Hydrochloric Acid

Hydrochloric Acid

SCHEMBL726

Cl.NCc1ccc([N+](=O)[O-])cc1

nearest known ligand 0.95

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
CA2 known ✓ P00918 3/20 0.49
KCNH2 known ✓ Q12809 1/20 0.48
ACHE known ✓ P22303 1/20 0.48
LOXL2 Q9Y4K0 1/20 0.95
IDO1 P14902 4/20 0.62
TSHR P16473 1/20 0.55
ALDH1A1 P00352 2/20 0.54
CYP2C19 P33261 3/20 0.52
POLB P06746 2/20 0.52
CA9 Q16790 3/20 0.49
CA1 P00915 3/20 0.49
CA12 O43570 2/20 0.49
CA14 Q9ULX7 2/20 0.49
MEN1 O00255 1/20 0.49
KMT2A Q03164 1/20 0.49
ATM Q13315 1/20 0.49
CYP1A2 P05177 2/20 0.48
CYP2C9 P11712 1/20 0.48
KCNJ1 P48048 1/20 0.48
MAPT P10636 1/20 0.48

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 SCHEMBL28059156 0.98 LOXL2 (0.91) LOXL2IDO1TSHRALDH1A1CYP2C19
Methane SCHEMBL29190749 0.98 LOXL2 (0.91) LOXL2IDO1TSHRALDH1A1CYP2C19
SCHEMBL354332 0.98 LOXL2 (1.00) LOXL2IDO1TSHRALDH1A1CYP2C19
Methane SCHEMBL11552193 0.95 LOXL2 (0.95) LOXL2IDO1TSHRALDH1A1CYP2C19
Bromide SCHEMBL31513716 0.95 LOXL2 (0.95) LOXL2IDO1TSHRALDH1A1CYP2C19
SCHEMBL4687550 0.91 LOXL2 (0.88) LOXL2IDO1TSHRALDH1A1CYP2C19
SCHEMBL11816242 0.88 LOXL2 (0.81) LOXL2IDO1TSHRALDH1A1CYP2C19
Phosphonic Acid SCHEMBL27895241 0.88 LOXL2 (0.81) LOXL2IDO1TSHRALDH1A1CYP2C19
Benzylamine SCHEMBL27935312 0.87 LOXL2 (0.80) LOXL2IDO1ALDH1A1CYP2C19MEN1
SCHEMBL12635614 0.86 LOXL2 (0.78) LOXL2IDO1TSHRALDH1A1CA9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20200131431-A1 CHEMICAL ADDITIVES AND SURFACTANT COMBINATIONS FOR FAVORABLE WETTABILITY ALTERATION AND IMPROVED HYDROCARBON RECOVERY FACTORS ALCHEMY SCIENCES INC (US) 2020-04-30 US claimed
CN-1186332-C Novel thyroid receptor ligands and method II KAROBIO AB (SE) 2005-01-26 CN claimed
CN-1337953-A Novel thyroid receptor ligands and method II KAROBIO AB (SE) 2002-02-27 CN claimed
US-4301196-A USING ACCELERATING OR DEPOLARIZING AGENTS WHICH ARE ORGANONITROGEN COMBOUNDS KOLLMORGEN TECHNOLOGIES CORP. (US) 1981-11-17 US claimed
EP-4073062-B1 FUNCTIONALIZED HETEROCYCLIC COMPOUNDS AS MODULATORS OF STIMULATOR OF INTERFERON GENES (STING) RYVU THERAPEUTICS S A (PL) 2026-04-29 EP disclosed
US-20250214963-A1 SULFONYL AMIDE DERIVATIVES FOR THE TREATMENT OF ABNORMAL CELL GROWTH PFIZER INC. 2025-07-03 US disclosed
WO-2024246857-A1 UREA COMPOUNDS, COMPOSITIONS, AND METHODS FOR TREATING ASTHMA AND PARKINSON'S DISEASE INNOPHARMASCREEN INC. (KR) 2024-12-05 WO disclosed
US-20240109862-A1 SULFONYL AMIDE DERIVATIVES FOR THE TREATMENT OF ABNORMAL CELL GROWTH PFIZER INC. 2024-04-04 US disclosed
EP-3280707-B1 BICYCLIC QUINAZOLINONE DERIVATIVES HOFFMANN LA ROCHE (CH) 2023-12-20 EP disclosed
US-11802108-B2 Compounds for the modulation of cyclophilins function THE UNIVERSITY COURT OF THE UNIVERSITY OF EDINBURGH (GB) 2023-10-31 US disclosed
CN-114315862-B Method for preparing penicillin sulfoxide ester by continuous flow 沈阳化工研究院有限公司 2023-08-08 CN disclosed
CN-114437110-B Application of supported catalyst in continuous preparation of penicillin sulfoxide ester 沈阳化工研究院有限公司 2023-07-11 CN disclosed
US-4820843-A Tetrazole intermediates to antihypertensive compounds E. I. DU PONT DE NEMOURS AND COMPANY (US) 1989-04-11 US disclosed
EP-0291969-A2 Tetrazole intermediates to antihypertensive compounds E.I. DU PONT DE NEMOURS AND COMPANY (US) 1988-11-23 EP disclosed
US-4741900-A Antibody-metal ion complexes CYTOGEN CORPORATION (US) 1988-05-03 US disclosed
EP-0253310-A2 Angiotensin II receptor blocking imidazoles E.I. DU PONT DE NEMOURS AND COMPANY (US) 1988-01-20 EP disclosed
US-4622217-A I-4-amino-3-iodobenzylguanidine as imaging and therapeutic agent THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 1986-11-11 US disclosed
US-4548904-A FORMING REACTION PRODUCT OF PROTEIN AND REAGENT, DEGRADATION TO REMOVE TERMINAL AMINO ACID, THEN CHROMATOGRAPHY ANALYSIS MOLECULAR GENETICS RESEARCH & DEVELOPMENT (US) 1985-10-22 US disclosed
EP-0113538-A2 Protein sequencing method and reagent MOLECULAR GENETICS RESEARCH & DEVELOPMENT LIMITED PARTNERSHIP (US) 1984-07-18 EP disclosed
US-4301196-A USING ACCELERATING OR DEPOLARIZING AGENTS WHICH ARE ORGANONITROGEN COMBOUNDS KOLLMORGEN TECHNOLOGIES CORP. (US) 1981-11-17 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-20250214963-A1 SULFONYL AMIDE DERIVATIVES FOR THE TREATMENT OF ABNORMAL CELL GROWTH GPR119, INSR, LYAR CA2 2580/4885KCNH2 845/4885ACHE 4528/4885
US-11802108-B2 Compounds for the modulation of cyclophilins function CBR1, CBR3, PPIC CA2 239/4885KCNH2 2338/4885ACHE 4422/4885
US-20240109862-A1 SULFONYL AMIDE DERIVATIVES FOR THE TREATMENT OF ABNORMAL CELL GROWTH GPR119, INSR, LYAR CA2 2580/4885KCNH2 845/4885ACHE 4528/4885

“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.