TFLLRN-NH2
Based on 1 Customer Validation
TFLLRN-NH2 is a PAR-1 peptide-selective agonist. TFLLRN-NH2 induces AMPK phosphorylation and attenuates LPS-induced osteoclastogenesis, NFATc1 expression, NF-κB activation, and IκBα degradation. TFLLRN-NH2 stimulates MAPK phosphorylation in hepatocellular carcinoma cells. TFLLRN-NH2 induces concentration-dependent contraction of isolated human renal artery rings, stimulates IL-6 release from human T cells, and also evokes intracellular Ca2+ mobilization in primary human renal tubular epithelial cells. TFLLRN-NH2 can be used in research related to hepatocellular carcinoma and acute lung injury.
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- Reinheit : 99.71%
- CAS. Nr.: 244095-36-1
- Formel: C35H59N11O8
- Molecular Weight:761.91
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Speicherung:
Sealed storage, away from moisture.
Powder -80°C, 2 years , -20°C, 1 year* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
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Biologische Aktivität
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Chemical Information
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Lösungsmittel & Löslichkeit
- Protokoll
- Reinheit & Dokumentation
- Verweise
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Help & FAQs
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Biologische Aktivität
Beschreibung
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PAR1 |
AMPK |
NF-κB |
IL-6 |
In Vitro
TFLLRN-NH2 (100 μM; 20 min) activates p42/p44 MAPKinase phosphorylation in HEP-3B cells[2].
TFLLRN-NH2 (100 μM) induces EGCG-sensitive p42/p44 MAPKinase activation in PHC1 and PHC2 primary HCC cultures[2].
TFLLRN-NH2 induces a significant, concentration-dependent contractile effect in isolated human renal artery rings[4].
TFLLRN-NH2 activates PAR-1 and induces intracellular Ca2+ mobilization in primary human tubular epithelial cells (HTECs); this peptide does not cross-activate PAR-2, cannot mediate PAR-1 transactivation of PAR-2, and fails to induce tissue factor (TF) synthesis in HTECs[5].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:RAW264.7 mouse monocyte/macrophage lineage cells
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Concentration:1 µg/mL (with LPS 1 µg/mL)
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Incubation Time:0, 5, 15 min
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Result:Attenuated LPS-induced IκBα degradation in RAW264.7 cells.
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Cell Line:human HCC cell line HEP-3B
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Concentration:100 μM
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Incubation Time:20 min
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Result:Caused an increase in phospho-p42/p44 MAPKinases in HEP-3B cells at 100 μM after 20 min.
- Kinase activity and phosphorylation assays
- Western Blot
- RNA extraction experimental
- Protocol for Kinase activity and phosphorylation assays
- Research Protocol for Inflammation-related Diseases
- Liver Cancer Modeling
- Ca2+ Staining Technique
- Inhalation Toxicity Study
- Osteoclast differentiation from monocyte/macrophage precursors
Chemical Information
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CAS. Nr. 244095-36-1
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Appearance Solid
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Molecular Weight 761.91
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Formel C35H59N11O8
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Color White to off-white
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Sequence
Thr-Phe-Leu-Leu-Arg-Asn-NH2
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Sequence Shortening
TFLLRN-NH2
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Versand
Room temperature in continental US; may vary elsewhere.
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Speicherung
Sealed storage, away from moisture
Powder -80°C 2 years -20°C 1 year * In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
Lösungsmittel & Löslichkeit
In Vitro:
DMSO : 50 mg/mL (65.62 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
Konzentration (Stammlösung) × Volumen (Stammlösung) = Konzentration (Ziellösung) × Volumen (Ziellösung)
In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:
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Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Working solution concentration: 0.22 mg/mL
Reinheit & Dokumentation
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Data Sheet (279 KB)
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SDS (254 KB)
- English - EN (254 KB)
- Français - FR (254 KB)
- Deutsch - DE (254 KB)
- Norwegian - NO (254 KB)
- Español - ES (254 KB)
- Swedish - SV (254 KB)
- Italian - IT (254 KB)
- Korean - KR (254 KB)
- Portuguese - PT (254 KB)
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Handling Instructions (2659 KB)
Verweise
Complete Stock Solution Preparation Table
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
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| DMSO | 1 mM | 1.3125 mL | 6.5625 mL | 13.1249 mL | 32.8123 mL |
| 5 mM | 0.2625 mL | 1.3125 mL | 2.6250 mL | 6.5625 mL | |
| 10 mM | 0.1312 mL | 0.6562 mL | 1.3125 mL | 3.2812 mL | |
| 15 mM | 0.0875 mL | 0.4375 mL | 0.8750 mL | 2.1875 mL | |
| 20 mM | 0.0656 mL | 0.3281 mL | 0.6562 mL | 1.6406 mL | |
| 25 mM | 0.0525 mL | 0.2625 mL | 0.5250 mL | 1.3125 mL | |
| 30 mM | 0.0437 mL | 0.2187 mL | 0.4375 mL | 1.0937 mL | |
| 40 mM | 0.0328 mL | 0.1641 mL | 0.3281 mL | 0.8203 mL | |
| 50 mM | 0.0262 mL | 0.1312 mL | 0.2625 mL | 0.6562 mL | |
| 60 mM | 0.0219 mL | 0.1094 mL | 0.2187 mL | 0.5469 mL |
TFLLRN-NH2 Related Classifications
HY-P5360 Related Classifications
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Keywords
- TFLLRN-NH2
- 244095-36-1
- Protease Activated Receptor (PAR)
- AMPK
- NF-κB
- p38 MAPK
- Interleukin Related
- Thrombin receptors
- AMP-activated protein kinase
- Nuclear factor-κB
- Nuclear factor-kappaB
- IL
- AMPK phosphorylation
- IL-6 release
- IκBα degradation
- LPS-induced osteoclastogenesis
- MAPK phosphorylation
- NF-κB activation
- NFATc1 expression
- PAR-1
- hepatocellular carcinoma
- intracellular calcium mobilization
- Inhibitor
- inhibitor
- inhibit