Hydrochloric Acid

Hydrochloric Acid

SCHEMBL6295669

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

nearest known ligand 0.32

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 19)

geneUniProtsupporting neighboursconfidence
HTR2A known ✓ P28223 1/20 0.32
CHRM2 known ✓ P08172 1/20 0.30
HTR1A known ✓ P08908 1/20 0.30
ADRA2A known ✓ P08913 1/20 0.30
CHRM1 known ✓ P11229 1/20 0.30
DRD1 known ✓ P21728 1/20 0.30
ACHE known ✓ P22303 1/20 0.30
SLC6A2 known ✓ P23975 1/20 0.30
SLC6A4 known ✓ P31645 1/20 0.30
ADRA1A known ✓ P35348 1/20 0.30
OPRM1 known ✓ P35372 1/20 0.30
DRD3 known ✓ P35462 1/20 0.30
SLC6A3 known ✓ Q01959 1/20 0.30
HRH3 known ✓ Q9Y5N1 1/20 0.30
GPR3 P46089 1/20 0.32
CYP3A4 P08684 1/20 0.32
CYP2D6 P10635 1/20 0.32
CYP2C9 P11712 1/20 0.32
CYP2C19 P33261 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
SCHEMBL7152500 0.98 GPR3 (0.32) GPR3HTR2ACYP3A4CYP2D6CYP2C9
Hydrochloric Acid SCHEMBL6727342 0.97 CYP3A4 (0.34) GPR3HTR2ACYP3A4CYP2D6CYP2C9
SCHEMBL8679648 0.97 GPR3 (0.33) GPR3HTR2ACYP3A4CYP2D6CYP2C9
Hydrochloric Acid SCHEMBL6295671 0.94 GPR3 (0.32) GPR3HTR2ACYP3A4CYP2D6CYP2C9
Hydrochloric Acid SCHEMBL6727344 0.94 GPR3 (0.32) GPR3HTR2ACYP3A4CYP2D6CYP2C9
Hydrochloric Acid SCHEMBL6731375 0.89 USP2 (0.33) CHRM2HTR1AADRA2ACHRM1DRD1
Hydrochloric Acid SCHEMBL6294799 0.88 USP2 (0.35) CHRM2HTR1AADRA2ACHRM1DRD1
SCHEMBL7158610 0.88 USP2 (0.33) GPR3HTR2ACYP3A4CYP2D6CYP2C9
Hydrochloric Acid SCHEMBL6727444 0.86 USP2 (0.33) CYP3A4CYP2D6CYP2C9CYP2C19CHRM2
SCHEMBL8609627 0.86 USP2 (0.36) CHRM2HTR1AADRA2ACHRM1DRD1

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 20 patents. 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
WO-1999043724-A1 METHOD FOR POLYMERIZING MONOMERS TO PRODUCE LINEAR, LOW DENSITY POLYMER PHILLIPS PETROLEUM COMPANY (US) 1999-09-02 WO claimed
EP-0685495-B1 Method for using a supported metallocene catalyst system PHILLIPS PETROLEUM CO (US) 1998-04-08 EP claimed
EP-0685495-A1 Method for making and using a supported metallocene catalyst system PHILLIPS PETROLEUM COMPANY (US) 1995-12-06 EP claimed
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
US-6677265-B1 THE METALLOCENE USED AS THE FEED HAVING IN THE MOLECULE AT LEAST ONE POLYMERIZABLE OLEFINIC SUBSTITUENT ALBEMARLE CORPORATION 2004-01-13 US disclosed
US-20030191254-A1 PARTICULATE GROUP 4 METALLOCENE-ALUMINOXANE CATALYST COMPOSITIONS DEVOID OF PREFORMED SUPPORT, AND THEIR PREPARATION AND THEIR USE ALBEMARLE CORPORATION 2003-10-09 US disclosed
US-20030105253-A1 Particulate group 4 metallocene-aluminoxane catalyst compositions devoid of preformed support, and their preparation and their use ALBEMARLE CORPORATION 2003-06-05 US disclosed
US-6551955-B1 Olefin polymerization catalysts; efficiency ALBEMARLE CORPORATION 2003-04-22 US disclosed
US-6521728-B1 Particulate group 4 metallocene-aluminoxane catalyst compositions devoid of preformed support, and their preparation and their use ALBEMARLE CORPORATION 2003-02-18 US disclosed
WO-2001098374-A2 PROCESS OF PRODUCING SELF-SUPPORTED CATALYSTS ALBEMARLE CORPORATION (US) 2001-12-27 WO disclosed
WO-2001098380-A2 PARTICULATE GROUP 4 METALLOCENE-ALUMINOXANE CATALYST COMPOSITIONS DEVOID OF PREFORMED SUPPORT, AND THEIR PREPARATION AND THEIR USE ALBEMARLE CORPORATION (US) 2001-12-27 WO disclosed
WO-2001098381-A2 POLYMERIZATION PROCESS USING SELF-SUPPORTED CATALYSTS ALBEMARLE CORPORATION (US) 2001-12-27 WO disclosed
US-6294496-B1 VERY HIGH PRODUCTIVITIES; PREPOLYMERIZING VINYLOLEFIN WITH A GROUP 4 METALLOCENE-ALUMINOXANE SOLUTION ALBEMARLE CORPORATION 2001-09-25 US disclosed
US-6166152-A Process to produce low density polymer in a loop reactor PHILLIPS PETROLEUM COMPANY (US) 2000-12-26 US disclosed
EP-1037931-A1 CATALYST COMPOSITIONS OF ENHANCED PRODUCTIVITY ALBEMARLE CORPORATION (US) 2000-09-27 EP disclosed
WO-1999029738-A1 CATALYST COMPOSITIONS OF ENHANCED PRODUCTIVITY ALBEMARLE CORPORATION (US) 1999-06-17 WO disclosed