Hydrochloric Acid

Hydrochloric Acid

SCHEMBL4848230

CC1=C(C)C([Hf])(C2C=Cc3ccccc32)C(C)=C1C.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
HTR6 known ✓ P50406 1/20 0.31
HTR2A known ✓ P28223 1/20 0.31
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
SCHEMBL3721982 0.98 HTR6 (0.32) HTR6HTR2A
Hydrochloric Acid SCHEMBL4852332 0.80 HTR6 (0.31) HTR6KDM4EMEN1PMP22KMT2A
SCHEMBL6378838 0.78 HTR6 (0.32) HTR6HTR2A
Hydrochloric Acid SCHEMBL27487479 0.77 HTR6 (0.31) HTR6HTR2A
Hydrochloric Acid SCHEMBL8623411 0.77 BRD4 (0.32) HTR6HTR2A
SCHEMBL7176934 0.76
Hydrochloric Acid SCHEMBL2785614 0.75
SCHEMBL2784485 0.73
SCHEMBL7046153 0.73
SCHEMBL6302806 0.72

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9416069-B2 Scalable production of precision hydrocarbons from trialkylaluminum via ternary living coordinative chain transfer polymerization UNIVERSITY OF MARYLAND, COLLEGE PARK (US) 2016-08-16 US disclosed
US-9175103-B2 Living coordinative chain transfer polymerization with dynamic counterion exchange UNIVERSITY OF MARYLAND, COLLEGE PARK (US) 2015-11-03 US disclosed
EP-2220128-B1 PROCESS FOR PREPARATION OF POLYOLEFINS VIA LIVING COORDINATIVE CHAIN TRANSFER POLYMERIZATION UNIV MARYLAND (US) 2014-10-22 EP disclosed
US-20140073752-A1 Living Coordinative Chain Transfer Polymerization with Dynamic Counterion Exchange UNIVERSITY OF MARYLAND, COLLEGE PARK (US) 2014-03-13 US disclosed
US-8188200-B2 Process for preparation of polyolefins via living coordinative chain transfer polymerization UNIVERSITY OF MARYLAND, COLLEGE PARK (US) 2012-05-29 US disclosed
US-7384884-B2 Catalyst preparation method UNIVATION TECHNOLOGIES, LLC (US) 2008-06-10 US disclosed
US-7053157-B2 Method for production of multimodal polyolefins of tunable composition, molecular weight, and polydispersity UNIVERSITY OF MARYLAND, COLLEGE PARK (US) 2006-05-30 US disclosed
US-6982236-B2 Process to polymerize olefins UNIVATION TECHNOLOGIES, LLC (US) 2006-01-03 US disclosed
US-20040198930-A1 Method for production of multimodal polyolefins of tunable composition, molecular weight, and polydispersity UNIVERSITY OF MARYLAND, COLLEGE PARK 2004-10-07 US disclosed
US-6624266-B2 Catalyst prepared by contacting unsupported olefin polymerization catalyst precursor, co-catalyst, and solvent for period of time sufficient to form preactivated unsupported olefin polymerization catalyst; nonfouling UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION 2003-09-23 US disclosed
US-6608149-B2 Continuously combining a catalyst slurry with a catalyst solution to form a catalyst formulation; combining the catalyst with olefin(s) in a polymerization reactor to form a polymer product; measuring sample of polymer; changing UNIVATION TECHNOLOGIES, LLC 2003-08-19 US disclosed
US-6605675-B2 Combines a catalyst component containing slurry and a catalyst component containing solution to form the completed catalyst composition for introduction into the polymerization reactor; polymerizing olefins UNIVATION TECHNOLOGIES, LLC 2003-08-12 US disclosed
US-6403518-B2 MADE BY REACTING AN INORGANIC OR POLYMERIC CARRIER CONTAINING REACTIVE FUNCTIONALITIES WITH A HALOGENATED ORGANIC IN THE PRESENCE OF A BASE; TRANSITION METAL CATALYSTS FURTHER SUPPORTED ON THE CARRIER W. R. GRACE & CO.-CONN. 2002-06-11 US disclosed