17094-86-9 Usage
Description
(22R,25R)-Spirosol-4-en-3-one is a natural compound found in the dried leaves and roots of Solanum lainanense. It is an alkaloid that crystallizes as colorless rods from ethanol. (22R,25R)-Spirosol-4-en-3-one has demonstrated effectiveness against various bacterial strains, including Bacillus subtilis, B. globifer, and Staphylococcus aureus, with a limiting concentration of 50 g/mL.
Uses
Used in Pharmaceutical Industry:
(22R,25R)-Spirosol-4-en-3-one is used as an antimicrobial agent for its effectiveness against Bacillus subtilis, B. globifer, and Staphylococcus aureus. Its ability to inhibit the growth of these bacteria makes it a potential candidate for the development of new antibiotics to combat drug-resistant infections.
Used in Research and Development:
(22R,25R)-Spirosol-4-en-3-one can be used as a research compound to study its antimicrobial properties and explore its potential applications in the development of new drugs and therapies. Further research may reveal additional benefits and uses for this compound in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 17094-86-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,9 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17094-86:
(7*1)+(6*7)+(5*0)+(4*9)+(3*4)+(2*8)+(1*6)=119
119 % 10 = 9
So 17094-86-9 is a valid CAS Registry Number.
InChI:InChI=1/C27H41NO2/c1-16-7-12-27(28-15-16)17(2)24-23(30-27)14-22-20-6-5-18-13-19(29)8-10-25(18,3)21(20)9-11-26(22,24)4/h13,16-17,20-24,28H,5-12,14-15H2,1-4H3/t16-,17+,20-,21+,22+,23+,24+,25+,26+,27-/m1/s1
17094-86-9Relevant articles and documents
TRANSFORMATIONS OF SOLASODINE AND DERIVATIVES OF HECOGENIN BY CUNNINGHAMELLA ELEGANS
Patel, Asmita V.,Blunden, Gerald,Crabb, Trevor A.
, p. 125 - 134 (2007/10/02)
Incubation of (25R)-5α-spirostane-3β,12β-diol (rickogenin) with the fungus Cunninghamella elegans led to the formation of (25R)-7β,12β-dihydroxy-5α-spirostan-3-one, (25R)-5α-spirostan-3β,7β,12β-triol and (25R)-5α-spirostan-3β,7α,12α-triol.Incubation of (25R)-5α-spirostan-3,12-dione (hecogenone) with the same fungus gave rise to (25R)-5α-spirostan-3,7,12-trione.When the (22R,25R)-spirosolane, solasod-5-en-3β-ol (solasodine) was incubated with C. elegans, solasod-5-ene-3β,7β-diol, solasod-5-ene-3β,7α-diol and 3β-hydroxysolasod-5-en-7-one were produced.In contrast, incubation of solasodine with Penicillium patulum gave solasod-4-en-3-one and the 6-methylsalicylic acid salt of solasodine.
ACTIVE MANGANASE DIOXIDE: A REAGENT FOR A BIOMIMETIC CYCLIZATION OF 16β-HYDROXYLATED 22.26-EPIMINOCHOLESTANES TO SPIROSOLANE ALKALOIDS
Adam, G.,Huong, H. Th.
, p. 1931 - 1932 (2007/10/02)
Treatment of the 16β-hydroxylated 22.26-epiminocholestanes 1 - 4 with activated MnO2 leads in a biogenetically remarkable cyclization directly and in good yields to the corresponding spirosolane alkaloids 5 - 8.
