Hydrochloric Acid

Hydrochloric Acid

SCHEMBL113583

Cl.Cl.Cl.O.O.O.O.O.O.O.[Ce]

nearest known ligand 0.33

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 3)

geneUniProtsupporting neighboursconfidence
CA4 P22748 1/20 0.33
CA5A P35218 1/20 0.33
CA5B Q9Y2D0 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 SCHEMBL29152314 1.00
Hydrochloric Acid SCHEMBL930844 1.00
Hydrochloric Acid SCHEMBL8720387 1.00
Hydrochloric Acid SCHEMBL9155128 1.00 CA4 (0.33) CA4CA5ACA5B
Hydrochloric Acid SCHEMBL25334179 1.00 CA4 (0.33) CA4CA5ACA5B
Hydrochloric Acid SCHEMBL10511168 1.00
Hydrochloric Acid SCHEMBL23295133 1.00
Hydrochloric Acid SCHEMBL5439759 1.00 CA4 (0.33) CA4CA5ACA5B
Hydrochloric Acid SCHEMBL225121 1.00
Hydrochloric Acid SCHEMBL29171175 1.00

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120121884-A Small molecule detection method and device based on photoelectric response gel substrate 南京师范大学 2025-06-10 CN claimed
CN-120126865-A Preparation method of aluminum-based enameled wire for automobile 铜陵兢强电子科技股份有限公司 2025-06-10 CN claimed
CN-120054547-A Ce-FeIn2S4-MoSe2Heterojunction photocatalyst and preparation method thereof 江苏理工学院 2025-05-30 CN claimed
CN-120039882-A Preparation method and application of lithium battery electrode material 江苏创能新能源科技有限公司 2025-05-27 CN claimed
CN-119978211-A CaF2:Ce3+,Tb3+Poly (acrylic acid-acrylamide) composite hydrogel and preparation method and application thereof 西安文理学院 2025-05-13 CN claimed
CN-119954593-A Method for producing chloroethylene by continuous photocatalytic hydrochlorination of acetylene at normal temperature 湖南大学 2025-05-09 CN claimed
CN-119797517-A Application of copper-loaded Ce-MOF derived cerium oxide carbon nano rod composite material in electrocatalytic reduction of Cr (VI) 南京大学 2025-04-11 CN claimed
CN-119330926-A Soyabean base ester compound and preparation and application thereof 华南理工大学 2025-01-21 CN claimed
CN-119194496-A Rare earth element doped Ru-based catalyst and preparation method and application thereof 中国科学院青岛生物能源与过程研究所 2024-12-27 CN claimed
CN-118871420-A Process for the preparation of codeine, its derivatives and intermediates 暨南大学 2024-10-29 CN claimed
CN-112280579-A Process method for preparing bio-oil by pyrolyzing straw-office waste paper 戴丹妮 2021-01-29 CN claimed
CN-112126286-A TiO-Ce @ PVDC composite emulsion based on cerium-titanium-oxygen cluster and preparation and application thereof 浙江工业大学 2020-12-25 CN claimed
CN-111766289-A Oxygen-enriched vacancy CeO2Preparation method and application of electrochemiluminescence immunosensor 济南大学 2020-10-13 CN claimed
CN-111363556-A Iron and cerium modified cellulose soil stabilizer and preparation method and application thereof 圣清环保股份有限公司 2020-07-03 CN claimed
CN-110841624-A Cerium-tin catalyst for low-temperature catalytic elimination of vinyl chloride and preparation method and application thereof 上海纳米技术及应用国家工程研究中心有限公司 2020-02-28 CN claimed
EP-2892909-B1 PROCESS FOR THE PREPARATION OF 11-METHYLENE-18-METHYLESTR-4-EN-3,17-DIONE, USEFUL AS AN INTERMEDIATE IN THE SYNTHESIS OF COMPOUNDS WITH PHARMACOLOGICAL ACTIVITY. IND CHIMICA SRL (IT) 2016-08-24 EP claimed
US-9422326-B2 Process for preparing 11-methylene-18-methyl-estr-4-en-3, 17-dione, useful as intermediate compound for the synthesis of molecules having pharmacological activity INDUSTRIALE CHIMICA S.R.L. (IT) 2016-08-23 US claimed
US-20150239925-A1 Process for Preparing 11-Methylene-18-Methyl-Estr-4-En-3, 17-Dione, Useful as Intermediate Compound for the Synthesis of Molecules Having Pharmacological Activity INDUSTRIALE CHIMICA S.R.L. (IT) 2015-08-27 US claimed
EP-2892909-A1 PROCESS FOR PREPARING 11 -METHYLENE-18-METHYL-ESTR-4-EN-3, 17- DIONE, USEFUL AS INTERMEDIATE COMPOUND FOR THE SYNTHESIS OF MOLECULES HAVING A PHARMACOLOGICAL ACTIVITY Industriale Chimica S.R.L. (IT) 2015-07-15 EP claimed
WO-2014037873-A1 PROCESS FOR PREPARING 11 -METHYLENE-18-METHYL-ESTR-4-EN-3, 17- DIONE, USEFUL AS INTERMEDIATE COMPOUND FOR THE SYNTHESIS OF MOLECULES HAVING A PHARMACOLOGICAL ACTIVITY INDUSTRIALE CHIMICA S.R.L. (IT) 2014-03-13 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-20150239925-A1 Process for Preparing 11-Methylene-18-Methyl-Estr-4-En-3, 17-Dione, Useful as Intermediate Compound for the Synthesis of Molecules Having Pharmacological Activity CYP19A1, HSD17B11, CYP17A1 CA4 4578/4885CA5A 3302/4885CA5B 3661/4885

“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.