Hydrochloric Acid

Hydrochloric Acid

SCHEMBL5092147

CCCCCCC(CCCC)C(P)(CCCC)CCCC.Cl

nearest known ligand 0.44

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 10)

geneUniProtsupporting neighboursconfidence
CA2 known ✓ P00918 1/20 0.34
OPRM1 known ✓ P35372 1/20 0.33
FDPS P14324 4/20 0.44
DNM1 Q05193 2/20 0.39
LMNA P02545 1/20 0.35
TSHR P16473 1/20 0.33
THRB P10828 1/20 0.33
GPR84 Q9NQS5 3/20 0.32
SPHK1 Q9NYA1 1/20 0.32
FFAR1 O14842 1/20 0.32

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 SCHEMBL5084790 1.00 FDPS (0.44) FDPSDNM1LMNACA2OPRM1
Hydrochloric Acid SCHEMBL377436 1.00 FDPS (0.44) FDPSDNM1LMNACA2OPRM1
Hydrochloric Acid SCHEMBL2886479 1.00 FDPS (0.44) FDPSDNM1LMNACA2OPRM1
Hydrochloric Acid SCHEMBL5085106 1.00 FDPS (0.44) FDPSDNM1LMNACA2OPRM1
Hydrochloric Acid SCHEMBL524626 1.00 FDPS (0.44) FDPSDNM1LMNACA2OPRM1
Hydrochloric Acid SCHEMBL5138884 1.00 FDPS (0.44) FDPSDNM1LMNACA2OPRM1
Hydrochloric Acid SCHEMBL5087140 1.00 FDPS (0.44) FDPSDNM1LMNACA2OPRM1
SCHEMBL1064108 0.98 FDPS (0.46) FDPSDNM1LMNACA2OPRM1
SCHEMBL1063958 0.98 FDPS (0.46) FDPSDNM1LMNACA2OPRM1
SCHEMBL1063393 0.98 FDPS (0.46) FDPSDNM1LMNACA2OPRM1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115449136-B Accelerator composition of rubber nanocomposite as well as preparation method and application thereof 浙江大学 2024-02-27 CN claimed
CN-115449136-A Accelerator composition of rubber nanocomposite and preparation method and application thereof 浙江大学 2022-12-09 CN claimed
CN-111389046-B Extraction agent and method for extracting astaxanthin by using same 广东海洋大学 2021-08-24 CN claimed
CN-111389046-A Extraction agent and method for extracting astaxanthin by using same 广东海洋大学 2020-07-10 CN claimed
EP-3371254-A1 METHOD FOR PREPARATION OF POLYMERIC MATERIALS Ustav Makromolekularni Chemie AV CR, v.v.i. (CZ) 2018-09-12 EP claimed
WO-2017076379-A1 METHOD FOR PREPARATION OF POLYMERIC MATERIALS USTAV MAKROMOLEKULARNI CHEMIE AV CR, V.V.I. (CZ) 2017-05-11 WO claimed
EP-4705389-A1 PROCESS FOR PRODUCING CYCLOSILOXANES FROM SILICONE WASTE Evonik Operations GmbH (DE) 2026-03-11 EP disclosed
WO-2024227761-A1 PROCESS FOR PRODUCING CYCLOSILOXANES FROM SILICONE WASTE EVONIK OPERATIONS GMBH (DE) 2024-11-07 WO disclosed
CN-118434793-A Main chain polymer, optical film, method for producing same, and multilayer film 东曹株式会社 2024-08-02 CN disclosed
CN-115449136-B Accelerator composition of rubber nanocomposite as well as preparation method and application thereof 浙江大学 2024-02-27 CN disclosed
US-20230011640-A1 METHODS FOR RECOVERING ORGANIC SALTS FROM INDUSTRIAL PROCESS STREAMS CYTEC INDUSTRIES INC. (US) 2023-01-12 US disclosed
EP-4073000-A1 METHODS FOR RECOVERING ORGANIC SALTS FROM INDUSTRIAL PROCESS STREAMS Cytec Industries, Inc. (US) 2022-10-19 EP disclosed
EP-4065738-A1 A METHOD AND AN APPARATUS OF PURIFYING A BAYER PROCESS STREAM Rio Tinto Alcan International Limited (CA) 2022-10-05 EP disclosed
US-20140001091-A1 HYDROCARBON CONVERSION PROCESS UOP LLC (US) 2014-01-02 US disclosed
US-20140001093-A1 HYDROCARBON CONVERSION PROCESS UOP LLC (US) 2014-01-02 US disclosed
US-20130199599-A1 POLYESTER FILM, BACK SHEET FOR SOLAR CELL, AND SOLAR CELL MODULE FUJIFILM CORPORATION (JP) 2013-08-08 US disclosed
US-20080214386-A1 Stability; easily separated from solution; surface treatment of catalyst with Group seven compound; reacting epoxide with carbon dioxide NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY (JP) 2008-09-04 US disclosed
US-6806387-B2 A STARTING MATERIAL FOR VITAMIN A DERIVATIVES AND VARIOUS TERPENE COMPOUNDS SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2004-10-19 US disclosed
EP-1426357-A1 PROCESS FOR PREPARATION OF ALLYL SULFONE DERIVATIVES AND INTERMEDIATES FOR THE PREPARATION Sumitomo Chemical Company, Limited (JP) 2004-06-09 EP disclosed
US-20040054233-A1 Process for preparation of allyl sulfone derivatives and intermediates for the preparation SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2004-03-18 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-20040054233-A1 Process for preparation of allyl sulfone derivatives and intermediates for the preparation ARSA, SULT1A1, SULT2A1 CA2 1143/4885OPRM1 2235/4885FDPS 3051/4885

“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.