Ablukast (Ro23-3544)

Alias: Ro-23-3544; Ro23-3544; Ablukast; Ro 23-3544/000; Ro 23-3544; Ro 233544; Ro-233544; Ro233544
Cat No.:V9950 Purity: ≥98%
Ablukast (Ro 23-3544) is a novel and potent leuktriene receptor antagonist with anti-asthmatic effects.
Ablukast (Ro23-3544) Chemical Structure CAS No.: 96566-25-5
Product category: Leukotriene Receptor
This product is for research use only, not for human use. We do not sell to patients.
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Product Description

Ablukast (Ro 23-3544) is a novel and potent leuktriene receptor antagonist with anti-asthmatic effects. It successfully lessens bronchoconstriction brought on by LTC4 and antigens.

Biological Activity I Assay Protocols (From Reference)
Targets
LTD4
ln Vitro
Ablukast (Ro 23-3544) is evaluated for its ability to mitigate allergic contact dermatitis caused by dinitrofluorobenzene (DNFB) and irritant contact dermatitis caused by croton oil in mouse ears. Treatment for dermatitis elicited within a few days and continued for up to five days after that was moderately effective in suppressing dose-dependent ear swelling caused by DNFB. The DNFB-induced ear swelling during the first 48 hours following elicitation is significantly reduced after daily pre-treatment of the ears for one week[2].
ln Vivo
Ablukast (Ro 23-3544) is evaluated for its ability to mitigate allergic contact dermatitis caused by dinitrofluorobenzene (DNFB) and irritant contact dermatitis caused by croton oil in mouse ears. Treatment for dermatitis elicited within a few days and continued for up to five days after that was moderately effective in suppressing dose-dependent ear swelling caused by DNFB. The DNFB-induced ear swelling during the first 48 hours following elicitation is significantly reduced after daily pre-treatment of the ears for one week[2].
Animal Protocol
Female BALB/c mice
Concentrations of 0.1 , 0.5 , 1.0 and 5.0 % of Ablukast
Applied to one of the pretreated ears 1 h after elicitation and at 24 h intervals on the following 4 days; three times daily
References

[1]. Pharmacological profile of Ro 23-3544, a new aerosol active leukotriene receptor antagonist. Adv Prostaglandin Thromboxane Leukot Res. 1987;17A:512-8.

[2]. Studies on the role of leukotrienes in murine allergic and irritant contact dermatitis. Br J Dermatol. 1988 Jan;118(1):1-6.

[3]. Pyrrolopyrimidines as phosphodiesterase VII inhibitors. US7498334B2.

These protocols are for reference only. InvivoChem does not independently validate these methods.
Physicochemical Properties
Molecular Formula
C28H34O8
Molecular Weight
498.57
Exact Mass
498.23
Elemental Analysis
C, 67.45; H, 6.87; O, 25.67
CAS #
96566-25-5
Related CAS #
96686-71-4 (S-isomer); 96686-73-6 (R-isomer); 96565-55-8 (sodium); 96566-25-5 (free acid)
Appearance
Solid powder
SMILES
CCCC1=C(C=CC(=C1O)C(=O)C)OCCCCCOC2=C(C=C3CCC(OC3=C2)C(=O)O)C(=O)C
InChi Key
FGGYJWZYDAROFF-UHFFFAOYSA-N
InChi Code
InChI=1S/C28H34O8/c1-4-8-21-23(12-10-20(17(2)29)27(21)31)34-13-6-5-7-14-35-26-16-25-19(15-22(26)18(3)30)9-11-24(36-25)28(32)33/h10,12,15-16,24,31H,4-9,11,13-14H2,1-3H3,(H,32,33)
Chemical Name
6-acetyl-7-[5-(4-acetyl-3-hydroxy-2-propylphenoxy)pentoxy]-3,4-dihydro-2H-chromene-2-carboxylic acid
Synonyms
Ro-23-3544; Ro23-3544; Ablukast; Ro 23-3544/000; Ro 23-3544; Ro 233544; Ro-233544; Ro233544
HS Tariff Code
2934.99.9001
Storage

Powder      -20°C    3 years

                     4°C     2 years

In solvent   -80°C    6 months

                  -20°C    1 month

Shipping Condition
Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)
Solubility Data
Solubility (In Vitro)
DMSO: ~100 mg/mL (~200.6 mM)
Solubility (In Vivo)
Solubility in Formulation 1: 2.5 mg/mL (5.01 mM) in 10% DMSO + 90% (20% SBE-β-CD in Saline) (add these co-solvents sequentially from left to right, and one by one), suspension solution; with sonication.
For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 25.0 mg/mL clear DMSO stock solution to 900 μL of 20% SBE-β-CD physiological saline solution and mix evenly.
Preparation of 20% SBE-β-CD in Saline (4°C,1 week): Dissolve 2 g SBE-β-CD in 10 mL saline to obtain a clear solution.

Solubility in Formulation 2: ≥ 2.5 mg/mL (5.01 mM) (saturation unknown) in 10% DMSO + 90% Corn Oil (add these co-solvents sequentially from left to right, and one by one), clear solution.
For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 25.0 mg/mL clear DMSO stock solution to 900 μL of corn oil and mix evenly.

 (Please use freshly prepared in vivo formulations for optimal results.)
Preparing Stock Solutions 1 mg 5 mg 10 mg
1 mM 2.0057 mL 10.0287 mL 20.0574 mL
5 mM 0.4011 mL 2.0057 mL 4.0115 mL
10 mM 0.2006 mL 1.0029 mL 2.0057 mL

*Note: Please select an appropriate solvent for the preparation of stock solution based on your experiment needs. For most products, DMSO can be used for preparing stock solutions (e.g. 5 mM, 10 mM, or 20 mM concentration); some products with high aqueous solubility may be dissolved in water directly. Solubility information is available at the above Solubility Data section. Once the stock solution is prepared, aliquot it to routine usage volumes and store at -20°C or -80°C. Avoid repeated freeze and thaw cycles.

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Note: Chemical formula is case sensitive: C12H18N3O4  c12h18n3o4
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In vivo Formulation Calculator (Clear solution)
Step 1: Enter information below (Recommended: An additional animal to make allowance for loss during the experiment)
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Calculation results

Working concentration mg/mL;

Method for preparing DMSO stock solution mg drug pre-dissolved in μL DMSO (stock solution concentration mg/mL). Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.

Method for preparing in vivo formulation:Take μL DMSO stock solution, next add μL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O,mix and clarify.

(1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
             (2) Be sure to add the solvent(s) in order.

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