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fadrozole

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  • Inhibitors & Agonists
    7
    TargetMol | Inhibitors_Agonists
Fadrozole
T7197102676-47-1
Fadrozole is a nonsteroidal aromatase inhibitor with potential antineoplastic activity(IC50 : 6.4 nM)
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Fadrozole hydrochloride
CGS 16949A
T7556102676-31-3
Fadrozole hydrochloride (CGS 16949A) is a model aromatase inhibitor that effectively suppresses estrogen production in fish ovaries.
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(R)-Fadrozole phosphate
Fadrozole phosphate, (R)-, 42REB33X4T
T2020072743427-54-3
Fadrozole is a selective aromatase inhibitor used effectively in the treatment of estrogen-dependent conditions, such as breast cancer.
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(R)-Fadrozole
FAD286,(R)-CGS 16949A free base,(R)-Fadrozole
T38424102676-87-9
(R)-Fadrozole ((R)-CGS 16949A; FAD286) is a potent nonsteroidal inhibitor. (R)-Fadrozole also inhibits human placental aromatase (pIC 50 = 6.17) and aldosterone biosynthesis. (R)-Fadrozole reverses cardiac fibrosis in spontaneously hypertensive heart failure rats..
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6-8 weeks
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Fadrozole HCl hydrate
Fadrozole,CGS-16949A,Fadrozole hydrochloride hemihydrate,CGS16949A,CGS 16949A
T7197L176702-70-8
Fadrozole is a selective inhibitor of aromatase. It also effective in the treatment of estrogen-dependent diseases including breast cancer.
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1-2 weeks
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(S)-Dexfadrostat
(S)-Fadrozole, (S)-FAD286, (S)-CGS 16949A free base
T200084102676-86-8
(S)-Dexfadrostat ((S)-Fadrozole), an aromatase inhibitor, exhibits an IC 50 of 4.6 nM in in vitro assays using human placental microsomes. It is applicable for research on estrogen-dependent breast cancer, gynecomastia, and systemic lupus erythematosus.
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6-8 weeks
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Dexfadrostat HCl
Fadrozole hydrochloride, (R)-, FAD-286, Dexfadrostat hydrochloride, 6T3TZF5EG8, (+)-Fadrozole hydrochloride
T202257131863-75-7
Dexfadrostat is an effective non-steroidal inhibitor of aldosterone synthase (CYP 11B2).
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