Hydrochloric Acid

Hydrochloric Acid

SCHEMBL447754

Cl.c1ccc(P(c2ccccc2)c2ccccc2)cc1.c1ccc(P(c2ccccc2)c2ccccc2)cc1

nearest known ligand 0.92

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
ESR1 known ✓ P03372 4/20 0.63
ESR2 known ✓ Q92731 4/20 0.63
GAA known ✓ P10253 1/20 0.48
DRD1 known ✓ P21728 2/20 0.35
CA2 known ✓ P00918 2/20 0.33
GLA known ✓ P06280 1/20 0.33
ACHE known ✓ P22303 1/20 0.33
TDP1 Q9NUW8 3/20 0.92
CYP3A4 P08684 1/20 0.92
KDM4E B2RXH2 1/20 0.48
ALDH1A1 P00352 4/20 0.38
NPSR1 Q6W5P4 1/20 0.37
TSHR P16473 4/20 0.33
CA1 P00915 2/20 0.33
CA9 Q16790 2/20 0.33
LMNA P02545 2/20 0.33
CA12 O43570 1/20 0.33
CA3 P07451 1/20 0.33
CA4 P22748 1/20 0.33
CA14 Q9ULX7 1/20 0.33

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 SCHEMBL28613396 1.00 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
Hydrochloric Acid SCHEMBL8372285 1.00 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
Hydrochloric Acid SCHEMBL28386435 1.00 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
Benzene SCHEMBL11521546 1.00 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
Hydrochloric Acid SCHEMBL7930992 1.00 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
Hydrochloric Acid SCHEMBL1584554 1.00 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
Hydrochloric Acid SCHEMBL288031 1.00 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
Hydrochloric Acid SCHEMBL288029 1.00 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
Hydrochloric Acid SCHEMBL9414432 1.00 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
Hydrochloric Acid SCHEMBL7786619 1.00 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119569553-A Preparation method and application of 3-methoxy-4-chlorobenzaldehyde 苏州亚科科技股份有限公司 2025-03-07 CN claimed
CN-118002199-A Composite catalyst and preparation method and application thereof 五邑大学 2024-05-10 CN claimed
CN-117996085-A Positive electrode material, preparation method and application thereof 荣耀终端有限公司 2024-05-07 CN claimed
CN-117466940-A Cyperus rotundus L ligand and application thereof in preparation of chiral beta-butyrolactone 万华化学集团股份有限公司 2024-01-30 CN claimed
CN-117199398-A Molybdenum-doped nickel-cobalt-copper lattice stretching alloy catalyst and preparation method thereof 广西大学 2023-12-08 CN claimed
CN-114605309-B Synthesis method of azabicyclo derivative 浙江新和成股份有限公司 2023-07-21 CN claimed
CN-112624211-B Graphene-loaded multi-metal oxide-coated cathode material, and preparation method and application thereof 天目湖先进储能技术研究院有限公司 2022-12-23 CN claimed
CN-114933556-B Preparation method of thioether compound 苏州照固新材料科技有限公司 2022-12-02 CN claimed
CN-115232126-A Beta-carbopol-1, 2, 3-triazole compound, preparation method thereof and application thereof in resisting Alzheimer disease 中国人民解放军北部战区总医院 2022-10-25 CN claimed
CN-114939438-B Method for selective hydrogenation of olefinic unsaturated carbonyl compound and catalyst thereof 山东新和成药业有限公司 2022-09-23 CN claimed
CN-113388117-A Cerium-containing multi-element metal organic compound modified dimethyl silicone oil and preparation method and application thereof 杭州师范大学 2021-09-14 CN claimed
CN-113388118-A Hafnium-containing multi-metal organic compound modified dimethyl silicone oil and preparation method and application thereof 杭州师范大学 2021-09-14 CN claimed
CN-113105504-A Remdesivir derivative, analogue thereof, preparation method and application thereof 澳门科技大学 2021-07-13 CN claimed
CN-109735107-B Method for improving thermal oxidation stability of low-viscosity dimethyl silicone oil in air by adopting organic metal compound of nickel and zirconium 宜昌科林硅材料有限公司 2021-05-18 CN claimed
CN-112624211-A Graphene-loaded multi-metal oxide-coated cathode material, and preparation method and application thereof 天目湖先进储能技术研究院有限公司 2021-04-09 CN claimed
CN-112121859-A Catalyst and preparation method thereof, and preparation method of 1,1,4, 4-tetramethoxy-2-butene 万华化学集团股份有限公司 2020-12-25 CN claimed
CN-111825552-A Preparation method of phenyl acrylate compound under palladium catalysis 哈尔滨工业大学(威海) 2020-10-27 CN claimed
EP-1226146-A2 QUINOLINE AND NAPHTHYRIDINE CARBOXYLIC ACID ANTIBACTERIALS ABBOTT LABORATORIES (US) 2002-07-31 EP claimed
US-20020049223-A1 Quinoline and naphthyridine carboxylic acid antibacterials ABBOTT LABORATORIES 2002-04-25 US claimed
WO-2001032655-A2 QUINOLINE AND NAPHTHYRIDINE CARBOXYLIC ACID ANTIBACTERIALS ABBOTT LABORATORIES (US) 2001-05-10 WO 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-20020049223-A1 Quinoline and naphthyridine carboxylic acid antibacterials NQO2, NQO1, NDUFA7 ESR1 1857/4885ESR2 3425/4885GAA 171/4885

“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.