28624-66-0 Usage
Uses
Used in Pharmaceutical Research:
(1S)-7α-Vinyl-1,2,3,4,4a,5,6,7,8,9,10,10aα-dodecahydro-2β-hydroxy-1,4aβ,7-trimethyl-1β-phenanthrenemethanol is used as a compound of interest in pharmaceutical research for its potential biological activity. The unique structure of this molecule may offer new avenues for the development of therapeutic agents, particularly given its phenanthrene ring and hydroxyl group, which are common features in bioactive molecules.
Used in Biochemical Studies:
In biochemical studies, (1S)-7α-Vinyl-1,2,3,4,4a,5,6,7,8,9,10,10aα-dodecahydro-2β-hydroxy-1,4aβ,7-trimethyl-1β-phenanthrenemethanol serves as a subject for investigation into its interactions with biological systems. Understanding how (1S)-7α-Vinyl-1,2,3,4,4a,5,6,7,8,9,10,10aα-dodecahydro-2β-hydroxy-1,4aβ,7-trimethyl-1β-phenanthrenemethanol engages with cellular components could provide insights into its potential applications in medicine and other biological applications.
Used in Organic Synthesis:
(1S)-7α-Vinyl-1,2,3,4,4a,5,6,7,8,9,10,10aα-dodecahydro-2β-hydroxy-1,4aβ,7-trimethyl-1β-phenanthrenemethanol is utilized in organic synthesis as a building block for the creation of more complex molecules. Its vinyl group at the 7α position may allow for further chemical reactions, making it a valuable component in the synthesis of novel organic compounds with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 28624-66-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,6,2 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 28624-66:
(7*2)+(6*8)+(5*6)+(4*2)+(3*4)+(2*6)+(1*6)=130
130 % 10 = 0
So 28624-66-0 is a valid CAS Registry Number.
28624-66-0Relevant academic research and scientific papers
Afiyatullov, Shamil Sh.,Kalinovsky, Anatoly I.,Kuznetsova, Tatyana A.,Isakov, Vladimir V.,Pivkin, Mikhail V.,Dmitrenok, Pavel S.,Elyakov, George B.
, p. 641 - 644 (2002)
Three new diterpene glycosides, virescenosides O (1), P (2), and Q (3), have been isolated from a marine strain of Acremonium striatisporum KMM 4401 associated with the holothurian Eupentactafraudatrix. Their structures were determined on the basis of HRMALDIMS and NMR data as β-D-altropyranosido-19-isopimara-8(14),15-diene-7α,3β-diol (1), β-D-altropyranosido-19-7-oxoisopimara-8(9),15-diene-3β-ol (2), and β-D-mannopyranosido-19-isopimara-7,15-diene-3β-ol (3). The cytotoxic activity of the virescenosides was examined.
New diterpenic altrosides of the fungus Acremonium striatisporum isolated from a sea cucumber
Afiyatullov, Shamil Sh.,Kuznetsova, Tatyana A.,Isakov, Vladimir V.,Pivkin, Mikhail V.,Prokofeva, Nina G.,Elyakov, George B.
, p. 848 - 850 (2007/10/03)
Two new diterpenic glycosides, virescenosides M (1) and N (2), have been isolated from a marine strain of Acremonium striatisporum KMM 4401 associated with the holothurian Eupentacta fraudatrix. Their structures were determined on the basis of MS and NMR data as β-D-altropyranosido-19-7-oxo-isopimara- 8,15-diene-2α,3β-diol (1) and β-D-altropyranosido-19-isopimara-7,15-diene- 2α,3β,6β-triol (2). Three other altrosides (3-5), identified as virescenosides A, B, and C from the terrestrial strain Acremonium luzulae, were also isolated. The cytotoxic activity of the virescenosides was examined.
