Milbemectin

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Milbemectin

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Cat No: 22003

Biochemicals - Ion Channel Modulation

Milbemectin is an insecticide used primarily to control mites.{36021} Milbemectin is a mixture of milbemycin A3 (30%; Item No. 18360) and milbemycin A4 (70%; Item No. 17155) that has acaricidal and nematocidal activity against adult spider mites, spid...

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Territorial Availability: Available through Bertin Technologies only in France

Synonyms:

Milbemycin A3: (6R,25R)-5-O-demethyl-28-deoxy-6,28-epoxy-25-methyl-milbemycin BMilbemycin A4: (6R,25R)-5-O-demethyl-28-deoxy-6,28-epoxy-25-ethyl-milbemycin B

Correlated keywords:

51596-10-2 51596-11-3 emamectin B-41A4 ?3 ?1 a1 caenorhabditis bursaphelenchus 6'-ethylmilbemycin milbemcin 41A3 anti-biotic GWN 1725 GWN1725 gowan koromite matsuguard mesa acaricide milbeknock ultiflora resistant to dieldrin gamma?aminobutyric aminobutyrate

Product Overview:
Milbemectin is an insecticide used primarily to control mites.{36021} Milbemectin is a mixture of milbemycin A3 (30%; Item No. 18360) and milbemycin A4 (70%; Item No. 17155) that has acaricidal and nematocidal activity against adult spider mites, spider mite eggs, and C. elegans with IC50 values of 5.3, 41.1, and 9.5 µg/ml, respectively.{28380} It acts as an allosteric agonist of the Drosophila RDL GABA receptor.{36022} It is also effective against the pinewood nematode, B. xylophilus with an LC20 of 0.0781 mg/liter.{36023}

Size	5 mg
Shipping	dry ice
CAS Number	1799297-76-9
Molecular Formula	C₃₁H₄₄O₇ (A₃) and C₃₂H₄₆O₇ (A₄)
SMILES	C/C(C[C@@H](C)/C=C/C=C(CO1)/[C@@]([C@@]1([H])[C@H](O)C(C)=C2)(O)[C@]2([H])C3=O)=C\C[C@]4([H])C[C@@](O3)([H])C[C@@]5(O[C@]([H])(C)[C@@H](C)CC5)O4.C/C(C[C@@H](C)/C=C/C=C(CO6)/[C@@]([C@@]6([H])[C@H](O)C(C)=C7)(O)[C@]7([H])C8=O)=C\C[C@]9([H])C[C@@](O8)([H])C[
Formulation	A solid
Purity	≥95%
Custom Code	2932.99
UNSPSC code	12352100

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Cayman Chemical's mission is to help make research possible by supplying scientists worldwide with the basic research tools necessary for advancing human and animal health. Our utmost commitment to healthcare researchers is to offer the highest quality products with an affordable pricing policy.

Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.

Accreditations
ISO/IEC 17025:2005
ISO Guide 34:2009

Cayman is a leader in the field of emerging drugs of abuse, providing high-purity Schedule I-V Controlled Substances to federally-licensed laboratories and qualified academic research institutions for forensic analyses. We are certified by ACLASS Accreditation Services with dual accreditation to ISO/IEC 17025:2005 and ISO Guide 34:2009.