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Kigamicin C

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    Kigamicin C
  • Kigamicin C
Cat No: 19445
Biochemicals - Natural Products
Cayman

Kigamicins are natural antitumor antibiotics that selectively kill pancreatic cancer PANC-1 cells only under nutrient-starved conditions.{31088} They also show antimicrobial activity against Gram-positive bacteria, including methicillin-resistant S. au...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • (1S,3R,4S,8aR,11aR)-3-[[(2S,5S,6R)-5-[(2,6-dideoxy-3-O-methyl-b-D-arabinohexopyranosyl)oxy]tetrahydro-6-methyl-2H-pyran-2-yl]oxy]-1,2,3,4,8a,9,11,11a,13,14-decahydro-1,4,17,18-tetrahydroxy-11a-methyl-oxazolo[3,2-b]xantheno[4',3',2':4,5][1,3]benzodioxino[7,6-g]isoquinoline-16,19-dione
Correlated keywords:
  • antitumor anti-tumor anti-biotic anti-microbial PANC-1 PANC1 Staphylococcus MRSA Amycolatopsis Micrococcus Bacillus
Product Overview:
Kigamicins are natural antitumor antibiotics that selectively kill pancreatic cancer PANC-1 cells only under nutrient-starved conditions.{31088} They also show antimicrobial activity against Gram-positive bacteria, including methicillin-resistant S. aureus. Kigamicin C is an antitumor antibiotic that has been found in A. regifaucium.{31088,62408} It is active against various strains of S. aureus, including methicillin-resistant S. aureus (MRSA; MICs = 0.05-0.2 µg/ml), as well as M. luteus and B. subtilis (MICs = 0.05-0.2 µg/ml).{31088} Kigamicin C is cytotoxic to PANC-1 pancreatic cancer cells in nutrient-deprived media at a 100-fold lower concentration than that required for cells cultured in nutrient-rich media.
Size 500 µg
Shipping dry ice
CAS Number 680571-51-1
Molecular Formula C41H47NO16
SMILES O=C1C2=C([C@@H](O)[C@H](O[C@]3([H])O[C@H](C)[C@@H](O[C@@]4([H])C[C@@H](OC)[C@H](O)[C@@H](C)O4)CC3)C[C@@H]2O)OC(C1=C5O)=C6OCO[C@@]7([H])C6=C5C(C(O)=C(C(N(CCO8)[C@@]8(C)C9)=O)C9=C%10)=C%10C7
Molecular Weight 809,8
Formulation A solid
Purity ≥98%
Custom Code 2907.19
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.

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