Hydrochloric Acid

Hydrochloric Acid

SCHEMBL200899

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

nearest known ligand 0.59

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 11)

geneUniProtsupporting neighboursconfidence
GAA known ✓ P10253 1/20 0.38
MARS1 P56192 6/20 0.43
METAP2 P50579 1/20 0.42
METAP1 P53582 1/20 0.42
ALDH1A1 P00352 1/20 0.41
L3MBTL1 Q9Y468 1/20 0.40
RNPEP Q9H4A4 1/20 0.39
CYP2C9 P11712 1/20 0.39
ANPEP P15144 1/20 0.38
ENPEP Q07075 1/20 0.38
HTT P42858 1/20 0.38

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 SCHEMBL3089952 1.00 MARS1 (0.43) MARS1METAP2METAP1ALDH1A1L3MBTL1
Hydrochloric Acid SCHEMBL27980313 1.00 MARS1 (0.43) MARS1METAP2METAP1ALDH1A1L3MBTL1
Hydrochloric Acid SCHEMBL200898 1.00 MARS1 (0.43) MARS1METAP2METAP1ALDH1A1L3MBTL1
Hydrochloric Acid SCHEMBL27980312 1.00 MARS1 (0.43) MARS1METAP2METAP1ALDH1A1L3MBTL1
SCHEMBL108559 0.98 MARS1 (0.44) MARS1METAP2METAP1ALDH1A1L3MBTL1
SCHEMBL108560 0.98 MARS1 (0.44) MARS1METAP2METAP1ALDH1A1L3MBTL1
SCHEMBL3089957 0.98 MARS1 (0.44) MARS1METAP2METAP1ALDH1A1L3MBTL1
Ammonia Solution, Strong SCHEMBL9081566 0.96 MARS1 (0.43) MARS1METAP2METAP1ALDH1A1L3MBTL1
Hydrogen Sulfide SCHEMBL9171273 0.96 MARS1 (0.43) MARS1METAP2METAP1ALDH1A1L3MBTL1
Sulfur Dioxide SCHEMBL28722439 0.94 MARS1 (0.42) MARS1METAP2METAP1ALDH1A1L3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025047832-A1 SKIN COSMETIC COMPOSITION CONTAINING BOTRYOCOCCENE AS ACTIVE INGREDIENT フィコケミー株式会社 2025-03-06 WO claimed
CN-119409588-A Caffeoyl amino acid methyl ester derivative and preparation method and application thereof 西北大学 2025-02-11 CN claimed
CN-118743985-B Solid waste-based modularized constructed wetland filler 皖创环保股份有限公司 2024-11-12 CN claimed
CN-118743985-A Novel solid waste-based modularized constructed wetland filler 皖创环保股份有限公司 2024-10-08 CN claimed
CN-118459369-A Synthetic method of N-Boc-vinyl glycine methyl ester and isomer thereof 成都师范学院 2024-08-09 CN claimed
CN-118290360-A Synthetic method of organic light response probe HBT-CN based on ESIPT effect, obtained probe and application thereof 临沂大学 2024-07-05 CN claimed
CN-117903078-A Amide derivative containing 3, 4-dichloro isothiazole, preparation method and application thereof 南开大学 2024-04-19 CN claimed
CN-117179320-A Gamma-aminobutyric acid collagen for promoting cartilage growth and preparation method thereof 武汉华源晨泰健康生物科技有限公司 2023-12-08 CN claimed
CN-113912524-B Polypeptide compound containing sulfur amide and synthesis method thereof 华东师范大学 2023-12-01 CN claimed
WO-2023167248-A1 NEW PEST CONTROL METHOD TARGETING RESPIRATORY ORGAN FORMING MECHANISM OF PESTS 国立研究開発法人産業技術総合研究所 2023-09-07 WO claimed
CN-113527399-A Ginsenoside CK derivative and application thereof in preparation of antitumor drugs 陕西巨子生物技术有限公司 2021-10-22 CN claimed
CN-110408584-B Left-handed chiral nanogel cell scaffold material and preparation method thereof 上海交通大学 2021-09-07 CN claimed
CN-111298768-A Diluted sulfuric acid and graphene oxide co-doped modified titanium dioxide composite material, preparation method and application thereof 武汉科技大学 2020-06-19 CN claimed
CN-110408584-A Left-handed chirality nanogel cell scaffold material and preparation method thereof UNIV SHANGHAI JIAOTONG 2019-11-05 CN claimed
CN-110343520-A Rhodamine mercury ion fluorescence probe and its application containing methionine hydrazide structure 辽宁大学 2019-10-18 CN claimed
US-10144914-B2 Modified substrates for protection of peptide-immobilized surfaces from gamma radiation degradation CORNING INCORPORATED (US) 2018-12-04 US claimed
US-20180070612-A1 RUMEN BY-PASS ANIMAL FEED COMPOSITION AND METHOD OF MAKING SAME WAN FENG (US) 2018-03-15 US claimed
CN-107708432-A Rumen bypass animal feed composition and preparation method thereof 拜内梅尔克公司 2018-02-16 CN claimed
US-20100145070-A1 ANTI-CANCER COMPOUND AND MANUFACTURING METHOD THEREOF NATIONAL DEFENSE MEDICAL CENTER (TW) 2010-06-10 US claimed
EP-0343654-A2 Diol-containing renin inhibitors WARNER-LAMBERT COMPANY (US) 1989-11-29 EP claimed

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-20100145070-A1 ANTI-CANCER COMPOUND AND MANUFACTURING METHOD THEREOF DCK, DHPS, DHX15 GAA 1862/4885MARS1 2408/4885METAP2 3710/4885

“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.