CAS 77658-38-9

Kaur-16-en-18-oic acid,9-hydroxy-, (4a)-(9CI)

Description:

Kaur-16-en-18-oic acid, 9-hydroxy-, also known by its CAS number 77658-38-9, is a naturally occurring compound classified as a diterpenoid. This substance is characterized by its complex carbon skeleton, which includes a fused ring structure typical of many terpenes. The presence of a hydroxyl group at the 9-position contributes to its reactivity and potential biological activity. Kaur-16-en-18-oic acid is often studied for its role in plant physiology and its potential applications in pharmaceuticals, particularly due to its anti-inflammatory and anticancer properties. The compound is typically found in various plant species, where it may play a role in growth regulation and defense mechanisms. Its structural features, including the specific arrangement of carbon atoms and functional groups, influence its chemical behavior and interactions with biological systems. As research continues, the full scope of its applications and mechanisms of action is being explored, highlighting its significance in both natural product chemistry and medicinal research.

Formula: C₂₀H₃₀O₃

Synonyms:

• 1H-2,10a-Ethanophenanthrene,kaur-16-en-18-oic acid deriv.
• 9b-Hydroxy-ent-kaur-16-en-oic acid
• Pterokaurane L3

Pterokaurene L3

CAS: 77658-38-9

Formula: C₂₀H₃₀O₃

Molecular weight: 318.4504

Ref: IN-DA00G68I

Pterokaurene L3

CAS: 77658-38-9

Pterokaurene L3 is a natural product for research related to life sciences. The catalog number is TN4854 and the CAS number is 77658-38-9.

Formula: C₂₀H₃₀O₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 318.45

Ref: TM-TN4854

Pterokaurene L3

CAS: 77658-38-9

Formula: C₂₀H₃₀O₃

Purity: 95%~99%

Color and Shape: Powder

Molecular weight: 318.457

Ref: BP-SBP02370

Pterokaurene L3

CAS: 77658-38-9

Pterokaurene L3 is a diterpene compound, which is a natural product isolated from gymnosperms. It exhibits unique biosynthesis pathways typical of these plants, highlighting its evolutionary origins and biochemical significance. The compound functions primarily through its mode of action as an antifungal agent. It disrupts the growth and proliferation of fungal cells by interfering with key biochemical pathways vital for their survival. This mode of action suggests potential for applications in managing fungal infections in both clinical and agricultural settings.

Formula: C₂₀H₃₀O₃

Purity: Min. 95%

Molecular weight: 318.4 g/mol

Ref: 3D-CDA65838