Hydrochloric Acid

Hydrochloric Acid

SCHEMBL377436

CCCCCCCCCCCCC(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 SCHEMBL5092147 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 410 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250381550-A1 CARBON DISULFIDE TREATED MATERIALS AND METHODS OF PURIFYING FLUIDS USING THE SAME ZENITH PURIFICATION LLC (US) 2025-12-18 US claimed
US-20250313540-A1 PROCESS FOR THE PREPARATION OF [1,4,5]-OXADIAZEPINE DERIVATIVES SYNGENTA CROP PROTECTION AG (CN) 2025-10-09 US claimed
CN-119156378-A Process for the preparation of [1,4,5] -oxadiazepine derivatives 先正达农作物保护股份公司 2024-12-17 CN claimed
US-20240010778-A1 CHARGED SURFACTANT PARTICLES AND BRUSH POLYMERIC PARTICLES, METHODS OF MAKING SAME, AND USES THEREOF CORNELL UNIVERSITY 2024-01-11 US claimed
WO-2023208706-A1 PROCESS FOR THE PREPARATION OF [1,4,5]-OXADIAZEPINE DERIVATIVES SYNGENTA CROP PROTECTION AG (CH) 2023-11-02 WO claimed
CN-113274980-B Vanadium oxide-organic molecular cage-based porous liquid and preparation method and application thereof 南京工业大学 2022-12-06 CN claimed
CN-114206115-A Compositions for treating and preventing bacterial growth on substrates 马来西亚国家石油公司 2022-03-18 CN claimed
WO-2022056175-A1 CHARGED SURFACTANT PARTICLES AND BRUSH POLYMERIC PARTICLES, METHODS OF MAKING SAME, AND USES THEREOF CORNELL UNIVERSITY (US) 2022-03-17 WO claimed
CN-114058020-A Preparation method and application of quaternary phosphonium salt 江苏康爱特环境工程集团有限公司 2022-02-18 CN claimed
CN-113274980-A Vanadium oxide-organic molecular cage-based porous liquid and preparation method and application thereof 南京工业大学 2021-08-20 CN claimed
US-7192776-B2 Synthetic urine and method of manufacturing same SPECTRUM LABORATORIES, LLC 2007-03-20 US claimed
US-20040005286-A1 Organic salt conditioner, organic salt-containing composition, and uses thereof L'OREAL (FR) 2004-01-08 US claimed
EP-0789595-A4 SYNERGISTIC BIOCIDAL COMBINATIONS BETZDEARBORN INC (US) 2000-11-02 EP claimed
EP-0789595-A1 SYNERGISTIC BIOCIDAL COMBINATIONS BetzDearborn Inc (US) 1997-08-20 EP claimed
WO-1996014092-A1 SYNERGISTIC BIOCIDAL COMBINATIONS BETZDEARBORN INC. (US) 1996-05-17 WO claimed
US-5468739-A Phosphonium BETZ LABORATORIES, INC. (US) 1995-11-21 US claimed
US-5372947-A Determining amount of aldehyde released by conversion with respect to a sample from which existing aldehydes have been separated CTS BIOCIDES LTD. (GB) 1994-12-13 US claimed
EP-0610302-A1 METHOD OF ANALYSIS CTS BIOCIDES LTD. (GB) 1994-08-17 EP claimed
WO-1993009430-A1 METHOD OF ANALYSIS CTS BIOCIDES LTD. (GB) 1993-05-13 WO claimed
US-5102874-A Synergistic ECOLAB INC. (US) 1992-04-07 US 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 (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-20040005286-A1 Organic salt conditioner, organic salt-containing composition, and uses thereof KRT18, HCN4, PRKDC CA2 290/4885OPRM1 2640/4885FDPS 4495/4885
US-20250313540-A1 PROCESS FOR THE PREPARATION OF [1,4,5]-OXADIAZEPINE DERIVATIVES ADH1C, ADH1A, ADH5 CA2 2478/4885OPRM1 67/4885FDPS 3814/4885

“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.