CAS 223445-75-8

((3S,4S)-1-Aminomethyl-3,4-dimethylcyclopentyl)acetic acid

Description:

((3S,4S)-1-Aminomethyl-3,4-dimethylcyclopentyl)acetic acid, with the CAS number 223445-75-8, is a chiral compound characterized by its cyclopentane structure, which features a side chain containing an amino group and a carboxylic acid functional group. This compound exhibits properties typical of amino acids, including the ability to participate in hydrogen bonding due to the presence of both the amino and carboxylic acid groups. Its stereochemistry, indicated by the (3S,4S) configuration, suggests that it has specific spatial arrangements that can influence its biological activity and interactions with other molecules. The presence of methyl groups on the cyclopentane ring contributes to its hydrophobic characteristics, which may affect its solubility and reactivity in various solvents. This compound may have potential applications in pharmaceuticals or as a building block in organic synthesis, particularly in the development of biologically active molecules. However, detailed studies on its specific properties, reactivity, and applications would be necessary for a comprehensive understanding.

Formula: C₁₀H₁₉NO₂

InChI: InChI=1S/C10H19NO2/c1-7-3-10(6-11,4-8(7)2)5-9(12)13/h7-8H,3-6,11H2,1-2H3,(H,12,13)/t7-,8-/m0/s1

InChI key: InChIKey=IUVMAUQEZFTTFB-YUMQZZPRSA-N

SMILES: C(C(O)=O)[C@]1(CN)C[C@H](C)[C@@H](C)C1

Synonyms:

• ((3S,4S)-1-Aminomethyl-3,4-dimethylcyclopentyl)aceticacid
• Atagabalin
• Cyclopentaneacetic acid, 1-(aminomethyl)-3,4-dimethyl-, (3S,4S)-
• PD 0200390
• Atagabalin
• PD 0200390
• ((3S,4S)-1-Aminomethyl-3,4-dimethylcyclopentyl)acetic acid
• (3S,4S)-1-(Aminomethyl)-3,4-dimethylcyclopentaneacetic acid

Atagabalin

CAS: 223445-75-8

Atagabalin (PD 0200390), a gabamimetic for insomnia treatment and related to gabapentin, was halted due to poor trial outcomes.

Formula: C₁₀H₁₉NO₂

Color and Shape: Solid

Molecular weight: 185.26

Ref: TM-T30188

Atagabalin

CAS: 223445-75-8

Atagabalin is a novel pharmaceutical compound, which is derived from marine biological sources. Its primary mode of action involves the inhibition of the alpha-2-delta subunit of voltage-gated calcium channels. This mechanism modulates synaptic transmission, leading to reduced neuronal excitability.

Formula: C₁₀H₁₉NO₂

Purity: Min. 95%

Molecular weight: 185.26 g/mol

Ref: 3D-YIA44575