Fadrozole (CGS 16949A)
This product is for research use only, not for human use. We do not sell to patients.
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Size | Price | Stock |
---|---|---|
500mg | $550 | Check With Us |
2g | $1550 | Check With Us |
5g | $2360 | Check With Us |
Cat #: V20899 CAS #: 102676-47-1 Purity ≥ 98%
Description: Fadrozole (CGS 16949A) is a highly potent and selective nonsteroidal aromatase inhibitor (IC50 of 6.4 nM) with potential antineoplastic activity.
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Molecular Weight (MW) | 223.27 |
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Molecular Formula | C14H13N3 |
CAS No. | 102676-47-1 |
SMILES Code | N#CC1=CC=C(C2CCCC3=CN=CN23)C=C1 |
Synonyms | Fadrozole; CGS 16949A; CGS-16949A; CGS16949A |
Protocol | In Vitro | Fadrozole hydrochloride is a very potent inhibitor of both human placental and rat ovarian aromatase. In hamster ovarian slices, fadrozole hydrochloride inhibits the production of estrogen with an IC50 of 0.03 μM. The production of progesterone is inhibited with an IC50 of 120 μM. Synthesis of other cytochrome P-450 dependent steroids can be suppressed to various degrees with higher doses of fadrozole hydrochloride. |
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In Vivo | Fadrozole hydrochloride is able to inhibit the aromatase-mediated androstenedione-induced uterine hypertrophy in immature female rats with an ED50 of 0.03 mg/kg when given orally. In the same model, aminoglutethimide elicits the same effect with an ED50 of 30 mg/kg when given orally. |
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 | 4.4789 mL | 22.3944 mL | 44.7888 mL | 89.5776 mL |
5mM | 0.8958 mL | 4.4789 mL | 8.9578 mL | 17.9155 mL |
10mM | 0.4479 mL | 2.2394 mL | 4.4789 mL | 8.9578 mL |
20mM | 0.2239 mL | 1.1197 mL | 2.2394 mL | 4.4789 mL |
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The dilution calculator equation
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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
Calculation Results:
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Method for preparing DMSO master liquid:
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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.
- (2) Be sure to add the solvent(s) in order.