MedKoo Cat#: 463081 | Name: 3-Acetyldeoxynivalenol

Description:

WARNING: This product is for research use only, not for human or veterinary use.

3-Acetyldeoxynivalenol is a natural inducer of DNA damage, cell cycle arrest, apoptosis, and autophagy in macrophages.

Chemical Structure

3-Acetyldeoxynivalenol
3-Acetyldeoxynivalenol
CAS#50722-38-8

Theoretical Analysis

MedKoo Cat#: 463081

Name: 3-Acetyldeoxynivalenol

CAS#: 50722-38-8

Chemical Formula: C17H22O7

Exact Mass: 338.1366

Molecular Weight: 338.36

Elemental Analysis: C, 60.35; H, 6.55; O, 33.10

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Related CAS #
No Data
Synonym
3-Acetyldeoxynivalenol; Deoxynivalenol 3-acetate;
IUPAC/Chemical Name
(2S,3'R,5'R,5a'R,6'S,9a'R)-6'-hydroxy-5a'-(hydroxymethyl)-5',8'-dimethyl-7'-oxo-2',3',4',5',5a',6',7',9a'-octahydrospiro[oxirane-2,10'-[2,5]methanobenzo[b]oxepin]-3'-yl acetate
InChi Key
ADFIQZBYNGPCGY-YMSRDNDKSA-N
InChi Code
InChI=1S/C17H22O7/c1-8-4-11-16(6-18,13(21)12(8)20)15(3)5-10(23-9(2)19)14(24-11)17(15)7-22-17/h4,10-11,13-14,18,21H,5-7H2,1-3H3/t10-,11-,13-,14?,15-,16-,17+/m1/s1
SMILES Code
O[C@@H]1C(C(C)=C[C@@H](OC2[C@H](OC(C)=O)C[C@@]3(C)[C@@]24OC4)[C@]13CO)=O
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 338.36 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
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PMID: 32653989. 4: Dong F, Zhang X, Xu JH, Shi JR, Lee YW, Chen XY, Li YP, Mokoena MP, Olaniran AO. Analysis of Fusarium graminearum Species Complex from Freshly Harvested Rice in Jiangsu Province (China). Plant Dis. 2020 Aug;104(8):2138-2143. doi: 10.1094/PDIS-01-20-0084-RE. Epub 2020 Jun 15. PMID: 32539593. 5: Mallmann CA, Tyska D, Almeida CAA, Oliveira MS, Gressler LT. Mycotoxicological monitoring of breakfast and infant cereals marketed in Brazil. Int J Food Microbiol. 2020 Oct 16;331:108628. doi: 10.1016/j.ijfoodmicro.2020.108628. Epub 2020 Apr 13. PMID: 32535523. 6: Panasiuk Ł, Jedziniak P, Pietruszka K, Posyniak A. Simultaneous Determination of Deoxynivalenol, Its Modified Forms, Nivalenol and Fusarenone-X in Feedstuffs by the Liquid Hromatography-Tandem Mass Spectrometry Method. Toxins (Basel). 2020 Jun 1;12(6):362. doi: 10.3390/toxins12060362. PMID: 32492900; PMCID: PMC7354445. 7: Liu N, Yang Y, Chen J, Jia H, Zhang Y, Jiang D, Wu G, Wu Z. 3-Acetyldeoxynivalenol induces lysosomal membrane permeabilization-mediated apoptosis and inhibits autophagic flux in macrophages. Environ Pollut. 2020 Oct;265(Pt B):114697. doi: 10.1016/j.envpol.2020.114697. Epub 2020 May 7. PMID: 32454357. 8: Spanic V, Katanic Z, Sulyok M, Krska R, Puskas K, Vida G, Drezner G, Šarkanj B. Multiple Fungal Metabolites Including Mycotoxins in Naturally Infected and Fusarium-Inoculated Wheat Samples. Microorganisms. 2020 Apr 17;8(4):578. doi: 10.3390/microorganisms8040578. PMID: 32316403; PMCID: PMC7232504. 9: Sneideris D, Ivanauskas A, Prakas P, Butkauskas D, Treikale O, Kadziene G, Rasiukeviciute N, Kelpsiene J, Suproniene S. Population Structure of Fusarium graminearum Isolated from Different Sources in One Area over the Course of Three Years. Phytopathology. 2020 Jul;110(7):1312-1318. doi: 10.1094/PHYTO-08-19-0298-R. Epub 2020 May 8. PMID: 32223642. 10: Maeda K, Tanaka Y, Matsuyama M, Sato M, Sadamatsu K, Suzuki T, Matsui K, Nakajima Y, Tokai T, Kanamaru K, Ohsato S, Kobayashi T, Fujimura M, Nishiuchi T, Takahashi-Ando N, Kimura M. Substrate specificities of Fusarium biosynthetic enzymes explain the genetic basis of a mixed chemotype producing both deoxynivalenol and nivalenol-type trichothecenes. Int J Food Microbiol. 2020 May 2;320:108532. doi: 10.1016/j.ijfoodmicro.2020.108532. Epub 2020 Jan 22. PMID: 32004825. 11: Huang C, Gangola MP, Ganeshan S, Hucl P, Kutcher HR, Chibbar RN. Spike culture derived wheat (Triticum aestivum L.) variants exhibit improved resistance to multiple chemotypes of Fusarium graminearum. PLoS One. 2019 Dec 19;14(12):e0226695. doi: 10.1371/journal.pone.0226695. PMID: 31856194; PMCID: PMC6922434. 12: Ksieniewicz-Woźniak E, Bryła M, Waśkiewicz A, Yoshinari T, Szymczyk K. Selected Trichothecenes in Barley Malt and Beer from Poland and an Assessment of Dietary Risks Associated with their Consumption. Toxins (Basel). 2019 Dec 9;11(12):715. doi: 10.3390/toxins11120715. PMID: 31835298; PMCID: PMC6949925. 13: Juan C, Oueslati S, Mañes J, Berrada H. Multimycotoxin Determination in Tunisian Farm Animal Feed. J Food Sci. 2019 Dec;84(12):3885-3893. doi: 10.1111/1750-3841.14948. Epub 2019 Nov 24. PMID: 31762027. 14: Tanaka N, Takushima R, Tanaka A, Okada A, Matsui K, Maeda K, Aikawa S, Kimura M, Takahashi-Ando N. Reduced Toxicity of Trichothecenes, Isotrichodermol, and Deoxynivalenol, by Transgenic Expression of the Tri101 3-O-Acetyltransferase Gene in Cultured Mammalian FM3A Cells. Toxins (Basel). 2019 Nov 10;11(11):654. doi: 10.3390/toxins11110654. PMID: 31717667; PMCID: PMC6891669. 15: Wipfler R, McCormick SP, Proctor R, Teresi J, Hao G, Ward T, Alexander N, Vaughan MM. Synergistic Phytotoxic Effects of Culmorin and Trichothecene Mycotoxins. Toxins (Basel). 2019 Sep 20;11(10):555. doi: 10.3390/toxins11100555. PMID: 31547160; PMCID: PMC6833022. 16: Arce-López B, Lizarraga E, Flores-Flores M, Irigoyen Á, González-Peñas E. Development and validation of a methodology based on Captiva EMR-lipid clean-up and LC-MS/MS analysis for the simultaneous determination of mycotoxins in human plasma. Talanta. 2020 Jan 1;206:120193. doi: 10.1016/j.talanta.2019.120193. Epub 2019 Jul 30. PMID: 31514835. 17: Wu L, Zhang H, Hu X, Zhang Y, Sun L, Li W, Wang B. Deacetylation of 3-acetyl-deoxynivalenol in wheat flour is mediated by water-soluble proteins during the making of Chinese steamed bread. Food Chem. 2020 Jan 15;303:125341. doi: 10.1016/j.foodchem.2019.125341. Epub 2019 Aug 8. PMID: 31442898. 18: Mokubedi SM, Phoku JZ, Changwa RN, Gbashi S, Njobeh PB. Analysis of Mycotoxins Contamination in Poultry Feeds Manufactured in Selected Provinces of South Africa Using UHPLC-MS/MS. Toxins (Basel). 2019 Aug 2;11(8):452. doi: 10.3390/toxins11080452. PMID: 31382387; PMCID: PMC6722855. 19: Tarazona A, Gómez JV, Mateo EM, Jiménez M, Mateo F. Antifungal effect of engineered silver nanoparticles on phytopathogenic and toxigenic Fusarium spp. and their impact on mycotoxin accumulation. Int J Food Microbiol. 2019 Oct 2;306:108259. doi: 10.1016/j.ijfoodmicro.2019.108259. Epub 2019 Jun 30. PMID: 31349113. 20: Molina A, Chavarría G, Alfaro-Cascante M, Leiva A, Granados-Chinchilla F. Mycotoxins at the Start of the Food Chain in Costa Rica: Analysis of Six Fusarium Toxins and Ochratoxin A between 2013 and 2017 in Animal Feed and Aflatoxin M1 in Dairy Products. Toxins (Basel). 2019 May 31;11(6):312. doi: 10.3390/toxins11060312. PMID: 31159287; PMCID: PMC6628313.