Amphotericin B (trihydrate)

CAT:
804-HY-B0221A
Size:
1 Each

For Laboratory Research Only. Not for Clinical or Personal Use.

  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Amphotericin B (trihydrate) - image 1

Amphotericin B (trihydrate)

  • Description :

    Amphotericin B trihydrate, a polyene antibiotic, is first isolated from fermenter cultures of Streptomyces nodosus. Amphotericin B trihydrate also possesses antileishmanial activity[1][2].
  • UNSPSC :

    12352005
  • Target :

    Antibiotic; Bacterial; Fungal; Parasite
  • Type :

    Natural Products
  • Related Pathways :

    Anti-infection
  • Applications :

    COVID-19-immunoregulation
  • Field of Research :

    Infection; Inflammation/Immunology; Cancer
  • Assay Protocol :

    https://www.medchemexpress.com/amphotericin-b-trihydrate.html
  • Solubility :

    10 mM in DMSO
  • Smiles :

    C[C@H]([C@@H](O)[C@@H](C)[C@H](C)OC1=O)/C=C/C=C/C=C/C=C/C=C/C=C/C=C/[C@H](O[C@]2([H])O[C@H](C)[C@@H](O)[C@H](N)[C@@H]2O)C[C@@]3([H])[C@H](C(O)=O)[C@@H](O)C[C@](C[C@@H](O)C[C@@H](O)[C@H](O)CC[C@@H](O)C[C@@H](O)C1)(O)O3.[H]O[H].[H]O[H].[H]O[H]
  • Molecular Formula :

    C47H79NO20
  • Molecular Weight :

    978.12
  • References & Citations :

    [1]A Lemke, et al. Amphotericin B Appl Microbiol Biotechnol. 2005 Aug;68 (2) :151-62.|[2]Andreza Rochelle do Vale Morais, et al. In-vitro and in-vivo antileishmanial activity of inexpensive Amphotericin B formulations: Heated Amphotericin B and Amphotericin B-loaded microemulsion. Exp Parasitol. 2018 Sep;192:85-92.|[3]Ramos H, et al. Amphotericin B kills unicellular leishmanias by forming aqueous pores permeable to small cations and anions. J Membr Biol. 1996 Jul;152 (1) :65-75.|[4]Demaimay R, et al. Pharmacological studies of a new derivative of amphotericin B, MS-8209, in mouse and hamster scrapie. J Gen Virol. 1994 Sep;75 (Pt 9) :2499-503.|[5]Adams ML, et al. Amphotericin B encapsulated in micelles based on poly (ethylene oxide) -block-poly (L-amino acid) derivatives exerts reduced in vitro hemolysis but maintains potent in vivo antifungal activity. Biomacromolecules. 2003 May-Jun;4 (3) :750-7.
  • Shipping Conditions :

    Room temperature
  • Scientific Category :

    Natural Products
  • Clinical Information :

    Launched
  • Isoform :

    Leishmania; Plasmodium
  • CAS Number :

    [1202017-46-6]