857395 | GT-11

N-[(1R,2S)-2-hydroxy-1-hydroxymethyl-2-(2-tridecyl-1-cyclopropenyl)ethyl]octanamide

GT-11

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1mg 857395P-1mg 857395P-1mg 1 x 1mg $304.90
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Info

GT-11

N-[(1R,2S)-2-hydroxy-1-hydroxymethyl-2-(2-tridecyl-1-cyclopropenyl)ethyl]octanamide

GT-11 Dihydroceramide Desaturase Inhibitor

GT-11, also N-[(1R,2S)-2-hydroxy-1-hydroxymethyl-2-(2-tridecyl-1-cyclopropenyl)ethyl]octanamide, is the first inhibitor of dihydroceramide desaturase, an enzyme that converts dihydroceramide into the bioactive compound ceramide.

Dihydroceramides desaturase is an enzyme involved in the biosynthesis of ceramides. Ceramides are important molecules in the structure of cell membranes that contribute to various cellular processes including cell signaling and apoptosis, also referred to as programmed cell death. By inhibiting the activity of dihydroceramides desaturase, GT-11 can affect the production of ceramides, altering various cellular processes and pathways in which ceramides are involved.

Application

GT-11 shows potential in use as a cell protective agent due to the proapoptotic and proinflammatory effect of ceramide. GT-11's ability to inhibit dihydroceramides desaturase activity could have several potential applications in neurological disorders like Parkinson's Disease, metabolic disorders, cancer therapy, and more.

Packaging

Turn to Avanti Research for clean, reliable GT-11 in 1 mg powder packaging.

Data
Hygroscopic
No
Light Sensitive
No
Molecular Formula
C28H53NO3
Percent Composition
C 74.45%, H 11.83%, N 3.10%, O 10.63%
Purity
>99%
Stability
1 Years
Storage Temperature
-20°C
CAS Number
649767-83-9
CAS Registry Number is a Registered Trademark of the American Chemical Society
Formula Weight
451.725
Exact Mass
451.403
Synonyms
GT-11 dihydroceramide desaturase inhibitor
References

Muñoz-Guardiola P, Casas J, Megías-Roda E, Solé S, Perez-Montoyo H, Yeste-Velasco M, Erazo T, Diéguez-Martínez N, Espinosa-Gil S, Muñoz-Pinedo C, Yoldi G, Abad JL, Segura MF, Moran T, Romeo M, Bosch-Barrera J, Oaknin A, Alfón J, Domènech C, Fabriàs G, Velasco G, Lizcano JM. The anti-cancer drug ABTL0812 induces ER stress-mediated cytotoxic autophagy by increasing dihydroceramide levels in cancer cells. Autophagy. 2020 May 25:1-18. doi: 10.1080/15548627.2020.1761651. Epub ahead of print. PMID: 32397857.

PubMed ID: 32397857

Triola G, Fabrias G, Dragusin M, Niederhausen L, Broere R, Llebaria A, van Echten-Deckert G. Specificity of the dihydroceramide desaturase inhibitor N-[(1R,2S)-2-hydroxy-1-hydroxymethyl-2-(2-tridecyl-1-cyclopropenyl)ethyl]octanamide (GT11) in primary cultured cerebellar neurons. Mol Pharmacol. 2004 Dec;66(6):1671-8. doi: 10.1124/mol.104.003681. Epub 2004 Sep 15. PMID: 15371559.

PubMed ID: 15371559

Orienti I, Francescangeli F, De Angelis ML, Fecchi K, Bongiorno-Borbone L, Signore M, Peschiaroli A, Boe A, Bruselles A, Costantino A, Eramo A, Salvati V, Sette G, Contavalli P, Zolla L, Oki T, Kitamura T, Spada M, Giuliani A, Baiocchi M, La Torre F, Melino G, Tartaglia M, De Maria R, Zeuner A. A new bioavailable fenretinide formulation with antiproliferative, antimetabolic, and cytotoxic effects on solid tumors. Cell Death Dis. 2019 Jul 23;10(7):529. doi: 10.1038/s41419-019-1775-y.

PubMed ID: 31332161
Certificates of Analysis

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