CAS 1423809-64-6

Formule : C15H20O3

InChI : InChI=1S/C15H20O3/c1-8(2)15(18)12-5-10(4)13(16)7-11(12)9(3)6-14(15)17/h5,9,11-12,18H,1,6-7H2,2-4H3/t9-,11+,12+,15-/m1/s1

Code InChI : GMEQWOXALWTOIS-CKRXIKOQSA-N

SMILES : C[C@@H]1CC(=O)[C@]([C@@H]2[C@H]1CC(=O)C(=C2)C)(C(=C)C)O

7α-Hydroxy-4,11-cadinadiene-3,8-dione

CAS : 1423809-64-6

7alpha-Hydroxy-4,11-cadinadiene-3,8-dione is a natural product for research related to life sciences.

Formule : C₁₅H₂₀O₃

Degré de pureté : 98%

Couleur et forme : Solid

Masse moléculaire : 248.322

Ref: TM-TN3253

7α-Hydroxy-4,11-cadinadiene-3,8-dione

CAS : 1423809-64-6

Formule : C₁₅H₂₀O₃

Degré de pureté : 95%~99%

Masse moléculaire : 248.322

Ref: BP-SBP01664

(4aS,5R,8S,8aR)-5-Hydroxy-3,8-dimethyl-5-prop-1-en-2-yl-4a,7,8,8a-tetrahydro-1H-naphthalene-2,6-dione

CAS : 1423809-64-6

(4aS,5R,8S,8aR)-5-Hydroxy-3,8-dimethyl-5-prop-1-en-2-yl-4a,7,8,8a-tetrahydro-1H-naphthalene-2,6-dione is a naturally occurring sesquiterpene lactone, which is derived from certain species of plants such as Artemisia and Tanacetum. This compound exhibits a range of biological activities, primarily attributed to its ability to modulate various biochemical pathways through its reactive lactone moiety. The mechanism of action involves inhibition of key enzymes and interaction with cellular proteins, leading to antiproliferative, anti-inflammatory, and antimicrobial effects.

Formule : C₁₅H₂₀O₃

Degré de pureté : Min. 95%

Masse moléculaire : 248.32 g/mol

Ref: 3D-YGC80964