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  • (2R)-6-acetamido-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}hexanoic acid

    Cas No: 320410-22-8

  • USD $ 1.9-2.9 / Gram

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  • 320410-22-8 Structure
  • Basic information

    1. Product Name: D-Nα-Fmoc-AcK
    2. Synonyms: D-Nα-Fmoc-AcK
    3. CAS NO:320410-22-8
    4. Molecular Formula:
    5. Molecular Weight: 410.47
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 320410-22-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 709.4±60.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: 1.239±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: D-Nα-Fmoc-AcK(CAS DataBase Reference)
    10. NIST Chemistry Reference: D-Nα-Fmoc-AcK(320410-22-8)
    11. EPA Substance Registry System: D-Nα-Fmoc-AcK(320410-22-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 320410-22-8(Hazardous Substances Data)

320410-22-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 320410-22-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,0,4,1 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 320410-22:
(8*3)+(7*2)+(6*0)+(5*4)+(4*1)+(3*0)+(2*2)+(1*2)=68
68 % 10 = 8
So 320410-22-8 is a valid CAS Registry Number.

320410-22-8Downstream Products

320410-22-8Relevant articles and documents

Substrate specificity of SIRT1-catalyzed lysine Nε-deacetylation reaction probed with the side chain modified Nε-acetyl-lysine analogs

Jamonnak, Nuttara,Hirsch, Brett M.,Pang, Yi,Zheng, Weiping

, p. 17 - 25 (2010)

Peptides containing l-Nε-acetyl-lysine (l-AcK) or its side chain modified analogs were prepared and assayed using SIRT1, the prototypical human silent information regulator 2 (Sir2) enzyme. While previous studies showed that the side chain acetyl group of l-AcK can be extended to bulkier acyl groups for Sir2 (including SIRT1)-catalyzed lysine Nε-deacylation reaction, our current study suggested that SIRT1-catalyzed deacetylation reaction had a very stringent requirement for the distance between the α-carbon and the side chain acetamido group, with that found in l-AcK being optimal. Moreover, our current study showed that SIRT1 catalyzed the stereospecific deacetylation of l-AcK versus its d-isomer. The results from our current study shall constitute another piece of important information to be considered when designing inhibitors for SIRT1 and Sir2 enzymes in general.

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