CAS 159190-45-1|L-NIL dihydrochloride

Introduction:Basic information about CAS 159190-45-1|L-NIL dihydrochloride, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameL-NIL dihydrochloride
CAS Number159190-45-1Molecular Weight260.161
Density/Boiling Point369ºC at 760 mmHg
Molecular FormulaC8H19Cl2N3O2Melting Point/
MSDSChineseUSAFlash Point177ºC
Symbol
GHS07
Signal WordWarning

Names

NameL-N6-(1-Iminoethyl)lysine dihydrochloride
SynonymMore Synonyms

L-NIL dihydrochloride BiologicalActivity

DescriptionL-NIL dihydrochloride is an inducible NO synthase inhibitor, with an IC50 of 3.3 μM for miNOS[1][2][3].
Related CatalogSignaling Pathways >>Immunology/Inflammation >>NO SynthaseResearch Areas >>Inflammation/Immunology
Target

IC50: 3.3 μM (mouse inducible NO synthase), 92 μM (rat brain constitutive NO synthase)[3].

In VitroL-NIL produces a concentration-dependent inhibition of both the mouse inducible NOS (miNOS) and the rat brain constitutive NOS (rcNOS) and is considerably more potent for miNOS. The IC50 values for L-NIL with miNOS and rcNOS are 3.3 and 92 pM, respectively, indicating that L-NIL is 28-fold more selective for miNOS. In addition, L-NIL has approximately 6-fold greater potency for miNOS than either L-NMA or L-NNA[2].
In VivoL-NIL (10 and 30 mg/kg, IP) prevents the inflammation, oxidative stress and autophagy induced by renal IR in mice[1]. Animal Model: Adult male Balb/c (20-25 g)[1]. Dosage: 10 and 30 mg/kg. Administration: Intraperitoneally at the end of CLP and at 6 h after sepsis induction. Result: Led to a negligible increase in plasma NGAL compared to sham mice. Led to a significant decrease in both TLR4 and IL1βprotein contents and clusterin transcript. Showed an increase in NFAT5 mRNA levels, as compared with mice treated with vehicle. Promoted a decrease in AR protein expression, as compared with animals treated with vehicle.
References

[1]. Consuelo Pasten, et al. l-NIL prevents the ischemia and reperfusion injury involving TLR-4, GST, clusterin, and NFAT-5 in mice. Am J Physiol Renal Physiol. 2019 Apr 1;316(4):F624-F634.

[2]. Sharon Angela Tanuseputero, et al. Intravenous Arginine Administration Downregulates NLRP3 Inflammasome Activity and Attenuates Acute Kidney Injury in Mice with Polymicrobial Sepsis. Mediators Inflamm. 2020 May 11;2020:3201635.

[3]. W M Moore, et al. L-N6-(1-iminoethyl)lysine: a selective inhibitor of inducible nitric oxide synthase. J Med Chem. 1994 Nov 11;37(23):3886-8.

Chemical & Physical Properties

Boiling Point369ºC at 760 mmHg
Molecular FormulaC8H19Cl2N3O2
Molecular Weight260.161
Flash Point177ºC
Exact Mass259.085419
PSA99.20000
LogP2.95030
InChIKeyOQIBCXRAFAHXMM-UHFFFAOYSA-N
SMILESCC(N)=NCCCCC(N)C(=O)O.Cl.Cl
Storage condition20°C

Safety Information

Symbol
GHS07
Signal WordWarning
Hazard StatementsH315-H319-H335
Precautionary StatementsP261-P305 + P351 + P338
Personal Protective Equipmentdust mask type N95 (US);Eyeshields;Gloves
Hazard CodesXi: Irritant;
Risk PhrasesR36/37/38
Safety PhrasesS37/39
RIDADRNONH for all modes of transport

Articles3

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L-N6-(1-iminoethyl)lysine: a selective inhibitor of inducible nitric oxide synthase.

J. Med. Chem. 37 , 3886, (1994)

L-N6-(1-Iminoethyl)lysine (L-NIL) has been synthesized and is shown to be both a potent and selective inhibitor of mouse inducible nitric oxide synthase (miNOS). L-NIL has an IC50 of 3.3 microM for mi...

Synonyms

N(6)-acetimidoyl-L-lysine dihydrochloride
N-Ethanimidoyl-L-lysine dihydrochloride
l-n6-(1-iminoethyl)lysine dihydrochloride
L-Lysine, N-(1-iminoethyl)-, hydrochloride (1:2)
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