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CRT0273750

🥰Excellent
Catalog No. T31101Cas No. 1979939-16-6
Alias CRT-0273750, CRT 0273750

CRT0273750 regulates plasma LPA levels and is suitable for in vivo studies. CRT0273750 is an autotaxin (ATX) inhibitor with IC50 of 0.014 μM.

CRT0273750

CRT0273750

🥰Excellent
Purity: 99.49%
Catalog No. T31101Alias CRT-0273750, CRT 0273750Cas No. 1979939-16-6
CRT0273750 regulates plasma LPA levels and is suitable for in vivo studies. CRT0273750 is an autotaxin (ATX) inhibitor with IC50 of 0.014 μM.
Pack SizePriceAvailabilityQuantity
1 mg$30In Stock
5 mg$71In Stock
10 mg$116In Stock
25 mg$238In Stock
50 mg$357In Stock
100 mg$535In Stock
1 mL x 10 mM (in DMSO)$77In Stock
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Purity:99.49%
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Product Introduction

Bioactivity
Description
CRT0273750 regulates plasma LPA levels and is suitable for in vivo studies. CRT0273750 is an autotaxin (ATX) inhibitor with IC50 of 0.014 μM.
Targets&IC50
ATX:0.014 μM
In vitro
CRT0273750 is also shown to inhibit the migration of 4T1 cells with an EC50 of 0.025μM[1]. CRT0273750 shows high potency in both the biochemical (IC50 = 0.01 μM) and plasma choline release assay(IC50 = 0.014 μM)[1].
In vivo
CRT0273750 treatment shows the Cmax, AUC and t1/2 values of 3.8 μM, 3.2 μM.h and 1.4 h, respectively and shows a proportional increase[1].CRT0273750 has a moderate blood clearance, with value of 41 mL/min/kg[1].
AliasCRT-0273750, CRT 0273750
Chemical Properties
Molecular Weight502.92
FormulaC25H22ClF3N4O2
Cas No.1979939-16-6
SmilesC[C@H](NC(=O)CCc1nc2cccnc2n1Cc1ccc(OC(F)(F)F)cc1)c1ccc(Cl)cc1
Relative Density.1.35 g/cm3 (Predicted)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 200 mg/mL (397.68 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.9884 mL9.9419 mL19.8839 mL99.4194 mL
5 mM0.3977 mL1.9884 mL3.9768 mL19.8839 mL
10 mM0.1988 mL0.9942 mL1.9884 mL9.9419 mL
20 mM0.0994 mL0.4971 mL0.9942 mL4.9710 mL
50 mM0.0398 mL0.1988 mL0.3977 mL1.9884 mL
100 mM0.0199 mL0.0994 mL0.1988 mL0.9942 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent 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 DMSOTargetMol | reagent (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 DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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