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PF-610355 HCl
Catalog No. T16509L
Alias PF-610355 HCl（4033-27-6 Free base）, PF610355 HCl, PF-610,355 HCl, PF-00610355 HCl
PF-610355 HCl is a selective and potent β2-adrenergic receptor agonist, a bronchodilator, and is used in the study of asthma and chronic obstructive pulmonary disease.
PF-610355 HCl
Catalog No. T16509LAlias PF-610355 HCl（4033-27-6 Free base）, PF610355 HCl, PF-610,355 HCl, PF-00610355 HCl
PF-610355 HCl is a selective and potent β2-adrenergic receptor agonist, a bronchodilator, and is used in the study of asthma and chronic obstructive pulmonary disease.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 1 mg | $95 | In Stock | |
| 5 mg | $210 | In Stock | |
| 10 mg | $315 | In Stock | |
| 25 mg | $585 | In Stock | |
| 50 mg | $856 | In Stock | |
| 100 mg | $1,125 | In Stock |
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Product Introduction
Bioactivity
Chemical Properties
| Description | PF-610355 HCl is a selective and potent β2-adrenergic receptor agonist, a bronchodilator, and is used in the study of asthma and chronic obstructive pulmonary disease. |
| In vivo | PF-610355 HCl is a once-daily, long-acting inhaled β2-adrenoceptor agonist. Oral bioavailability is limited due to low intestinal absorption and high first-pass metabolism, and further studies are warranted.The short half-life of PF-610355 HCl (Clint = 33 (μL/min)/mg) suggests an unconjugated intrinsic clearance of more than 10,000 (mL/min)/kg.Overall, PF-610355 HCl demonstrates desirable inhalant pharmacokinetic properties. [1] |
| Alias | PF-610355 HCl（4033-27-6 Free base）, PF610355 HCl, PF-610,355 HCl, PF-00610355 HCl |
| Molecular Weight | 479.87 |
| Formula | C19H22ClN7O6 |
Storage & Solubility Information
| Storage | store at low temperature,keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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For example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . A total of 10 animals were administered, and the formula you used is 5% 
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 DMSO (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.
(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 DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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