Anisomycin from Streptomyces griseolus

• Catalog No.: A9789
• CAS Number: 22862-76-6
• M. F.: C14H19NO4
• M. W.: 265.30496
• Purity: ≥98% (HPLC)

SYNONYMS

• IUPAC name: (2R,3S,4S)-4-hydroxy-2-[(4-methoxyphenyl)methyl]pyrrolidin-3-yl acetate
• IUPAC Traditional name: anisomycin
• Synonyms: (2R,3S,4S)-2-(4-Methoxybenzyl)-3,4-pyrrolidinediol-3-acetate; 2-[(4-Methoxyphenyl)methyl]-3,4-pyrrolidinediol 3-acetate; Flagecidin

DATABASE IDS

• EC Number: 245-269-7
• MDL Number: MFCD00077650
• Beilstein Number: 20705
• CAS Number: 22862-76-6
• PubChem SID: 24891496

PROPERTIES

• Purity: ≥98% (HPLC)
• Quality Level: PREMIUM
• Apperance: white to faint yellow solid
• Solubility: H2O: soluble2 mg/mL (Aqueous solutions are stable over a wide range of pH at room temperature.)
• Solubility: DMSO: soluble20 mg/mL
• Solubility: methanol: soluble20 mg/mL
• GHS Signal Word: Danger
• GHS Hazard statements: H301
• European Hazard Symbols: Toxic (T)
• Personal Protective Equipment: Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
• GHS Precautionary statements: P301 + P310
• RID/ADR: UN 3462 6.1/PG 3
• Risk Statements: 25
• RTECS: BZ9800000
• Safety Statements: 45
• Storage Temperature: 2-8°C
• Hazard Class: 6.1
• UN Number: 3462
• Packing Group: 3
• German water hazard class: 3

DETAILS

Description (English)

Caution
Hygroscopic
Biochem/physiol Actions
Antibiotic isolated from Streptomyces griseolus that inhibits protein synthesis. Acts by inhibiting peptidyl transferase activity in eukaryote ribosomes. Reported to induce apoptosis in a variety of cells including promyelocytic leukemia cells, Jurkat cells, ventricular myocytes, and colon adenocarcinoma cells. Initiates intracellular signals and immediate early gene induction. Selective signaling agonist. Potent Jun-NH2 terminal kinase (JNK) agonist. Activates mitogen-activated protein (MAP) kinases (JNK/SAPK and p38/RK). Antiprotozoal agent.