JAK2/FLT3-IN-1

Cat No.:V51499 Purity: ≥98%
JAK2/FLT3-IN-1 is an orally bioactive dual JAK2/FLT3 conjugate with IC50s of 0.7 nM, 4 nM, 26 nM and 39 nM for JAK2, FLT3, JAK1 and JAK3, respectively.
JAK2/FLT3-IN-1 Chemical Structure CAS No.: 2387765-27-5
Product category: JAK
This product is for research use only, not for human use. We do not sell to patients.
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100mg
250mg
500mg

Other Forms of JAK2/FLT3-IN-1:

  • JAK2/FLT3-IN-1 TFA
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Top Publications Citing lnvivochem Products
Product Description
JAK2/FLT3-IN-1 is an orally bioactive dual JAK2/FLT3 conjugate with IC50s of 0.7 nM, 4 nM, 26 nM and 39 nM for JAK2, FLT3, JAK1 and JAK3, respectively. JAK2/FLT3-IN- 1 has anti-cancer activity.
Biological Activity I Assay Protocols (From Reference)
ln Vitro
JAK2/FLT3-IN-1 dose-dependently downregulates p-FLT3 (0.008-1 μM; for 2 hours)[1]. JAK2/FLT3-IN-1 (5-100 nM; for 2 hours) induces apoptosis in MV4-11 cells in a dose-dependent manner [1]. With a G1/G0 percentage of 85% at 100 nM, JAK2/FLT3-IN-1 (5-100 nM; for 2 hours) significantly induces cell cycle arrest in MV4-11 cells [1].
ln Vivo
JAK2/FLT3-IN-1 (30 and 60 mg/kg/day; orally; for 14 days) displays substantial anti-tumor effects [1].
Cell Assay
Western Blot Analysis[1]
Cell Types: MV4-11 and SET-2 Cell
Tested Concentrations: 0.008, 0.04, 0.2, 1 μM
Incubation Duration: 2 hrs (hours)
Experimental Results: p-FLT3 was downregulated from 0.008 to 1μM in a dose-dependent manner.

Apoptosis analysis [1]
Cell Types: MV4-11 Cell
Tested Concentrations: 5, 10, 50, 100 nM
Incubation Duration: 2 hrs (hours)
Experimental Results: It has a dose-dependent effect on inducing apoptosis of MV4-11 cells.

Cell cycle analysis[1]
Cell Types: MV4-11 Cell
Tested Concentrations: 5, 10, 50, 100 nM
Incubation Duration: 2 hrs (hours)
Experimental Results: Induced cell cycle arrest at 100 nM with a G1/G0 percentage of 85%.
Animal Protocol
Animal/Disease Models: NOD/SCID mouse model [1]
Doses: 30 and 60 mg/kg
Route of Administration: oral; daily; 14-day
Experimental Results: demonstrated significant anti-tumor effect. In the MV4-11-carrying mouse model, the tumor growth inhibition rates (TGI) were 58% and 93%, respectively.
References
[1]. Yang T, et al. Discovery of Potent and Orally Effective Dual JAK2/FLT3 Inhibitors for the Treatment of AcuteMyelogenous Leukemia and Myeloproliferative Neoplasms. J Med Chem. 2019 Oct 31.
These protocols are for reference only. InvivoChem does not independently validate these methods.
Physicochemical Properties
Molecular Formula
C25H34FN7O
Molecular Weight
467.582
CAS #
2387765-27-5
Related CAS #
JAK2/FLT3-IN-1 TFA;2928093-29-0
SMILES
C1CC(CCN1C1C=CC(=CC=1F)NC1=NC=C(C)C(C2C=NN(C(C)C)C=2)=N1)N(C)CCO
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 : ~35 mg/mL (~74.85 mM)
Solubility (In Vivo)
Solubility in Formulation 1: 2.08 mg/mL (4.45 mM) in 10% DMSO + 40% PEG300 + 5% Tween80 + 45% 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 20.8 mg/mL clear DMSO stock solution to 400 μL PEG300 and mix evenly; then add 50 μL Tween-80 to the above solution and mix evenly; then add 450 μL normal saline to adjust the volume to 1 mL.
Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH₂ O to obtain a clear solution.

Solubility in Formulation 2: ≥ 2.08 mg/mL (4.45 mM) (saturation unknown) in 10% DMSO + 90% (20% SBE-β-CD in Saline) (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 20.8 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.

 (Please use freshly prepared in vivo formulations for optimal results.)
Preparing Stock Solutions 1 mg 5 mg 10 mg
1 mM 2.1387 mL 10.6934 mL 21.3867 mL
5 mM 0.4277 mL 2.1387 mL 4.2773 mL
10 mM 0.2139 mL 1.0693 mL 2.1387 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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