Hydrochloric Acid

Hydrochloric Acid

SCHEMBL134493

CCOC(=O)[C@@H](N)CCSC.Cl

nearest known ligand 0.57

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 12)

geneUniProtsupporting neighboursconfidence
METAP2 P50579 4/20 0.51
METAP1 P53582 2/20 0.51
PPID Q08752 1/20 0.41
MARS1 P56192 6/20 0.40
NOD1 Q9Y239 2/20 0.39
RNPEP Q9H4A4 1/20 0.38
ALOX15 P16050 1/20 0.37
CYP2D6 P10635 1/20 0.37
CYP2C9 P11712 1/20 0.37
CYP2C19 P33261 1/20 0.37
ANPEP P15144 1/20 0.36
ENPEP Q07075 1/20 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 SCHEMBL2031642 1.00 METAP2 (0.51) METAP2METAP1PPIDMARS1NOD1
Hydrochloric Acid SCHEMBL8014832 1.00 METAP2 (0.51) METAP2METAP1PPIDMARS1NOD1
SCHEMBL113611 0.98 METAP2 (0.53) METAP2METAP1PPIDMARS1NOD1
SCHEMBL113612 0.98 METAP2 (0.53) METAP2METAP1PPIDMARS1NOD1
SCHEMBL5443843 0.98 METAP2 (0.53) METAP2METAP1PPIDMARS1NOD1
SCHEMBL6461273 0.94 METAP2 (0.50) METAP2METAP1PPIDMARS1NOD1
SCHEMBL1252426 0.94 METAP2 (0.50) METAP2METAP1PPIDMARS1NOD1
Hydrochloric Acid SCHEMBL27497759 0.85 MARS1 (0.43) METAP2METAP1MARS1NOD1RNPEP
SCHEMBL1839254 0.84 NOD1 (0.40) METAP2METAP1NOD1ALOX15CYP2D6
SCHEMBL1839255 0.84 NOD1 (0.40) METAP2METAP1NOD1ALOX15CYP2D6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115644297-A Candy and preparation method thereof 何桂霞 2023-01-31 CN claimed
CN-114344230-A Composition for inhibiting bacteria, removing mites and removing acnes, and preparation method and application thereof 广州美果生物科技有限公司 2022-04-15 CN claimed
CN-109234343-B Methionine oligopeptide and preparation method and application thereof 中国海洋大学 2020-12-01 CN claimed
US-20150045496-A1 THERMO-REVERSIBLE POLYBUTADIENE RUBBER BLEND WITH SELF-HEALING NATURE RELIANCE INDUSTRIES LIMITED (IN) 2015-02-12 US claimed
WO-2013164843-A1 THERMO-REVERSIBLE POLYBUTADIENE RUBBER BLEND WITH SELF-HEALING NATURE RELIANCE INDUSTRIES LTD. (IN) 2013-11-07 WO claimed
WO-2010117258-A1 A METHOD OF SYNTHESISING AN AMINO ACID DERIVATIVE OF AZELAIC ACID MALAYSIAN PALM OIL BOARD (MY) 2010-10-14 WO claimed
US-6372788-B1 None US disclosed
EP-4680222-A1 N-BETA-HYDROXYBUTYRYL-AMINO ACIDS AND RELATED COMPOSITIONS AND METHODS The Board of Trustees of the Leland Stanford Junior University (US) 2026-01-21 EP disclosed
CN-119868228-A Acne-removing composition capable of achieving targeted bacteriostasis and application thereof 诺斯贝尔化妆品股份有限公司 2025-04-25 CN disclosed
US-12221445-B2 Crystalline salts of 5-methyl-(6S)-tetrahydrofolic acid and amino ethyl esters MERCK PATENT GMBH (DE) 2025-02-11 US disclosed
US-12161620-B2 Devices and methods for facilitating and controlling use of a medication Jazz Pharmaceuticals, Inc. (US) 2024-12-10 US disclosed
WO-2024192165-A1 N-BETA-HYDROXYBUTYRYL-AMINO ACIDS AND RELATED COMPOSITIONS AND METHODS THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY (US) 2024-09-19 WO disclosed
EP-4425181-A1 COMPOSITION FOR DETECTING OR MEASURING ANALYTE Bertis Inc (KR) 2024-09-04 EP disclosed
EP-0309766-A2 N-acylamino acid derivatives and their use BANYU PHARMACEUTICAL CO., LTD. (JP) 1989-04-05 EP disclosed
WO-1988006187-A1 A PROCESS FOR ENZYMATIC PRODUCTION PRODUCTION OF DIPEPTIDES CARLSBERG BIOTECHNOLOGY LTD. A/S (DK) 1988-08-25 WO disclosed
EP-0278787-A1 A process for enzymatic production of dipeptides CARLBIOTECH LTD. A/S (DK) 1988-08-17 EP disclosed
EP-0056565-B1 DERIVATIVES OF DI(-2-CHLOROETHYL) AMINOPHENYL ALANINE WITH ANTITUMOUR ACTIVITY PROTER S.p.A. (IT) 1984-12-05 EP disclosed
US-4428875-A TRIPEPTIDES INCLUDING METHIONINE PROTER S.P.A. (IT) 1984-01-31 US disclosed
EP-0056565-A1 Derivatives of di(-2-chloroethyl) aminophenyl alanine with antitumour activity PROTER S.p.A. (IT) 1982-07-28 EP disclosed
US-4325954-A ANTIDEPRESSANTS LABORATOIRES JACQUES LOGEAIS (FR) 1982-04-20 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 (1 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-12161620-B2 Devices and methods for facilitating and controlling use of a medication CES2, OPRM1, UGT1A10 METAP2 579/4885METAP1 750/4885PPID 3015/4885

“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.