Hydrochloric Acid

Hydrochloric Acid

SCHEMBL3199181

Cl.O=C(O)c1cccc([N+](=O)[O-])c1

nearest known ligand 0.96

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
HSP90AA1 known ✓ P07900 1/20 0.58
GAA known ✓ P10253 1/20 0.56
TP53 P04637 1/20 0.96
CES2 O00748 1/20 0.72
CES1 P23141 1/20 0.72
TSHR P16473 3/20 0.68
ALDH1A1 P00352 3/20 0.68
PRSS1 P07477 1/20 0.64
PRSS2 P07478 1/20 0.64
PRSS3 P35030 1/20 0.64
PTPN1 P18031 1/20 0.61
PTPN12 Q05209 1/20 0.61
PTPN22 Q9Y2R2 1/20 0.61
MEN1 O00255 2/20 0.60
KMT2A Q03164 2/20 0.60
KDM4E B2RXH2 1/20 0.59
LMNA P02545 1/20 0.59
MAPT P10636 2/20 0.58
MITF O75030 1/20 0.58
HTT P42858 1/20 0.58

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
SCHEMBL27709081 0.98 TP53 (1.00) TP53CES2CES1TSHRALDH1A1
SCHEMBL132618 0.98 TP53 (1.00) TP53CES2CES1TSHRALDH1A1
SCHEMBL29490968 0.98 TP53 (1.00) TP53CES2CES1TSHRALDH1A1
Fluoride SCHEMBL28228052 0.96 TP53 (0.96) TP53CES2CES1TSHRALDH1A1
SCHEMBL11320128 0.96 TP53 (0.96) TP53CES2CES1TSHRALDH1A1
Ammonia Solution, Strong SCHEMBL1734091 0.96 TP53 (0.96) TP53CES2CES1TSHRALDH1A1
SCHEMBL11534873 0.96 TP53 (0.96) TP53CES2CES1TSHRALDH1A1
SCHEMBL10415666 0.96 TP53 (0.96) TP53CES2CES1TSHRALDH1A1
Methane SCHEMBL27901093 0.96 TP53 (0.96) TP53CES2CES1TSHRALDH1A1
SCHEMBL8816405 0.96 TP53 (0.96) TP53CES2CES1TSHRALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0284422-B1 4,5-DIHYDRO-1H-1,2,4-TRIAZOLE-3-CARBOXAMIDE DERIVATIVES AND HERBICIDAL COMPOSITION CONTAINING THE SAME KUREHA KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1992-07-15 EP claimed
US-20240383844-A1 META-ESTER AROMATIC DIAMINES, METHOD FOR PRODUCING SAME, AND POLYIMIDE HAVING SAID META-ESTER AROMATIC DIAMINES AS RAW MATERIAL SEIKA CORPORATION (JP) 2024-11-21 US disclosed
US-20240239741-A1 META-ESTER AROMATIC DIAMINES, METHOD FOR PRODUCING SAME, AND POLYIMIDE HAVING SAID META-ESTER AROMATIC DIAMINES AS RAW MATERIAL SEIKA CORPORATION (JP) 2024-07-18 US disclosed
WO-2022239534-A1 META-ESTER AROMATIC DIAMINES, METHOD FOR PRODUCING SAME, AND POLYIMIDE HAVING SAID META-ESTER AROMATIC DIAMINES AS RAW MATERIAL セイカ株式会社 2022-11-17 WO disclosed
EP-3548534-A1 METHOD FOR PRODUCING TDI-BASED FLEXIBLE POLYURETHANE FOAMS CONTAINING ORGANIC ACID ANHYDRIDES AND/OR ORGANIC ACID CHLORIDES Covestro Deutschland AG (DE) 2019-10-09 EP disclosed
CN-101351443-B Process for preparing sulfonamides BASF SE 2012-11-28 CN disclosed
US-8263806-B2 Method for producing sulfonamides BASF SE (DE) 2012-09-11 US disclosed
US-20100228054-A1 Method for Producing Sulfonamides BASF SE (DE) 2010-09-09 US disclosed
CN-101351443-A Process for preparing sulfonamides BASF AG (DE) 2009-01-21 CN disclosed
EP-1957443-A2 METHOD FOR PRODUCING SULFONAMIDES BASF SE (DE) 2008-08-20 EP disclosed
WO-2007063028-A3 METHOD FOR PRODUCING SULFONAMIDES BASF AG (DE) 2007-08-23 WO disclosed
WO-2007063028-A2 METHOD FOR PRODUCING SULFONAMIDES BASF SE (DE) 2007-06-07 WO disclosed
JP-2001055362-A AROMATIC DIAMINO COMPOUND MITSUI CHEMICALS INC 2001-02-27 JP disclosed
US-4388246-A THERMAL SPLITTING OF CARBAMATES BAYER AKTIENGESELLSCHAFT (DE) 1983-06-14 US disclosed
US-4339455-A 1-(3-Pyridyl)-2,2,2-trihaloethyl compounds and fungicidal compositions containing the same CONSORTIUM FUR ELEKTROCHEMISCHE INDUSTRIE GMBH (DE) 1982-07-13 US disclosed
US-4189486-A FUNGICIDES CONSORTIUM FUR ELEKTROCHEMISCHE INDUSTRIE GMBH (DE) 1980-02-19 US disclosed
US-4179436-A DYEING POLYESTERS BAYER AKTIENGESELLSCHAFT (DE) 1979-12-18 US disclosed
US-3971741-A DISPERSION PIGMENTS BAYER AKTIENGESELLSCHAFT (DT) 1976-07-27 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 (3 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-20100228054-A1 Method for Producing Sulfonamides STS, MSRB3, SQOR HSP90AA1 2892/4885GAA 3021/4885TP53 4495/4885
US-20240239741-A1 META-ESTER AROMATIC DIAMINES, METHOD FOR PRODUCING SAME, AND POLYIMIDE HAVING SAID META-ESTER AROMATIC DIAMINES AS RAW MATERIAL PRMT9, DDC, AOC1 HSP90AA1 4655/4885GAA 2963/4885TP53 4294/4885
US-20240383844-A1 META-ESTER AROMATIC DIAMINES, METHOD FOR PRODUCING SAME, AND POLYIMIDE HAVING SAID META-ESTER AROMATIC DIAMINES AS RAW MATERIAL PRMT9, DDC, AOC1 HSP90AA1 4655/4885GAA 2963/4885TP53 4294/4885

“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.