Hydrochloric Acid

Hydrochloric Acid

SCHEMBL2760912

Cl.O=C(O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F

nearest known ligand 0.94

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 10/20 0.34
MMP1 known ✓ P03956 2/20 0.34
MMP8 known ✓ P22894 2/20 0.34
MMP13 known ✓ P45452 2/20 0.34
GAA known ✓ P10253 1/20 0.32
HDAC3 known ✓ O15379 1/20 0.31
HDAC4 known ✓ P56524 1/20 0.31
HDAC1 known ✓ Q13547 1/20 0.31
HDAC7 known ✓ Q8WUI4 1/20 0.31
HDAC2 known ✓ Q92769 1/20 0.31
HDAC10 known ✓ Q969S8 1/20 0.31
HDAC11 known ✓ Q96DB2 1/20 0.31
HDAC8 known ✓ Q9BY41 1/20 0.31
HDAC6 known ✓ Q9UBN7 1/20 0.31
HDAC9 known ✓ Q9UKV0 1/20 0.31
HDAC5 known ✓ Q9UQL6 1/20 0.31
THRB P10828 1/20 0.94
ACLY P53396 2/20 0.36
LMNA P02545 1/20 0.35
CA1 P00915 9/20 0.34

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 SCHEMBL23706471 1.00 THRB (0.94) THRBACLYLMNACA2CA1
Hydrochloric Acid SCHEMBL2760998 1.00 THRB (0.94) THRBACLYLMNACA2CA1
Hydrochloric Acid SCHEMBL2761043 1.00 THRB (0.94) THRBACLYLMNACA2CA1
Hydrochloric Acid SCHEMBL9659602 1.00 THRB (0.94) THRBACLYLMNACA2CA1
Hydrochloric Acid SCHEMBL31397825 0.97 THRB (0.90) THRBACLYLMNACA2CA1
SCHEMBL3628434 0.97 THRB (1.00) THRBACLYLMNACA2CA1
SCHEMBL24715 0.97 THRB (1.00) THRBACLYLMNACA2CA1
SCHEMBL20657170 0.97 THRB (1.00) THRBACLYLMNACA2CA1
SCHEMBL62447 0.97 THRB (1.00) THRBACLYLMNACA2CA1
SCHEMBL25223581 0.97 THRB (1.00) THRBACLYLMNACA2CA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110465271-B Synthetic method and application of temperature-controlled targeted capture material 四川轻化工大学 2022-06-03 CN claimed
CN-111961381-A anti-H2Long-acting paint film of S gas erosion 江苏华夏制漆科技有限公司 2020-11-20 CN claimed
CN-110656492-A High-performance oil-water separation material based on polyether-ether-ketone, preparation method and application thereof 吉林大学 2020-01-07 CN claimed
CN-113416336-B Fluorine-containing end group active hydroxyl friction-resistant high-shear-resistant composite rubber material 四川大学 2022-06-07 CN disclosed
CN-110465271-B Synthetic method and application of temperature-controlled targeted capture material 四川轻化工大学 2022-06-03 CN disclosed
CN-110656492-B High-performance oil-water separation material based on polyether-ether-ketone, preparation method and application thereof 吉林大学 2022-03-08 CN disclosed
CN-113773750-A Water-soluble flame-retardant super-amphiphobic coating, preparation method and coating 四川大学 2021-12-10 CN disclosed
CN-113416336-A Fluorine-containing end group active hydroxyl friction-resistant high-shear-resistant composite rubber material 四川大学 2021-09-21 CN disclosed
CN-112110839-B High-fluorine-containing interface compatibilizer and preparation method and application thereof 四川大学 2021-07-27 CN disclosed
CN-112110838-B Hydroxyl-containing high-fluorine-containing interface compatibilizer and preparation method and application thereof 四川大学 2021-07-27 CN disclosed
CN-112110838-A Hydroxyl-containing high-fluorine-containing interface compatibilizer and preparation method and application thereof 四川大学 2020-12-22 CN disclosed
US-20040072987-A1 3,4-Alkylenedioxythiophene compounds and polymers thereof AGFA-GEVAERT (BE) 2004-04-15 US disclosed
WO-2004031192-A1 3,4-ALKYLENEDIOXYTHIOPHENE COMPOUNDS AND POLYMERS THEREOF AGFA-GEVAERT (BE) 2004-04-15 WO disclosed
US-6711336-B2 MIXTURE OF FLUORINATED UNSATURATED COMPOUND AND ACRYLATED ESTER E.I. DU PONT DE NEMOURS AND COMPANY 2004-03-23 US disclosed
EP-1362071-A2 LOW OPTICAL LOSS POLYMERS E.I. DU PONT DE NEMOURS AND COMPANY (US) 2003-11-19 EP disclosed
US-20030108326-A1 Low optical loss polymers ENABLENCE TECHNOLOGIES USA INC. (CA) 2003-06-12 US disclosed
US-6496637-B2 Low optical loss polymers CORNING INCORPORATED 2002-12-17 US disclosed
US-20020122647-A1 Low optical loss polymers ENABLENCE TECHNOLOGIES USA INC. (CA) 2002-09-05 US disclosed
WO-2002051927-A2 LOW OPTICAL LOSS POLYMERS E.I. DU PONT DE NEMOURS AND COMPANY (US) 2002-07-04 WO disclosed
US-4839256-A Perfluoroalkyl group-containing 1,2-napthoquinone daizide compounds and reproduction materials produced therefrom HOECHST AKTIENGESELLSCHAFT (DE) 1989-06-13 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-20040072987-A1 3,4-Alkylenedioxythiophene compounds and polymers thereof CCNT1, TTI1, SULT1E1 CA2 4708/4885MMP1 957/4885MMP8 3709/4885

“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.