Hydrochloric Acid

Hydrochloric Acid

SCHEMBL6295599

C=CC[Si](C)(C1c2ccccc2-c2ccccc21)C1c2ccccc2-c2ccccc21.Cl.Cl.[Zr]

nearest known ligand 0.37

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
HTR2A known ✓ P28223 1/20 0.37
ACHE known ✓ P22303 2/20 0.32
CHRM2 known ✓ P08172 1/20 0.32
HTR1A known ✓ P08908 1/20 0.32
ADRA2A known ✓ P08913 1/20 0.32
CHRM1 known ✓ P11229 1/20 0.32
DRD1 known ✓ P21728 1/20 0.32
SLC6A2 known ✓ P23975 1/20 0.32
SLC6A4 known ✓ P31645 1/20 0.32
ADRA1A known ✓ P35348 1/20 0.32
OPRM1 known ✓ P35372 1/20 0.32
DRD3 known ✓ P35462 1/20 0.32
SLC6A3 known ✓ Q01959 1/20 0.32
HRH3 known ✓ Q9Y5N1 1/20 0.32
BCHE known ✓ P06276 1/20 0.31
GPR3 P46089 1/20 0.33
SLC22A2 O15244 1/20 0.31
SLC22A3 O75751 1/20 0.31
PRCP P42785 1/20 0.30
CYP3A4 P08684 1/20 0.30

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
SCHEMBL7561178 0.98 HTR2A (0.38) HTR2AGPR3ACHECHRM2HTR1A
Hydrochloric Acid SCHEMBL6732020 0.97 HTR2A (0.37) HTR2AGPR3ACHECHRM2HTR1A
SCHEMBL20986960 0.96 HTR2A (0.39) HTR2AGPR3ACHECHRM2HTR1A
Hydrochloric Acid SCHEMBL6295601 0.93 HTR2A (0.37) HTR2AGPR3ACHECHRM2HTR1A
Hydrochloric Acid SCHEMBL6732026 0.93 HTR2A (0.37) HTR2AGPR3ACHECHRM2HTR1A
Hydrochloric Acid SCHEMBL6295669 0.83 GPR3 (0.32) HTR2AGPR3ACHECHRM2HTR1A
SCHEMBL7152500 0.81 GPR3 (0.32) HTR2AGPR3ACHECHRM2HTR1A
Hydrochloric Acid SCHEMBL6727342 0.80 CYP3A4 (0.34) HTR2AGPR3ACHECHRM2HTR1A
Hydrochloric Acid SCHEMBL6731375 0.80 USP2 (0.33) ACHECHRM2HTR1AADRA2ACHRM1
SCHEMBL7627897 0.79 ACHE (0.34) HTR2AGPR3ACHECHRM2HTR1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6852660-B2 Solid metallocene catalyst system CHEVRON PHILLIPS CHEMICAL COMPANY, LP (US) 2005-02-08 US claimed
US-20030144436-A1 Coorination catalyst for polyalpha-olefins MITCHELL KENT E (US) 2003-07-31 US claimed
US-6534609-B2 Making by combining an organoaluminoxane and a metallocene having olefinic unsaturated substituent(s) in an aliphatic liquid, prepolymerizing olefin(s) to produce a prepolymerized solid catalyst and separating from the liquid CHEVRON PHILLIPS CHEMICAL COMPANY LP 2003-03-18 US claimed
US-20020177676-A1 Method for making and using a metallocene catalyst system CHEVRON PHILLIPS CHEMICAL COMPANY LP, A DELAWARE LIMITED PARTNERSHIP 2002-11-28 US claimed
WO-2002072641-A1 METHOD FOR MAKING AND USING A METALLOCENE CATALYST SYSTEM CHEVRON PHILLIPS CHEMICAL COMPANY LP (US) 2002-09-19 WO claimed
WO-1999043724-A1 METHOD FOR POLYMERIZING MONOMERS TO PRODUCE LINEAR, LOW DENSITY POLYMER PHILLIPS PETROLEUM COMPANY (US) 1999-09-02 WO claimed
WO-1998052686-A1 METHOD FOR MAKING AND USING A PREPOLYMERIZED OLEFIN POLYMERIZATION CATALYST PHILLIPS PETROLEUM COMPANY (US) 1998-11-26 WO claimed
EP-0685495-B1 Method for using a supported metallocene catalyst system PHILLIPS PETROLEUM CO (US) 1998-04-08 EP claimed
US-5498581-A OLEFIN POLYMERIZATION PHILLIPS PETROLEUM COMPANY (US) 1996-03-12 US claimed
EP-0685495-A1 Method for making and using a supported metallocene catalyst system PHILLIPS PETROLEUM COMPANY (US) 1995-12-06 EP claimed
US-20050171305-A1 Solid metallocene catalyst system MITCHELL KENT E (US) 2005-08-04 US disclosed
US-6852660-B2 Solid metallocene catalyst system CHEVRON PHILLIPS CHEMICAL COMPANY, LP (US) 2005-02-08 US disclosed
US-6746981-B2 OLEFIN POLYMERIZATION CATALYSTS WITH PRODUCTIVITY WHEN FRESH OF >/= 18,000 GRAMS OF POLYETHYLENE PER GRAM OF CATALYST IN ONE HOUR, AND A SPECIFIC SURFACE AREA OF </= 20 M2/G ALBEMARLE CORPORATION 2004-06-08 US disclosed
US-6730758-B2 ADDITION POLYMERIZATION OF ALPHA-OLEFIN HYDROCARBON IN PRESENCE OF SELF-SUPPORTED VINYLOLEFIN-PREPOLYMERIZED CATALYST ALBEMARLE CORPORATION 2004-05-04 US disclosed
EP-1037931-B1 CATALYST COMPOSITIONS OF ENHANCED PRODUCTIVITY ALBEMARLE CORP (US) 2004-02-04 EP disclosed
WO-1999043724-A1 METHOD FOR POLYMERIZING MONOMERS TO PRODUCE LINEAR, LOW DENSITY POLYMER PHILLIPS PETROLEUM COMPANY (US) 1999-09-02 WO disclosed
WO-1999029738-A1 CATALYST COMPOSITIONS OF ENHANCED PRODUCTIVITY ALBEMARLE CORPORATION (US) 1999-06-17 WO disclosed
WO-1998052686-A1 METHOD FOR MAKING AND USING A PREPOLYMERIZED OLEFIN POLYMERIZATION CATALYST PHILLIPS PETROLEUM COMPANY (US) 1998-11-26 WO disclosed
EP-0685495-B1 Method for using a supported metallocene catalyst system PHILLIPS PETROLEUM CO (US) 1998-04-08 EP disclosed
US-5498581-A OLEFIN POLYMERIZATION PHILLIPS PETROLEUM COMPANY (US) 1996-03-12 US disclosed