BRL-15572 dihydrochloride
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 |
---|---|---|
250mg | $476 | Check With Us |
500mg | $760 | Check With Us |
1g | $1140 | Check With Us |
Cat #: V0978 CAS #: 193611-72-2 Purity ≥ 98%
Description: BRL-15572 (BRL-15,572; BRL-15572; BRL 15,572; BRL15,572) dihydrochloride salt is a potent and selective 5-HT1D receptor antagonist with important biological activity.
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- Physicochemical and Storage Information
- Protocol
- Related Biological Data
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Molecular Weight (MW) | 479.87 |
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Molecular Formula | C25H27ClN2O.2HCl |
CAS No. | 193611-72-2 |
Storage | -20℃ for 3 years in powder formr |
-80℃ for 2 years in solvent | |
Solubility In Vitro | DMSO: 96 mg/mL (200.1 mM)r |
Water: <1 mg/mLr | |
Ethanol: 40 mg/mL (83.4 mM) | |
Solubility In Vivo | 30% Propylene glycol, 5% Tween 80, 65% D5W: 20 mg/mL |
SMILES Code | OC(CN1CCN(C2=CC(Cl)=CC=C2)CC1)C(C3=CC=CC=C3)C4=CC=CC=C4.[H]Cl.[H]Cl |
Synonyms | BRL15572; BRL 15572 HCl; BRL-15,572; BRL-15572; BRL 15,572; BRL15,572. |
Protocol | In Vitro | BRL-15572 has 60-fold higher affinity for h5-HT1D (pKi=7.9) than 5-HT1B receptors on human receptors expressed in CHO cells. BRL-15572 (0.1 nM-10 μM) stimulates [35S]GTPγS binding in CHO cell membranes expressing h5-HT1B and h5-HT1D receptors |
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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 | 2.0839 mL | 10.4195 mL | 20.8390 mL | 41.6780 mL |
5mM | 0.4168 mL | 2.0839 mL | 4.1678 mL | 8.3356 mL |
10mM | 0.2084 mL | 1.0419 mL | 2.0839 mL | 4.1678 mL |
20mM | 0.1042 mL | 0.5210 mL | 1.0419 mL | 2.0839 mL |
The molarity calculator equation
Mass(g) = Concentration(mol/L) × Volume(L) × Molecular Weight(g/mol)
Mass
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Concentration
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Volume
×
Molecular Weight*
The dilution calculator equation
Concentration(start)
×
Volume(start)
=
Concentration(final)
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Volume(final)
This equation is commonly abbreviated as: C1 V1 = C2 V2
Concentration(start)
C1
×
Volume(start)
V1
=
Concentration(final)
C2
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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.