Hydrochloric Acid

Hydrochloric Acid

SCHEMBL996153

Cl.Cl.N=P(c1ccccc1)(c1ccccc1)c1ccccc1.N=P(c1ccccc1)(c1ccccc1)c1ccccc1

nearest known ligand 0.41

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 1/20 0.41
ESR1 known ✓ P03372 3/20 0.36
ESR2 known ✓ Q92731 2/20 0.36
GAA known ✓ P10253 2/20 0.35
PTGS1 known ✓ P23219 1/20 0.33
SLC6A2 known ✓ P23975 1/20 0.33
PTGS2 known ✓ P35354 1/20 0.33
HTR2B known ✓ P41595 1/20 0.33
CA4 P22748 1/20 0.41
CA5A P35218 1/20 0.41
CFTR P13569 1/20 0.36
ALDH1A1 P00352 5/20 0.35
L3MBTL1 Q9Y468 3/20 0.35
MAPT P10636 2/20 0.35
TDP1 Q9NUW8 2/20 0.35
ALOX12 P18054 2/20 0.35
NPSR1 Q6W5P4 2/20 0.35
ALPG P10696 1/20 0.35
NPY1R P25929 1/20 0.35
HTT P42858 1/20 0.35

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 SCHEMBL2582115 1.00 CA2 (0.41) CA2CA4CA5AESR1ESR2
SCHEMBL361668 0.97 CA2 (0.43) CA2CA4CA5AESR1ESR2
Bromide SCHEMBL2185231 0.93 CA2 (0.41) CA2CA4CA5AESR1ESR2
Fluoride SCHEMBL11191593 0.93 CA2 (0.41) CA2CA4CA5AESR1ESR2
Iodide SCHEMBL27336456 0.93 CA2 (0.41) CA2CA4CA5AESR1ESR2
SCHEMBL6316218 0.93 CA2 (0.41) CA2CA4CA5AESR1ESR2
Water SCHEMBL7532602 0.93 CA2 (0.41) CA2CA4CA5AESR1ESR2
SCHEMBL10710709 0.93 CA2 (0.41) CA2CA4CA5AESR1ESR2
Iodide SCHEMBL3694471 0.93 CA2 (0.41) CA2CA4CA5AESR1ESR2
Carbon Monoxide SCHEMBL10708053 0.89 CA2 (0.40) CA2CA4CA5AESR1ESR2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4743505-A2 NOVEL PHOTOSENSITIVE CARBON DIOXIDE BASED POLYCARBONATE DERIVATIVES AND METHOD FOR PREPARATION OF PHOTO-ANTIMICROBIAL POLYCARBONATE-BIOPLASTICIZER COMPOSITES AND THEIR USE Universidade de Coimbra (PT) 2026-05-20 EP claimed
EP-4731688-A1 METHOD FOR THE PRODUCTION OF A HYDROXYL-GROUP TERMINATED OXAZOLIDINONE COMPOSITION Covestro Deutschland AG (DE) 2026-04-29 EP claimed
EP-4731689-A1 METHOD FOR THE PRODUCTION OF THERMOPLASTIC POLYOXAZOLIDINONE Covestro Deutschland AG (DE) 2026-04-29 EP claimed
US-12496575-B2 Catalyst composition for cyclic carbonate production from CO2 and epoxides PTT GLOBAL CHEMICAL PUBLIC COMPANY LIMITED (TH) 2025-12-16 US claimed
US-20250362302-A1 INTRACELLULAR LIGATION OF PHOTOCATALYSTS FOR PHOTO-RESPONSIVE, PROBE-MEDIATED PROTEIN LABELING SEED THERAPEUTICS US INC (US) 2025-11-27 US claimed
EP-4448605-B1 PROCESS FOR THE PRODUCTION OF A THERMOPLASTIC POLYOXAZOLIDINONE COVESTRO DEUTSCHLAND AG (DE) 2025-11-19 EP claimed
EP-4200351-B1 METHOD FOR THE PRODUCTION OF A THERMOPLASTIC POLYOXAZOLIDINONE COVESTRO DEUTSCHLAND AG (DE) 2025-11-19 EP claimed
EP-4200352-B1 METHOD FOR THE PRODUCTION OF A THERMOPLASTIC POLYOXAZOLIDINONE COVESTRO DEUTSCHLAND AG (DE) 2025-11-19 EP claimed
EP-4200353-B1 METHOD FOR THE PRODUCTION OF A THERMOPLASTIC POLYOXAZOLIDINONE COVESTRO DEUTSCHLAND AG (DE) 2025-11-19 EP claimed
US-12466913-B2 Method for the production of a thermoplastic polyoxazolidinone COVESTRO DEUTSCHLAND AG (DE) 2025-11-11 US claimed
US-8252891-B2 Purification of polycarbonates NOVOMER, INC. (US) 2012-08-28 US claimed
US-20110201779-A1 PURIFICATION OF POLYCARBONATES NOVOMER, INC. (US) 2011-08-18 US claimed
EP-2342258-A1 PURIFICATION OF POLYCARBONATES Novomer, Inc. (US) 2011-07-13 EP claimed
WO-2010033703-A1 PURIFICATION OF POLYCARBONATES NOVOMER, INC. (US) 2010-03-25 WO claimed
EP-0507616-B1 Process for the preparation of trisubstituted ureas by reductive carbonylation ARCO CHEM TECH (US) 1996-02-07 EP claimed
EP-0273520-B1 A COMPOSITION COMPRISING A POLYEPOXIDE AND A EPOXY ADVANCEMENT CATALYST, AND A PROCESS FOR PREPARING ADVANCED EPOXY RESINS SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) 1993-09-22 EP claimed
US-5241118-A Reacting nitroarene with carbon monoxide ARCO CHEMICAL TECHNOLOGY, L.P. (US) 1993-08-31 US claimed
EP-0507616-A1 Process for the preparation of trisubstituted ureas by reductive carbonylation ARCO Chemical Technology, L.P. (US) 1992-10-07 EP claimed
EP-0273520-A2 A composition comprising a polyepoxide and a epoxy advancement catalyst, and a process for preparing advanced epoxy resins SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) 1988-07-06 EP claimed
US-4732958-A BIS(TRIHYDROCARBYL PHOSPHINE) IMINIUM CATALYSTS SHELL OIL COMPANY (US) 1988-03-22 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 (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-12496575-B2 Catalyst composition for cyclic carbonate production from CO2 and epoxides CA3, INO80C, KCNN4 CA2 5/4885ESR1 42/4885ESR2 305/4885

“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.