A selective inhibitor of the 20S proteasome
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Lactacystin

Item No. 70980

Technical Information
Formal Name
3S-hydroxy-2R-(1-hydroxy-2-methylpropyl)-4R-methyl-5-oxo-2-pyrrolidinecarboxylate-N-acetyl-L-cysteine
CAS Number
133343-34-7
Molecular Formula
C15H24N2O7S
Formula Weight
Purity
≥95%
Formulation
A clear film
DMF: 20 mg/mlDMSO: 20 mg/mlEthanol: 1 mg/mlMethanol: 1 mg/mlPBS (7.2): 2 mg/mlWater: 10 mg/ml
SMILES
O=C(SC[C@@H](C(O)=O)N(C(C)=O)[H])[C@@]1(N([H])C([C@H](C)[C@@H]1O)=O)[C@H](C(C)C)O
InChi Code
InChI=1S/C15H24N2O7S/c1-6(2)10(19)15(11(20)7(3)12(21)17-15)14(24)25-5-9(13(22)23)16-8(4)18/h6-7,9-11,19-20H,5H2,1-4H3,(H,16,18)(H,17,21)(H,22,23)/t7-,9?,10+,11+,15-/m1/s1
InChi Key
DAQAKHDKYAWHCG-MJZHQVMOSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Lactacystin is a microbial metabolite isolated from Streptomyces that is now widely used as a selective inhibitor of the 20S proteasome.1,2,3 Lactacystin was first characterized by its ability to induce differentiation and inhibit cell cycle progression in several tumor cell lines. At concentrations from 2 to 10 µM, lactacystin induces the outgrowth of neurites in the neuroblastoma cell line Neuro2a.4 Lactacystin irreversibly alkylates subunit X of the 20S proteasome.3 The concomitant inhibition of proteasome peptidase activity results in the accumulation of a variety of ubiquitinated proteins which would normally undergo rapid degradation. Thus, the effects of lactacystin are pleiotropic and depend substantially on the expression pattern of signalling proteins within the treated cell.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Omura, S., Fujimoto, T.T., Otoguro, K., et alLactacystin, a novel microbial metabolite, induces neuritogenesis of neuroblastoma cells. J. Antibiot. (Tokyo) 44, 113-116 (1991).

    2. Corey, E.J., and Reichard, G.A. Total synthesis of lactacystin. J. Am. Chem. Soc. 114, 10677-10678 (1992).

    3. Fenteany, G., and Schreiber, S.L. Lactacystin, proteasome function, and cell fate. The Journal of Biological Chemisty 273(15), 8545-8548 (1998).

    4. Fenteany, G., Standaert, R.F., Reichard, G.A., et alA β-lactone related to lactacystin induces neurite outgrowth in a neuroblastoma cell line and inhibits cell cycle progression in an osteosarcoma cell line. Proc. Natl. Acad. Sci. USA 91, 3358-3362 (1994).