CAS 124027-47-0
:1-Acridinol,9-amino-1,2,3,4-tetrahydro-
Description:
1-Acridinol, 9-amino-1,2,3,4-tetrahydro- is a chemical compound characterized by its structure, which includes an acridine core modified with a hydroxyl group and an amino group. This compound is part of a class of heterocyclic organic compounds known for their diverse biological activities. The presence of the hydroxyl (-OH) and amino (-NH2) functional groups suggests potential for hydrogen bonding, which can influence its solubility and reactivity. Typically, such compounds may exhibit properties like antimicrobial, antitumor, or anti-inflammatory activities, making them of interest in medicinal chemistry. The tetrahydro configuration indicates that the compound is saturated, which can affect its stability and interaction with biological targets. Additionally, the molecular weight and specific stereochemistry can play crucial roles in determining its pharmacokinetic and pharmacodynamic profiles. Overall, 1-Acridinol, 9-amino-1,2,3,4-tetrahydro- represents a unique structure that may have significant implications in pharmaceutical research and development.
Formula:C13H14N2O
InChI:InChI=1S/C13H14N2O/c14-13-8-4-1-2-5-9(8)15-10-6-3-7-11(16)12(10)13/h1-2,4-5,11,16H,3,6-7H2,(H2,14,15)
InChI key:InChIKey=HLVVITIHAZBPKB-UHFFFAOYSA-N
SMILES:NC1=C2C(=NC=3C1=CC=CC3)CCCC2O
Synonyms:- (?à)-9-Amino-1,2,3,4-tetrahydroacridin-1-ol
- 1-Hydroxytacrine
- 9-Amino-1,2,3,4-tetrahydro-1-acridinol
- 9-Amino-1,2,3,4-tetrahydroacridin-1-ol
- Hydroxytacrine
- Velnacrine
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Found 6 products.
1-Acridinol, 9-amino-1,2,3,4-tetrahydro-
CAS:Formula:C13H14N2OPurity:95%Color and Shape:SolidMolecular weight:214.2631Velnacrine
CAS:<p>Velnacrine (1,2,3,4-tetrahydro-9-aminoacridin-1-ol maleate) is a biochemical.</p>Formula:C13H14N2OPurity:99.83%Color and Shape:SolidMolecular weight:214.26Velnacrine
CAS:<p>Velnacrine is a reversible monoamine oxidase B (MAO-B) inhibitor, which is a synthetic compound derived from acridine. Its mode of action involves inhibiting the enzyme MAO-B, which is responsible for the breakdown of monoamines in the central nervous system. This inhibition leads to increased levels of monoamines, such as dopamine, which are crucial for cognitive and motor function.</p>Formula:C13H14N2OPurity:Min. 95%Molecular weight:214.26 g/mol






