© 2008 Alexis Corporation
ALX-380-099 Revised 03-Apr-08
Concanamycin C
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PRODUCT LINE Natural Products / Antibiotics
PRODUCT CATEGORY Antibiotics - ATPase Inhibitors
Ordering Information
Product Numbers: Format: Size: Unit Price: Quantity: Add To Cart
ALX-380-099-C100   100 µg 30.00 USD Add To Cart
ALX-380-099-C500   500 µg 90.00 USD Add To Cart
Product Specification
FORMULA: C45H74O13
MW: 823.1
CAS NUMBER: 81552-34-3
RTECS: GK6887000
SOURCE/HOST: Isolated from Streptomyces sp.
PURITY: ≥96%
APPEARANCE: White to off-white solid.
SOLUBILITY: Soluble in chloroform, methanol, acetonitrile or DMSO. Insoluble in water.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C
HANDLING: Protect from light.
HAZARD: VERY TOXIC.

Product Description
Antibiotic. Inhibits vacuolar-type H+-ATPase. Potential antiosteoporotic agent. Shows antiviral and immunosuppressive activity. Active against fungi and yeasts.
Product Specific Literature References
Structures of concanamycins B and C: H. Kinashi, et al.; J. Antibiot. (Tokyo) 35, 1618 (1982) Abstract
Isolation and characterization of concanamycins A, B and C: H. Kinashi, et al.; J. Antibiot. (Tokyo) 37, 1333 (1984) Abstract
Inhibitory effect of modified bafilomycins and concanamycins on P- and V-type adenosinetriphosphatases: S. Drose, et al.; Biochemistry 32, 3902 (1993) Abstract
Disruption of vma-1, the gene encoding the catalytic subunit of the vacuolar H(+)-ATPase, causes severe morphological changes in Neurospora crassa: E.J. Bowman, et al.; J. Biol. Chem. 275, 167 (2000) Abstract
Semisynthetic derivatives of concanamycin A and C, as inhibitors of V- and P-type ATPases: structure-activity investigations and developments of photoaffinity probes: S. Drose, et al.; Biochemistry 40, 2816 (2001) Abstract