Hydrochloric Acid

Hydrochloric Acid

SCHEMBL156231

CCCCCCCC[SiH2][Zr](C)(C1c2ccccc2-c2ccccc21)C1c2ccccc2-c2ccccc21.Cl.Cl

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 16)

geneUniProtsupporting neighboursconfidence
ACHE known ✓ P22303 2/20 0.41
BCHE known ✓ P06276 1/20 0.41
CHRM2 known ✓ P08172 1/20 0.35
HTR1A known ✓ P08908 1/20 0.35
ADRA2A known ✓ P08913 1/20 0.35
CHRM1 known ✓ P11229 1/20 0.35
DRD1 known ✓ P21728 1/20 0.35
SLC6A2 known ✓ P23975 1/20 0.35
SLC6A4 known ✓ P31645 1/20 0.35
ADRA1A known ✓ P35348 1/20 0.35
OPRM1 known ✓ P35372 1/20 0.35
DRD3 known ✓ P35462 1/20 0.35
SLC6A3 known ✓ Q01959 1/20 0.35
HRH3 known ✓ Q9Y5N1 1/20 0.35
CNR2 P34972 3/20 0.36
CNR1 P21554 1/20 0.36

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
SCHEMBL7195138 0.98 ACHE (0.41) ACHEBCHECNR2CNR1CHRM2
SCHEMBL30596219 0.98 ACHE (0.41) ACHEBCHECNR2CNR1CHRM2
Hydrochloric Acid SCHEMBL7581041 0.73 ACHE (0.41) ACHEBCHECHRM2HTR1AADRA2A
SCHEMBL6638015 0.70 ACHE (0.44) ACHEBCHECHRM2HTR1AADRA2A
SCHEMBL797705 0.68 ACHE (0.49) ACHEBCHECHRM2HTR1AADRA2A
SCHEMBL6060938 0.68 HTR2A (0.54) ACHEBCHE
SCHEMBL1449246 0.68 HTR2A (0.54) ACHEBCHE
SCHEMBL6060915 0.68 HTR2A (0.54) ACHEBCHE
SCHEMBL6061312 0.68 HTR2A (0.54) ACHEBCHE
SCHEMBL6061696 0.68 HTR2A (0.54) ACHEBCHE

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2460834-B1 Improved acidic activator-supports and catalysts for olefin polymerization CHEVRON PHILLIPS CHEMICAL CO (US) 2015-08-12 EP claimed
EP-1807456-B1 ORGANOCHROMIUM/METALLOCENE COMBINATION CATALYST FOR PRODUCING BIMODAL RESINS CHEVRON PHILLIPS CHEMICAL CO (US) 2012-07-11 EP claimed
EP-2460834-A1 Improved acidic activator-supports and catalysts for olefin polymerization Chevron Phillips Chemical Company LP (US) 2012-06-06 EP claimed
US-7622414-B2 Organometal catalyst compositions CHEVRON PHILLIPS CHEMICAL COMPANY, LP (US) 2009-11-24 US claimed
US-20080281063-A9 Ethylene polymers and copolymers with high optical opacity and methods of making the same SUKHADIA ASHISH M 2008-11-13 US claimed
JP-2008519092-A 2008-06-05 JP claimed
WO-2006052232-A9 ORGANOCHROMIUM/ METALLOCENE COMBINATION CATALYST FOR PRODUCING BIMODAL RESINS CHEVRON PHILLIPS CHEMICAL CO (US) 2008-02-07 WO claimed
US-20080026934-A1 ACIDIC ACTIVATOR SUPPORTS AND CATALYSTS FOR OLEFIN POLYMERIZATION CHEVRON PHILLIPS CHEMICAL COMPANY (US) 2008-01-31 US claimed
EP-1807456-A1 ORGANOCHROMIUM/ METALLOCENE COMBINATION CATALYST FOR PRODUCING BIMODAL RESINS CHEVRON PHILLIPS CHEMICAL COMPANY LP (US) 2007-07-18 EP claimed
EP-1773897-A2 IMPROVED ACIDIC ACTIVATOR-SUPPORTS AND CATALYSTS FOR OLEFIN POLYMERIZATION Chevron Phillips Chemical Company LP (US) 2007-04-18 EP claimed
WO-2006012321-A2 IMPROVED ACIDIC ACTIVATOR-SUPPORTS AND CATALYSTS FOR OLEFIN POLYMERIZATION CHEVRON PHILLIPS CHEMICAL COMPANY, LP (US) 2006-02-02 WO claimed
US-6992032-B2 Organometal catalyst compositions PHILLIPS PETROLEUM COMPANY (US) 2006-01-31 US claimed
US-20050288178-A1 Acidic activator-supports and catalysts for olefin polymerization CHEVRON PHILLIPS CHEMICAL COMPANY 2005-12-29 US claimed
US-20050203261-A1 Ethylene polymers and copolymers with high optical opacity and methods of making the same CHEVRON PHILLIPS CHEMICAL COMPANY, L.P. 2005-09-15 US claimed
US-20050137366-A1 Organometal compound catalyst MCDANIEL MAX P (US) 2005-06-23 US claimed
US-6858687-B2 Catalyst compositions that are useful for polymerizing at least one monomer to produce a polymer. This invention also provides catalyst compositions that are useful for polymerizing at least one monomer to produce a polymer, PHILLIPS PETROLEUM COMPANY (US) 2005-02-22 US claimed
US-6838533-B2 Organometal catalyst composition PHILIPS PETROLEUM COMPANY (US) 2005-01-04 US claimed
US-6548441-B1 Polymerization catalysts comprises an organometal compound, an organoaluminum compound, and a halogenated nickel solid oxide compound; heterogeneous catalysts can lead to form uniform polymer particles that have a high bulk density PHILLIPS PETROLEUM COMPANY 2003-04-15 US claimed
US-6548442-B1 Polymerization catalysts comprises an organometal compound, an organoaluminum compound, and a halogenated solid zirconium oxide compound; heterogeneous catalysts can lead to form uniform polymer particles that have a high bulk density PHILLIPS PETROLEUM COMPANY 2003-04-15 US claimed
US-6355594-B1 CONTACTING AT LEAST ONE ORGANOMETAL COMPOUND, AT LEAST ONE ORGANOALUMINUM COMPOUND, AND AT LEAST ONE FLUORIDED SILICA-ALUMINA TO PRODUCE POLYMERIZATION CATALYST COMPOSITION PHILLIPS PETROLEUM COMPANY 2002-03-12 US claimed