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L -Arginine

Our experience conditions us to focus on the organic components of the reaction—l arginine and l citrul line—and to give less attention to the inorganic one—nitric oxide (nitrogen monoxide NO) To do so however would lead us to overlook one of the most important discoveries in biology in the last quarter of the twentieth century... [Pg.1149]

Three years later Robert F Furchgott discov ered that the relaxing of smooth muscles such as blood vessel walls was stimulated by an unknown substance produced in the lining of the blood vessels (the endothelium) He called this substance the endothelium-dependent relaxing factor or EDRF and in 1986 showed that EDRF was NO Louis J Ignarro reached the same conclusion at about the same time Further support was provided by Salvador Moncada who showed that endothelial cells did in deed produce NO and that the l arginine to l citrulline conversion was responsible... [Pg.1149]

Most NOS inhibitors are stmcturaHy related to L-arginine and do not differentiate between the isoforms (Table 15). t - / 7-Methy1 arginine (l-NMA) (264) is a competitive inhibitor and also irreversibly inhibits NOS. T.-/ 7-Nitroarginine (l-NNA) (265), L-AP -nitroarginine methyl ester (t.-NAMF) (266),... [Pg.564]

For any measurement of optical rotation, the wavelength of the light used and the temperature must both be specified. In this case, D refers to the d line of sodium at 589 nm and 25 refers to a measurement temperature of 25°C. Calculate the concentration of a solution of L-arginine that rotates the incident light by 0.35° in an optical path length of 1 dm (decimeter). [Pg.106]

Chemical Name Glutamic Acid Compound with L-Arginine Common Name —... [Pg.102]

It is a peptide containing 27 amino acid residues containing the amino acids L-histidine (His) L-aspartic acid (Asp) L-serine (Ser) glycine (Gly) L-threonine (Thr) L-phenyl-alanine (Phe) L-glutamic acid (Glu) L-glutamine [Glu(NHj)] L-leucine (Leu) L-arginine (Arg) L-alanine (Ala) and L-valinamide (Va -NHj). [Pg.1371]

L-Arginine Arginase + Urease (double reaction) nh3, co2 Tris pH 7 NHj-airgap ... [Pg.255]

L-NAME (N-nitro-L-arginine methyl ester), like L-NMMA, is a structural analogue of L-arginine and competes with L-arginine for NO-synthase, which uses L-arginine as a substrate for the formation of NO. L-NMMA and L-NAME are very effective NO-synthesis inhibitors, both in vitro and in vivo. [Pg.679]


See other pages where L -Arginine is mentioned: [Pg.1149]    [Pg.1149]    [Pg.1149]    [Pg.857]    [Pg.486]    [Pg.69]    [Pg.146]    [Pg.312]    [Pg.564]    [Pg.270]    [Pg.282]    [Pg.282]    [Pg.289]    [Pg.289]    [Pg.290]    [Pg.290]    [Pg.292]    [Pg.293]    [Pg.297]    [Pg.122]    [Pg.307]    [Pg.308]    [Pg.521]    [Pg.340]    [Pg.1149]    [Pg.1149]    [Pg.1149]    [Pg.96]    [Pg.118]    [Pg.102]    [Pg.102]    [Pg.1615]    [Pg.63]    [Pg.15]    [Pg.406]    [Pg.233]    [Pg.218]    [Pg.856]   
See also in sourсe #XX -- [ Pg.1112 , Pg.1114 , Pg.1119 ]

See also in sourсe #XX -- [ Pg.110 ]




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A -Benzoyl-L-arginine-p-nitroanilide

A -nitro-L-arginine methyl ester

A-Acyl-L-arginine

A-Hydroxy-L-arginine

A-Methyl-L-arginine

Arginine (L-Arg)

Benzoyl-L-arginine amide

Difluoro-L-arginine

L- Arginine-nitric oxide pathway

L-Arginine Monohydrochloride

L-Arginine hydrochloride

L-Arginine, methyl ester

L-Deamino-8-D-Arginine Vasopressin

L-arginine amidinohydrolase

L-arginine derivative

L-arginine-guanidino

L-arginine:glycine amidinotransferase

Monomethyl-L-arginine

N-hydroxy-L-arginine

N-monomethyl-L-arginine

N-nitro-L-arginine methyl ester

NG-Monomethyl-L-arginine

Nitric oxide from L-arginine

N®-Nitro-L-arginine

Poly-L-arginine

Secondary Products Derived from l-Arginine

Superoxide Anion in the Enzymatic Conversion of L-Arginine to NO

The l-Arginine-Nitric Oxide Pathway

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