Hydrochloric Acid

Hydrochloric Acid

SCHEMBL954680

CCC(C)C(N)C(=O)OC(C)(C)C.Cl

nearest known ligand 0.51

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 9)

geneUniProtsupporting neighboursconfidence
DPP4 known ✓ P27487 13/20 0.40
NOS1 P29475 2/20 0.51
NOS3 P29474 1/20 0.51
NOS2 P35228 1/20 0.51
DPP8 Q6V1X1 8/20 0.40
DPP9 Q86TI2 7/20 0.40
CTSS P25774 1/20 0.38
CTSK P43235 1/20 0.38
DPP7 Q9UHL4 7/20 0.36

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 SCHEMBL919003 1.00 NOS1 (0.51) NOS1NOS3NOS2DPP4DPP8
Hydrochloric Acid SCHEMBL919002 1.00 NOS1 (0.51) NOS1NOS3NOS2DPP4DPP8
SCHEMBL919004 0.98 NOS1 (0.53) NOS1NOS3NOS2DPP4DPP8
SCHEMBL1952051 0.98 NOS1 (0.53) NOS1NOS3NOS2DPP4DPP8
SCHEMBL6224216 0.98 NOS1 (0.53) NOS1NOS3NOS2DPP4DPP8
SCHEMBL4425446 0.98 NOS1 (0.53) NOS1NOS3NOS2DPP4DPP8
SCHEMBL1952544 0.98 NOS1 (0.53) NOS1NOS3NOS2DPP4DPP8
SCHEMBL1841059 0.98 NOS1 (0.53) NOS1NOS3NOS2DPP4DPP8
Acetic Acid SCHEMBL9342261 0.93 NOS1 (0.49) NOS1NOS3NOS2DPP4DPP8
Leucine SCHEMBL29264283 0.84 SLC7A5 (0.53) NOS1NOS3NOS2CTSSCTSK

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114163507-B Recombinant antigen protein rP44-60 for detecting granulocytoplasmatic disease and kit containing antigen 河套学院 2023-06-20 CN claimed
CN-114163507-A Recombinant antigen protein rP44-60 for detecting granulocytic anaplasmosis and kit containing antigen 河套学院 2022-03-11 CN claimed
CN-110269858-A It is a kind of to treat twin medicine of cerebral arterial thrombosis and preparation method thereof 贵州医科大学 2019-09-24 CN claimed
EP-4719602-A1 ANTI-HIV COMPOUNDS GILEAD SCIENCES, INC. (US) 2026-04-08 EP disclosed
US-20250051375-A1 ANTI-HIV COMPOUNDS GILEAD SCIENCES, INC. 2025-02-13 US disclosed
WO-2024249517-A1 ANTI-HIV COMPOUNDS GILEAD SCIENCES, INC. (US) 2024-12-05 WO disclosed
EP-4441070-A1 MODIFIED AMATOXINS AND USES THEREOF The University of British Columbia (CA) 2024-10-09 EP disclosed
CN-114163507-B Recombinant antigen protein rP44-60 for detecting granulocytoplasmatic disease and kit containing antigen 河套学院 2023-06-20 CN disclosed
WO-2023097407-A1 MODIFIED AMATOXINS AND USES THEREOF THE UNIVERSITY OF BRITISH COLUMBIA (CA) 2023-06-08 WO disclosed
EP-4051269-A1 D-AMPHETAMINE COMPOUNDS, COMPOSITIONS, AND PROCESSES FOR MAKING AND USING THE SAME KemPharm, Inc. (US) 2022-09-07 EP disclosed
CN-114746091-A D-amphetamine compounds, compositions, and methods of making and using the same 肯法姆股份有限公司 2022-07-12 CN disclosed
EP-1697348-A1 HIV PROTEASE INHIBITING COMPOUNDS ABBOTT LABORATORIES (US) 2006-09-06 EP disclosed
US-20060166985-A1 Pyrrolydin-2-one derivatives as inhibitors of thrombin and factor xa GLAXO GROUP LIMITED (GB) 2006-07-27 US disclosed
EP-1476427-A4 PEPTIDE BETA-STRAND MIMICS BASED ON 1,2-DIHYDRO-3(6H)-PYRIDINONE UNIV CALIFORNIA (US) 2006-04-19 EP disclosed
WO-2005061487-A1 HIV PROTEASE INHIBITING COMPOUNDS ABBOTT LABORATORIES (US) 2005-07-07 WO disclosed
US-20050043538-A1 Peptide beta-strand mimics based on 1,2-dihydro-3(6H)-pyridinone THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2005-02-24 US disclosed
EP-1476427-A2 PEPTIDE BETA-STRAND MIMICS BASED ON 1,2-DIHYDRO-3(6H)-PYRIDINONE The Regents of the University of California (US) 2004-11-17 EP disclosed
US-20030073721-A1 Peptide beta-strand mimics based on 1,2-dihydro-3(6H)-pyridinone THE REGENTS OF THE UNIVERSITY OF CALIFORNIA, A CALIFORNIA CORPORATION (US) 2003-04-17 US disclosed
WO-2002099045-A2 PEPTIDE BETA-STRAND MIMICS BASED ON 1,2-DIHYDRO-3(6H)-PYRIDINONE THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2002-12-12 WO disclosed
WO-2000061631-A1 MODIFIED PENTAPEPTIDE ANTAGONISTS OF THE ATRIAL NATRIURETIC PEPTIDE CLEARANCE RECEPTOR ASTRAZENECA AB (SE) 2000-10-19 WO 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 (4 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-20030073721-A1 Peptide beta-strand mimics based on 1,2-dihydro-3(6H)-pyridinone IAPP, VIP, APP DPP4 91/4885NOS1 3744/4885NOS3 2786/4885
US-20050043538-A1 Peptide beta-strand mimics based on 1,2-dihydro-3(6H)-pyridinone IAPP, APP, VIP DPP4 68/4885NOS1 4073/4885NOS3 3318/4885
US-20250051375-A1 ANTI-HIV COMPOUNDS CCR5, CD4, NFATC1 DPP4 348/4885NOS1 1530/4885NOS3 1338/4885
US-20060166985-A1 Pyrrolydin-2-one derivatives as inhibitors of thrombin and factor xa TFPI, TFPI2, SERPINC1 DPP4 383/4885NOS1 1566/4885NOS3 2260/4885

“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.