Hydrochloric Acid

Hydrochloric Acid

SCHEMBL18476

CC(C)(C)OC(=O)CC[C@H](N)C(=O)OC(C)(C)C.Cl

nearest known ligand 0.42

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
HDAC3 known ✓ O15379 1/20 0.34
HDAC1 known ✓ Q13547 1/20 0.34
HDAC2 known ✓ Q92769 1/20 0.34
HDAC8 known ✓ Q9BY41 1/20 0.34
HDAC6 known ✓ Q9UBN7 1/20 0.34
GRIN2D known ✓ O15399 1/20 0.32
GRIN3B known ✓ O60391 1/20 0.32
GRIN1 known ✓ Q05586 1/20 0.32
GRIN2A known ✓ Q12879 1/20 0.32
GRIN2B known ✓ Q13224 1/20 0.32
GRIN2C known ✓ Q14957 1/20 0.32
GRIN3A known ✓ Q8TCU5 1/20 0.32
GAA known ✓ P10253 1/20 0.31
LTA4H P09960 1/20 0.42
NOS1 P29475 2/20 0.37
NOS3 P29474 1/20 0.37
NOS2 P35228 1/20 0.37
SLC1A1 P43005 2/20 0.34
PMP22 Q01453 2/20 0.33
LMNA P02545 1/20 0.33

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 SCHEMBL1517836 1.00 LTA4H (0.42) LTA4HNOS1NOS3NOS2SLC1A1
Hydrochloric Acid SCHEMBL4654220 1.00 LTA4H (0.42) LTA4HNOS1NOS3NOS2SLC1A1
SCHEMBL18477 0.98 LTA4H (0.43) LTA4HNOS1NOS3NOS2SLC1A1
SCHEMBL1841835 0.98 LTA4H (0.43) LTA4HNOS1NOS3NOS2SLC1A1
SCHEMBL1654337 0.98 LTA4H (0.43) LTA4HNOS1NOS3NOS2SLC1A1
Water SCHEMBL3912787 0.96 LTA4H (0.42) LTA4HNOS1NOS3NOS2SLC1A1
SCHEMBL6893763 0.96 LTA4H (0.42) LTA4HNOS1NOS3NOS2SLC1A1
Water SCHEMBL27596082 0.96 LTA4H (0.42) LTA4HNOS1NOS3NOS2SLC1A1
Hydrochloric Acid SCHEMBL23042780 0.89 SLC1A1 (0.46) LTA4HNOS1NOS3NOS2SLC1A1
Hydrochloric Acid SCHEMBL1143881 0.89 SLC1A1 (0.39) LTA4HNOS1NOS3NOS2SLC1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122031415-A Curcumin peptide dendrimer-Prussian blue nano enzyme-MSCs self-assembled preparation and preparation method and application thereof 南京工业大学 2026-05-15 CN claimed
US-20250367332-A1 PSMA-TARGETED RADIOACTIVE METAL COMPLEX CONTAINING NITROAROMATIC HETEROCYCLIC GROUP AND PREPARATION METHOD UNIV BEIJING NORMAL (CN) 2025-12-04 US claimed
CN-119301141-A Compound of double-targeting tumor cells, preparation method and application thereof 中国医学科学院北京协和医院 2025-01-10 CN claimed
CN-118924682-A Difunctional dendritic lipopeptide nano micelle and preparation method and application thereof 中国药科大学 2024-11-12 CN claimed
CN-118546180-A Small molecule prodrug of clofarabine, preparation method and application thereof 中国科学院苏州生物医学工程技术研究所 2024-08-27 CN claimed
CN-118546192-A Cordycepin prodrug for resisting cancer, preparation method and application thereof 中国科学院苏州生物医学工程技术研究所 2024-08-27 CN claimed
WO-2023231452-A1 PSMA-TARGETING RADIOACTIVE METAL COMPLEX CONTAINING NITRO AROMATIC HETEROCYCLIC GROUP AND PREPARATION THEREOF 北京师范大学 2023-12-07 WO claimed
CN-116903495-A Preparation method of radioactive diagnostic drug ligand 江苏华益科技有限公司 2023-10-20 CN claimed
CN-116507630-A PSMA targeted radioactive metal complex containing nitro aromatic heterocyclic group and preparation thereof 北京师范大学 2023-07-28 CN claimed
CN-109384715-B Preparation method of small molecule inhibitor of prostate specific membrane antigen 复旦大学附属肿瘤医院 2021-09-03 CN claimed
CN-110982012-B Amphoteric acrylamide polymer flocculant and preparation method thereof 江西科技师范大学 2021-08-06 CN claimed
CN-109134602-B Solid phase preparation method of efficient prostate specific membrane antigen ligand PSMA-617 兰州大学 2021-07-02 CN claimed
CN-107245082-B Synthesis method of 6-pterin folic acid 天津阿尔塔科技有限公司 2020-04-17 CN claimed
CN-110982012-A Novel amphoteric acrylamide polymer flocculant and preparation method thereof 江西科技师范大学 2020-04-10 CN claimed
EP-1391449-A1 Hydrolysis of amino acid diesters PCBU Services, Inc. (US) 2004-02-25 EP claimed
US-20040030177-A1 Hydrolysis of amino acid diesters PCBU SERVICES, INC. 2004-02-12 US claimed
CN-122059928-A Bifunctional chelators, PSMA ligand compounds, radiolabeled compounds and uses thereof 广州医科大学附属第一医院(广州呼吸中心) 2026-05-19 CN disclosed
CN-122031415-A Curcumin peptide dendrimer-Prussian blue nano enzyme-MSCs self-assembled preparation and preparation method and application thereof 南京工业大学 2026-05-15 CN disclosed
US-4845216-A ANTITUMOR AGENTS THE TRUSTEES OF PRINCETON UNIVERSITY (US) 1989-07-04 US disclosed
US-4684653-A ANTITUMOR AGENTS THE TRUSTEES OF PRINCETON UNIVERSITY (US) 1987-08-04 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-20250367332-A1 PSMA-TARGETED RADIOACTIVE METAL COMPLEX CONTAINING NITROAROMATIC HETEROCYCLIC GROUP AND PREPARATION METHOD PSMA1, PSMA2, PSMA7 HDAC3 1787/4885HDAC1 222/4885HDAC2 1534/4885
US-20040030177-A1 Hydrolysis of amino acid diesters DNPEP, ANPEP, DAO HDAC3 4528/4885HDAC1 4072/4885HDAC2 3400/4885

“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.