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7200-31-9

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7200-31-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7200-31-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,0 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7200-31:
(6*7)+(5*2)+(4*0)+(3*0)+(2*3)+(1*1)=59
59 % 10 = 9
So 7200-31-9 is a valid CAS Registry Number.

7200-31-9Relevant articles and documents

(S)-3′-methyl-abscisic acid and esters thereof

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Page/Page column 8-9, (2016/05/24)

The invention relates to (S)-3′-methyl-abscisic acid, and esters thereof, and methods of using and making these compounds.

(S)-2′-vinyl-abscisic acid derivatives

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Page/Page column 6, (2016/10/17)

The invention relates to a novel class of (S)-2′-vinyl-substituted-abscisic acid derivatives, and to methods of synthesizing and using the derivatives.

Synthesis, structural characterization and effect on human granulocyte intracellular cAMP levels of abscisic acid analogs

Bellotti, Marta,Salis, Annalisa,Grozio, Alessia,Damonte, Gianluca,Vigliarolo, Tiziana,Galatini, Andrea,Zocchi, Elena,Benatti, Umberto,Millo, Enrico

, p. 22 - 32 (2015/02/19)

The phytohormone abscisic acid (ABA), in addition to regulating physiological functions in plants, is also produced and released by several mammalian cell types, including human granulocytes, where it stimulates innate immune functions via an increase of the intracellular cAMP concentration ([cAMP]i). We synthesized several ABA analogs and evaluated the structure-activity relationship, by the systematical modification of selected regions of these analogs. The resulting molecules were tested for their ability to inhibit the ABA-induced increase of [cAMP]i in human granulocytes. The analogs with modified configurations at C-2′ and C-3′ abrogated the ABA-induced increase of the [cAMP]i and also inhibited several pro-inflammatory effects induced by exogenous ABA on granulocytes and monocytes. Accordingly, these analogs could be suitable as novel putative anti-inflammatory compounds.

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