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(4R,5S)-4,5-dihydroxy-(2E)-hexenoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

931426-07-2

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931426-07-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 931426-07-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,1,4,2 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 931426-07:
(8*9)+(7*3)+(6*1)+(5*4)+(4*2)+(3*6)+(2*0)+(1*7)=152
152 % 10 = 2
So 931426-07-2 is a valid CAS Registry Number.

931426-07-2Upstream product

931426-07-2Downstream Products

931426-07-2Relevant academic research and scientific papers

Absolute stereostructures of cell-adhesion inhibitors, macrosphelides C, E-G and I, produced by a Periconia species separated from an Aplysia sea hare

Yamada,Iritani,Doi,Minoura,Ito,Numata

, p. 3046 - 3053 (2001)

Macrosphelides E-I have been isolated, along with known macrosphelides A and C, from a strain of Periconia byssoides originally separated from the sea hare Aplysia kurodai, and the absolute stereostructures of macrosphelides E-G and I have been elucidated on the basis of spectroscopic analyses using 1D and 2D NMR techniques and some chemical transformations. In addition, the absolute configuration of macrosphelide C, previously undetermined, has been established by X-ray analysis and application of the modified Mosher method. Macrosphelides E-H inhibited the adhesion of human-leukaemia HL-60 cells to HUVEC.

Novel antitumour metabolites produced by a fungal strain from a sea hare

Numata, Atsushi,Iritani, Masashi,Yamada, Takeshi,Minoura, Katsuhiko,Matsumura, Eiko,Yamori, Takao,Tsuruo, Takashi

, p. 8215 - 8218 (2007/10/03)

Pericosines A (1) and B (2), and macrosphelides E - H (3 - 6) have been isolated, along with known macrosphelide C (7), from a strain of Periconia byssoides originally separated from the sea hare Aplysia kurodai, and their structures have been established on the basis of spectral analyses. Compounds 1 and 2 exhibited significant inhibitory activity in vitro against tumour cells, and the former also showed significant in vivo tumour-inhibitory activity.

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