research use only
Cat.No.S8960
| Related Targets | CFTR CRM1 AChR Calcium Channel Sodium Channel Potassium Channel GABA Receptor TRP Channel ATPase GluR |
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| Other CD markers Inhibitors | SodiuM Metatungstate LY-3475070 Cynarin AX-024 HCl NQ301 ADH-503 (GB1275) AB680 Angstrom6 MK-0159 RBN013209 |
| Molecular Weight | 413.53 | Formula | C22H27N3O3S |
Storage (From the date of receipt) | 3 years -20°C powder |
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| CAS No. | 1700637-55-3 | -- | Storage of Stock Solutions |
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| Synonyms | CD38-IN-78c, MDK-7553 | Smiles | CN1C2=C(C=C(C=C2)C3=CN=CS3)C(=CC1=O)NC4CCC(CC4)OCCOC | ||
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In vitro |
DMSO
: 42 mg/mL
(101.56 mM)
Water : Insoluble Ethanol : Insoluble |
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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.
| Targets/IC50/Ki |
mCD38
(Cell-free assay) 1.9 nM
hCD38
(Cell-free assay) 7.3 nM
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| In vitro |
CD38 inhibitor 1 (compound 78c) increases NAD+ levels, resulting in activation of pro-longevity and health span-related factors including sirtuins, AMPK, and PARPs. |
| In vivo |
CD38 inhibitor 1 (compound 78c) is found to not only be a very potent inhibitor, but also had suitable physiochemical properties to serve as a robust tool for in vivo studies. In addition, this compound is able to elevate NAD in both liver and gastrocnemius tissue when dosed orally in a DIO mouse. |
References |
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