Thermo Scientific Chemicals

Tunicamycin, 95%, Thermo Scientific Chemicals

Catalog number: J62217.MA
10 mg, Each
Thermo Scientific Chemicals

Tunicamycin, 95%, Thermo Scientific Chemicals

Catalog number: J62217.MA
10 mg, Each
Quantity
Informational:Informational:This chemical may require us to obtain additional information for our regulatory and chemical compliance records. If required, we will contact you for this information once your order is placed.
Catalog number: J62217.MA
also known as J62217-MA
Price (EUR)
Price: 217,00
Online price: 195,30
Your price:
Quantity
-

Chemical Identifiers

CAS
11089-65-9
IUPAC Name
(2E)-N-[(2R,3R,4R,5R,6R)-6-{2-[(2R,3S,4R,5R)-5-(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl}-2-{[(2R,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4,5-dihydroxyoxan-3-yl]-5-methylhex-2-enamide
Molecular Formula
C30H46N4O16
InChI Key
ZHSGGJXRNHWHRS-PEALBESXSA-N
SMILES
CC(C)C\C=C\C(=O)N[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CC(O)[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=CC(=O)NC2=O)O[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1NC(C)=O
Assay from Suppliers CofA
≥94.0%
Form
Powder

Description

Tunicamycin has been widely used in the study of glycoprotein synthesis in various biological systems. During protein glycosylation, tunicamycin is noted to be an inhibitor of the transfer of saccharide moieties to dolichol during dolichol-linked glycoprotein synthesis. Dose-dependent inhibition of DNA synthesis may be related to the alteration of glycoproteins, which thereby affects the transport of thymidine into cells. Additionally, tunicamycin has been reported to prevent cell cycle progression in primary cultures of rat glial cells, as well as inhibit lipid-mediated protein glycosylation in chick or mouse fibroblasts in a dose-dependent manner.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Tunicamycin has been widely used in the study of glycoprotein synthesis in various biological systems. During protein glycosylation, tunicamycin is noted to be an inhibitor of the transfer of saccharide moieties to dolichol during d
RUO – Research Use Only

Figures

Documents & Downloads

Certificates

    Frequently asked questions (FAQs)

    Citations & References

    Search citations by name, author, journal title or abstract text

    Safety and Handling


    Classification of the substance or mixture
    CLP classification - Regulation(EC) No 1272/2008
    Acute oral toxicity
    Category 2
    Acute Inhalation Toxicity - Dusts and Mists
    Category 1
    Specific target organ toxicity - (repeated exposure)
    Category 2
    Label Elements
    Signal Word

    Danger

    Hazard Statements

    H300 + H330 - Fatal if swallowed or if inhaled

    H373 - May cause damage to organs through prolonged or repeated exposure

    Precautionary Statements

    P260 - Do not breathe dust/fume/gas/mist/vapors/spray

    P264 - Wash face, hands and any exposed skin thoroughly after handling

    P304 + P340 - IF INHALED: Remove person to fresh air and keep comfortable for breathing

    P310 - Immediately call a POISON CENTER or doctor/physician

    P330 - Rinse mouth

    P403 + P233 - Store in a well-ventilated place. Keep container tightly closed