Izonsteride

TargetMol
Product Code: TAR-T27643
Supplier: TargetMol
CodeSizePrice
TAR-T27643-1mg1mg£199.00
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TAR-T27643-5mg5mg£392.00
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Quantity:
TAR-T27643-10mg10mg£552.00
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Quantity:
TAR-T27643-25mg25mg£841.00
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Quantity:
TAR-T27643-50mg50mg£1,099.00
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Quantity:
TAR-T27643-100mg100mg£1,476.00
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Quantity:
Prices exclude any Taxes / VAT

Overview

Regulatory Status: RUO
Shipping:
cool pack
Storage:
-20℃

Images

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Further Information

Bioactivity:
Izonsteride is a selective and potent inhibitor of the 5α-reductase with dual effects on both the type I and type II isoforms of the enzyme.
CAS:
176975-26-1
Formula:
C24H26N2OS2
Molecular Weight:
422.61
Pathway:
Endocrinology/Hormones|Metabolism
Purity:
0.98
SMILES:
CCc1cccc2sc(Sc3ccc4c(CC[C@H]5N(C)C(=O)CC[C@]45C)c3)nc12
Target:
Reductase

References

1. Eisenberger MA, Laufer M, Vogelzang NJ, Sartor O, Thornton D, Neubauer BL, Sinibaldi V, Lieskovsky G, Carducci MA, Zahurak M, Raghavan D. Phase I and clinical pharmacology of a type I and II, 5-alpha-reductase inhibitor (LY320236) in prostate cancer: elevation of estradiol as possible mechanism of action. Urology. 2004 Jan;63(1):114-9. PubMed PMID: 14751361. 2. Trump DL, Waldstreicher JA, Kolvenbag G, Wissel PS, Neubauer BL. Androgen antagonists: Potential role in prostate cancer prevention. Urology. 2001 Apr;57(4 Suppl 1):64-7. PubMed PMID: 11295597. 3. McNulty AM, Audia JE, Bemis KG, Goode RL, Rocco VP, Neubauer BL. Kinetic analysis of LY320236: competitive inhibitor of type I and non-competitive inhibitor of type II human steroid 5alpha-reductase. J Steroid Biochem Mol Biol. 2000 Jan-Feb;72(1-2):13-21. PubMed PMID: 10731633.