Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1665136

Cl.NNc1ccc([N+](=O)[O-])cc1[N+](=O)[O-]

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 20)

geneUniProtsupporting neighboursconfidence
GAA known ✓ P10253 1/20 0.46
MAPT P10636 6/20 0.59
MEN1 O00255 6/20 0.59
KMT2A Q03164 6/20 0.59
MAPK1 P28482 5/20 0.59
TDP1 Q9NUW8 4/20 0.58
TXNRD1 Q16881 1/20 0.55
TXNRD3 Q86VQ6 1/20 0.55
TXNRD2 Q9NNW7 1/20 0.55
ALDH1A1 P00352 4/20 0.52
SMN1; SMN2 Q16637 2/20 0.52
GPR35 Q9HC97 2/20 0.52
TP53 P04637 1/20 0.52
HPGD P15428 1/20 0.52
TSHR P16473 1/20 0.52
HIF1A Q16665 1/20 0.52
L3MBTL1 Q9Y468 3/20 0.51
CTDSP1 Q9GZU7 1/20 0.51
CRHBP P24387 1/20 0.51
CRHR2 Q13324 1/20 0.51

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 SCHEMBL11150669 1.00 MAPT (0.59) MAPTMEN1KMT2AMAPK1TDP1
SCHEMBL16140 0.98 MAPT (0.61) MAPTMEN1KMT2AMAPK1TDP1
SCHEMBL29352891 0.98 MAPT (0.61) MAPTMEN1KMT2AMAPK1TDP1
SCHEMBL27470180 0.98 MAPT (0.61) MAPTMEN1KMT2AMAPK1TDP1
SCHEMBL28247841 0.98 MAPT (0.61) MAPTMEN1KMT2AMAPK1TDP1
Water SCHEMBL9233283 0.96 MAPT (0.59) MAPTMEN1KMT2AMAPK1TDP1
Methane SCHEMBL28068825 0.96 MAPT (0.59) MAPTMEN1KMT2AMAPK1TDP1
Formaldehyde SCHEMBL28414752 0.95 MAPT (0.58) MAPTMEN1KMT2AMAPK1TDP1
Methyl Alcohol SCHEMBL27980452 0.93 MAPT (0.56) MAPTMEN1KMT2AMAPK1TDP1
Phosphoric Acid SCHEMBL30231818 0.90 MAPT (0.54) MAPTMEN1KMT2AMAPK1TDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116804661-A Method for measuring formaldehyde content in antiviral drug of lovir raw material drug by HPLC 湖北省宏源药业科技股份有限公司 2023-09-26 CN claimed
CN-113281421-A Efficient determination method for formaldehyde in starch food 贵州省产品质量检验检测院 2021-08-20 CN claimed
CN-111693632-A Method for extracting total formaldehyde in cosmetics and rapid detection method 上海市食品药品检验所 2020-09-22 CN claimed
CN-108828089-A The method that derivatization HPLC-UV/Vis method measures 4- nitrobenzaldehyde in chloramphenicol or its preparation 中国药科大学 2018-11-16 CN claimed
EP-4443155-B1 ENCAPSULATED PRE-ANALYTIC WORKFLOWS FOR FLOW-THROUGH DEVICES, LIQUID CHROMATOGRAPHY AND MASS SPECTROMETRIC ANALYSIS WATERS TECHNOLOGIES CORP (US) 2026-05-13 EP disclosed
US-12616220-B2 Method for producing plant-based milk-fermented liquid ASAHI GROUP HOLDINGS, LTD. (JP) 2026-05-05 US disclosed
US-12487210-B2 Encapsulated pre-analytic workflows for flow-through devices, liquid chromatography and mass spectrometric analysis WATERS TECHNOLOGIES CORPORATION (US) 2025-12-02 US disclosed
EP-4443155-A2 ENCAPSULATED PRE-ANALYTIC WORKFLOWS FOR FLOW-THROUGH DEVICES, LIQUID CHROMATOGRAPHY AND MASS SPECTROMETRIC ANALYSIS Waters Technologies Corporation (US) 2024-10-09 EP disclosed
EP-3491374-B1 ENCAPSULATED PRE-ANALYTIC WORKFLOW REAGENTS FOR FLOW-THROUGH DEVICES, LIQUID CHROMATOGRAPHY AND MASS SPECTROMETRIC ANALYSIS WATERS TECHNOLOGIES CORP (US) 2024-10-09 EP disclosed
WO-2024162063-A1 AQUEOUS DISPERSION AND RESIN FILM FORMED FROM SAID AQUEOUS DISPERSION 住友化学株式会社 2024-08-08 WO disclosed
US-20240172780-A1 METHOD FOR PRODUCING PLANT-BASED MILK-FERMENTED LIQUID ASAHI GROUP HOLDINGS, LTD. (JP) 2024-05-30 US disclosed
US-20240172767-A1 METHOD FOR PRODUCING PLANT-BASED MILK-FERMENTED LIQUID ASAHI GROUP HOLDINGS, LTD. (JP) 2024-05-30 US disclosed
US-5512466-A EXPRESSION OF A 1-AMINOCYCLOPROPANE-1-CARBOXYLIC ACID METABOLIZING ENZYME TO INHIBIT PRODUCTION OF ETHYLENE MONSANTO COMPANY (US) 1996-04-30 US disclosed
US-5300497-A Broad spectrum antibiotics and bactericides; stable to beta-lactamase; effective against antibiotic-resistant bacteria TOYAMA CHEMICAL CO., LTD. (JP) 1994-04-05 US disclosed
EP-0564524-A1 CONTROL OF FRUIT RIPENING AND SENESCENCE IN PLANTS MONSANTO COMPANY (US) 1993-10-13 EP disclosed
US-5185330-A Penicillins/ad/ TOYAMA CHEMICAL CO., LTD. (JP) 1993-02-09 US disclosed
WO-1992012249-A1 CONTROL OF FRUIT RIPENING AND SENESCENCE IN PLANTS MONSANTO COMPANY (US) 1992-07-23 WO disclosed
EP-0010615-B1 METHOD AND REAGENT FOR DETERMINING IONS, POLAR AND/OR LIPOPHILIC COMPOUNDS IN LIQUIDS Roche Diagnostics GmbH (DE) 1984-07-25 EP disclosed
US-4367072-A Ligands assayed by host molecules including cyclophanes, crown ethers, crypstands and podands BOEHRINGER MANNHEIM GMBH (DE) 1983-01-04 US disclosed
US-3950427-A ANTIINFLAMMATORY, ANTIPYRETIC BOEHRINGER INGELHEIM GMBH (DT) 1976-04-13 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-12616220-B2 Method for producing plant-based milk-fermented liquid LPO, LCT, CA9 GAA 290/4885MAPT 711/4885MEN1 3797/4885

“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.