Stigmastane-3,6-diol
Stigmastane-3 beta, 6 alpha-diol and stigmastane-3 beta, 6 beta-diol possess marked inhibitory activity against 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced
inflammation in mice, the 50% inhibitory dose is 0.5--1.0 mg/ear.
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Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to
24 months(2-8C).
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.
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The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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European Journal of Integrative Medicine2018, 20:165-172
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Biol Pharm Bull. 1995 Nov;18(11):1617-9.
Inhibitory effect of some oxygenated stigmastane-type sterols on 12-O-tetradecanoylphorbol-13-acetate-induced inflammation in mice.[Pubmed:
8593493]
METHODS AND RESULTS:
The oxygenated stigmastane-type sterols stigmastane-3 beta, 6 alpha-diol(Stigmastane-3,6-diol), stigmastane-3 beta, 6 beta-diol, 7 alpha-hydroxysitosterol and its diacetyl derivative, 7 beta-hydroxysitosterol and its diacetyl derivative, 7-oxositosterol, 4 beta-hydroxysitosterol, and stigmast-4-ene-3 beta, 6 beta-diol were evaluated with respect to their anti-inflammatory activity against 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced inflammation in mice.
CONCLUSIONS:
All of the sterols, with the exception of 7 alpha-hydroxysitosterol and its diacetyl derivative, were found to possess marked inhibitory activity. The 50% inhibitory dose of these compounds for TPA-inflammation (1 microgram) was 0.5--1.0 mg/ear.
Planta Med 2008; 74 - P-101
Chemical Studies of Casearia sylvestris Swartz[Reference:
WebLink]
METHODS AND RESULTS:
In the present report, the isolation and structure elucidation of two new highly oxygenated clerodane diterpenes casearins U and V (1 and 2) and two new ent -kauranoid diterpene glycosides sylvestriside A and B (3 and 4) were described from C. sylvestris (see Fig. 1), together with 3 known diterpenes, namely, (−)-hardwickic acid (5), (−)-patagonic acid (6) and ent-3β, 18-dihydroxykaur-16-ene (7), as well as 11 other known compounds, namely, spathulenol (8), 7, 8-dihydrovomifoliol (blumenol B 9), N-methyl-trans-4-hydroxy-L-proline (10), Cinnamic acid (11), Soyacerebroside I (12), methypheophorbides (13), pheophorbide a (14), chlorophyll (15), β-sitosterol (16), Stigmastane-3,6-diol (17), daucosterol (18), β-D-glucopyranoside, (3β)-stigmast-5-en-3-yl, 6-nonadecanoate (19).
