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Tridihexethyl Chloride , Muscarinic acetylcholine receptor M1 antagonist, CAS No.4310-35-4, Muscarinic acetylcholine receptor M1 antagonist

    Grade & Purity:
  • ≥96%
  • Cas Number:  4310-35-4
  • Molecular Weight:  353.97
  • PubChem CID: 20298
In stock
Item Number
T346648
Grouped product items
SKU Size
Availability
Price Qty
T346648-1mg
1mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$199.90
T346648-5mg
5mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$399.90
T346648-10mg
10mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$599.90
T346648-25mg
25mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$899.90
T346648-50mg
50mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$1,199.90

Basic Description

Synonyms 4310-35-4 (chloride) | AKOS040754253 | SR-01000838833 | TRIDIHEXETHYL IODIDE TRIDIHEXETHYL CHLORIDE | (3-Cyclohexyl-3-hydroxy-3-phenylpropyl)triethylammonium chloride | Pathilon (TN) | DTXCID103701 | Tridihexethyl (Chloride) | AMMONIUM, (3-CYCLOHEXYL-3-HY
Specifications & Purity ≥96%
Storage Temp Store at 2-8°C,Protected from light,Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Action Type ANTAGONIST
Mechanism of action Muscarinic acetylcholine receptor M1 antagonist
Product Description

Tridihexethyl (Pathilon) chloride is an orally active anticholinergic agent and mAChR antagonist, shows activities of antimuscarinic and anticholinergic. Tridihexethyl chloride shows pronounced antispasmodic and antisecretory effects on the gastrointestinal tract. Tridihexethyl chloride can be used in studies of peptic ulcer disease and acquired nystagmus.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic nitrogen compounds
Class Organonitrogen compounds
Subclass Amines
Intermediate Tree Nodes Not available
Direct Parent Aralkylamines
Alternative Parents Benzene and substituted derivatives  Tetraalkylammonium salts  Tertiary alcohols  1,3-aminoalcohols  Organopnictogen compounds  Organic zwitterions  Organic chloride salts  Hydrocarbon derivatives  Aromatic alcohols  
Molecular Framework Aromatic homomonocyclic compounds
Substituents Aralkylamine - Monocyclic benzene moiety - Benzenoid - 1,3-aminoalcohol - Tetraalkylammonium salt - Quaternary ammonium salt - Tertiary alcohol - Organic oxygen compound - Organic salt - Organic zwitterion - Aromatic alcohol - Organic chloride salt - Hydrocarbon derivative - Organooxygen compound - Organopnictogen compound - Alcohol - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as aralkylamines. These are alkylamines in which the alkyl group is substituted at one carbon atom by an aromatic hydrocarbyl group.
External Descriptors organic chloride salt

Associated Targets(Human)

TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

ampC Beta-lactamase AmpC (62480 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name (3-cyclohexyl-3-hydroxy-3-phenylpropyl)-triethylazanium;chloride
INCHI InChI=1S/C21H36NO.ClH/c1-4-22(5-2,6-3)18-17-21(23,19-13-9-7-10-14-19)20-15-11-8-12-16-20;/h7,9-10,13-14,20,23H,4-6,8,11-12,15-18H2,1-3H3;1H/q+1;/p-1
InChIKey XJGONMZLEDGBRM-UHFFFAOYSA-M
Smiles CC[N+](CC)(CC)CCC(C1CCCCC1)(C2=CC=CC=C2)O.[Cl-]
Isomeric SMILES CC[N+](CC)(CC)CCC(C1CCCCC1)(C2=CC=CC=C2)O.[Cl-]
PubChem CID 20298
Molecular Weight 353.97

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

Sensitivity Light sensitive
Molecular Weight 354.000 g/mol
XLogP3
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 8
Exact Mass 353.249 Da
Monoisotopic Mass 353.249 Da
Topological Polar Surface Area 20.200 Ų
Heavy Atom Count 24
Formal Charge 0
Complexity 318.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 1
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 2

Solution Calculators

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