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Latanoprostene bunod

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Catalog No. T15719Cas No. 860005-21-6
Alias NCX116, LBN

Latanoprostene bunod (LBN) is nitric oxide (NO)-donating prostaglandin F2a analog and is a topical ophthalmic therapeutic. It is used for the reduction of intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension (OHT).

Latanoprostene bunod

Latanoprostene bunod

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Purity: 99.69%
Catalog No. T15719Alias NCX116, LBNCas No. 860005-21-6
Latanoprostene bunod (LBN) is nitric oxide (NO)-donating prostaglandin F2a analog and is a topical ophthalmic therapeutic. It is used for the reduction of intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension (OHT).
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$73In Stock-
5 mg$189In Stock-
10 mg$297In Stock-
25 mg$492In Stock-
50 mg$717In Stock-
100 mg$988In Stock-
200 mg$1,330InquiryInquiry
500 mg$1,980InquiryInquiry
1 mL x 10 mM (in DMSO)$209In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.69%
Appearance:Oil
Color:Transparent
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Product Introduction

Latanoprostene bunod AI Summary
Latanoprostene bunod exhibits a broad spectrum of bioactivities with relatively weak binding affinity and inhibition activities. It has a half-life of 1.8 hours in rabbits. The compound interacts with various human receptors and enzymes, including but not limited to DRD1, SLC6A3, ADORA1, and Gabra1, with most binding affinity (AC50) values being greater than 30,000.0 nM. It shows moderate to weak inhibition against enzymes like ACHE, MAOA, and PDE3A, with AC50 values also above 30,000.0 nM, except for PTGS1 inhibition measured by fluorescence, which has an AC50 of 13,489.9 nM. Additionally, the compound displays antagonist and agonist activities at some receptors, notably TBXA2R and ADRA1A, with AC50 values just over 10,000.0 nM..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Latanoprostene bunod (LBN) is nitric oxide (NO)-donating prostaglandin F2a analog and is a topical ophthalmic therapeutic. It is used for the reduction of intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension (OHT).
SynonymsNCX116, LBN
Chemical Properties
Molecular Weight507.62
FormulaC27H41NO8
Cas No.860005-21-6
SmilesO[C@H](CC[C@H]1[C@H](O)C[C@H](O)[C@@H]1C\C=C/CCCC(=O)OCCCCO[N+]([O-])=O)CCc1ccccc1
Relative Density.1.178 g/cm3 (Predicted)
Storage & Solubility Information
StoragePure form: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 100 mg/mL (197 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 4 mg/mL (7.88 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.9700 mL9.8499 mL19.6998 mL98.4989 mL
5 mM0.3940 mL1.9700 mL3.9400 mL19.6998 mL
10 mM0.1970 mL0.9850 mL1.9700 mL9.8499 mL
20 mM0.0985 mL0.4925 mL0.9850 mL4.9249 mL
50 mM0.0394 mL0.1970 mL0.3940 mL1.9700 mL
100 mM0.0197 mL0.0985 mL0.1970 mL0.9850 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
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%
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