CAS 1169805-98-4

Kaurane-7,16,17-triol,17-(3-methyl-2-butenoate), (7b)-

Description:

Kaurane-7,16,17-triol, 17-(3-methyl-2-butenoate), also known by its CAS number 1169805-98-4, is a chemical compound belonging to the class of kaurane diterpenoids, which are derived from the kaurene skeleton. This compound features multiple hydroxyl groups, indicating its potential for hydrogen bonding and solubility in polar solvents. The presence of the 3-methyl-2-butenoate moiety suggests that it may exhibit unique reactivity and properties associated with ester functionalities. Kaurane derivatives are often studied for their biological activities, including potential anti-inflammatory and anti-cancer properties. The structural complexity of this compound, characterized by its specific stereochemistry and functional groups, may influence its interactions with biological targets. As with many natural products, the synthesis and extraction of kaurane derivatives can be challenging, making their study significant in both synthetic and medicinal chemistry. Further research may elucidate its pharmacological potential and applications in various fields, including pharmaceuticals and agrochemicals.

Formula: C₂₅H₄₀O₄

Synonyms:

• SculponeatinN

Sculponeatin N

CAS: 1169805-98-4

Formula: C₂₅H₄₀O₄

Purity: 97.5%

Molecular weight: 404.5827

Ref: IN-DA008YCN

Sculponeatin N

CAS: 1169805-98-4

Sculponeatin N

Purity: ≥95%

Molecular weight: 404.58g/mol

Ref: 54-BUP22058

Sculponeatin N

CAS: 1169805-98-4

Formula: C₂₅H₄₀O₄

Purity: 95%~99%

Color and Shape: Powder

Molecular weight: 404.591

Ref: BP-SBP00126

Sculponeatin N

CAS: 1169805-98-4

Sculponeatin N may have protective effects on the lipid peroxidation-damaged live cells.

Formula: C₂₅H₄₀O₄

Purity: 97.00%

Color and Shape: Solid

Molecular weight: 404.58

Ref: TM-TN4972

Sculponeatin N

CAS: 1169805-98-4

Sculponeatin N is a hypothetical biochemical compound, which is theorized to be synthesized from marine microorganisms. The source of this compound is potentially derived through a biosynthetic process involving unique metabolic pathways present in specific oceanic bacteria. The mode of action of Sculponeatin N is proposed to involve the inhibition of specific enzymatic activities, disrupting targeted metabolic cycles by interfering with enzyme-substrate interactions at a molecular level.

Formula: C₂₅H₄₀O₄

Purity: Min. 95%

Molecular weight: 404.6 g/mol

Ref: 3D-UWB80598