Inhibitor of Ras farnesyltransferase.
AChE inhibitor (more selective over BuChE).
Active against Gram-positive bacteria.
Shows apoptosis inhibiting activity.
Product Specification
| Formula: | C28H34N2O7 |
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| MW: | 510.6 |
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| Source: | Isolated from Streptomyces parvulus. |
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| CAS: | 139023-58-8 |
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| Purity: | ≥98% (HPLC) |
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| Identity: | Identity determined by 1H-NMR and UV. |
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| Appearance: | Yellow to brown powder. |
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| Solubility: | Soluble in methanol or DMSO. |
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| Long Term Storage: | -20°C |
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| Use/Stability: | Store, as supplied, at -20°C for up to 1 year. Store solutions at -20°C for up to 3 months. |
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| Handling: | Protect from light. |
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Product Literature References
Pathobiology of renal-specific oxidoreductase/myo-inositol oxygenase in diabetic nephropathy: its implications in tubulointerstitial fibrosis: P. Xie, et al.; Am. J. Physiol. Renal Physiol.
298, F1393 (2010),
Abstract;
Full Text
An HTS approach to screen for antagonists of the nuclear export machinery using high content cell-based assays: F. Zanella, et al.; Assay Drug Dev. Technol.
5, 333 (2007),
Abstract;
Isolation and characterization of N98-1272 A, B and C, selective acetylcholinesterase inhibitors from metabolites of an actinomycete strain: Z.H. Zheng, et al.; J. Enzyme Inhib. Med. Chem.
22, 43 (2007),
Abstract;
Binding of manumycin A inhibits IkappaB kinase beta activity: M. Bernier, et al.; J. Biol. Chem.
281, 2551 (2006),
Abstract;
Enhancement of manumycin A-induced apoptosis by methoxyamine in myeloid leukemia cells: M. She, et al.; Leukemia
19, 595 (2005),
Abstract;
Manumycin A and its analogues are irreversible inhibitors of neutral sphingomyelinase: C. Arenz, et al.; ChemBioChem
2, 141 (2001),
Abstract;
Manumycin inhibits ras signal transduction pathway and induces apoptosis in COLO320-DM human colon tumour cells: A. Di Paolo, et al.; Br. J. Cancer
82, 905 (2000),
Abstract;
Protein kinase C, but not tyrosine kinases or Ras, plays a critical role in angiotensin II-induced activation of Raf-1 kinase and extracellular signal-regulated protein kinases in cardiac myocytes: Y. Zou et al.; J. Biol. Chem.
271, 33592 (1996),
Abstract;
Farnesyltransferase inhibitors: Ras research yields a potential cancer therapeutic: J.B. Gibbs, et al.; Cell
77, 175 (1994),
Abstract;
Identification of Ras farnesyltransferase inhibitors by microbial screening: M. Hara et al.; PNAS
90, 2281 (1993),
Abstract;
Inhibitors of Ras farnesyltransferases: F. Tamanoi; TIBS
18, 349 (1993), (Review),
Abstract;