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Nisin Z

🥰Excellent
Catalog No. T76264Cas No. 137061-46-2

Nisin Z has anti-inflammatory activity and reduces pro-inflammatory cytokine release by inhibiting activation of the ERK1/2 and p38 mitogen-activated protein kinase (MAPK) signaling pathways, attenuating lipopolysaccharide-induced mastitis through inhibition of the ERK1/2 and p38 mitogen-activated protein kinase signaling pathways.

Nisin Z

Nisin Z

🥰Excellent
Catalog No. T76264Cas No. 137061-46-2
Nisin Z has anti-inflammatory activity and reduces pro-inflammatory cytokine release by inhibiting activation of the ERK1/2 and p38 mitogen-activated protein kinase (MAPK) signaling pathways, attenuating lipopolysaccharide-induced mastitis through inhibition of the ERK1/2 and p38 mitogen-activated protein kinase signaling pathways.
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5 g$40In Stock
10 g$56In Stock
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Product Introduction

Bioactivity
Description
Nisin Z has anti-inflammatory activity and reduces pro-inflammatory cytokine release by inhibiting activation of the ERK1/2 and p38 mitogen-activated protein kinase (MAPK) signaling pathways, attenuating lipopolysaccharide-induced mastitis through inhibition of the ERK1/2 and p38 mitogen-activated protein kinase signaling pathways.
In vitro
Nisin Z (10 μg/mL, 24 h) promoted the detachment and differentiation of gingival fibroblasts.Nisin Z (25-75 μg/mL, 24 h) inhibited the adhesion of C. albicans to gingival cells. [2]
Nisin Z (500 and 1000 μg/mL, 24 hours) inhibited the formation of germ tubes in C. albicans. [3]
Nisin Z (100 μg/mL, 12 h) decreased LPS-induced secretion of pro-inflammatory cytokines (e.g., IL-6, TNF-α, IL-1β) in MCF10A cells Nisin Z (10-100 μg/mL, 12 h) inhibited LPS-induced activation of the ERK1/2 and p38 MAPK signaling pathways in MCF10A cells. [4]
In vivo
Nisin Z (1, 5 and 10 mg/kg, intraperitoneal injection) helps to prevent pathological damage in LPS-induced mouse mastitis model. [4]
Chemical Properties
Molecular Weight3331.03
FormulaC141H229N41O38S7
Cas No.137061-46-2
SmilesO=C(NC(C(=O)O)CCCCN)C(=C)NC(=O)C(NC(=O)C(NC(=O)C(NC(=O)C(NC(=O)C1NC(=O)C(NC(=O)C2NC(=O)C(NC(=O)C(NC(=O)C(NC(=O)C(NC(=O)C(NC(=O)C(NC(=O)C3NC(=O)CNC(=O)C(NC(=O)C(NC(=O)C(NC(=O)CNC(=O)C(NC(=O)C(NC(=O)C4NC(=O)CNC(=O)C5N(C(=O)C(NC(=O)C6NC(=O)C(NC(=O)C(=C)NC(=O)C(NC(=O)C(NC(=O)C(=CC)NC(=O)C(N)C(C)CC)CSC6)C(C)CC)CC(C)C)C(SC4)C)CCC5)CCCCN)C(SC3)C)C)CC(C)C)CCSC)CC(=O)N)CCSC)CCCCN)C(SC2)C)C)C(SC1)C)CC(=O)N)CO)C(C)CC)CC7=CN=CN7)C(C)C
Storage & Solubility Information
Storagekeep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
H2O: 8.00 mg/mL (2.40 mM), Sonication is recommended.
DMSO: 1.00 mg/mL (0.30 mM), Sonication is recommended.

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TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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