SBP-7455
This product is for research use only, not for human use. We do not sell to patients.
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Size | Price | Stock |
---|---|---|
250mg | $1350 | Check With Us |
500mg | $2160 | Check With Us |
1g | $3240 | Check With Us |
Cat #: V2248 CAS #: 1884222-74-5 Purity ≥ 99%
Description: SBP-7455 is a potent dual inhibitors of ULK1 and ULK2 (ULK1/2),It potently inhibited ULK1/2 enzymatic activity.
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Molecular Weight (MW) | 354.33 |
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Molecular Formula | C16H17F3N4O2 |
CAS No. | 1884222-74-5 |
SMILES Code | COC1=C(OC)C=CC(NC2=NC(NC3CC3)=C(C(F)(F)F)C=N2)=C1 |
Synonyms | SBP-7455; SBP7455; SBP 7455; |
Protocol | In Vitro | SBP-7455 (compound 26; 72 h) treatment inhibits cell growth with an IC50 of 0.3 μM for MDA-MB-468 cells. SBP-7455 inhibits starvation-induced autophagic flux in TNBC cells that are dependent on autophagy for survival. |
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In Vivo | A single dose of SBP-7455 (compound 26) (30 mg/kg) is orally administered to mice. The Tmax for SBP-7455 is approximately 1 h, the Cmax is 990 nM and the T1/2 is 1.7 h. The plasma concentration of SBP-7455 remains above the ULK1 IC50 for almost 4 h after oral dosing. The mice are dosed with SBP-7455 (compound 26) (10 mg/kg) by oral gavage, and liver samples were collected after 2 h. The results reveals robust inhibition of pATG13 (Ser318), as well as downregulation of total ATG13 and ULK1 levels by SBP-7455. |
These protocols are for reference only. InvivoChem does not
independently validate these methods.
Solvent volume to be added | Mass (the weight of a compound) | |||
---|---|---|---|---|
Mother liquor concentration | 1mg | 5mg | 10mg | 20mg |
1mM | 2.8222 mL | 14.1111 mL | 28.2223 mL | 56.4446 mL |
5mM | 0.5644 mL | 2.8222 mL | 5.6445 mL | 11.2889 mL |
10mM | 0.2822 mL | 1.4111 mL | 2.8222 mL | 5.6445 mL |
20mM | 0.1411 mL | 0.7056 mL | 1.4111 mL | 2.8222 mL |
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Step One: Enter information below
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Average weight of animals g
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Step Two: Enter the in vivo formulation
%DMSO
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%ddH2O
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Method for preparing DMSO master liquid:
mg
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,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 add
µL
PEG300, mix and clarify, next add
µL
Tween 80,mix and clarify, next add
µL
ddH2O,mix and clarify.
Note:
- (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.
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