Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1064640

CCOC(=O)[C@@H](N)Cc1ccc(F)cc1.Cl

nearest known ligand 0.50

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
PPARG known ✓ P37231 2/20 0.50
DPP4 known ✓ P27487 2/20 0.42
OPRM1 known ✓ P35372 1/20 0.42
KCNQ3 known ✓ O43525 1/20 0.41
KCNQ2 known ✓ O43526 1/20 0.41
GAA known ✓ P10253 1/20 0.41
EPHX2 P34913 1/20 0.50
TPH1 P17752 4/20 0.44
MAPT P10636 3/20 0.44
MEN1 O00255 2/20 0.44
LMNA P02545 2/20 0.44
KMT2A Q03164 2/20 0.44
NPSR1 Q6W5P4 2/20 0.44
KDM4E B2RXH2 2/20 0.44
ALDH1A1 P00352 1/20 0.44
HPGD P15428 1/20 0.44
ALOX12 P18054 1/20 0.44
CCR6 P51684 1/20 0.44
HKDC1 Q2TB90 1/20 0.44
KDM4C Q9H3R0 1/20 0.44

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 SCHEMBL2108091 1.00 PPARG (0.50) PPARGEPHX2TPH1MAPTMEN1
SCHEMBL838697 0.98 PPARG (0.51) PPARGEPHX2TPH1MAPTMEN1
SCHEMBL839736 0.98 PPARG (0.51) PPARGEPHX2TPH1MAPTMEN1
SCHEMBL1064642 0.98 PPARG (0.51) PPARGEPHX2TPH1MAPTMEN1
Hydrochloric Acid SCHEMBL7224972 0.95 DPP4 (0.48) PPARGEPHX2TPH1MAPTMEN1
SCHEMBL7224977 0.94 DPP4 (0.49) PPARGEPHX2TPH1MAPTMEN1
SCHEMBL7960935 0.90 SLC7A5 (0.48) PPARGEPHX2TPH1ALDH1A1SLC7A5
L-Tyrosine Ethylester SCHEMBL9331146 0.85 SLC7A5 (0.59) TPH1SLC7A5
Hydrochloric Acid SCHEMBL7152109 0.85 LMNA (0.50) PPARGTPH1MAPTMEN1LMNA
L-Tyrosine Ethylester SCHEMBL595118 0.85 SLC7A5 (0.59) TPH1SLC7A5

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4347615-B1 PROCESS FOR MAKING MELFLUFEN OR A SALT THEREOF SYNTHON BV (NL) 2025-05-21 EP disclosed
CN-116348109-B Piperazine derivative, and preparation method and application thereof 浙江海正药业股份有限公司 2025-01-21 CN disclosed
US-20240358838-A1 LYOPHILIZED PREPARATION OF CYTOTOXIC DIPEPTIDES ONCOPEPTIDES AB (SE) 2024-10-31 US disclosed
US-20240270680-A1 PROCESS FOR MAKING MELFLUFEN OR A SALT THEREOF SYNTHON B.V. (NL) 2024-08-15 US disclosed
EP-4347615-A1 PROCESS FOR MAKING MELFLUFEN OR A SALT THEREOF Synthon B.V. (NL) 2024-04-10 EP disclosed
EP-3015488-B1 PRODUCTION METHOD FOR POLYAMINO ACID TAKEDA PHARMACEUTICALS CO (JP) 2024-03-06 EP disclosed
US-11896668-B2 Lyophilized preparation of cytotoxic dipeptides ONCOPEPTIDES AB (SE) 2024-02-13 US disclosed
CN-116348109-A Piperazine derivative, and preparation method and application thereof 浙江海正药业股份有限公司 2023-06-27 CN disclosed
EP-4122482-A1 LYOPHILIZED PREPARATION OF CYTOTOXIC DIPEPTIDES Oncopeptides AB (SE) 2023-01-25 EP disclosed
WO-2022253894-A1 PROCESS FOR MAKING MELFLUFEN OR A SALT THEREOF SYNTHON B.V. (NL) 2022-12-08 WO disclosed
CN-1155612-C Endothelin antagon 中国人民解放军军事医学科学院毒物药 2004-06-30 CN disclosed
CN-1155611-C Endothelin antagon 中国人民解放军军事医学科学院毒物药 2004-06-30 CN disclosed
US-20040097421-A1 Melphalan derivatives and their use as cancer chemotherapeutic drugs ONCOPEPTIDES INNOVATION AB (SE) 2004-05-20 US disclosed
US-20040038906-A1 Tripeptides; acidification; saponification INSTITUTE OF PHARMACOLOGY AND TOXICOLOGY ACADEMY OF MILITARY MEDICAL SCIENCES, P.L.A. (CN) 2004-02-26 US disclosed
US-20030162721-A1 PHARMACEUTICAL COMPOSITION CONTAINING PEPTICHEMIO PTC PHARMA AG (CH) 2003-08-28 US disclosed
EP-1290011-A1 MELPHALAN DERIVATIVES AND THEIR USE AS CANCER CHEMOTHERAPEUTIC DRUGS Oncopeptides AB (SE) 2003-03-12 EP disclosed
CN-1330076-A Endothelin antagon INST OF TOXIC MEDICINES PLA S (CN) 2002-01-09 CN disclosed
CN-1330077-A Endothelin antegon INST OF TOXIC MEDICINES PLA S (CN) 2002-01-09 CN disclosed
CN-1330075-A Endothelin antagon INST OF TOXIC MEDICINES PLA S (CN) 2002-01-09 CN disclosed
WO-2001096367-A1 MELPHALAN DERIVATIVES AND THEIR USE AS CANCER CHEMOTHERAPEUTIC DRUGS ONCOPEPTIDES AB (SE) 2001-12-20 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 (6 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-11896668-B2 Lyophilized preparation of cytotoxic dipeptides TREH, SORD, SI PPARG 4006/4885DPP4 30/4885OPRM1 2040/4885
US-20240270680-A1 PROCESS FOR MAKING MELFLUFEN OR A SALT THEREOF CYP2F1, CYP4F3, CYP4F2 PPARG 3983/4885DPP4 1532/4885OPRM1 1624/4885
US-20040097421-A1 Melphalan derivatives and their use as cancer chemotherapeutic drugs MCL1, LNPEP, MYADM PPARG 4666/4885DPP4 242/4885OPRM1 3504/4885
US-20240358838-A1 LYOPHILIZED PREPARATION OF CYTOTOXIC DIPEPTIDES TREH, TYMP, SI PPARG 4302/4885DPP4 754/4885OPRM1 1027/4885
US-20040038906-A1 Tripeptides; acidification; saponification VIP, DNPEP, ECE1 PPARG 4051/4885DPP4 13/4885OPRM1 4752/4885
US-20030162721-A1 PHARMACEUTICAL COMPOSITION CONTAINING PEPTICHEMIO VIP, HBB, PTMS PPARG 4061/4885DPP4 1967/4885OPRM1 1645/4885

“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.