Hydrochloric Acid

Hydrochloric Acid

SCHEMBL4846513

Cl.Cl.[SiH3][Zr](C1CC1)(C1C=Cc2ccccc21)C1C=Cc2ccccc21

nearest known ligand 0.32

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 2)

geneUniProtsupporting neighboursconfidence
HTR6 known ✓ P50406 1/20 0.32
HTR2A known ✓ P28223 1/20 0.32

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 SCHEMBL7615277 0.77 RET (0.35) HTR6HTR2A
Ethane SCHEMBL8628956 0.75 RET (0.34) HTR6HTR2A
SCHEMBL18952179 0.74 RET (0.36) HTR6HTR2A
Hydrochloric Acid SCHEMBL8733929 0.74 HTR6 (0.33) HTR6HTR2A
Hydrochloric Acid SCHEMBL7945370 0.74 SIGMAR1 (0.33) HTR6HTR2A
Hydrochloric Acid SCHEMBL441680 0.72 HTR2A (0.32) HTR2A
Hydrochloric Acid SCHEMBL4457343 0.72 KDM4E (0.40) HTR6HTR2A
Ethane SCHEMBL8634247 0.71 HTR2A (0.34) HTR6HTR2A
SCHEMBL550007 0.70 HTR2A (0.38) HTR6HTR2A
SCHEMBL3685967 0.70 HTR2A (0.38) HTR6HTR2A

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-6344577-B1 COMPLEXING METAL, SILICON HYDROCARBYL COMPOUNDS AND CYCLOPENTADIENE FINA TECHNOLOGY, INC. 2002-02-05 US claimed
US-6117957-A COORDINATION CATALYST FINA TECHNOLOGY, INC. (US) 2000-09-12 US claimed
US-5846896-A Metallocene catalyst systems FINA TECHNOLOGY, INC. (US) 1998-12-08 US claimed
EP-0284708-B1 Metallocene catalyst systems for olefin polymerization having a silicon hydrocarbyl bridge. FINA TECHNOLOGY (US) 1996-01-31 EP claimed
US-12071502-B2 Method of making an ethylene-propylene copolymer KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) 2024-08-27 US disclosed
US-20240228677-A9 METHOD OF MAKING AN ETHYLENE-PROPYLENE COPOLYMER KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) 2024-07-11 US disclosed
US-20240132635-A1 METHOD OF MAKING AN ETHYLENE-PROPYLENE COPOLYMER KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) 2024-04-25 US disclosed
US-11926691-B2 Method for making and using a supported zinc aluminum layered double hydroxide catalyst KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) 2024-03-12 US disclosed
US-20240034818-A1 METHOD FOR MAKING AND USING A SUPPORTED ZINC ALUMINUM LAYERED DOUBLE HYDROXIDE CATALYST KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) 2024-02-01 US disclosed
US-11827734-B1 Method of making a polyolefin KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) 2023-11-28 US disclosed
US-11746164-B1 Method of making a polyolefin nanocomposite KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) 2023-09-05 US disclosed
US-7332456-B2 Varying the melting points and molecular weights of polyolefins in a process of addition polymerization using metallocene catalyst which are chiral and stereorigid and include a bridge between the cyclopentadienyl groups FINA TECHNOLOGY, INC. (US) 2008-02-19 US disclosed
US-6649712-B2 Changing the components and structure of the metallocene catalysts; melting point is controlled by the number of inversions in the xylene insoluble fraction of the polymer FINA TECHNOLOGY, INC. 2003-11-18 US disclosed
US-20020193537-A1 Method for varying the melting points and molecular weights of polyolefins using metallocene catalyst systems EWEN JOHN A (US) 2002-12-19 US disclosed
US-20020111444-A1 Alpha olefin polymer products and catalyst systems EWEN JOHN A (US) 2002-08-15 US disclosed
US-6344577-B1 COMPLEXING METAL, SILICON HYDROCARBYL COMPOUNDS AND CYCLOPENTADIENE FINA TECHNOLOGY, INC. 2002-02-05 US disclosed
US-6117957-A COORDINATION CATALYST FINA TECHNOLOGY, INC. (US) 2000-09-12 US disclosed
US-5846896-A Metallocene catalyst systems FINA TECHNOLOGY, INC. (US) 1998-12-08 US disclosed
EP-0284708-B1 Metallocene catalyst systems for olefin polymerization having a silicon hydrocarbyl bridge. FINA TECHNOLOGY (US) 1996-01-31 EP disclosed
EP-0284708-A1 Metallocene catalyst systems for olefin polymerization having a silicon hydrocarbyl bridge. FINA TECHNOLOGY, INC. (US) 1988-10-05 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20020193537-A1 Method for varying the melting points and molecular weights of polyolefins using metallocene catalyst systems MRPS22, MRPS35, MCRS1 HTR6 2528/4885HTR2A 1388/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.