|Source: ||Fusarium moniliforme|
|Description: ||Moniliformin is a mycotoxin, formed in many cereals by a number of Fusarium species that include, besides moniliforme, Fusarium avenaceum. Fusarium subglutinans, Fusarium proliferatum and others. Moniliformin is supplied as sodium salt of 1-hydroxycyclobut-1-ene-3,4-dione.|
|CAS number: ||71376-34-6 |
|Merck index: || |
|Molecular weight: ||120|
|Molecular Formula: ||C4HO3Na |
|Moniliformin is soluble in water and polar solvents, such as methanol.|
|Appearance: ||Yellow crystalline solid|
|Purity: ||Not less than 95% by HPLC, TLC. |
|λmax:||226, 259 in methanol|
|Melting point||Decomposes at 345-355oC without melting.|
|Solubility||Clear, yellowish solution at 10 mg in 1 ml of water |
| ||For Research use only. Not for Human or Drug use|
GMP/API grade available on request
Moniliformin by Fermentek is not produced from or contains any ingredients from animal origin.
No genetically modified organisms are used.
| ||Kristensen R, Berdal KG, Holst-Jensen A.|
Simultaneous detection and identification of trichothecene- and moniliformin - producing Fusarium species based on multiplex SNP analysis.
J Appl Microbiol. 2007 Apr;102(4):1071-81.
| ||Harvey B, Edrington TS, Kubena LF, Rottinghaus GE, Turk JR, Genovese KJ, Ziprin RL, Nisbet DJ.|
Toxicity of fumonisin from Fusarium verticillioides culture material and moniliformin from Fusarium fujikuroi culture material when fed singly and in combination to growing barrows.
J Food Prot. 2002 Feb;65(2):373-7.
| ||Desjardins AE, Maragos CM, Proctor RH.|
Maize ear rot and moniliformin contamination by cryptic species of Fusarium subglutinans.
J Agric Food Chem. 2006 Sep 20;54(19):7383-90.
| ||Kamyar MR, Kouri K, Rawnduzi P, Studenik C, Lemmens-Gruber R.|
Effects of moniliformin in presence of cyclohexadepsipeptides on isolated mammalian tissue and cells.
Toxicol In Vitro. 2006 Dec;20(8):1284-91