Hydrochloric Acid

Hydrochloric Acid

SCHEMBL8527173

C[SiH](C)[Ti](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
ACHE known ✓ P22303 2/20 0.37
CHRM2 known ✓ P08172 1/20 0.37
HTR1A known ✓ P08908 1/20 0.37
ADRA2A known ✓ P08913 1/20 0.37
CHRM1 known ✓ P11229 1/20 0.37
DRD1 known ✓ P21728 1/20 0.37
SLC6A2 known ✓ P23975 1/20 0.37
SLC6A4 known ✓ P31645 1/20 0.37
ADRA1A known ✓ P35348 1/20 0.37
OPRM1 known ✓ P35372 1/20 0.37
DRD3 known ✓ P35462 1/20 0.37
SLC6A3 known ✓ Q01959 1/20 0.37
HRH3 known ✓ Q9Y5N1 1/20 0.37
HTR2A known ✓ P28223 1/20 0.35
BCHE known ✓ P06276 1/20 0.32
HDAC3 known ✓ O15379 1/20 0.31
HDAC4 known ✓ P56524 1/20 0.31
HDAC7 known ✓ Q8WUI4 1/20 0.31
HDAC8 known ✓ Q9BY41 1/20 0.31
HDAC6 known ✓ Q9UBN7 1/20 0.31

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
Methyl Alcohol SCHEMBL8160175 0.94 GPR3 (0.39) GPR3ACHECHRM2HTR1AADRA2A
SCHEMBL8194634 0.80 GPR3 (0.31) GPR3ACHECHRM2HTR1AADRA2A
SCHEMBL8166078 0.77 GPR3 (0.31) GPR3CHRM2CHRM1SLC6A2ADRA1A
Methyl Alcohol SCHEMBL8155526 0.75 CYP2D6 (0.31) CYP2D6
SCHEMBL9409548 0.72 GPR3 (0.46) GPR3ACHECHRM2HTR1AADRA2A
Hydrochloric Acid SCHEMBL7946463 0.70 GPR3 (0.44) GPR3ACHECHRM2HTR1AADRA2A
Hydrochloric Acid SCHEMBL30300599 0.70 GPR3 (0.44) GPR3ACHECHRM2HTR1AADRA2A
SCHEMBL8203373 0.68
SCHEMBL4277063 0.67 GPR3 (0.46) GPR3ACHECHRM2HTR1AADRA2A
SCHEMBL6910181 0.67 GPR3 (0.41) GPR3ACHECHRM2HTR1AADRA2A

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 9 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0793679-B1 ETHYLENE HOMOPOLYMERIZATION USING GROUP 3 METAL COMPLEXES DOW CHEMICAL CO (US) 1998-11-25 EP disclosed
EP-0781299-B1 SILYLIUM CATIONIC POLYMERIZATION ACTIVATORS FOR METALLOCENE COMPLEXES DOW CHEMICAL CO (US) 1998-09-09 EP disclosed
EP-0827962-A2 Preparation of silylium salts THE DOW CHEMICAL COMPANY (US) 1998-03-11 EP disclosed
EP-0793679-A1 ETHYLENE HOMOPOLYMERIZATION USING GROUP 3 METAL COMPLEXES THE DOW CHEMICAL COMPANY (US) 1997-09-10 EP disclosed
EP-0781299-A2 SILYLIUM CATIONIC POLYMERIZATION ACTIVATORS FOR METALLOCENE COMPLEXES THE DOW CHEMICAL COMPANY (US) 1997-07-02 EP disclosed
US-5625087-A Silylium cationic polymerization activators for metallocene complexes THE DOW CHEMICAL COMPANY (US) 1997-04-29 US disclosed
WO-1996016095-A1 ETHYLENE HOMOPOLYMERIZATION USING GROUP 3 METAL COMPLEXES THE DOW CHEMICAL COMPANY (US) 1996-05-30 WO disclosed
WO-1996008519-A2 SILYLIUM CATIONIC POLYMERIZATION ACTIVATORS FOR METALLOCENE COMPLEXES THE DOW CHEMICAL COMPANY (US) 1996-03-21 WO disclosed
US-5464906-A Polymerization catalyst THE DOW CHEMICAL COMPANY (US) 1995-11-07 US disclosed