85124-22-7
Chemical Structure
Roridin L2
- CAS. Nr.: 85124-22-7
- Formula:C29H38O9
- Molecular Weight:530.61
IUPAC Name: (2S,2'R,4'R,5'S,5a'R,9a'R)-5a'-(hydroxymethyl)-5',8'-dimethyl-2',3',4',5',5a',6',7',9a'-octahydrospiro[oxirane-2,10'-[2,5]methanobenzo[b]oxepin]-4'-yl (2Z,4E)-7-hydroxy-6-(2-(5-oxo-2,5-dihydrofuran-3-yl)ethoxy)octa-2,4-dienoate
InChIKey: JGIYRVDWRBKREW-JNMAXWDTSA-N
SMILES: CC1=C[C@@]2([C@](CO)(CC1)[C@@]3([C@]4([C@]([H])(O2)C[C@H]3OC(/C=C\C=C\C(C(C)O)OCCC5=CC(OC5)=O)=O)OC4)C)[H]
Biological Activity: Roridin L2 is an inhibitor of the peptidyl transferase center of the 60S ribosomal subunit. Roridin L2 irreversibly binds to this center and inhibits protein biosynthesis[1][2].
| Art. -Nr. | Produktname | Reinheit | Beschreibung | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Roridin L2 | 99.9% | Roridin L2 is an inhibitor of the peptidyl transferase center of the 60S ribosomal subunit. Roridin L2 irreversibly binds to this center and inhibits protein biosynthesis. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
References
- [1]. Islam Z, et al. Purification and comparative neurotoxicity of the trichothecenes satratoxin G and roridin L2 from Stachybotrys chartarum. Journal of Toxicology and Environmental Health, Part A. 2009 Sep 16;72(20):1242-51. [Content Brief]
- [2]. Wolff A, et al. Establishment of a Human Cell-Based In Vitro Test System for Investigating and Evaluating Cytotoxic and Immunomodulatory Effects of Indoor Mold. Environmental toxicology. 2026 Jul 22.
