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L-NIL [I1001]
Description: L-NIL.dihydrochloride is a selective inhibitor of inducible Nitric Oxide Synthase (iNOS).
Chemical Formula: C8H17N3O2.2HCl
Chemical Name: : N6-(1-Iminoethyl)-L-lysine.dihydrochloride
Molecular Weight: M.W. 223.7
Solubility: Soluble in Water.
CAS Number: CAS [150403-89-7]
Active Product: N
Appearance: White Solid
Purity: >98%
Handling: Extremely Hygroscopic. Protect from Moisture. Store in Tightly Sealed Vial.
Storage: -20°C.
Shipping: Express Courier
General Comments: Please inquire for D-NIL, D-N6-(1-Iminoethyl)-lysine.hydrochloride.
Literature Reference: 1. Moore, W.M., R.K. Webber, G.M. Jerome, F.S. Tjoeng, T.P. Misko, M.G. Currie., L-N6-(1-Iminoethyl)-lysine: A Selective Inhibitor of Inducible Nitric Oxide Synthase., 1994., 23:, 3886-3888., 2. Stenger, S., H. Thuring, M. Rollinghoff, P. Manning, C. Bogdan..
Literature Reference: L-N6-(1-Iminoethyl)-lysine Potently Inhibits Inducible Nitric Oxide Synthase and is Superior to NG-Monomethyl-arginine In Vitro and In Vivo., European Journal of Pharmacology., 1995., 294(2-3):, 703-712., 3. Bustamonte, S.A., et al...
Literature Reference: Inducible Nitric Oxide Synthase and the Regulation of Central Vessel Caliber in the Fetal Rat., Circulation., 1996., 94(8):, 1948-1953., 4. Southan, G.J., C. Szabo..
Literature Reference: Selective Pharmacological Inhibition of Distinct Nitric Oxide Synthase Isoforms., Biochemical Pharmacology., 1996., 51(4):, 383-394., 5. Connor, J.R., et al..
Literature Reference: Suppression of Adjuvant-Induced Arthritis by Selective Inhibition of Inducible Nitric Oxide Synthase., European Journal of Pharmacology., 1995., 273(1-2):, 15-24., 6. Handy, R.L., P.K. Moore...
Literature Reference: A Comparison of the Effects of L-NAME, 7-NI and L-NIL on Carrageenan-Induced Hindpaw Oedema and NOS Activity., British Journal of Pharmacology., 1998., 123(6):, 1119-1126..
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