Milbemycin A3 (Standard)
Milbemycin A3 (Standard) is the analytical standard of Milbemycin A3 (HY-130423). This product is intended for research and analytical applications. Milbemycin A3 is a 16-membered macrocyclic lactone compound found in the soil bacterium Saccharopolyspora hygroscopicus subsp. aureolacrimosus. Milbemycin A3 enhances the opening of glutamate- and GABA-gated chloride channels and exhibits insecticidal activity. Milbemycin A3 can be used in insect resistance-related research.
For research use only. We do not sell to patients.
- CAS No.: 51596-10-2
- Formula: C31H44O7
- Molecular Weight:528.68
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
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Product Information
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Chemical Information
- Purity & Documentation
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Help & FAQs
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HY-130423
Milbemycin A3
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HY-15308
Avermectin B1a
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HY-126906
Milbemycin A4
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HY-18982
Anisomycin
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HY-B0767
Spinosyn A
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HY-N7071A
Maduramicin ammonium
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HY-126906R
Milbemycin A4 (Standard)
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HY-18982R
Anisomycin (Standard)
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HY-B1864A
Kasugamycin hydrochloride
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HY-15308R
Avermectin B1a (Standard)
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HY-125326
Spinosyn D
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HY-N7071AR
Maduramicin ammonium (Standard)
Product Information
The compound is the grade of analytical standard, which is the reference standard supplied assay. It is commonly used in qualitative, quantitative and methodological research experiments in HPLC, GC and MS.
Chemical Information
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CAS No. 51596-10-2
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Molecular Weight 528.68
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Formula C31H44O7
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SMILES
C[C@H]1CC[C@@]2(O[C@@H]1C)C[C@@H]3C[C@@H](C/C=C(C)/C[C@@H](C)/C=C/C=C4CO[C@H]5[C@]\4(O)[C@H](C(O3)=O)C=C(C)[C@H]5O)O2
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
[1]. Yang L Y, et al. New nemadectin congeners with acaricidal and nematocidal activity from Streptomyces microflavus neau3 Y-3[J]. Bioorganic & medicinal chemistry letters, 2013, 23(20): 5710-5713. [Content Brief]
[2]. Nakagawa K, et al. Microbial conversion of milbemycins: hydroxylation of milbemycin A4 and related compounds by Cunninghamella echinulata ATCC 9244. J Antibiot (Tokyo). 1991;44(2):232-240. [Content Brief]
[3]. Zhang J, et al. Genetic engineering of Streptomyces bingchenggensis to produce milbemycins A3/A4 as main components and eliminate the biosynthesis of nanchangmycin. Appl Microbiol Biotechnol. 2013;97(23):10091-10101. [Content Brief]
[4]. Duke SO, et al. Natural toxins for use in pest management. Toxins (Basel). 2010;2(8):1943-1962. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Milbemycin A3 (Standard) Related Classifications
HY-130423R Related Classifications
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