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Toyocamycin is a natural adenosine analog first isolated from Streptomyces and shown in early studies to be cytotoxic to bacteria, fungi, and cancer cells and to have antiviral activities. Toyocamycin prevents IRE1alpha-induced mRNA cleavage (IC50 = 80 nM) and inhibits constitutive activation of XBP1 in multiple myeloma cell lines. It is used to study IRE1alpha action in the endoplasmic reticulum stress response, particularly in the context of cancer. It also inhibits phosphatidylinositol kinase in vitro (IC50 = 3.3 µg/ml), but not in cells, and blocks the ribosomal RNA-processing kinase Rio1 (IC50 = ~30 nM).Formal Name: 4-amino-7-beta-D-ribofuranosyl-7H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile, hydrate. Synonyms: NSC 63701, NSC 99843. Molecular Formula: C12H13N5O4 . XH2O. Formula Weight: 291.3. Purity: >98%. Formulation: (Request formulation change), A crystalline solid. Solubility: :, DMF: 50 mg/mL, DMF:PBS(pH 7.2)(1:1): 0.5 mg/mL, DMSO: 30 mg/mL, Ethanol: 0.5 mg/mL. lambdamax: 232, 280 nm. SMILES: O[C@H]1[C@H](N2C=C(C#N)C3=C2N=CN=C3N)O[C@H](CO)[C@H]1O. InChi Code: InChI=1S/C12H13N5O4/c13-1-5-2-17(11-7(5)10(14)15-4-16-11)12-9(20)8(19)6(3-18)21-12/h2,4,6,8-9,12,18-20H,3H2,(H2,14,15,16)/t6-,8-,9-,12-/m1/s1. InChi Key: XOKJUSAYZUAMGJ-WOUKDFQISA-N.
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