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130607-26-0

130607-26-0 Structure

130607-26-0 Structure
IdentificationBack Directory
[Name]

hydantocidin
[CAS]

130607-26-0
[Synonyms]

hydantocidin
(+)-Hidantocidin
(5S,7R,8S,9R)-8,9-dihydroxy-7-(hydroxymethyl)-6-oxa-1,3-diazaspiro[4.4]nonane-2,4-dione
6-Oxa-1,3-diazaspiro[4.4]nonane-2,4-dione, 8,9-dihydroxy-7-(hydroxymethyl)-, (5S,7R,8S,9R)-
(2S)-4,5-Dihydro-3α,4α-dihydroxy-5β-(hydroxymethyl)spiro[furan-2(3H),4'-imidazolidine]-2',5'-dione
(4S)-3'α,4'α-Dihydroxy-5'β-(hydroxymethyl)-4',5'-dihydrospiro[imidazolidine-4,2'(3'H)-furan]-2,5-dione
[Molecular Formula]

C7H10N2O6
[MDL Number]

MFCD01722994
[MOL File]

130607-26-0.mol
[Molecular Weight]

218.16
Chemical PropertiesBack Directory
[Boiling point ]

358.84°C (rough estimate)
[density ]

1.5295 (rough estimate)
[refractive index ]

1.4880 (estimate)
Hazard InformationBack Directory
[Description]

Hydantocidin (52), a microbial spironucleoside, selectively inhibits plant adenylsuccinate synthetase only after in vivo phosphorylation, resulting in the 5 -monophosphate 52, an analog of adenosine 5 -monophosphate (74) .
[Uses]

Hydantocidin is an adenylosuccinate synthetase inhibitor and a spiroribofuranose. Hydantocidin can be produced by Streptomyces hygroscopicus. Hydantocidin has strong herbicidal activity toward annual, biennial and perennial weeds[1].
[References]

[1] Shiozaki M. Synthesis of hydantocidin and C-2-thioxo-hydantocidin. Carbohydr Res. 2001 Oct 8;335(3):147-50. DOI:10.1016/s0008-6215(01)00239-7
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