1058-61-3 Usage
Uses
Used in Pharmaceutical Industry:
B-Sitostenone is used as a medicinal compound for its anti-inflammatory and anti-cancer effects. It modulates various biological pathways, contributing to the inhibition of tumor growth and progression, as well as reducing inflammation in the body.
Used in Nutrition Industry:
B-Sitostenone is used as a dietary supplement for its cholesterol-lowering properties. It helps in maintaining healthy cholesterol levels, which is essential for cardiovascular health.
Used in Cosmetic Industry:
B-Sitostenone is used as an active ingredient in hair care products for its hair growth-promoting properties. It stimulates hair follicle activity, leading to increased hair growth and reduced hair loss.
Used in Men's Health Industry:
B-Sitostenone is used as a therapeutic agent for reducing prostate enlargement. It helps in alleviating symptoms associated with benign prostatic hyperplasia (BPH) and improving overall prostate health.
Check Digit Verification of cas no
The CAS Registry Mumber 1058-61-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,5 and 8 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1058-61:
(6*1)+(5*0)+(4*5)+(3*8)+(2*6)+(1*1)=63
63 % 10 = 3
So 1058-61-3 is a valid CAS Registry Number.
InChI:InChI=1/C29H48O/c1-7-21(19(2)3)9-8-20(4)25-12-13-26-24-11-10-22-18-23(30)14-16-28(22,5)27(24)15-17-29(25,26)6/h18-21,24-27H,7-17H2,1-6H3/t20-,21-,24+,25-,26+,27+,28+,29-/m1/s1
1058-61-3Relevant academic research and scientific papers
Chemical Constituents of Piper betle Linn. (Piperaceae) roots
Ghosh, K.,Bhattacharya, T. K.
, p. 782 - 786 (2007/10/03)
Column chromatography of the alcoholic extract of Piper betle roots furnished aristololactam A-II and a new phenyl propene, characterized as 4-allyl resorcinol, while the petroleum-ether extract yielded a diketosteroid, viz. stigmast-4-en-3,6-dione. All these compounds were characterized by spectroscopic means. Isolation of these compounds from this source is being reported here for the first time.
Stereospecific oxidation of 3β-hydroxysteroids by persolvent fermentation with Pseudomonas sp. ST-200
Aono, Rikizo,Doukyu, Noriyuki
, p. 1146 - 1151 (2007/10/03)
Pseudomonas sp. strain ST-200 isolated from a humus soil effectively oxidizes cholesterol dissolved in organic solvents but not that suspended in the growth medium. The organism does not assimilate cholesterol. This organism oxidized a variety of 5α- or 5-ene-steroids dissolved in organic solvent. First, the 3β-OH group was oxidized to a ketone group. The 3α-OH group was scarcely oxidized. Successively, C-6 position of 5-ene-steroids was hydroxylated, and a double bond of 5-ene-steroids was transferred from Δ5 to Δ4. Then, the 6-OH group was oxidized to a ketone group. Persolvent fermentation with ST-200 would provide an effective, convenient, and stereospecific method to oxidize the C-3 and C-6 positions of steroids.
