35761-54-7 Usage
Uses
Used in Pharmaceutical Applications:
(24S)-20,24-Epoxy-25-hydroxy-5α-dammaran-3-one is used as a bioactive compound for its potential anti-inflammatory, antitumor, and antimicrobial properties. Its ability to inhibit the growth of certain cancer cell lines and modulate various biological pathways makes it a candidate for the development of new therapeutic agents.
Used in Cancer Treatment:
In the field of oncology, (24S)-20,24-Epoxy-25-hydroxy-5α-dammaran-3-one is used as a potential antitumor agent, targeting the growth and proliferation of cancer cells. Its research indicates that it may be effective against a variety of cancer types, offering a new avenue for cancer treatment strategies.
Used in Osteoporosis Treatment:
(24S)-20,24-Epoxy-25-hydroxy-5α-dammaran-3-one is used as a therapeutic agent for osteoporosis, as it has been shown to stimulate osteoblast differentiation and inhibit osteoclast formation. This dual action makes it a promising candidate for the treatment and management of bone loss associated with osteoporosis.
Used in Agricultural Applications:
In agriculture, (24S)-20,24-Epoxy-25-hydroxy-5α-dammaran-3-one is used for its antimicrobial properties, potentially serving as a natural pesticide or fungicide to protect crops from various pathogens, thereby enhancing crop yield and quality.
Overall, (24S)-20,24-Epoxy-25-hydroxy-5α-dammaran-3-one's multifaceted pharmacological activities position it as a versatile compound with broad applications in medicine and agriculture, warranting further exploration and development.
Check Digit Verification of cas no
The CAS Registry Mumber 35761-54-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,7,6 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 35761-54:
(7*3)+(6*5)+(5*7)+(4*6)+(3*1)+(2*5)+(1*4)=127
127 % 10 = 7
So 35761-54-7 is a valid CAS Registry Number.
35761-54-7Relevant academic research and scientific papers
Dammarane Triterpenes of Trevoa trinervis: Structure and Absolute Stereochemistry of Trevoagenins A, B, and C
Betancor, Carmen,Freire, Raimundo,Hernandez, Rosendo,Suarez, Ernesto,Cortes, Manuel,et al.
, p. 1119 - 1126 (2007/10/02)
Trevoagenins A, B, and C, extracted from Trevoa trinervis Miers, are shown, by chemical and spectral means, to be isomeric dammarane triterpenes posessing the general 3β,25,30-trihydroxy-(20,24)-epoxydammaran-16-one structure with stereoisomeric side-chains of the ocotillol type.Trevoagenin A (20R,24R)-(1),, whose stereochemistry has been esteblished by chemical methods and confirmed by X-ray analysis, was transformed into (20R,24ξ)-ocotillone (26) and the C-24 stereochemistry was assigned as R.As a consequence, the C-24 stereochemistry for ocotillol-related compounds of the (20R)-series, unestablished so far, has been determined.The stereochemistry of trevoagenin B, (20S,24R)-(13), was established by chemical correlation with trevoagenin A.Moreover, trevoagenin B was transformed into ocotillol (20S,24R)-(21) and its recently questioned C-24 stereochemistry has been reaffirmed.Trevoagenin C, (20S,24S)-(17), is the C-24 isomer of trevoagenin B as shown by degradation of both compounds to the lactone (16).
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.
