NIGERICIN SODIUM SALT manufacturers
- Nigericin
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- $250.00 / 25mg
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2026-01-15
- CAS:28380-24-7
- Min. Order:
- Purity: 98.50%
- Supply Ability: 10g
- NIGERICIN SODIUM SALT
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- $1.00 / 1KG
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2020-01-13
- CAS:28380-24-7
- Min. Order: 1KG
- Purity: 98%-99.9%
- Supply Ability: 200kg
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| | NIGERICIN SODIUM SALT Basic information |
| Product Name: | NIGERICIN SODIUM SALT | | Synonyms: | (2R)-2-((3S)-6-{[2-((5S)-5-{(3S)-5-[(3S,5R,6R)-6-Hydroxy-6-(hydroxymethyl)-3,5-dimethylperhydro-2H-pyran-2-yl]-3-methyloxolan-2-yl}-5-methyloxolan-2-yl)(2S,4R,9R,10R)-9-methoxy-2,4,10-trimethyl-1,6-dioxaspiro[4.5]dec-7-yl]methyl}-3-methylperhydro-2H-pyran-2-yl)propanoic acid;28643-80-3 (Sodium salt);Aids003767;Aids-003767;Helix c;AZALOMYCIN M;HELIXIN C;ANTIBIOTIC K178 | | CAS: | 28380-24-7 | | MF: | C40H68O11 | | MW: | 724.96 | | EINECS: | | | Product Categories: | antibiotic | | Mol File: | 28380-24-7.mol |  |
| | NIGERICIN SODIUM SALT Chemical Properties |
| Melting point | 183.5-185° | | alpha | D24 +36.2° (c = 0.842 in CHCl3) | | Boiling point | 779.9±60.0 °C(Predicted) | | density | 1.19±0.1 g/cm3(Predicted) | | storage temp. | 2-8°C | | solubility | chloroform: 10 mg/mL, clear, colorless | | pka | 4.39±0.10(Predicted) | | form | Solid | | color | White to off-white | | InChIKey | DANUORFCFTYTSZ-ANZYULKNSA-N |
| Hazard Codes | T,Xi | | Risk Statements | 25-36/37/38 | | Safety Statements | 26-36/37/39-45-36 | | RIDADR | UN 3462 6.1/PG 3 | | WGK Germany | 3 | | RTECS | QT6840000 | | F | 10 | | HazardClass | 6.1(b) | | PackingGroup | III | | HS Code | 29419090 | | Toxicity | LD50 in mice (mg/kg): 10-15 i.p. (Shoji); also reported as 2.5 i.p. (Harned) |
| | NIGERICIN SODIUM SALT Usage And Synthesis |
| Uses | Nigericin is a polyether antibiotic produced by Streptomyces, notably S. hygroscopicus, isolated in the 1950s. Its complex structure was finally elucidated in 1968. Nigericin is an ionophore, possessing very high affinity for monovalent cations such as Na+ and K+. Nigericin disrupts membrane potential and Golgi apparatus in mitochondria. Although nigericin can be isolated as the free acid (under acidic conditions), like most ionophores it is extracted into organic solvents and is most conveniently isolated as a salt. In vitro, nigericin has broad biological activity against Gram positive bacteria, fungi, tumour cell lines and some viruses, including HIV. Nigericin is the most common member of the polyether class which are common false positives in in vitro screening bioassays using crude microbial extracts. They are thus important standards for dereplication. | | Definition | ChEBI: A polyether antibiotic which affects ion transport and ATPase activity in mitochondria. It is produced by Streptomyces hygroscopicus. | | in vivo | Nigericin (1 mg/kg; i.p.; every 12 h for 3 D) reduces the infection of S. aureus USA300 in mice[4].
Nigericin (0.025 mg/kg; s.c.; every two days in 4 weeks) plus anti-PD-1 shows synergistic anti-cancer effect[6].
| Animal Model: | BALB/c Mice injected orthotopically with 4T1 cells[6] | | Dosage: | 0.025 mg/kg | | Administration: | Subcutaneous injection (s.c.) | | Result: | Showed combination with anti-PD-1 antibody almost completely suppressed tumor growth. |
| Animal Model: | Mice Infected with S. aureus USA300[4] | | Dosage: | 1 mg/kg | | Administration: | Intraperitoneal injection (i.p.) | | Result: | Showed reduction in the bacterial burden to 1,000-10,000-fold in the major organs. |
| | IC 50 | NLRP3 |
| | NIGERICIN SODIUM SALT Preparation Products And Raw materials |
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