Hydrochloric Acid

Hydrochloric Acid

SCHEMBL6897360

[Cl-].[Cl-].[Zr+2]C1C=Cc2ccccc21.b1ccccc1

nearest known ligand 0.33

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEBDKRB2CHRM1CHRM2CHRM3CHRNA1CHRNB1CHRNDCHRNECHRNGGUCY1A1GUCY1A2GUCY1B1GUCY1B2NAMPTPTAFRSLC10A2SLC6A2SLC6A3TACR1dacAdacBdacCftsImrcAmrcBmrdA

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 3)

geneUniProtsupporting neighboursconfidence
HTR6 P50406 1/20 0.33
HTR2A P28223 1/20 0.32
SIGMAR1 Q99720 2/20 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 SCHEMBL812668 0.87 HTR2A (0.40) HTR6HTR2ASIGMAR1
Hydrochloric Acid SCHEMBL6908577 0.85 HTR2A (0.39) HTR6HTR2ASIGMAR1
Bromide SCHEMBL6440191 0.82 HTR2A (0.45) HTR6HTR2ASIGMAR1
Fluoride Ion SCHEMBL5183634 0.82 HTR2A (0.40) HTR6HTR2ASIGMAR1
Phenol SCHEMBL4827336 0.78 HTR6 (0.38) HTR6HTR2ASIGMAR1
SCHEMBL7107703 0.77 HTR2A (0.36) HTR6HTR2ASIGMAR1
Ethylbenzene SCHEMBL6930967 0.76 TP53 (0.47) HTR6HTR2ASIGMAR1
Hydrochloric Acid SCHEMBL182284 0.72 SIGMAR1 (0.32) HTR6HTR2ASIGMAR1
Hydrochloric Acid SCHEMBL6559467 0.70 HTR2A (0.38) HTR6HTR2ASIGMAR1
Hydrochloric Acid SCHEMBL6903962 0.69

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1373334-A1 ETHYLENE POLYMERIZATION PROCESS Equistar Chemicals, LP (US) 2004-01-02 EP disclosed
US-6664349-B2 Using coordination polymerization catalyst EQUISTAR CHEMICALS, LP 2003-12-16 US disclosed
US-6583240-B2 In the presence of an activator and a Group 4 metal catalyst having at least one boraaryl ligand; wherein the catalyst is alkylated iwth triisobutyl aluminum; polyethylene with higher long chain branching index (LCBI) EQUISTAR CHEMICALS, LP 2003-06-24 US disclosed
EP-1290044-A1 ETHYLENE POLYMERIZATON PROCESS Equistar Chemicals L.P. (US) 2003-03-12 EP disclosed
US-20020177675-A1 Ethylene polymerization process EQUISTAR CHEMICALS, LP 2002-11-28 US disclosed
WO-2002094888-A1 ETHYLENE POLYMERIZATION PROCESS EQUISTAR CHEMICALS, LP (US) 2002-11-28 WO disclosed
US-20020161144-A1 Ethylene polymerization process EQUISTAR CHEMICALS, LP 2002-10-31 US disclosed
WO-2002079277-A1 ETHYLENE POLYMERIZATION PROCESS EQUISTAR CHEMICALS, LP (US) 2002-10-10 WO disclosed
US-6403736-B1 SUPPORTING GROUP 3-10 METAL CATALYST CONTAINING BORAARYL LIGAND ONTO INORGANIC OXIDE OR CHLORIDE OR POLYMER, PREMIXING WITH TRIETHYLALUMINUM, POLYMERIZING OLEFIN IN PRESENCE OF CATALYST, ACTIVATOR AND TRIISOBUTYLALUMINUM SCAVENGER EQUISTAR CHEMICALS, LP 2002-06-11 US disclosed
WO-2001096420-A1 ETHYLENE POLYMERIZATON PROCESS EQUISTAR CHEMICALS, L.P. (US) 2001-12-20 WO disclosed