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(2S,3R,4R,5S,6R)-6-Benzyloxycarbonyloxymethyl-5-(diphenoxy-phosphoryloxy)-3-tetradecanoylamino-4-((R)-3-tetradecanoyloxy-tetradecanoyloxy)-tetrahydro-pyran-2-carboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

183479-79-0

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183479-79-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 183479-79-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,4,7 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 183479-79:
(8*1)+(7*8)+(6*3)+(5*4)+(4*7)+(3*9)+(2*7)+(1*9)=180
180 % 10 = 0
So 183479-79-0 is a valid CAS Registry Number.

183479-79-0Upstream product

183479-79-0Relevant academic research and scientific papers

Syntheses of 2,6-anhydro-3-deoxy-5-O-phosphono-3-tetradecanamido-4-O- [(R)-3-(tetradecanoyloxy)tetradecanoyl]-D-glycero-D-ido-heptonic acid, its dimeric analogue, and related compounds

Shiozaki, Masao,Kurakata, Shin-Ichi,Tatsuta, Tohru,Maeda, Hiroaki,Nishijima, Masahiro

, p. 16041 - 16060 (2007/10/03)

Pyran carboxylic acid analogues of GLA-60 (12a, 12b, and 17) and their dimeric analogues (21 and 24) were synthesized in a stereocontrolled manner. Compounds 12a and 17 showed endotoxin antagonistic activity toward human monoblastic U937 cells as an index of the inhibition of LPS-induced TNFα production. Compounds 12b and 24 were less active than 12a and 17, Dimeric ester 21 was practically inactive.

Synthesis of 2,6-anhydro-3-deoxy-5-O-phosphono-3-tetradecanamido-4-O-[(R)-3-(tetrad ecanoyloxy)tetradecanoyl]-D-glycero-D-ido-heptonic acid as a new potent endotoxin antagonist and its dimeric analogue

Shiozaki, Masao,Mochizuki, Takashi,Wakabayashi, Takanori,Kurakata, Shin-Ichi,Tatsuta, Tohru,Nishijima, Masahiro

, p. 7271 - 7274 (2007/10/03)

A pyran carboxylic acid analogue of GLA-60 (14) and its dimeric analogue 18 were synthesized in a stereocontrolled manner. Compound 14 showed strong LPS-antagonistic activity.

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