Hydrochloric Acid

Hydrochloric Acid

SCHEMBL3182704

Cl.Nc1cc(N)c(O)cc1O

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
GAA known ✓ P10253 7/20 0.48
HSP90AA1 known ✓ P07900 1/20 0.39
CA2 known ✓ P00918 1/20 0.39
ALDH1A1 P00352 9/20 0.48
MAPT P10636 6/20 0.48
MEN1 O00255 5/20 0.48
KMT2A Q03164 5/20 0.48
KDM4E B2RXH2 4/20 0.48
PKM P14618 2/20 0.48
L3MBTL1 Q9Y468 1/20 0.48
ALOX15 P16050 5/20 0.48
HSD17B10 Q99714 5/20 0.48
CYP3A4 P08684 2/20 0.48
PTK2 Q05397 1/20 0.47
ALOX12 P18054 3/20 0.43
SMN1; SMN2 Q16637 2/20 0.43
HPGD P15428 2/20 0.43
MAPK1 P28482 1/20 0.43
RECQL P46063 2/20 0.42
THRB P10828 1/20 0.42

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 SCHEMBL41565 1.00 ALDH1A1 (0.48) ALDH1A1GAAMAPTMEN1KMT2A
Hydrochloric Acid SCHEMBL10348271 0.97 PTK2 (0.53) ALDH1A1GAAMAPTMEN1KMT2A
Hydrochloric Acid SCHEMBL28456008 0.97 ALDH1A1 (0.46) ALDH1A1GAAMAPTMEN1KMT2A
SCHEMBL106886 0.96 ALDH1A1 (0.50) ALDH1A1GAAMAPTMEN1KMT2A
SCHEMBL28229778 0.96 ALDH1A1 (0.50) ALDH1A1GAAMAPTMEN1KMT2A
SCHEMBL28190785 0.93 ALDH1A1 (0.48) ALDH1A1GAAMAPTMEN1KMT2A
SCHEMBL2675947 0.93 ALDH1A1 (0.48) ALDH1A1GAAMAPTMEN1KMT2A
Water SCHEMBL27493672 0.93 ALDH1A1 (0.48) ALDH1A1GAAMAPTMEN1KMT2A
Hydrochloric Acid SCHEMBL2146037 0.90 PTK2 (0.53) ALDH1A1GAAMAPTMEN1KMT2A
Methyl Alcohol SCHEMBL27532918 0.90 ALDH1A1 (0.48) ALDH1A1GAAMAPTMEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122082149-A Ultraviolet-resistant PBO fiber with excellent mechanical properties and preparation method thereof 2026-05-26 CN claimed
CN-120134776-A Preparation method of high-strength multilayer composite fabric 江苏佩浦高分子科技有限公司 2025-06-13 CN claimed
CN-119859105-A Preparation method of 4, 6-diaminoresorcinol hydrochloride crystal 中国石油化工股份有限公司 2025-04-22 CN claimed
CN-119684604-A Flexible temperature-resistant PBO polymer and preparation process thereof 中蓝晨光化工研究设计院有限公司 2025-03-25 CN claimed
CN-119640624-A High-strength PBO composite insulating paper and preparation method thereof 山东非金属材料研究所 2025-03-18 CN claimed
CN-119640581-A Preparation method of modified PBO fiber toughening agent for well cementation under high-frequency alternating injection and production conditions 西南石油大学 2025-03-18 CN claimed
CN-119593096-A Ultraviolet radiation resistant PBOH fiber and preparation method thereof 哈尔滨工业大学 2025-03-11 CN claimed
CN-119571491-A High-strength high-modulus PBO fiber and preparation method thereof 中国石油化工股份有限公司 2025-03-07 CN claimed
CN-119571492-A Ultraviolet aging resistant high-strength high-modulus PBO fiber and preparation method thereof 中国石油化工股份有限公司 2025-03-07 CN claimed
CN-119194654-B Preparation method of low-dielectric PBO fiber 山东非金属材料研究所 2025-02-18 CN claimed
CN-103880767-A Preparation method for 2-(p-formylchloropropyl)-5-amino-6-hydroxyl benzoxazole HARBIN INST OF TECHNOLOGY 2014-06-25 CN claimed
CN-103709404-A PBO (poly(p-phenylene-2,6-benzobisoxazole)) copolycondensation modification method CHONGQING INST GREEN & INTELLIGENT TECHNOLOGY CAS 2014-04-09 CN claimed
US-20130298933-A1 METHOD FOR STRAIGHTENING KERATINOUS FIBERS USING HEATING MEANS AND AN AROMATIC COMPOUND L'OREAL (FR) 2013-11-14 US claimed
CN-103160950-A Preparation method for ultraviolet-resistant PBO fibers KINGFA SCIENCE & TECHNOLOGY CO 2013-06-19 CN claimed
CN-103013113-A Preparation method of graphene/PBO polymer HARBIN INST OF TECHNOLOGY 2013-04-03 CN claimed
CN-103014901-A Preparation method of graphene/PBO (Poly-P-Phenylene Benzobisoxazazole) composite fiber HARBIN INST OF TECHNOLOGY 2013-04-03 CN claimed
CN-102992312-A Preparation method of graphene monomer complex HARBIN INST OF TECHNOLOGY 2013-03-27 CN claimed
CN-102296376-B Production method of poly-p-phenylene benzodioxazole fibers SINOSELEN HI TECH CO LTD 2013-01-09 CN claimed
US-20100300472-A1 METHOD FOR STRAIGHTENING KERATINOUS FIBERS USING HEATING MEANS AND AN AROMATIC COMPOUND L'OREAL S.A. (FR) 2010-12-02 US claimed
CN-1583752-A Synthesis of benzoxazole UNIV HARBIN POLYTECHNIC (CN) 2005-02-23 CN 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-20100300472-A1 METHOD FOR STRAIGHTENING KERATINOUS FIBERS USING HEATING MEANS AND AN AROMATIC COMPOUND KRT18, TUBB4A, TUBB4B GAA 3877/4885HSP90AA1 404/4885CA2 2393/4885

“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.