JNJ-1661010
This product is for research use only, not for human use. We do not sell to patients.
For small sizes, please check our retail website as below: www.invivochem.com
| Size | Price | Stock |
|---|---|---|
| 500mg | $1350 | Check With Us |
| 1g | $2100 | Check With Us |
| 5g | $5315 | Check With Us |
: Cat #: V0910 CAS #: 681136-29-8 Purity ≥ 98%
Description: JNJ-1661010 (JNJ 1661010; Takeda-25; JNJ1661010; Takeda25), a piperazinyl phenyl urea compound, is a selective and reversible inhibitor of Fatty acid amide hydrolase/FAAH with important biological activity.
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- Physicochemical and Storage Information
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- Related Biological Data
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| Molecular Weight (MW) | 365.45 |
|---|---|
| Molecular Formula | C19H19N5OS |
| CAS No. | 681136-29-8 |
| Storage | -20℃ for 3 years in powder formr |
| -80℃ for 2 years in solvent | |
| Solubility In Vitro | DMSO: 36 mg/mL (98.5 mM)r |
| Water: <1 mg/mLr | |
| Ethanol: <1 mg/mL | |
| Solubility In Vivo | 5% DMSO+95% Corn oil: 5 mg/mL |
| SMILES Code | O=C(N1CCN(C2=NC(C3=CC=CC=C3)=NS2)CC1)NC4=CC=CC=C4 |
| Synonyms | Takeda 25; JNJ-1661010; Takeda-25; Takeda25; JNJ 1661010; JNJ1661010. |
| Protocol | In Vivo | JNJ-1661010 (i.p.; 10 mg/kg) has a T1/2 of 35 mins, a CL of 0.032 mL/min/kg, and a Cmax of 1.58 μM for rats. |
|---|
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 | 2.7364 mL | 13.6818 mL | 27.3635 mL | 54.7270 mL |
| 5mM | 0.5473 mL | 2.7364 mL | 5.4727 mL | 10.9454 mL |
| 10mM | 0.2736 mL | 1.3682 mL | 2.7364 mL | 5.4727 mL |
| 20mM | 0.1368 mL | 0.6841 mL | 1.3682 mL | 2.7364 mL |
The molarity calculator equation
Mass(g) = Concentration(mol/L) × Volume(L) × Molecular Weight(g/mol)
Mass
=
Concentration
×
Volume
×
Molecular Weight*
The dilution calculator equation
Concentration(start)
×
Volume(start)
=
Concentration(final)
×
Volume(final)
This equation is commonly abbreviated as: C1 V1 = C2 V2
Concentration(start)
C1
×
Volume(start)
V1
=
Concentration(final)
C2
×
Volume(final)
V2
Step One: Enter information below
Dosage mg/kg
Average weight of animals g
Dosing volume per animal µL
Number of animals
Step Two: Enter the in vivo formulation
%DMSO
+
%
+
%Tween 80
+
%ddH2O
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 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.
- (2) Be sure to add the solvent(s) in order.