research use only
Cat.No.S5003
| Related Targets | PI3K Akt mTOR GSK-3 ATM/ATR DNA-PK AMPK PDPK1 PTEN PP2A |
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| Other FKBP Inhibitors | dTAG-13 Rimiducid (AP1903) Shield-1 (Shld1) AP20187 (B/B Homodimerizer) S107 hydrochloride dTAGV-1 TFA SAFit2 |
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In vitro |
DMSO
: 120 mg/mL
(149.25 mM)
Ethanol : 100 mg/mL Water : Insoluble The solubility data above are all experimental results (not literature values). |
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In vivo |
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Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)
Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)
Calculation results:
Working concentration: mg/ml;
Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid 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 master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.
Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.
Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.
Read more about FK506 (Tacrolimus) solubility in DMSO or water
Read more about FK506 (Tacrolimus) working concentrations for cell culture treatment
| Information | FK506 is a potent calcineurin inhibitor. It affects NFAT signaling pathways, by binding to FKBP12, inhibiting T-cell activation. |
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Read more about FK506 (Tacrolimus) IC50 for cell-based and cell-free assays |
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| Primary Applications and Mechanism of Action | |
| Molecular Weight | 804.02 | Formula | C44H69NO12 |
Storage (From the date of receipt) | |
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| CAS No. | 104987-11-3 | Download SDF | Storage of Stock Solutions |
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| Synonyms | FR900506, Fujimycin | Smiles | CC1CC(C2C(CC(C(O2)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C(CC(=O)C(C=C(C1)C)CC=C)O)C)C(=CC4CCC(C(C4)OC)O)C)O)C)OC)OC | ||
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Question 1:
We would like to inject it subcutaneously into rats. Can we mix it with 5% dextrose to a concentration of 5mg/ml to prepare the solution?
Answer:
You can dissolve it with DMSO to prepare the stock solution, and then dilute by 5% dextrose. However, we don't have the information about the solubility in this condition. Or you can use the vehicle we tested: 30% PEG400/0.5% Tween80/5% propylene glycol (Solubility: 30mg/ml).