Hydrochloric Acid

Hydrochloric Acid

SCHEMBL8705751

CCN(CC)CCCCCCCCCCCCC1CCCCC1.Cl

nearest known ligand 0.63

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 13)

geneUniProtsupporting neighboursconfidence
SIGMAR1 known ✓ Q99720 3/20 0.63
CHRM2 known ✓ P08172 2/20 0.39
CHRM4 known ✓ P08173 2/20 0.39
CHRM1 known ✓ P11229 2/20 0.39
CHRM3 known ✓ P20309 2/20 0.39
BCHE known ✓ P06276 3/20 0.37
CYP1A2 P05177 1/20 0.52
LSS P48449 2/20 0.42
KDM5A P29375 3/20 0.41
PHF8 Q9UPP1 3/20 0.41
KDM2A Q9Y2K7 3/20 0.41
KDM4C Q9H3R0 2/20 0.41
KDM4A O75164 1/20 0.41

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 SCHEMBL9520541 1.00 SIGMAR1 (0.63) SIGMAR1CYP1A2LSSKDM5APHF8
Hydrochloric Acid SCHEMBL9518737 1.00 SIGMAR1 (0.63) SIGMAR1CYP1A2LSSKDM5APHF8
Hydrochloric Acid SCHEMBL9516639 1.00 SIGMAR1 (0.63) SIGMAR1CYP1A2LSSKDM5APHF8
Hydrochloric Acid SCHEMBL9516763 1.00 SIGMAR1 (0.63) SIGMAR1CYP1A2LSSKDM5APHF8
Hydrochloric Acid SCHEMBL9516659 1.00 SIGMAR1 (0.63) SIGMAR1CYP1A2LSSKDM5APHF8
SCHEMBL8711529 0.98 SIGMAR1 (0.66) SIGMAR1CYP1A2LSSKDM5APHF8
SCHEMBL8855135 0.98 SIGMAR1 (0.66) SIGMAR1CYP1A2LSSKDM5APHF8
Water SCHEMBL9249880 0.96 SIGMAR1 (0.63) SIGMAR1CYP1A2LSSKDM5APHF8
Water SCHEMBL9246810 0.96 SIGMAR1 (0.63) SIGMAR1CYP1A2LSSKDM5APHF8
Water SCHEMBL9249103 0.96 SIGMAR1 (0.63) SIGMAR1CYP1A2LSSKDM5APHF8

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12447699-B2 Anisotropic composite materials based on polyisocyanates COVESTRO DEUTSCHLAND AG (DE) 2025-10-21 US disclosed
EP-3085718-B1 SILOXANE GROUPS CONTAINING POLYISOCYANURATE PLASTIC AND METHOD FOR PRODUCING THE SAME COVESTRO DEUTSCHLAND AG (DE) 2024-04-17 EP disclosed
EP-3286244-B1 POLYISOCYANURATE POLYMERS AND PROCESS FOR THE PRODUCTION OF POLYISOCYANURATE POLYMERS COVESTRO INTELLECTUAL PROPERTY GMBH & CO KG (DE) 2023-11-01 EP disclosed
EP-3452529-B1 METHOD FOR PRODUCING A POLYISOCYANURATE COMPOSITE MATERIAL COVESTRO INTELLECTUAL PROPERTY GMBH & CO KG (DE) 2023-08-16 EP disclosed
CN-112204065-B Process for preparing polyisocyanate polymers and polyisocyanurate plastics 科思创知识产权两合公司 2023-03-28 CN disclosed
US-11530290-B2 Method for producing a polyisocyanurate composite material COVESTRO DEUTSCHLAND AG (DE) 2022-12-20 US disclosed
US-11453739-B2 Use of thermally decomposable acid as inhibitor for preparing polyisocyanurate composites COVESTRO LLC (US) 2022-09-27 US disclosed
CN-109071768-B Process for preparing polyisocyanurate composites 科思创德国股份有限公司 2022-09-23 CN disclosed
CN-109642015-B Method for producing polyisocyanurate plastics by means of phosphine catalysis 科思创德国股份有限公司 2022-09-23 CN disclosed
WO-2022155295-A1 POLYISOCYANURATE THERMOSETS WITH IMPROVED MECHANICAL PROPERTIES COVESTRO LLC (US) 2022-07-21 WO disclosed
US-4946923-A S-alkyl thiocarbamate base resin, plastic lens comprising the resin, and process for making the lens MITSUI TOATSU CHEMICALS, INC. (JP) 1990-08-07 US disclosed
EP-0374258-A1 HIGH REFRACTIVE INDEX LENS AND METHOD FOR ITS PRODUCTION MITSUI CHEMICALS, INC. (JP) 1990-06-27 EP disclosed
US-4929707-A Polyurethane base lens resin, plastic lens comprising the resin and preparation method of the lens MITSUI TOATSU CHEMICALS, INC. (JP) 1990-05-29 US disclosed
US-4908122-A Contacting hydrocarbon in the presence of an oxidizing agent with a catalytic composite to oxidize mercaptans to disulfides UOP (US) 1990-03-13 US disclosed
EP-0351073-A2 Lens comprising a resin having a large refractive index and process for preparing the lens MITSUI TOATSU CHEMICALS, Inc. (JP) 1990-01-17 EP disclosed
EP-0329387-A2 Plastic lens, and method for its preparation MITSUI TOATSU CHEMICALS, Inc. (JP) 1989-08-23 EP disclosed
EP-0329389-A2 Polyurethane base lens and its preparation method MITSUI TOATSU CHEMICALS, Inc. (JP) 1989-08-23 EP disclosed
EP-0329386-A2 S-alkyl thiocarbamate base resin, plastic lens comprising the resin, and process for making the lens MITSUI TOATSU CHEMICALS, Inc. (JP) 1989-08-23 EP disclosed
EP-0271839-A2 Casting polymerisation process for preparing sulfur-containing urethane resin lens MITSUI TOATSU CHEMICALS, Inc. (JP) 1988-06-22 EP disclosed
US-4124493-A Catalytic oxidation of mercaptan in petroleum distillate including alkaline reagent and substituted ammonium halide UOP INC. (US) 1978-11-07 US disclosed