-09-20 CN disclosed
EP-4038052-A2 PROSTAGLANDIN E2 (PGE2) EP4 RECEPTOR ANTAGONISTS Domain Therapeutics (FR) 2022-08-10 EP disclosed
US-6420380-B2 FOR TREATMENT OF HEPATITIS C VIRUS (HCV) INFECTION BOEHRINGER INGELHEIM (CANADA) LTD. (CA) 2002-07-16 US disclosed
US-6410531-B1 FOR THERAPY OF HEPATITIS C VIRUS (HCV) INFECTION BOEHRINGER INGELHEIM (CANADA) LTD. (CA) 2002-06-25 US disclosed
US-20020037998-A1 Hepatitis C inhibitor tri-peptides LLINAS-BRUNET MONTSE (CA) 2002-03-28 US disclosed
US-20020016442-A1 Hepatitis C inhibitor tri-peptides LLINAS-BRUNET MONTSE (CA) 2002-02-07 US disclosed
US-6329417-B1 RACEMATES, DIASTEREOISOMERS AND OPTICAL ISOMERS; PROTEASE INHIBITOR PEPTIDE ANALOG BOEHRINGER INGELHEIM (CANADA) LTD. (CA) 2001-12-11 US disclosed
US-6329379-B1 OLIGOPEPTIDES FOR INHIBITING HEPATITIS BOEHRINGER INGELHEIM (CANADA) LTD. (CA) 2001-12-11 US disclosed
US-6323180-B1 PROTEASE INHIBITORS; INHIBIT REPLICATION OF HEPATITIS C VIRUS BOEHRINGER INGELHEIM (CANADA) LTD (CA) 2001-11-27 US disclosed
US-6268207-B1 RESOLUTION OF ENANTIOMERS FROM A MIXTURE OF (1R,2S)/(1S,2S)-1-AMINO-2-VINYLCYCLOPROPYL CARBOXYLIC ACID METHYL ESTER COMPRISING THE STEP OF TREATING SAID MIXTURE WITH AN ESTERASE TO OBTAIN THE CORRESPONDING (1R,2S) ENANTIOMER BOEHRINGER INGELHEIM (CANADA) LTD. (CA) 2001-07-31 US disclosed
US-4570014-A Cycloalkanecarboxylic acid compounds BAYER AKTIENGESELLSCHAFT (DE) 1986-02-11 US disclosed
US-4554017-A Method and compositions for regulating plant growth using cycloalkane-carboxylic acid compounds BAYER AKTIENGESELLSCHAFT (DE) 1985-11-19 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 (3 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-12209081-B2 Heterocycle derivatives for treating TRPM3 mediated disorders TRPM4, TRPM6, TRPM2 NPSR1 507/4885CYP4F2 3261/4885CYP4A11 3126/4885
US-20020037998-A1 Hepatitis C inhibitor tri-peptides LIPC, HAVCR2, HCCS NPSR1 627/4885CYP4F2 1871/4885CYP4A11 335/4885
US-20020016442-A1 Hepatitis C inhibitor tri-peptides HAVCR2, LIPC, HCCS NPSR1 831/4885CYP4F2 1395/4885CYP4A11 353/4885

“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.