Potent and specific inhibitor of arginase. Does not inhibit NO synthases.
Product Specification
| Alternative Name: | 2(S)-Amino-6-boronohexanoic acid . NH4 |
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| Formula: | C6H13BNO4 . NH4 |
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| MW: | 174.0 . 18.0 |
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| Purity: | ≥95.0% (1H-NMR) |
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| Appearance: | White to off-white powder. |
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| Solubility: | Soluble in water. |
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| Short Term Storage: | +4°C |
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| Long Term Storage: | -20°C |
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| Use/Stability: | Solutions are stable for 6 months when stored at -20°C. |
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| Handling: | After reconstitution, prepare aliquots and store at -20°C. Hygroscopic. |
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| Background / Technical Information: | Note: Can contain up to 15% ammonium chloride. This does not affect activity, but must be taken into account for calculation of concentrations. |
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Product Literature References
Crystal structure of human arginase I at 1.29-A resolution and exploration of inhibition in the immune response: L. Di Costanzo, et al.; PNAS
102, 13058 (2005),
Abstract;
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Role of arginase in the male and female sexual arousal response: N.N. Kim, et al.; J. Nutr.
134, 2873S (2004),
Abstract;
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Arginase and autoimmune inflammation in the central nervous system: L. Xu, et al.; Immunology
110, 141 (2003),
Abstract;
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Arginase expression and modulation of IL-1beta-induced nitric oxide generation in rat and human islets of Langerhans: P. Stickings, et al.; Nitric Oxide
7, 289 (2002),
Abstract;
Classical and slow-binding inhibitors of human type II arginase: D.M. Colleluori and D.E. Ash; Biochemistry (Mosc).
40, 9356 (2001),
Abstract;
Increased expression of arginase II in human diabetic corpus cavernosum: in diabetic-associated erectile dysfunction: T.J. Bivalacqua, et al.; BBRC
283, 923 (2001),
Abstract;
Arginase-boronic acid complex highlights a physiological role in erectile function: J.D. Cox, et al.; Nat. Struct. Biol.
6, 1043 (1999),
Abstract;
Biochemical and functional profile of a newly developed potent and isozyme-selective arginase inhibitor: R. Baggio, et al.; J. Pharmacol. Exp. Ther.
290, 1409 (1999),
Abstract;
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Inhibition of Mn2+ 2-arginase by borate leads to the design of a transition state analog inhibitor, 2(S)-amino-6-boronohexanoic acid: R. Baggio, et al.; J. Am. Chem. Soc. 119, 8107 (1997),