Hydrochloric Acid

Hydrochloric Acid

SCHEMBL906469

C[SiH](C)[Zr](C1c2ccccc2-c2ccccc21)C1c2ccccc2-c2ccccc21.Cl.Cl

nearest known ligand 0.40

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 0.35
HDAC3 known ✓ O15379 1/20 0.35
HDAC4 known ✓ P56524 1/20 0.35
HDAC7 known ✓ Q8WUI4 1/20 0.35
HDAC8 known ✓ Q9BY41 1/20 0.35
HDAC6 known ✓ Q9UBN7 1/20 0.35
HDAC9 known ✓ Q9UKV0 1/20 0.35
HDAC5 known ✓ Q9UQL6 1/20 0.35
ACHE known ✓ P22303 2/20 0.33
CHRM2 known ✓ P08172 1/20 0.33
HTR1A known ✓ P08908 1/20 0.33
ADRA2A known ✓ P08913 1/20 0.33
CHRM1 known ✓ P11229 1/20 0.33
DRD1 known ✓ P21728 1/20 0.33
SLC6A2 known ✓ P23975 1/20 0.33
SLC6A4 known ✓ P31645 1/20 0.33
ADRA1A known ✓ P35348 1/20 0.33
OPRM1 known ✓ P35372 1/20 0.33
DRD3 known ✓ P35462 1/20 0.33
SLC6A3 known ✓ Q01959 1/20 0.33

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
SCHEMBL814191 0.98 GPR3 (0.41) GPR3HTR2AHDAC3HDAC4HDAC7
Chloromethane SCHEMBL7037925 0.94 GPR3 (0.39) GPR3HTR2AHDAC3HDAC4HDAC7
Hydrochloric Acid SCHEMBL1978361 0.83 GPR3 (0.30) GPR3
SCHEMBL814590 0.81 GPR3 (0.31) GPR3
SCHEMBL8202195 0.80 GPR3 (0.31) GPR3
SCHEMBL6917289 0.77 GPR3 (0.31) GPR3HTR2ACHRM2CHRM1SLC6A2
SCHEMBL7066602 0.74 GPR3 (0.35) GPR3HTR2AHDAC3HDAC4HDAC7
Hydrochloric Acid SCHEMBL10181364 0.74 ACHE (0.41) ACHECHRM2HTR1AADRA2ACHRM1
SCHEMBL7103508 0.72 GPR3 (0.46) GPR3HTR2AHDAC3HDAC4HDAC7
SCHEMBL7195132 0.71 ACHE (0.42) ACHECHRM2HTR1AADRA2ACHRM1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7217676-B2 Hydrophobization and silica for supported catalyst EXXON MOBIL CHEMICAL PATENTS INC. (US) 2007-05-15 US claimed
US-20060264320-A1 Hydrophobization and silica for supported catalyst RODRIGUEZ GEORGE 2006-11-23 US claimed
EP-1704171-A2 HYDROPHOBIZATION AND SILICA FOR SUPPORTED CATALYST ExxonMobil Chemical Patents Inc. (US) 2006-09-27 EP claimed
WO-2005075526-A2 HYDROPHOBIZATION AND SILICA FOR SUPPORTED CATALYST EXXONMOBIL CHEMICAL PATENTS INC. (US) 2005-08-18 WO claimed
US-20050159299-A1 Hydrophobization and silica for supported catalyst EXXONMOBIL CHEMICAL PATENTS INC. 2005-07-21 US claimed
EP-0524624-B1 Use of organometallic flurorenyl compounds. PHILLIPS PETROLEUM CO (US) 2002-05-15 EP claimed
EP-2277928-B1 Shear thinning ethylene/alpha-olefin interpolymers and their preparation DOW GLOBAL TECHNOLOGIES LLC (US) 2018-02-21 EP disclosed
EP-2277928-A1 Shear thinning ethylene/alpha-olefin interpolymers and their preparation DOW GLOBAL TECHNOLOGIES INC. (US) 2011-01-26 EP disclosed
EP-1159320-B1 SHEAR THINNING ETHYLENE/ALPHA-OLEFIN/DIENE INTERPOLYMERS AND THEIR PREPARATION DOW GLOBAL TECHNOLOGIES INC (US) 2011-01-12 EP disclosed
US-7750104-B2 E.g.., ethylene-ethylidenenorbornene-propylene terpolymer, characterized by a Processing Rheology Ratio of at least 8; the polymers do not include a traditional branch-inducing monomer such as norbornadiene; prepared without H2 using a constrained geometry complex catalyst and an activating cocatalyst Dow Global Technologie Inc. (US) 2010-07-06 US disclosed
US-20070203314-A1 E.g.., ethylene-ethylidenenorbornene-propylene terpolymer, characterized by a Processing Rheology Ratio of at least 8; the polymers do not include a traditional branch-inducing monomer such as norbornadiene; prepared without H2 using a constrained geometry complex catalyst and an activating cocatalyst DUPONT DOW ELASTOMERS, LLC 2007-08-30 US disclosed
US-7217676-B2 Hydrophobization and silica for supported catalyst EXXON MOBIL CHEMICAL PATENTS INC. (US) 2007-05-15 US disclosed
US-20060264320-A1 Hydrophobization and silica for supported catalyst RODRIGUEZ GEORGE 2006-11-23 US disclosed
EP-0940412-A1 Atactic propylene (co)polymers Bayer Aktiengesellschaft (DE) 1999-09-08 EP disclosed
WO-1999015534-A1 MODIFIED ALUMOXANE CATALYST ACTIVATOR THE DOW CHEMICAL COMPANY (US) 1999-04-01 WO disclosed
EP-0793679-B1 ETHYLENE HOMOPOLYMERIZATION USING GROUP 3 METAL COMPLEXES DOW CHEMICAL CO (US) 1998-11-25 EP disclosed
US-5814714-A INTERPOLYMER COMPRISING POLYMERIZED ETHYLENE, ALPHA-OLEFIN, NON-CONJUGATED ALPHA,OMEGA DIENE THE DOW CHEMICAL COMPANY (US) 1998-09-29 US disclosed
EP-0793679-A1 ETHYLENE HOMOPOLYMERIZATION USING GROUP 3 METAL COMPLEXES THE DOW CHEMICAL COMPANY (US) 1997-09-10 EP disclosed
WO-1996016095-A1 ETHYLENE HOMOPOLYMERIZATION USING GROUP 3 METAL COMPLEXES THE DOW CHEMICAL COMPANY (US) 1996-05-30 WO disclosed
US-5464906-A Polymerization catalyst THE DOW CHEMICAL COMPANY (US) 1995-11-07 US disclosed