For research use only. Not for therapeutic Use.
3-Dehydrotrametenolic Acid(Cat No.:I018549)is a natural triterpenoid compound derived from mushrooms, particularly those in the Trametes genus. Known for its biological activities, it has been studied for its potential in metabolic health, showing promise in regulating glucose and lipid metabolism. 3-Dehydrotrametenolic acid is believed to stimulate adipocyte differentiation and improve insulin sensitivity, making it relevant in diabetes and obesity research. Additionally, its anti-inflammatory and anticancer properties contribute to its value in pharmaceutical research, particularly for developing therapies targeting metabolic disorders and related inflammatory conditions.
Catalog Number | I018549 |
CAS Number | 29220-16-4 |
Molecular Formula | C₃₀H₄₆O₃ |
Purity | ≥95% |
Storage | Sealed in dry,Room Temperature |
IUPAC Name | (2R)-2-[(3S,5R,10S,13R,14R,17R)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methylhept-5-enoic acid |
InChI | InChI=1S/C30H46O3/c1-19(2)9-8-10-20(26(32)33)21-13-17-30(7)23-11-12-24-27(3,4)25(31)15-16-28(24,5)22(23)14-18-29(21,30)6/h9,11,14,20-21,24-25,31H,8,10,12-13,15-18H2,1-7H3,(H,32,33)/t20-,21-,24+,25+,28-,29-,30+/m1/s1 |
InChIKey | QFPLAAZRZNKRRY-GIICLEHTSA-N |
SMILES | CC(=CCC[C@H]([C@H]1CC[C@@]2([C@@]1(CC=C3C2=CC[C@@H]4[C@@]3(CC[C@@H](C4(C)C)O)C)C)C)C(=O)O)C |
Reference | [1]. De Nicola GR, et al. Novel gram-scale production of enantiopure R-sulforaphane from Tuscan black kale seeds. Molecules. 2014 May 27;19(6):6975-86.<br>[2]. Abdull Razis AF, et al. The natural chemopreventive phytochemical R-sulforaphane is a far more potent inducer of the carcinogen-detoxifying enzyme systems in rat liver and lung than the S-isomer. Int J Cancer. 2011 Jun 15;128(12):2775-82. |