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Acetic acid (1S,2R,3R)-3,4-diacetoxy-1-[(R)-acetoxy-(2-benzyloxycarbonylamino-ethylcarbamoyl)-methyl]-2-((2R,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

126829-56-9

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126829-56-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126829-56-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,8,2 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 126829-56:
(8*1)+(7*2)+(6*6)+(5*8)+(4*2)+(3*9)+(2*5)+(1*6)=149
149 % 10 = 9
So 126829-56-9 is a valid CAS Registry Number.

126829-56-9Downstream Products

126829-56-9Relevant academic research and scientific papers

Interaction of α-helical glycopeptides with lipid bilayer membrane

Otoda,Kimura,Imanishi

, p. 489 - 496 (2007/10/02)

α-Helical polypeptides having a glyco moiety at one end and a fluorescent probe at the other were prepared and investigated on the interaction with a lipid bilayer membrane. A glycopeptide composed of poly(alanine) and maltose was incorporated into the lipid membrane with the glyco moiety exposed to the aqueous phase and the peptide chain buried in membrane above the phase-transition temperature of the lipid membrane. However, below the phase-transition temperature, the glycopeptide induced the aggregation of dimyristoyl-phosphatidylcholine (DMPC) small unilamellar vesicles (SUV). Another glycopeptide composed of poly(γ-benzyl glutamate) and glucose also induced the aggregation of DMPC SUV, indicating that such the hydrophobic peptide tends to disturb the membrane structure significantly upon binding. The arrangement of the glycopeptide in a membrane was investigated by using a fluorescent probe connected to the end of the peptide chain. The terminal region of the peptide chain was located at the hydrophobic core of lipid membrane. However, the glycopeptide composed of 25 Ala residues had a smaller fraction taking perpendicular orientation to the membrane than that composed of 15 Ala residues. It was therefore considered that a part of the former glycopeptide molecules exists on the membrane surface, forming aggregates.

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