Hydrochloric Acid

Hydrochloric Acid

SCHEMBL153249

CCCCCCCC[Hf]([SiH2]c1ccccc1)(C1C=Cc2ccccc21)C1C=Cc2ccccc21.Cl.Cl

nearest known ligand 0.31

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 7)

geneUniProtsupporting neighboursconfidence
SIGMAR1 known ✓ Q99720 2/20 0.30
HTR2A known ✓ P28223 1/20 0.30
KDM4E B2RXH2 1/20 0.31
MEN1 O00255 1/20 0.31
PMP22 Q01453 1/20 0.31
KMT2A Q03164 1/20 0.31
SMN1; SMN2 Q16637 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
Hydrochloric Acid SCHEMBL1655213 1.00 KDM4E (0.31) KDM4EMEN1PMP22KMT2ASMN1; SMN2
SCHEMBL7129635 0.99 HTR2A (0.31) SIGMAR1HTR2A
Hydrochloric Acid SCHEMBL217343 0.75 SIGMAR1 (0.31) KDM4EMEN1PMP22KMT2ASMN1; SMN2
SCHEMBL796452 0.69 KDM4E (0.32) KDM4EMEN1PMP22KMT2ASMN1; SMN2
SCHEMBL4565253 0.66
SCHEMBL6674209 0.65 HTR6 (0.45) KDM4EMEN1PMP22KMT2ASMN1; SMN2
Hydrochloric Acid SCHEMBL4466250 0.65 RET (0.36) KDM4EMEN1PMP22KMT2ASMN1; SMN2
SCHEMBL10359804 0.65 HTR6 (0.45) KDM4EMEN1PMP22KMT2ASMN1; SMN2
SCHEMBL31185871 0.65 HTR6 (0.45) KDM4EMEN1PMP22KMT2ASMN1; SMN2
SCHEMBL6055948 0.65 HTR6 (0.45) KDM4EMEN1PMP22KMT2ASMN1; SMN2

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 66 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
US-7417097-B2 Organometal compound catalyst PHILLIPS PETROLEUM COMPANY (US) 2008-08-26 US claimed
US-20080026934-A1 ACIDIC ACTIVATOR SUPPORTS AND CATALYSTS FOR OLEFIN POLYMERIZATION CHEVRON PHILLIPS CHEMICAL COMPANY (US) 2008-01-31 US claimed
US-7163906-B2 provide polyolefins having very broad molecular weight distribution; comprise the contact product of at least one metallocene compound, at least one organochromium compound, at least one chemically-treated solid oxide, and at least one organoaluminum compound CHEVRON PHILLIPS CHEMICAL COMPANY, LLP (US) 2007-01-16 US claimed
US-20060094590-A1 Organochromium/metallocene combination catalysts for producing bimodal resins CHEVRON PHILLIPS CHEMICAL COMPANY, LP 2006-05-04 US claimed
US-6984603-B2 Organometal catalyst compositions PHILLIPS PETROLEUM COMPANY (US) 2006-01-10 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-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-10982023-B2 Process to produce modified clay, supported metallocene polymerization catalyst W. R. GRACE & CO.-CONN. (US) 2021-04-20 US disclosed
US-10940460-B2 Process to produce modified clay, modified clay produced and use thereof W. R. GRACE & CO.-CONN. (US) 2021-03-09 US disclosed
EP-2611861-B1 POLYMER RESINS HAVING IMPROVED BARRIER PROPERTIES AND METHODS OF MAKING SAME CHEVRON PHILLIPS CHEMICAL CO LP (US) 2019-01-02 EP disclosed
EP-1226180-A1 ORGANOMETAL CATALYST COMPOSITIONS Phillips Petroleum Company (US) 2002-07-31 EP disclosed
WO-2001041920-A1 ORGANOMETAL COMPOUND CATALYST PHILLIPS PETROLEUM COMPANY (US) 2001-06-14 WO disclosed
WO-2001023433-A1 ORGANOMETAL CATALYST COMPOSITIONS PHILLIPS PETROLEUM COMPANY (US) 2001-04-05 WO disclosed