ACHN-975 TFA
Based on 1 publication(s) in Google Scholar
ACHN-975 TFA is a selective LpxC inhibitor and exhibits a subnanomolar LpxC inhibitory activity. ACHN-975 TFA is against a wide range of gram-negative bacterias with low MIC values (≤1 μg/mL).
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- Pureza: 99.02%
- No. CAS: 1410809-37-8
- Fòrmula: C22H24F3N3O6
- Peso molecular:483.44
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Almacenamiento:
4°C, sealed storage, away from moisture
* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
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Actividad biológica
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Chemical Information
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Solvente y solubilidad
- Pureza y Documentación
- Referencias
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Help & FAQs
Publications Citing Use of MedChemExpress (MCE) ACHN-975 TFA
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Actividad biológica
IC50: LpxC[1]
ACHN-975 is against Enterobacteriaceae spp with an IC50 of 0.02 nM[1].ACHN-975 is against Enterobacteriaceae spp, Pa, and Ab with MIC90 values of 1, 0.5, and >64 μg/mL, respectively[1].ACHN-975 is potently against the?P. aeruginosa?isolates tested, inhibiting 100% of the isolates at an MIC of ≤2?μg/ml. It against?Pseudomonas aeruginosa?with an MIC50?and MIC90?of 0.06 and 0.25?μg/ml, respectively[2].ACHN-975?is?against six?P. aeruginosa?isolates, it against P. aeruginosa?APAE1064, APAE1232, and APAE1064?isolates with MIC values of 0.12, 0.06?and 0.06??μg/ml, respectively[2].LpxC is highly conserved in gram-negative bacteria and catalyzes the first committed step of lipid A biosynthesis. LpxC is the bacterial enzyme Zinc-dependent metalloamidase UDP-3-O-[(R)-3-hydroxymyristoyl]-N-acetylglucosamine deacetylase[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Neutropenic mouse thigh model with P. aeruginosa ATCC 27853[2]
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Dosage:5-30 mg/kg
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Administration:Intraperitoneal administration; single dose
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Result:Had a bactericidal activity and was against the P. aeruginosa ATCC27853 strain in vivo.
Chemical Information
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No. CAS 1410809-37-8
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Appearance Solid
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Peso molecular 483.44
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Fòrmula C22H24F3N3O6
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Color Light yellow to yellow
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SMILES
O=C(N[C@H](C(NO)=O)C(C)(N)C)C1=CC=C(C#CC#C[C@H]2[C@H](CO)C2)C=C1.O=C(O)C(F)(F)F
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Envío
Room temperature in continental US; may vary elsewhere.
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Almacenamiento
4°C, sealed storage, away from moisture
* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
Publications (1)
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Journal Impact Factor
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Most Recent
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ACS Infect Dis
Genetic and Chemical Screening Reveals Targets and Compounds to Potentiate Gram-Positive Antibiotics against Gram-Negative Bacteria. [Abstract]2022 Oct 14;8(10):2187-2197. PMID: 36098580
Solvente y solubilidad
DMSO : 100 mg/mL (206.85 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.
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Pureza y Documentación
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Ficha de datos (273 KB)
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SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 KB)
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Instrucciones de manejo (2659 KB)
Referencias
[1]. Kalinin DV, et al. Insights into the Zinc-Dependent Deacetylase LpxC: Biochemical Properties and Inhibitor Design. Curr Top Med Chem. 2016;16(21):2379-430. [Content Brief]
[2]. Krause KM,et al. Potent LpxC Inhibitors with In Vitro Activity against Multidrug-Resistant Pseudomonas aeruginosa.Antimicrob Agents Chemother. 2019 Oct 22;63(11). pii: e00977-19. [Content Brief]
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 |
|---|---|---|---|---|---|
| DMSO | 1 mM | 2.0685 mL | 10.3425 mL | 20.6851 mL | 51.7127 mL |
| 5 mM | 0.4137 mL | 2.0685 mL | 4.1370 mL | 10.3425 mL | |
| 10 mM | 0.2069 mL | 1.0343 mL | 2.0685 mL | 5.1713 mL | |
| 15 mM | 0.1379 mL | 0.6895 mL | 1.3790 mL | 3.4475 mL | |
| 20 mM | 0.1034 mL | 0.5171 mL | 1.0343 mL | 2.5856 mL | |
| 25 mM | 0.0827 mL | 0.4137 mL | 0.8274 mL | 2.0685 mL | |
| 30 mM | 0.0690 mL | 0.3448 mL | 0.6895 mL | 1.7238 mL | |
| 40 mM | 0.0517 mL | 0.2586 mL | 0.5171 mL | 1.2928 mL | |
| 50 mM | 0.0414 mL | 0.2069 mL | 0.4137 mL | 1.0343 mL | |
| 60 mM | 0.0345 mL | 0.1724 mL | 0.3448 mL | 0.8619 mL | |
| 80 mM | 0.0259 mL | 0.1293 mL | 0.2586 mL | 0.6464 mL | |
| 100 mM | 0.0207 mL | 0.1034 mL | 0.2069 mL | 0.5171 mL |
ACHN-975 TFA Related Classifications
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