Hydrochloric Acid

Hydrochloric Acid

SCHEMBL4849700

CC1=C(C)C(C)(C2C=Cc3ccccc32)C([Zr])=C1C.Cl.Cl

nearest known ligand 0.00

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.

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
SCHEMBL2784485 0.98
Hydrochloric Acid SCHEMBL2785614 0.82
SCHEMBL7176934 0.81
SCHEMBL7046153 0.81
Hydrochloric Acid SCHEMBL6469236 0.79
Hydrochloric Acid SCHEMBL2153741 0.77
Hydrochloric Acid SCHEMBL2153146 0.77
Hydrochloric Acid SCHEMBL4852332 0.75 HTR6 (0.31)
Hydrochloric Acid SCHEMBL4848230 0.75 HTR6 (0.31)
Hydrochloric Acid SCHEMBL6524498 0.74

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6897273-B2 Catalyst composition, method of polymerization and polymer therefrom UNIVATION TECHNOLOGIES, LLC (US) 2005-05-24 US claimed
US-20020103310-A1 Catalyst composition, method of polymerization and polymer therefrom UNIVATION TECHNOLOGIES, LLC 2002-08-01 US claimed
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
WO-2003008459-A9 METHOD FOR PRODUCTION OF MULTIMODAL POLYOLEFINS OF TUNABLE COMPOSITION, MOLECULAR WEIGHT, AND POLYDISPERSITY UNIV MARYLAND (US) 2003-10-16 WO 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
WO-2003008459-A1 METHOD FOR PRODUCTION OF MULTIMODAL POLYOLEFINS OF TUNABLE COMPOSITION, MOLECULAR WEIGHT, AND POLYDISPERSITY UNIVERSITY OF MARYLAND, COLLEGE PARK (US) 2003-01-30 WO disclosed
US-20020119890-A1 Catalyst preparation method WENZEL TIMOTHY T (US) 2002-08-29 US disclosed
US-6432863-B2 FOR TRANSITION METAL CATALYST W. R. GRACE & CO.-CONN. 2002-08-13 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
US-6136747-A SOLID ZIEGLER-NATTA CATALYST; A LIQUID SINGLE SITE CATALYST; AND AT LEAST ONE ACTIVATING COCATALYST IS PROVIDED. POLYMERS HAVING A BROAD OR BIMODAL MOLECULAR WEIGHT DISTRIBUTION MAY BE MADE UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION (US) 2000-10-24 US disclosed