Shopping Cart
- Remove All
Your shopping cart is currently empty
Fadrozole hydrochloride
🥰Excellent
Catalog No. T7556Cas No. 102676-31-3
Alias CGS 16949A
Fadrozole hydrochloride (CGS 16949A) is a model aromatase inhibitor that effectively suppresses estrogen production in fish ovaries.
Fadrozole hydrochloride
🥰Excellent
Catalog No. T7556Alias CGS 16949ACas No. 102676-31-3
Fadrozole hydrochloride (CGS 16949A) is a model aromatase inhibitor that effectively suppresses estrogen production in fish ovaries.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 5 mg | $42 | In Stock | |
| 10 mg | $66 | In Stock | |
| 25 mg | $128 | In Stock | |
| 50 mg | $227 | In Stock | |
| 100 mg | $398 | In Stock | |
| 1 mL x 10 mM (in DMSO) | $46 | In Stock |
Bulk & Custom
Add to Cart
Questions
View MoreInhibitors Related to "Fadrozole hydrochloride"
YM 511
T23549148869-05-0
YM 511 is a highly specific non-steroidal aromatase inhibitor. YM 511 inhibits aromatase activities in microsomes from rat ovary and human placenta competitively (IC50s of 0.4 and 0.12 nM, respectively). YM 511 slightly inhibits production of other steroid hormones. YM 511 has the potential for suppressing estrogen-dependent action research without affecting serum levels of other steroid hormones.
- $32
Size
QTY
3-(3,4-Dimethoxyphenyl)propanoic acid
3,4-Dimethoxyhydrocinnamic acid
T16922107-70-2
3-(3,4-Dimethoxyphenyl)propanoic acid (3,4-Dimethoxyhydrocinnamic acid) is an orally active short-chain fatty acid (SCFAs) that promotes γ-globin gene expression and erythropoiesis in vivo, making it useful in treating beta hemoglobinopathies and other anemias.
- $29
Size
QTY
Finrozole
MPV-2213ad, MPV2213ad, MPV-2213, MPV 2213ad, MPV 2213
T27320160146-17-8In house
Finrozole (MPV 2213ad) is a novel selective aromatase inhibitor that is partially reversible for breast development.
- $130
Size
QTY
Exemestane
PNU155971, FCE 24304, EXE
T1587107868-30-4
Exemestane (EXE) is an Aromatase Inhibitor. The mechanism of action of exemestane is as an Aromatase Inhibitor.
Inquiry
Minamestane
T71708105051-87-4In house
Minamestane is a novel irreversible aromatase inhibitor.Minamestane induces time-dependent inhibition of human placental aromatase with a half-life of 4 minutes and a K of 59 nM.Minamestane has antitumor activity.
- $128
Size
QTY
Aminoglutethimide
NSC-330915, DL-Aminoglutethimide, BA-16038
T1103125-84-8
Aminoglutethimide (BA-16038), an aromatase inhibitor, is used in the therapy of advanced BREAST Y.
- $54
Size
QTY
Vorozole
R83842, R-83839, R83839, R 83839, (+)-Vorozole
T26322129731-10-8In house
Vorozole (R83842) is an orally active, potent, and selective nonsteroidal aromatase inhibitor.Vorozole exhibits antitumor activity in vivo and may be used in the study of breast cancer.
- $191
Size
QTY
Letrozole
Cited
CGS 20267
T1590112809-51-5
Letrozole (CGS 20267) is an Aromatase Inhibitor. The mechanism of action of letrozole is as an Aromatase Inhibitor.
- $31
Size
QTY
CitedAnastrozole
ZD1033
T0393120511-73-1
Anastrozole (ZD1033)(ZD1033), a potent and highly selective aromatase (CYP19) inhibitor (IC50 = 15 nM), has no obvious effect on adrenocorticoid hormone synthesis.
- $45
Size
QTY
Flavanone
4-Flavanone, 2-Phenylchroman-4-one, 2-Phenyl-4-chromanone, 2,3-Dihydroflavone
T0530487-26-3
Flavanone (2-Phenylchroman-4-one)s from citrus fruits have also been shown to exert beneficial effects on human vascular function. In particular, chronic interventions with orange juice, or the pure flavanone hesperidin, resulted in a decrease in blood pressure in overweight volunteers and acute improvements in microvascular reactivity.
- $40
Size
QTY
Oleuropein
T691732619-42-4
Oleuropein is an antioxidant polyphenol isolated from olive leaf.
- $33
Size
QTY
LY 43578
LY-43578, LY43578
T2791826766-35-8
LY 43578 is an orally active aromatase inhibitor. LY43578 could inhibit O-demethylation of P-450-dependent p-nitroanisole and N-demethylation of ethylmorphine (IC50 of 0.3 and 5 μm, respectively) in rat liver microsomes. LY 43578 can be used to study neurological and cardiovascular diseases.
- $30
Size
QTY
Select Batch
Purity:≥95%
Contact us for more batch information
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.Product Introduction
Bioactivity
Chemical Properties
| Description | Fadrozole hydrochloride (CGS 16949A) is a model aromatase inhibitor that effectively suppresses estrogen production in fish ovaries. |
| Targets&IC50 | Aromatase:1.4 nM (rat), Aromatase:5 nM(human) |
| In vivo | Fadrozole hydrochloride inhibits growth of androstenedione-stimulated mammary D2 cells implanted into thoracic mammary fat pads of mice by 95% when administered at a dose of 0.5 mg per animal per day. |
| Alias | CGS 16949A |
| Molecular Weight | 259.73 |
| Formula | C14H14ClN3 |
| Cas No. | 102676-31-3 |
| Smiles | Cl.N#Cc1ccc(cc1)C1CCCc2cncn12 |
| Relative Density. | no data available |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 100 mg/mL (385.02 mM), Sonication is recommended. H2O: 100 mg/mL (385.02 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO/H2O
| ||||||||||||||||||||||||||||||||||||
Sci Citations
Calculator
In Vivo Formulation Calculator (Clear solution)
Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
For example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . A total of 10 animals were administered, and the formula you used is 5% 
DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSO (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
(mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.Preparation method for in vivo formula: Take 50 μL DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
Dose Conversion
You can also refer to dose conversion for different animals. More Dose Conversion
Tech Support
Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
Keywords
Preview
Related Tags: buy Fadrozole hydrochloride | purchase Fadrozole hydrochloride | Fadrozole hydrochloride cost | order Fadrozole hydrochloride | Fadrozole hydrochloride chemical structure | Fadrozole hydrochloride in vivo | Fadrozole hydrochloride formula | Fadrozole hydrochloride molecular weight
- TOP
Feedback
Hello! How can I help you today? 
Copyright © 2015-2025 TargetMol Chemicals Inc. All Rights Reserved.