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- Amphotericin B
Amphotericin B
Amphotericin B, a polyene antifungal antibiotic, has been produced from a strain of Streptomyces nodosus with an IC50 of 0.028–0.290 μg/ml.
In vitro: Amphotericin B was the most effective drug for treating many life-threatening fungal infections. In cells expressing TLR2 and CD14, amphotericin B induced signal transduction and inflammatory cytokine release. In primary murine macrophages and human cell lines expressing TLR2, CD14, and the adapter protein MyD88, amphotericin induced NF-κB-dependent reporter activity and cytokine release, whereas cells deficient in any of these failed to respond. Cells with TLR4 mutation were less responsive to amphotericin B stimulation than cells expressing normal TLR4 [1]. Amphotericin B could interact with cholesterol, the major sterol of mammal membranes, thus limiting the usefulness of Amphotericin B due to its relatively high toxicity [2]. Low AmB concentrations (≤ 0.1 μM) induced a polarization potential in KCl-loaded liposomes suspended in an iso-osmotic sucrose solution, indicating K+ leakage. AmB (> 0.1 μM) allowed cations and anions movements. LPs suspended in an iso-osmotic NaCl solution and exposed to AmB (0.05 μM) exhibited a nearly total collapse of the negative membrane potential, indicated that Na+ entered into the cells [3].
In vivo: Amphotericin B prolonged the incubation time and decreased PrPSc accumulation in the hamster scrapie model. Amphotericin B markedly resulted in reduction of PrPSc levels in mice with transmissible subacute spongiform encephalopathies (TSSE) [4].
References:
[1].?Sau K1,Mambula SS,Latz E,Henneke P,Golenbock DT,Levitz SM.The antifungal drug amphotericin B promotes inflammatory cytokine release by a Toll-like receptor- and CD14-dependent mechanism.J Biol Chem.2003 Sep 26;278(39):37561-8. Epub 2003 Jul 14.
[2].?Barwicz J1,Tancrède P.The effect of aggregation state of amphotericin-B on its interactions with cholesterol- or ergosterol-containing phosphatidylcholine monolayers.Chem Phys Lipids.1997 Feb 28;85(2):145-55.
[3].?Ramos H1,Valdivieso E,Gamargo M,Dagger F,Cohen BE.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 R1,Adjou K,Lasmézas C,Lazarini F,Cherifi K,Seman M,Deslys JP,Dormont D.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.
- 1. Lukas Hafner, Maxime Pichon, et al. "Listeria monocytogenes faecal carriage is common and depends on the gut microbiota." Nat Commun. 2021 Nov 24;12(1):6826. PMID: 34819495
- 2. Xue-Ming Zhu , Lin Li, et al. "A VASt-domain protein regulates autophagy, membrane tension, and sterol homeostasis in rice blast fungus." Autophagy. 2020 Nov 11. PMID: 33176558
- 3. Perni S, Lavorato M, Beam KG. "De novo reconstitution reveals the proteins required for skeletal muscle voltage-induced Ca(2+) release." Proc Natl Acad Sci U S A. 2017 Dec 26;114(52):13822-13827. PMID: 29229815
Storage | Store at -20°C |
M.Wt | 924.08 |
Cas No. | 1397-89-3 |
Formula | C47H73NO17 |
Solubility | ≥46.2 mg/mL in DMSO; insoluble in EtOH; insoluble in H2O |
SDF | Download SDF |
Canonical SMILES | O=C(C[C@@H](C[C@@H](CC[C@@H](O)[C@@H]1O)O)O)O[C@@H](C)[C@H](C)[C@H](O)[C@@H](C)/C=C/C=C/C=C/C=C/C=C/C=C/C=C/[C@H](O[C@H]2[C@@H](O)[C@@H](N)[C@H](O)[C@@H](C)O2)C[C@@H]([C@H](C(O)=O)[C@@H](O)C3)OC3(O)C[C@H](C1)O |
Shipping Condition | Small Molecules with Blue Ice, Modified Nucleotides with Dry Ice. |
General tips | We do not recommend long-term storage for the solution, please use it up soon. |
Cell experiment [1]: | |
Cell lines |
peritoneal macrophages; HEK293 cells expressing TLR2 and CD14 |
Preparation method |
The solubility of this compound in DMSO is >46.2mg/mL. General tips for obtaining a higher concentration: Please warm the tube at 37℃ for 10 minutes and/or shake it in the ultrasonic bath for a while. Stock solution can be stored below -20℃ for several months. |
Reacting condition |
1, 2, and 4 μg/ml |
Applications |
In peritoneal macrophages from CD14 knockout mice (C57BL/6 CD14–/–) and CD14 wild-type (C57BL/6 CD14+/+) mice, Amphotericin B failed to induce the production of TNF-α in macrophages from CD14–/– mice. HEK293 cells expressing TLR2 and CD14 responded more strongly to Amphotericin B (1, 2, and 4 μg/ml). |
Animal experiment [2]: | |
Animal models |
hamster scrapie model |
Dosage form |
2.5 mg/kg; p.i. injection from 0 to 7 days |
Application |
In hamsters infected intracerebrally with scrapie, Amphotericin B significantly prolonged the survival time by 14.7 days. |
Other notes |
Please test the solubility of all compounds indoor, and the actual solubility may slightly differ with the theoretical value. This is caused by an experimental system error and it is normal. |
References: [1]. Sau K1,Mambula SS,Latz E,Henneke P,Golenbock DT,Levitz SM.The antifungal drug amphotericin B promotes inflammatory cytokine release by a Toll-like receptor- and CD14-dependent mechanism.J Biol Chem.2003 Sep 26;278(39):37561-8. Epub 2003 Jul 14. [2]. Demaimay R1,Adjou K,Lasmézas C,Lazarini F,Cherifi K,Seman M,Deslys JP,Dormont D.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. |
Quality Control & MSDS
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