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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532935Generated: October 30, 2026

Acetic Acid → FR-179642

https://huagongshe.com/reaction/1532935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant[5-[(1S,2S)-2-[(3S,6S,9S,11R,15S,18S,20R,21S,24S,25S,26S)-3-[(1R)-3-amino-1-hydroxy-3-oxopropyl]-18-(hexadecanoylamino)-11,20,21,25-tetrahydroxy-15-[(1R)-1-hydroxyethyl]-26-methyl-2,5,8,14,17,23-hexaoxo-1,4,7,13,16,22-hexazatricyclo[22.3.0.09,13]heptacosan-6-yl]-1,2-dihydroxyethyl]-2-hydroxyphenyl] hydrogen sulfateHCID 44352613—
ReactantDisodium hydrogenphosphate potassium dihydrogenphosphateHCID 71312623—
SolventMethanolHCID 887—
ProductFR-179642HCID 71714631—

Reaction Steps

To 700 μl of the fermentation broth of Streptomyces anulatus No. 8703 obtained in Example 1-2 was added 100 μl of an aqueous solution of Substance FR901379 (100 mg/ml) (10 mg as Substance FR901379; 8.35 μmol) together with 100 μl of methanol and 100 μl of buffer (0.5 M potassium dihydrogen phosphate-disodium hydrogen phosphate buffer; pH 6.0), and the reaction was carried out at 30° C. for 30 minutes. The reaction was then stopped with 1 ml of 4% acetic acid and following addition of 2 ml of methanol, the mixture was filtered through a membrane filter (0.45 μm) to remove the macromolecular protein and other fraction and subjected to HPLC and the acylase activity of the skeletal substance FR179642 produced was monitored and assayed at 210 nm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06207434B1
Source datasetuspto-grants-2001_03
ORD IDord-775144a4b47641dd95bcaff664033844
Source noteuspto-grants-2001_03