BIA10-2474
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 | $750 | Check With Us |
500mg | $1285 | Check With Us |
1g | $1935 | Check With Us |
Cat #: V4091 CAS #: 1233855-46-3 Purity ≥ 98%
Description: BIA 10-2474 is a novel, potent, long-acting and reversible inhibitor of fatty acid amide hydrolase (FAAH) with IC50 values of 50 to 70mg/kg in various rat brain regions.
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Molecular Weight (MW) | 300.36 |
---|---|
Molecular Formula | C16H20N4O2 |
CAS No. | 1233855-46-3 |
Storage | -20℃ for 3 years in powder formr |
-80℃ for 2 years in solvent | |
Solubility In Vitro | DMSO: ≥ 4 mg/mLr |
Water: < 1mg/mLr | |
Ethanol: N/A | |
SMILES Code | O=C(N1C=C(C2=C[N+]([O-])=CC=C2)N=C1)N(C3CCCCC3)C |
Synonyms | BIA 10-2474; BIA-10-2474; BIA10-2474 |
Protocol | In Vitro | ExVivo: BIA 10-2474 proves to be a potent FAAH inhibitor with IC50s of 50-70mg/kg (i.p.) in various brain regions. IC50 values for brain regions are 52 (cerebellum), 67 (rest of brain), 68 (cortex), and 71 mg/kg (hypothalamus). |
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In Vivo | In January 2016, severe adverse events (SAE) occurs in the Phase I clinical trial using the drug BIA 10-2474 including one death. The possibilities for failure of trials such as off-target effect, dose calculation, unexpected immune response, species variation, and cumulative dose toxicity would be sought. |
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 | 3.3293 mL | 16.6467 mL | 33.2934 mL | 66.5868 mL |
5mM | 0.6659 mL | 3.3293 mL | 6.6587 mL | 13.3174 mL |
10mM | 0.3329 mL | 1.6647 mL | 3.3293 mL | 6.6587 mL |
20mM | 0.1665 mL | 0.8323 mL | 1.6647 mL | 3.3293 mL |
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Step One: Enter information below
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Step Two: Enter the in vivo formulation
%DMSO
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%ddH2O
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Working concentration:
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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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