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Benzaldehyde, 3-bromo-2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-4,5-dimethoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

905291-15-8

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905291-15-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 905291-15-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,5,2,9 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 905291-15:
(8*9)+(7*0)+(6*5)+(5*2)+(4*9)+(3*1)+(2*1)+(1*5)=158
158 % 10 = 8
So 905291-15-8 is a valid CAS Registry Number.

905291-15-8Relevant academic research and scientific papers

Synthesis of phosphatidylinositol 3-kinase (PI3K) inhibitory analogues of the sponge meroterpenoid liphagal

Pereira, Alban R.,Strangman, Wendy K.,Marion, Frederic,Feldberg, Larry,Roll, Deborah,Mallon, Robert,Hollander, Irwin,Andersen, Raymond J.

supporting information; experimental part, p. 8523 - 8533 (2011/02/26)

Analogues of the sponge meroterpenoid liphagal (1) have been synthesized and evaluated for inhibition of PI3Kα and PI3Kα as part of a program aimed at developing new isoform-selective PI3K inhibitors. One of the analogues, compound 24, with IC50/sub

Liphagal, a selective inhibitor of PI3 kinase α isolated from the sponge Aka coralliphaga: Structure elucidation and biomimetic synthesis

Marion, Frederic,Williams, David E.,Patrick, Brian O.,Hollander, Irwin,Mallon, Robert,Kim, Steven C.,Roll, Deborah M.,Feldberg, Larry,Van Soest, Rob,Andersen, Raymond J.

, p. 321 - 324 (2007/10/03)

Liphagal (1), a selective inhibitor of PI3K α, has been isolated from the marine sponge Aka coralliphaga collected in Dominica. The "liphagane" meroterpenoid carbon skeleton of liphagal (1) is new. A biomimetic total synthesis has been used to confirm the

MEROTERPENOID INHIBITORS OF PHOSPHOINOSITIDE 3 KINASE (PI3K)

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Page/Page column 29-32; 41-42, (2008/06/13)

Compounds with unique liphagane meroterpenoid carbon skeleton are described (structures I, II, III) together with pharmaceutical compositions and their use. A method of inhibiting the activity of phosphoinositide 3 kinase (PBK) is disclosed. In particular

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