Hydrochloric Acid

Hydrochloric Acid

SCHEMBL22346017

CCc1ccccc1NC(=O)O.Cl

nearest known ligand 0.71

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
GAA known ✓ P10253 2/20 0.58
HDAC3 known ✓ O15379 1/20 0.57
HDAC4 known ✓ P56524 1/20 0.57
HDAC1 known ✓ Q13547 1/20 0.57
HDAC7 known ✓ Q8WUI4 1/20 0.57
HDAC2 known ✓ Q92769 1/20 0.57
HDAC10 known ✓ Q969S8 1/20 0.57
HDAC11 known ✓ Q96DB2 1/20 0.57
HDAC8 known ✓ Q9BY41 1/20 0.57
HDAC6 known ✓ Q9UBN7 1/20 0.57
HDAC9 known ✓ Q9UKV0 1/20 0.57
HDAC5 known ✓ Q9UQL6 1/20 0.57
KCNK3 known ✓ O14649 1/20 0.55
KCNK9 known ✓ Q9NPC2 1/20 0.55
GRIN2D known ✓ O15399 1/20 0.53
GRIN3B known ✓ O60391 1/20 0.53
GRIN1 known ✓ Q05586 1/20 0.53
GRIN2A known ✓ Q12879 1/20 0.53
GRIN2B known ✓ Q13224 1/20 0.53
GRIN2C known ✓ Q14957 1/20 0.53

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
SCHEMBL948318 0.98 MAPT (0.59) MAPTALDH1A1GAAPOLBHDAC3
Acrylic Acid SCHEMBL3955124 0.87 MAPT (0.52) MAPTALDH1A1GAAPOLBHDAC3
SCHEMBL2022897 0.86 POLB (0.53) MAPTALDH1A1GAAPOLBHDAC3
Hydrochloric Acid SCHEMBL28825350 0.86 MAPT (0.61) MAPTALDH1A1GAAPOLBHDAC3
SCHEMBL9717979 0.85 HTT (0.72) MAPTALDH1A1GAAPOLBHDAC3
SCHEMBL2349955 0.85 MAPT (0.61) MAPTALDH1A1GAAPOLBHDAC3
SCHEMBL4622869 0.85 L3MBTL1 (0.56) MAPTALDH1A1GAAPOLBHDAC3
SCHEMBL29580443 0.85 HTT (0.72) MAPTALDH1A1GAAPOLBHDAC3
SCHEMBL21551505 0.84 MAPT (0.60) MAPTALDH1A1GAAPOLBHDAC3
SCHEMBL2019462 0.83 POLB (0.58) MAPTALDH1A1GAAPOLBHDAC3

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 10 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4678626-A1 LONG-CHAIN ALKENYLOXY-SUBSTITUTED BENZOYL DERIVATIVE AND OLIGONUCLEOTIDE SYNTHESIS METHOD USING SAME Spera Pharma, Inc. (JP) 2026-01-14 EP disclosed
US-12509484-B2 Method of producing nucleic acid compound, and nucleic acid compound FUJIFILM CORPORATION (JP) 2025-12-30 US disclosed
WO-2024185775-A1 LONG-CHAIN ALKENYLOXY–SUBSTITUTED BENZOYL DERIVATIVE AND OLIGONUCLEOTIDE SYNTHESIS METHOD USING SAME スペラファーマ株式会社 2024-09-12 WO disclosed
WO-2022220019-A1 LONG-CHAIN DNA SYNTHESIS USING NON-NATURAL BASE 国立大学法人東京工業大学 2022-10-20 WO disclosed
US-20220259255-A1 METHOD OF PRODUCING NUCLEIC ACID COMPOUND, AND NUCLEIC ACID COMPOUND FUJIFILM CORPORATION (JP) 2022-08-18 US disclosed
WO-2022172994-A1 OLIGONUCLEOTIDE PRODUCTION METHOD 味の素株式会社 2022-08-18 WO disclosed
EP-4006045-A1 NUCLEIC ACID COMPOUND MANUFACTURING METHOD AND NUCLEIC ACID COMPOUND FUJIFILM Corporation (JP) 2022-06-01 EP disclosed
WO-2021039935-A1 NUCLEIC ACID COMPOUND MANUFACTURING METHOD AND NUCLEIC ACID COMPOUND 富士フイルム株式会社 2021-03-04 WO disclosed
WO-2020196890-A1 METHOD FOR PRODUCING OLIGONUCLEOTIDE HAVING PHOSPHOROTHIOATE SITE 味の素株式会社 2020-10-01 WO disclosed
WO-2020166705-A1 PRODUCTION METHOD FOR OLIGONUCLEOTIDES 味の素株式会社 2020-08-20 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 (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-20220259255-A1 METHOD OF PRODUCING NUCLEIC ACID COMPOUND, AND NUCLEIC ACID COMPOUND XRN2, RNASEH1, NSUN2 GAA 4572/4885HDAC3 849/4885HDAC4 1297/4885
US-12509484-B2 Method of producing nucleic acid compound, and nucleic acid compound NSUN2, RNASEH1, XRN2 GAA 4194/4885HDAC3 1561/4885HDAC4 2300/4885

“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.