Fumonisin B2-¹³C₃₄

Cat. No.: HY-N6723S: FAQs
Data Sheet Handling Instructions

Molarity Calculator

Fumonisin B2-¹³C₃₄ is the ¹³C labeled Fumonisin B2 (HY-N6723). Fumonisin B2, a mycotoxin produced by Fusarium moniliforme in various grains, is a potent inhibitor of sphingosine N-acyltransferase (ceramide synthase) and disrupts de novo sphingolipid biosynthesis.

For research use only. We do not sell to patients.

Fumonisin B2-<sup>13</sup>C<sub>34</sub> Chemical Structure

Fumonisin B2-¹³C₃₄ Chemical Structure

CAS No. : 1217481-36-1

Size	Price	Stock
Solvent
12 μg (13.52 μM * 1.2 mL in Acetonitrile)	USD 1100	Ask For Quote & Lead Time

Synthetic products have potential research and development risk.

* Please select Quantity before adding items.

This product is a controlled substance and not for sale in your territory.

Other Forms of Fumonisin B2-¹³C₃₄:

Fumonisin B2 Get quote

Featured Recommendations

•Related Small Molecules:

•Related Proteins:

Biological Activity
Purity & Documentation
References
Customer Review

Description	Fumonisin B2-¹³C₃₄ is the ¹³C labeled Fumonisin B2 (HY-N6723)^[1]. Fumonisin B2, a mycotoxin produced by Fusarium moniliforme in various grains, is a potent inhibitor of sphingosine N-acyltransferase (ceramide synthase) and disrupts de novo sphingolipid biosynthesis^[2]^[3].
IC₅₀ & Target	Sphingosine N-acyltransferase^[2]
In Vitro	Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs^[1]. MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Fumonisin B2-¹³C₃₄ Related Antibodies
Molecular Weight	739.58
Formula	¹³C₃₄H₅₉NO₁₄
CAS No.	1217481-36-1
Unlabeled CAS	116355-84-1
SMILES	O[13C]([13CH2][13C@@H]([13C](O)=O)[13CH2][13C](O[13C@@H]([13CH2][13C@@H]([13CH3])[13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13C@@H](O)[13CH2][13C@H](O)[13C@@H](N)[13CH3])[13C@@H]([13C@H]([13CH3])[13CH2][13CH2][13CH2][13CH3])O[13C]([13CH2][13C@H]([13C](O)=O)[13CH2][13C](O)=O)=O)=O)=O
Shipping	Room temperature in continental US; may vary elsewhere.
Storage	Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation	Data Sheet (275 KB) Handling Instructions (2659 KB)
References	[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-220. [Content Brief] [2]. Henry MH, et al. The toxicity of fumonisin B1, B2, and B3, individually and in combination, in chicken embryos. Poult Sci. 2001 Apr;80(4):401-7. [Content Brief] [3]. Wei T, et al. Natural occurrence of fumonisins B1 and B2 in corn in four provinces of China. Food Addit Contam Part B Surveill. 2013;6(4):270-4. [Content Brief]