Malonyl Coenzyme A (lithium salt

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Malonyl Coenzyme A (lithium salt)

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Cat No: 16455

Biochemicals - More Biochemicals

Malonyl coenzyme A is a coenzyme A (CoA; Item No. 16147) derivative that is used in fatty acid and polyketide synthesis and in the transport of α-ketoglutarate across the mitochondrial membrane.{30631,30632} Malonyl-CoA is formed by acetyl-CoA carboxy...

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Territorial Availability: Available through Bertin Technologies only in France

Synonyms:

S-(hydrogen propanedioate) coenzyme A, lithium salt

Correlated keywords:

524-14-1 fatty acid synthesis polyketide mitochondria lipids substrate a-ketoglutarate

Product Overview:
Malonyl coenzyme A is a coenzyme A (CoA; Item No. 16147) derivative that is used in fatty acid and polyketide synthesis and in the transport of α-ketoglutarate across the mitochondrial membrane.{30631,30632} Malonyl-CoA is formed by acetyl-CoA carboxylase-mediated carboxylation of acetyl-CoA (Item No. 16160).{30631} Fatty acid synthase catalyzes the NADPH-dependent condensation of malonyl-CoA and acetyl-CoA to produce palmitate. Proliferating human cancer cells upregulate this fatty acid synthesis pathway as a strategy for survival. High levels of malonyl-CoA, achieved through fatty acid synthase inhibition, have been proposed to contribute to cancer cell apoptosis.{11993} Manlonyl-CoA is exclusively used as the extender unit in the synthesis of bacterial aromatic polyketides.{30632,30633}

Size	1 mg
Shipping	dry ice
CAS Number	108347-84-8
Molecular Formula	C₂₄H₃₈N₇O₁₉P₃S • XLi
SMILES	O[C@H]1[C@H](N2C=NC3=C2N=CN=C3N)O[C@H](COP(OP(OCC(C)(C)[C@@H](O)C(NCCC(NCCSC(CC(O)=O)=O)=O)=O)(O)=O)(O)=O)[C@H]1OP(O)(O)=O.[Li]
Molecular Weight	860,5
Formulation	A crystalline solid
Purity	≥90%
Custom Code	2930.90
UNSPSC code	12352100

Technical File

MSDS

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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.

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ISO Guide 34:2009

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