GeldanamycinGeldanamycin - High-quality laboratory reagent available from Gentaur. Catalog: 400-SIH-111A.400-SIH-111A400-SIH-111ABusiness & Industrial > Science & LaboratoryGeldanamycin
Gentaur
EUR12027-02-23

Geldanamycin

CAT:
400-SIH-111A
Size:
1 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
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Geldanamycin

  • Background:

    Glendanamycin (GA), a benzoquinone ansamycin antibiotic, interferes with the action of Hsp90 leading to degradation of Hsp90 client proteins. GA itself however has undesirable properties such as poor aqueous solubility and liver toxicity; therefore, numerous analogs have been synthesized, such as 17-AAG(1). 17-AAG is an HSP-90 inhibitor that displays a 100-fold higher affinity for HSP-90 derived from tumor cells compared to HSP-90 from normal cells(2). 17-AAG inhibits Akt activation and expression in tumors and synergizes with a number of antitumor agents such as taxol(3), cisplatin(4) and UCN-01 (400 nM 17-AAG, U937 cells)(5). Looking for more information on HSP90? Visit our new HSP90 Scientific Resource Guide at http://www.HSP90.ca.
  • Description:

    Hsp90 inhibitor
  • Product Name Alternative:

    (4E,6Z,8S,9S,10E,12S,13R,14S,16R) -13-hydroxy-8,14,19-trimethoxy-4,10,12,16-tetramethyl-3,20,22-trioxo-2-azabicyclo[16.3.1] docosa-1 (21),4,6,10,18-pentaen-9-yl carbamate
  • UNSPSC:

    41116105
  • Type:

    Inhibitor
  • Source:

    Produced by fermentation
  • Field of Research:

    Cancer | Heat Shock
  • Purity:

    >95%
  • Weight:

    0.001
  • Format:

    Yellow Solid
  • Solubility:

    Slightly soluble in methanol, chloroform or DMSO (10 mg/ml); insoluble in water
  • Molecular Formula:

    C29H40N2O9
  • Molecular Weight:

    560.6
  • Precautions:

    Not for use in humans. Not for use in diagnostics or therapeutics. For in vitro research use only.
  • References & Citations:

    1. Whitesell L., et al. (1994) Proc. Natl. Acad. Sci. USA 91:8324. 2. Neckers L. (2002) Trends Mol. Med. 8: S55. 3. Mabjeesh N.J., et al. (2002) Cancer Res. 62: 2478. 4. Chavany C., et al. 1996) Amer. Society Biochem Mol Bio. 9: 4974-4977. 5. Villa R., et al. (2003) Carcinogenesis. 24(5): 851-9. 6. Yamaki H., Iguchi-Ariga S.M., and Ariga H. (1989) J Antibiot (Tokyo). 42(4): 604-10.
  • CAS Number:

    30562-34-6