Cart
sales@molnova.com
Etoxazole
CAS No. 153233-91-1
Etoxazole( Etoxazole | YI 5301 | YI-5301 )
Catalog No. M18070 CAS No. 153233-91-1
Etoxazole is an acaricide/insecticide that works via chitin biosynthesis inhibition for the control of mites. Used as a standard for Pesticide detection.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 10MG | 33 | In Stock |
|
| 25MG | 51 | In Stock |
|
| 50MG | 96 | In Stock |
|
| 100MG | 149 | In Stock |
|
| 500MG | 374 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameEtoxazole
-
NoteResearch use only, not for human use.
-
Brief DescriptionEtoxazole is an acaricide/insecticide that works via chitin biosynthesis inhibition for the control of mites. Used as a standard for Pesticide detection.
-
DescriptionEtoxazole is an acaricide/insecticide that works via chitin biosynthesis inhibition for the control of mites. Used as a standard for Pesticide detection.
-
In Vitro——
-
In Vivo——
-
SynonymsEtoxazole | YI 5301 | YI-5301
-
PathwayCell Cycle/DNA Damage
-
TargetHDAC
-
Recptorchitin biosynthesi
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number153233-91-1
-
Formula Weight359.41
-
Molecular FormulaC21H23F2NO2
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESCCOc1c(ccc(c1)C(C)(C)C)C1COC(=N1)c1c(cccc1F)F
-
Chemical NameOxazole, 2-(2,6-difluorophenyl)-4-(4-(1,1-dimethylethyl)-2-ethoxyphenyl)-4,5-dihydro-
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Uesugi R, et al. Genetic basis of resistances to chlorfenapyr and etoxazole in the two-spotted spider mite (Acari: Tetranychidae). J Econ Entomol. 2002 Dec;95(6):1267-74.
molnova catalog
related products
-
HDAC-IN-57
HDAC-IN-57 is an orally active pan-inhibitor of histone deacetylase (HDAC), inhibiting HDAC1, HDAC2, HDAC6, and HDAC8 with IC50 values of 2.07 nM, 4.71 nM, 2.4 nM, and 107 nM, respectively.
-
R306465
R306465 (JNJ-16241199) is an orally active and selective class I histone deacetylase (HDAC 1) inhibitor with an IC50 of 3.3 nM.
-
Tubacin
Tubacin is a potent, selective inhibitor of class II histone deacetylase 6 (HDAC6) with IC50 of 4 nM.
