Hydrochloric Acid

Hydrochloric Acid

SCHEMBL3501117

CC(C)(C)OC(=O)[C@@H](N)CCC(=O)OCc1ccccc1.Cl

nearest known ligand 0.60

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
LTA4H P09960 3/20 0.60
ALDH1A1 P00352 3/20 0.45
MAPK1 P28482 1/20 0.45
L3MBTL1 Q9Y468 1/20 0.45
SLC15A1 P46059 2/20 0.44
SYK P43405 1/20 0.44
LMNA P02545 1/20 0.42
MEN1 O00255 1/20 0.42
HPGD P15428 1/20 0.42
KMT2A Q03164 1/20 0.42
SLC7A5 Q01650 1/20 0.41
POLB P06746 1/20 0.40
PSMB5 P28074 1/20 0.40

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 SCHEMBL15387431 1.00 LTA4H (0.60) LTA4HALDH1A1MAPK1L3MBTL1SLC15A1
Hydrochloric Acid SCHEMBL25286512 1.00 LTA4H (0.60) LTA4HALDH1A1MAPK1L3MBTL1SLC15A1
SCHEMBL12155266 0.99 LTA4H (0.61) LTA4HALDH1A1MAPK1L3MBTL1SLC15A1
SCHEMBL7740145 0.99 LTA4H (0.61) LTA4HALDH1A1MAPK1L3MBTL1SLC15A1
SCHEMBL7740147 0.99 LTA4H (0.61) LTA4HALDH1A1MAPK1L3MBTL1SLC15A1
SCHEMBL8698981 0.91 LTA4H (0.56) LTA4HALDH1A1MAPK1L3MBTL1SLC15A1
Hydrochloric Acid SCHEMBL29400992 0.90 LTA4H (0.55) LTA4HALDH1A1MAPK1L3MBTL1SLC15A1
SCHEMBL28119343 0.89 LTA4H (0.52) LTA4HALDH1A1MAPK1L3MBTL1SLC15A1
SCHEMBL28119342 0.89 LTA4H (0.52) LTA4HALDH1A1MAPK1L3MBTL1SLC15A1
SCHEMBL9716820 0.88 LTA4H (0.56) LTA4HALDH1A1MAPK1L3MBTL1SLC15A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12576169-B2 Silicon-fluoride acceptor substituted radiopharmaceuticals and precursors thereof Technische Universität München (DE) 2026-03-17 US disclosed
US-20260001914-A1 MACROCYCLIC PEPTIDES TARGETING KRAS MERCK SHARP & DOHME LLC (US) 2026-01-01 US disclosed
US-20250295819-A1 PSMA binding dual mode radiotracer and therapeutics UNIV MUENCHEN TECH (DE) 2025-09-25 US disclosed
US-12377175-B2 Trifunctional constructs with tunable pharmacokinetics useful in imaging and anti-tumor therapies CORNELL UNIVERSITY (US) 2025-08-05 US disclosed
US-12377176-B2 Cancer diagnostic imaging agents Technische Universität München (DE) 2025-08-05 US disclosed
US-12357711-B2 PSMA binding dual mode radiotracer and therapeutic Technische Universität München (DE) 2025-07-15 US disclosed
US-12268759-B2 Trifunctional constructs with tunable pharmacokinetics useful in imaging and anti-tumor therapies CORNELL UNIVERSITY (US) 2025-04-08 US disclosed
EP-4520745-A2 DOUBLE TARGETED CONSTRUCTS TO AFFECT TUMOR KILL Cornell University (US) 2025-03-12 EP disclosed
US-12220419-B2 BCL-2 inhibitors NEWAVE PHARMACEUTICAL INC. (US) 2025-02-11 US disclosed
EP-3474903-B1 DOUBLE TARGETED CONSTRUCTS TO AFFECT TUMOR KILL UNIV CORNELL (US) 2025-01-22 EP disclosed
US-20170057912-A1 PROCESS FOR MAKING LYSINE-GLUTAMIC ACID DIPEPTIDE DERIVATIVES HOFFMANN-LA ROCHE INC. (US) 2017-03-02 US disclosed
EP-3127604-A1 LYSIN-GLUTAMIC ACID DIPEPTIDE DERIVATIVES F. Hoffmann-La Roche AG (CH) 2017-02-08 EP disclosed
US-9522874-B2 Lysine-glutamic acid dipeptide derivatives HOFFMANN-LA ROCHE INC. (US) 2016-12-20 US disclosed
EP-2849882-A1 LYSIN-GLUTAMIC ACID DIPEPTIDE DERIVATIVES F. Hoffmann-La Roche AG (CH) 2015-03-25 EP disclosed
US-20150073173-A1 LYSINE-GLUTAMIC ACID DIPEPTIDE DERIVATIVES HOFFMANN-LA ROCHE INC. (US) 2015-03-12 US disclosed
CN-104271227-A Lysin-glutamic acid dipeptide derivatives HOFFMANN LA ROCHE 2015-01-07 CN disclosed
WO-2013171135-A1 LYSIN-GLUTAMIC ACID DIPEPTIDE DERIVATIVES F. HOFFMANN-LA ROCHE AG (CH) 2013-11-21 WO disclosed
EP-2664374-A1 Lysin-glutamic acid dipeptide derivatives F. Hoffmann-La Roche AG (CH) 2013-11-20 EP disclosed
US-20100130737-A1 Regulating Agent of GPR34 Receptor Function TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2010-05-27 US disclosed
EP-1849465-A1 AGENT FOR CONTROLLING FUNCTION OF GPR34 RECEPTOR Takeda Pharmaceutical Company Limited (JP) 2007-10-31 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 (11 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-12377176-B2 Cancer diagnostic imaging agents FOLH1, FOLR1, KLK3 LTA4H 4594/4885ALDH1A1 1382/4885MAPK1 3975/4885
US-20100130737-A1 Regulating Agent of GPR34 Receptor Function GPR34, GPR4, GPR6 LTA4H 1788/4885ALDH1A1 3047/4885MAPK1 1691/4885
US-12357711-B2 PSMA binding dual mode radiotracer and therapeutic PSMA2, FOLH1, PSMA1 LTA4H 4230/4885ALDH1A1 2013/4885MAPK1 3294/4885
US-12377175-B2 Trifunctional constructs with tunable pharmacokinetics useful in imaging and anti-tumor therapies VHL, GLS, GPER1 LTA4H 3191/4885ALDH1A1 1271/4885MAPK1 4664/4885
US-12220419-B2 BCL-2 inhibitors BCL2L10, BCL2, BCL2L11 LTA4H 2762/4885ALDH1A1 3743/4885MAPK1 2202/4885
US-20250295819-A1 PSMA binding dual mode radiotracer and therapeutics FOLH1, PSMA2, PSMA1 LTA4H 4176/4885ALDH1A1 2008/4885MAPK1 3257/4885
US-20260001914-A1 MACROCYCLIC PEPTIDES TARGETING KRAS KRAS, NRAS, HRAS LTA4H 3810/4885ALDH1A1 3909/4885MAPK1 470/4885
US-12268759-B2 Trifunctional constructs with tunable pharmacokinetics useful in imaging and anti-tumor therapies VHL, GLS, GPER1 LTA4H 3191/4885ALDH1A1 1271/4885MAPK1 4664/4885
US-12576169-B2 Silicon-fluoride acceptor substituted radiopharmaceuticals and precursors thereof KLK3, FOLH1, SLC7A1 LTA4H 3407/4885ALDH1A1 2396/4885MAPK1 1950/4885
US-20170057912-A1 PROCESS FOR MAKING LYSINE-GLUTAMIC ACID DIPEPTIDE DERIVATIVES GLUL, ASNS, QPCT LTA4H 475/4885ALDH1A1 2242/4885MAPK1 1610/4885
US-20150073173-A1 LYSINE-GLUTAMIC ACID DIPEPTIDE DERIVATIVES GLUL, ASNS, QPCT LTA4H 431/4885ALDH1A1 2435/4885MAPK1 1503/4885

“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.