Silodosin
CAS No. 160970-54-7
Silodosin ( KAD 3213;KMD 3213 )
Catalog No. M12319 CAS No. 160970-54-7
A highly potent, uroselective α1a-adrenoceptor antagonist with Ki of 36 pM; displays 583- and 56-fold lower potency against α1b and α1d respectors, respectively.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 29 | In Stock |
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10MG | 47 | In Stock |
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25MG | 68 | In Stock |
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50MG | 82 | In Stock |
|
100MG | 97 | In Stock |
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200MG | 122 | In Stock |
|
500MG | Get Quote | In Stock |
|
1G | Get Quote | In Stock |
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Biological Information
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Product NameSilodosin
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NoteResearch use only, not for human use.
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Brief DescriptionA highly potent, uroselective α1a-adrenoceptor antagonist with Ki of 36 pM; displays 583- and 56-fold lower potency against α1b and α1d respectors, respectively.
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DescriptionA highly potent, uroselective α1a-adrenoceptor antagonist with Ki of 36 pM; displays 583- and 56-fold lower potency against α1b and α1d respectors, respectively; inhibits norepinephrine-induced increases intracellular Ca2+ concentrations in CHO cells with IC50 of 0.32 nM; inhibits intraurethral pressure (IUP) response in vivo.Other Indication Approved
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SynonymsKAD 3213;KMD 3213
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PathwayAngiogenesis
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TargetAdrenergic Receptor
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Recptorβ-adrenergicreceptor
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Research AreaOther Indications
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IndicationOther Disease
Chemical Information
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CAS Number160970-54-7
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Formula Weight495.53
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Molecular FormulaC25H32F3N3O4
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Purity>98% (HPLC)
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Solubility10 mM in DMSO
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SMILESO=C(C1=CC(C[C@H](NCCOC2=CC=CC=C2OCC(F)(F)F)C)=CC3=C1N(CCCO)CC3)N
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Chemical Name1H-Indole-7-carboxamide, 2,3-dihydro-1-(3-hydroxypropyl)-5-[(2R)-2-[[2-[2-(2,2,2-trifluoroethoxy)phenoxy]ethyl]amino]propyl]-
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Shibata K, et al. Mol Pharmacol. 1995 Aug;48(2):250-8.
2. Yamagishi R, et al. Eur J Pharmacol. 1996 Nov 7;315(1):73-9.
3. Yamada S, et al. Life Sci. 1998;62(17-18):1585-9.
4. Akiyama K, et al. J Pharmacol Exp Ther. 1999 Oct;291(1):81-91.
2. Yamagishi R, et al. Eur J Pharmacol. 1996 Nov 7;315(1):73-9.
3. Yamada S, et al. Life Sci. 1998;62(17-18):1585-9.
4. Akiyama K, et al. J Pharmacol Exp Ther. 1999 Oct;291(1):81-91.
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