19942-04-2 Usage
Uses
Used in Pharmaceutical Industry:
(20S,24S)-20,24-Epoxydammarane-3β,25-diol is used as a potential therapeutic agent for its anti-inflammatory, anti-tumour, and neuroprotective properties. It is being studied for its potential to modulate various biological pathways and provide health benefits in the treatment of different diseases.
Used in Alternative Medicine:
(20S,24S)-20,24-Epoxydammarane-3β,25-diol is used as an active ingredient in certain types of ginseng-based alternative remedies, where it is believed to contribute to the overall health-promoting effects of these traditional treatments.
Used in Research Applications:
(20S,24S)-20,24-Epoxydammarane-3β,25-diol is used as a subject of study in various scientific research projects, where its potential health benefits and mechanisms of action are being investigated to further understand its therapeutic potential and possible applications in medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 19942-04-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,4 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19942-04:
(7*1)+(6*9)+(5*9)+(4*4)+(3*2)+(2*0)+(1*4)=132
132 % 10 = 2
So 19942-04-2 is a valid CAS Registry Number.
InChI:InChI=1/C30H52O3/c1-25(2)21-12-17-29(7)22(27(21,5)15-13-23(25)31)10-9-19-20(11-16-28(19,29)6)30(8)18-14-24(33-30)26(3,4)32/h19-24,31-32H,9-18H2,1-8H3/t19-,20+,21+,22-,23+,24?,27+,28-,29-,30+/m1/s1
19942-04-2Relevant academic research and scientific papers
TRITERPENOIDS FROM THE LEAVES OF Betula lanata
Pokhilo, N. D.,Malinovskaya, G. V.,Makhan'kov, V. V.,Anufriev, V. F.,Uvarova, N. I.
, p. 368 - 372 (2007/10/02)
From the unsaponifiable fraction of an ethereal extract of the leaves of Betula lanata, in addition to 3-epiocotillol (I) we have isolated a new triterpene, 20(S),24(R)-epoxydammarane-3α,11α,25-triol (V) and also derivatives of it - the monoacetates at C-3 (II) and C-11 (III), and the monoketone at C-3 (IV).The structures of compounds (I-V) have been established on the basis of the results of physicochemical investigations.
