Hydrochloric Acid

Hydrochloric Acid

SCHEMBL307401

CCCCCCCCCCCC(=O)OC(CC(=O)[O-])C[N+](C)(C)C.Cl

nearest known ligand 0.97

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 2/20 0.74
GLA known ✓ P06280 1/20 0.72
HRH1 known ✓ P35367 1/20 0.56
MAPT P10636 5/20 0.97
MEN1 O00255 5/20 0.97
KMT2A Q03164 5/20 0.97
SLC25A20 O43772 3/20 0.97
TP53 P04637 3/20 0.97
TSHR P16473 3/20 0.97
CYP2D6 P10635 2/20 0.97
SLC6A5 Q9Y345 2/20 0.97
CYP2C9 P11712 2/20 0.97
HIF1A Q16665 2/20 0.97
CYP2C19 P33261 2/20 0.97
KDM4E B2RXH2 1/20 0.97
CYP3A4 P08684 1/20 0.97
NFKB1 P19838 1/20 0.97
THPO P40225 1/20 0.97
HSD17B10 Q99714 1/20 0.97
MAPK1 P28482 5/20 0.74

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 SCHEMBL5499648 1.00 MAPT (0.97) MAPTMEN1KMT2ASLC25A20TP53
Octanoylcarnitine SCHEMBL2784153 1.00 MAPT (0.97) MAPTMEN1KMT2ASLC25A20TP53
Palmitoyl-Carnitine SCHEMBL1332594 1.00 MAPT (0.97) MAPTMEN1KMT2ASLC25A20TP53
Hydrochloric Acid SCHEMBL6676390 1.00 MAPT (0.97) MAPTMEN1KMT2ASLC25A20TP53
Palmitoyl-Carnitine SCHEMBL1332983 1.00 MAPT (0.97) MAPTMEN1KMT2ASLC25A20TP53
Palmitoyl-Carnitine SCHEMBL2785481 1.00 MAPT (0.97) MAPTMEN1KMT2ASLC25A20TP53
Hydrochloric Acid SCHEMBL6658904 1.00 MAPT (0.97) MAPTMEN1KMT2ASLC25A20TP53
Hydrochloric Acid SCHEMBL17395722 1.00 MAPT (0.97) MAPTMEN1KMT2ASLC25A20TP53
Octanoylcarnitine SCHEMBL2787592 1.00 MAPT (0.97) MAPTMEN1KMT2ASLC25A20TP53
Palmitoyl-Carnitine SCHEMBL527281 1.00 MAPT (0.97) MAPTMEN1KMT2ASLC25A20TP53

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4642440-A1 COMPOSITIONS AND METHODS TO INCREASE THE SYSTEMIC BIOAVAILABILITY OF A POLYPEPTIDE THERAPEUTIC AGENT UNDERGOING ORAL ADMINISTRATION ALGIPHARMA AS (NO) 2025-11-05 EP claimed
WO-2024141760-A1 COMPOSITIONS AND METHODS TO INCREASE THE SYSTEMIC BIOAVAILABILITY OF A POLYPEPTIDE THERAPEUTIC AGENT UNDERGOING ORAL ADMINISTRATION ALGIPHARMA AS (NO) 2024-07-04 WO claimed
CN-114076701-A Dried blood spot quality control product for newborn screening and preparation method thereof 上海安谱实验科技股份有限公司 2022-02-22 CN claimed
CN-111196764-A Method for synthesizing lauroyl L-carnitine hydrochloride 黄冈华阳药业有限公司 2020-05-26 CN claimed
CN-109498559-A A kind of oral preparation and preparation method thereof loading treating diabetes polypeptide 复旦大学 2019-03-22 CN claimed
US-20160082026-A1 Ganglioside Transmucosal Formulations LZ THERAPEUTICS INC (US) 2016-03-24 US claimed
US-20150283158-A1 Ganglioside Transmucosal Formulations LZ THERAPEUTICS INC (US) 2015-10-08 US claimed
CN-101774934-B Method for synthesizing lauroyl L-carnitine hydrochloride HUBEI HILE CHEMICAL TECHNOLOGY CO LTD 2012-12-12 CN claimed
US-20120220544-A1 Ganglioside Transmucosal Formulations LZ THERAPEUTICS, INC. 2012-08-30 US claimed
EP-2473174-A2 GANGLIOSIDE TRANSMUCOSAL FORMULATIONS LZ Therapeutics, Inc. (US) 2012-07-11 EP claimed
WO-2011028799-A2 GANGLIOSIDE TRANSMUCOSAL FORMULATIONS LAZARUS THERAPEUTICS, INC. (US) 2011-03-10 WO claimed
CN-101774934-A Method for synthesizing lauroyl L-carnitine hydrochloride HUBEI HILE CHEMICAL TECHNOLOGY 2010-07-14 CN claimed
US-20260077020-A1 ORAL PEPTIDE PHARMACEUTICAL COMPOSITION THAT FACILITATES ENHANCED ORAL ABSORPTION LE ROUX DANIELLE MARIE (US) 2026-03-19 US disclosed
US-20260027062-A1 IMPROVED ORAL PHARMACEUTICAL FORMULATIONS OF THERAPEUTIC PEPTIDES AND PROTEINS CYPRUMED GMBH (AT) 2026-01-29 US disclosed
EP-4680265-A1 PHARMACEUTICAL COMPOSITIONS AND METHODS FOR THE TREATMENT OF METABOLIC AND LIVER DISORDERS Viking Therapeutics, Inc. (US) 2026-01-21 EP disclosed
EP-4658374-A1 METHODS FOR PREPARING CRYSTALLINE PEPTIDE INHIBITORS OF INTERLEUKIN-23 RECEPTOR Janssen Pharmaceutica NV (BE) 2025-12-10 EP disclosed
EP-0929270-A1 ORAL PEPTIDE PHARMACEUTICAL PRODUCTS Unigene Laboratories, Inc. (US) 1999-07-21 EP disclosed
US-5912014-A COMPOUNDS FOR TREATMENT OF BONE DISORDERS UNIGENE LABORATORIES, INC. (US) 1999-06-15 US disclosed
CN-1213282-A Oral peptide pharmaceutical products UNIGENE LAB INC (US) 1999-04-07 CN disclosed
WO-1997033531-A1 ORAL PEPTIDE PHARMACEUTICAL PRODUCTS UNIGENE LABORATORIES, INC. (US) 1997-09-18 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 (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-20260027062-A1 IMPROVED ORAL PHARMACEUTICAL FORMULATIONS OF THERAPEUTIC PEPTIDES AND PROTEINS ADM2, TAS2R42, ACP1 HSP90AA1 216/4885GLA 3979/4885HRH1 2561/4885
US-20260077020-A1 ORAL PEPTIDE PHARMACEUTICAL COMPOSITION THAT FACILITATES ENHANCED ORAL ABSORPTION VIP, GIPR, SLC10A2 HSP90AA1 2907/4885GLA 983/4885HRH1 193/4885

“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.