Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2861056

Cc1ccc(N)c(C)c1.Cl

nearest known ligand 0.62

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 0.42
TDP1 Q9NUW8 7/20 0.62
CYP3A4 P08684 7/20 0.62
ALOX15 P16050 3/20 0.62
TP53 P04637 2/20 0.62
THRB P10828 2/20 0.62
SMN1; SMN2 Q16637 1/20 0.62
ALDH1A1 P00352 7/20 0.59
TSHR P16473 3/20 0.59
HSD17B10 Q99714 1/20 0.48
CA1 P00915 1/20 0.46
MAPK1 P28482 2/20 0.46
NPC1 O15118 2/20 0.45
RAB9A P51151 2/20 0.45
S100B P04271 1/20 0.45
MAPT P10636 2/20 0.43
PKM P14618 1/20 0.43
ATM Q13315 1/20 0.43
L3MBTL1 Q9Y468 1/20 0.43
SKP2 Q13309 1/20 0.43

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 SCHEMBL6141790 1.00 TDP1 (0.62) TDP1CYP3A4ALOX15TP53THRB
Hydrochloric Acid SCHEMBL27406515 1.00 TDP1 (0.62) TDP1CYP3A4ALOX15TP53THRB
SCHEMBL33980 0.97
SCHEMBL29366708 0.97
Ammonia Solution, Strong SCHEMBL1548755 0.94 TDP1 (0.62) TDP1CYP3A4ALOX15TP53THRB
SCHEMBL11239230 0.94 TDP1 (0.62) TDP1CYP3A4ALOX15TP53THRB
Fluoride SCHEMBL18789317 0.94 TDP1 (0.62) TDP1CYP3A4ALOX15TP53THRB
Methyl Alcohol SCHEMBL11681113 0.92 TDP1 (0.59) TDP1CYP3A4ALOX15TP53THRB
2,5-Xylidine SCHEMBL9494012 0.87 TDP1 (0.81) TDP1CYP3A4ALOX15TP53THRB
SCHEMBL6834418 0.87 TDP1 (0.54) TDP1CYP3A4ALOX15TP53THRB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4626874-A1 PROCESSES AND INTERMEDIATES FOR THE PREPARATION OF SPIROCYCLIC KRAS INHIBITORS Boehringer Ingelheim International GmbH (DE) 2025-10-08 EP claimed
WO-2025074394-A1 A PROCESS FOR THE PREPARATION OF BELZUTIFAN AND ITS NOVEL INTERMEDIATES THEREOF NATCO PHARMA LIMITED (IN) 2025-04-10 WO claimed
CN-117361825-B Heavy metal treatment method for livestock and poultry manure 江西正合生态农业有限公司 2024-10-01 CN claimed
US-20240199569-A1 PROCESS FOR THE MANUFACTURE OF INHIBITORS OF KRAS BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2024-06-20 US claimed
WO-2024115529-A1 PROCESSES AND INTERMEDIATES FOR THE PREPARATION OF SPIROCYCLIC KRAS INHIBITORS BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2024-06-06 WO claimed
CN-117361825-A Heavy metal treatment method for livestock and poultry manure 江西正合生态农业有限公司 2024-01-09 CN claimed
CN-107778200-B Process for the preparation of amitraz 东莞市东阳光动物保健药品有限公司 2020-11-24 CN claimed
CN-1800185-A Substituted sulfonamide compounds, process for their use as medicament for the treatment of CNS disorders, obesity and type II diabetes. BIOVITRUM AB (SE) 2006-07-12 CN claimed
CN-1522245-A Substituted sulfonamide compounds, process for their preparation and their use as medicaments for the treatment of CNS disorders, obesity and type II diabetes �Ȱ�ά����ķ�ɷݹ�˾ 2004-08-18 CN claimed
EP-4720678-A1 SURVIVIN AS A BIOMARKER FOR PREDICTING THE RESPONSIVENESS OF CANCER TREATMENT Boehringer Ingelheim International GmbH (DE) 2026-04-08 EP disclosed
EP-4719603-A1 SPIROCYCLIC ANNULATED 2-AMINO-3-CYANO THIOPHENES AND DERIVATIVES FOR THE TREATMENT OF CANCER Boehringer Ingelheim International GmbH (DE) 2026-04-08 EP disclosed
EP-4626874-A1 PROCESSES AND INTERMEDIATES FOR THE PREPARATION OF SPIROCYCLIC KRAS INHIBITORS Boehringer Ingelheim International GmbH (DE) 2025-10-08 EP disclosed
WO-2025201480-A1 SPIRO COMPOUND AS KRAS MUTANT INHIBITOR 苏州浦合医药科技有限公司 2025-10-02 WO disclosed
US-20250153157-A1 PALLADIUM PRECATALYST EMBODIMENTS FOR ENANTIOSELECTIVE CHEMICAL REACTIONS AND METHODS OF MAKING AND USING THE SAME UVIC IND PARTNERSHIPS INC (CA) 2025-05-15 US disclosed
CN-1522245-A Substituted sulfonamide compounds, process for their preparation and their use as medicaments for the treatment of CNS disorders, obesity and type II diabetes �Ȱ�ά����ķ�ɷݹ�˾ 2004-08-18 CN disclosed
EP-1384998-A1 EYESTRAIN MODEL, METHOD OF CONSTRUCTING THE SAME, EVALUATION METHOD WITH THE USE OF THE MODEL AND DRUGS SCREENED BY USING THE EVALUATION METHOD Biochemical and Pharmacological Laboratories Inc. (JP) 2004-01-28 EP disclosed
EP-0849292-B1 Olefin polymerisation catalysts and processes for producing olefin polymers TOSOH CORP (JP) 2002-08-21 EP disclosed
US-6110858-A AN OLEFIN POLYMERIZATION CATALYST CONSISTS OF A TRANSITION METAL COMPOUND, A MODIFIED CLAY COMPOUND CONTAINING CLAY MINERAL AND AN AMINE COMPOUND AND AN ORGANOALUMINUM COMPOUND TOSOH CORPORATION (JP) 2000-08-29 US disclosed
EP-0849292-A1 Olefin polymerisation catalysts and processes for producing olefin polymers TOSOH CORPORATION (JP) 1998-06-24 EP disclosed
US-4963691-A Spirodilactam derivatives SHELL OIL COMPANY (US) 1990-10-16 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 (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-20240199569-A1 PROCESS FOR THE MANUFACTURE OF INHIBITORS OF KRAS KRAS, NRAS, HRAS GAA 820/4885TDP1 2755/4885CYP3A4 2474/4885
US-20250153157-A1 PALLADIUM PRECATALYST EMBODIMENTS FOR ENANTIOSELECTIVE CHEMICAL REACTIONS AND METHODS OF MAKING AND USING THE SAME PPOX, PDCD1, DDT GAA 2177/4885TDP1 1189/4885CYP3A4 803/4885

“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.