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  • 西洛多辛

    Silodosin

    西洛多辛
    产品编号 CFN90002
    CAS编号 160970-54-7
    分子式 = 分子量 C25H32F3N3O4 = 495.53
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Alkaloids
    植物来源
    ChemFaces的产品在影响因子大于5的优秀和顶级科学期刊中被引用
    提供自定义包装
    产品名称 产品编号 CAS编号 包装 QQ客服
    西洛多辛 CFN90002 160970-54-7 1mg QQ客服:2159513211
    西洛多辛 CFN90002 160970-54-7 5mg QQ客服:2159513211
    西洛多辛 CFN90002 160970-54-7 10mg QQ客服:2159513211
    西洛多辛 CFN90002 160970-54-7 20mg QQ客服:2159513211
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    ChemFaces的产品在许多优秀和顶级科学期刊中被引用

    Cell. 2018 Jan 11;172(1-2):249-261.e12.
    doi: 10.1016/j.cell.2017.12.019.
    IF=36.216(2019)

    PMID: 29328914

    Cell Metab. 2020 Mar 3;31(3):534-548.e5.
    doi: 10.1016/j.cmet.2020.01.002.
    IF=22.415(2019)

    PMID: 32004475

    Mol Cell. 2017 Nov 16;68(4):673-685.e6.
    doi: 10.1016/j.molcel.2017.10.022.
    IF=14.548(2019)

    PMID: 29149595

    ACS Nano. 2018 Apr 24;12(4): 3385-3396.
    doi: 10.1021/acsnano.7b08969.
    IF=13.903(2019)

    PMID: 29553709

    Nature Plants. 2016 Dec 22;3: 16206.
    doi: 10.1038/nplants.2016.205.
    IF=13.297(2019)

    PMID: 28005066

    Sci Adv. 2018 Oct 24;4(10): eaat6994.
    doi: 10.1126/sciadv.aat6994.
    IF=12.804(2019)

    PMID: 30417089
    我们的产品现已经出口到下面的研究机构与大学,并且还在增涨
  • Gyeongsang National University (Korea)
  • Korea Institute of Oriental Medicine (Korea)
  • FORTH-IMBB (Greece)
  • Washington State University (USA)
  • Centralised Purchases Unit (CPU), B.I.T.S (India)
  • University of Stirling (United Kingdom)
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  • Universiti Kebangsaan Malaysia (Malaysia)
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  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Korea Institute of Oriental Medicine2020, doi: 10.21203.
  • Molecules.2019, 24(11):E2044
  • Int. J. of Pha. and Phy. Res.2015, 7(1):144-149
  • PLoS One.2021, 16(9):e0257243.
  • Journal of Plant Growth Regulation2022, 10705-2.
  • Molecular & Cellular Toxicology2022, 10.1007:s13273-022-00277-3
  • J Food Sci Technol.2019, 56(5):2712-2720
  • J Nat Prod.2021, 84(9):2544-2553.
  • J Neuroinflammation.2020, 17(1):75.
  • Nutrients.2023, 15(6):1335.
  • Journal of Chromatography A2020, 460942
  • Planta Med.2018, 84(15):1101-1109
  • Nutrients.2021, 13(12):4364.
  • Phytomedicine.2022, 99:154025.
  • Exp Ther Med.2019, 18(6):4388-4396
  • Phytother Res.2016, 30(12):2020-2026
  • Pharmaceutics.2022, 14(3):564.
  • Biofactors.2018, 44(2):168-179
  • Vojnosanit Pregl2016, 75(00):391-391
  • Plants (Basel).2021, 10(7):1376.
  • Eur J Pharmacol.2020, 889:173589.
  • Phytomedicine.2021, 93:153796.
  • Life (Basel).2022, 12(10):1630.
  • ...
  • 生物活性
    Description: Silodosin, a selective α-1a receptor antagonist, can increase passage of distal ureteral stones. Silodosin can temporarily improve lower urinary tract symptoms (LUTS), but do not improve the bladder outlet obstruction index (BOOI) after implantation in the prostate, it is a useful option for the treatment of lower urinary tract symptoms associated with benign prostatic hyperplasia .Silodosin appears to suppress ejaculation in a relatively higher percent of trial participants, this suppression of ejaculation by silodosin suggested its potential for treating premature ejaculation.
    Targets: Adrenergic Receptor
    In vivo:
    Eur Urol. 2015 May;67(5):959-64.
    Silodosin to facilitate passage of ureteral stones: a multi-institutional, randomized, double-blinded, placebo-controlled trial.[Pubmed: 25465978]
    Using a selective α-blocker for medical expulsive therapy (MET) is a cost-effective treatment approach widely used for ureteral stones. To evaluate the efficacy of Silodosin, a selective α-1a receptor antagonist, in this setting.
    METHODS AND RESULTS:
    This was a multicenter, phase 2 study conducted in adult patients with a unilateral ureteral calculus of 4-10mm. Of 239 patients in the safety population, six discontinued due to adverse events. Patients were randomized 1:1 to receive Silodosin 8 mg or placebo for up to 4 wk. The primary outcome was spontaneous stone passage, analyzed using logistic regression. Secondary outcomes included time to stone passage, emergency room (ER) visits, hospital admissions, analgesic use, and incidence and severity of pain. No significant differences between the Silodosin and placebo groups were observed for passage rate of all stones (52% vs 44%, respectively; p=0.2). However, Silodosin achieved a significantly greater rate of distal ureter stone passage than placebo (p=0.01). Significant differences were not observed for ER visits, hospital admission, or use of analgesics. The number of patients in the intent-to-treat population was slightly below the calculated sample size (232 vs 240) and sample sizes were not calculated for subgroup analyses.
    CONCLUSIONS:
    This is among the first prospective, randomized, multi-institutional trials to examine the efficacy of a selective α-1a antagonist as MET in patients with ureteral calculi and did not demonstrate a benefit to the entire ureter. However, Silodosin was found to be well tolerated and beneficial in facilitating the passage of distal ureteral stones, warranting additional future studies on distal stone elimination. In this report, we looked at the efficacy of Silodosin for the treatment of ureteral stones. We found that Silodosin increased passage of distal ureteral stones.
    Int J Urol. 2012 Mar;19(3):268-72.
    Silodosin and its potential for treating premature ejaculation: a preliminary report.[Pubmed: 22188258]
    However, compared with other α1-adrenoceptor antagonists, Silodosin appeared to suppress ejaculation in a relatively higher percent of trial participants. This suppression of ejaculation by Silodosin suggested its potential for treating premature ejaculation. Consequently, we evaluated the feasibility of off-label Silodosin as a new treatment option for premature ejaculation.
    METHODS AND RESULTS:
    Eight patients suffering premature ejaculation were treated with Silodosin. Silodosin (4 mg) was given 2 h before sexual intercourse. Intravaginal ejaculatory latency time, premature ejaculation profile item, clinical global impression change in premature ejaculation and systemic adverse events were recorded. Intravaginal ejaculatory latency time was significantly prolonged (from 3.4 min to 10.1 min, P = 0.003). All patients answered better (much better) or slightly better for their own premature ejaculation problem compared with pretreatment condition in the clinical global impression change. Premature ejaculation profile also significantly improved. Two (25%), three (37.5%) and seven patients (87.5%) experienced anejaculation, reduced semen volume and discomfort during orgasm, respectively. However, these problems were not of major concern for the participants. No systemic adverse effects were reported.
    CONCLUSIONS:
    The current results support the possible use of Silodosin as a new treatment option for premature ejaculation, and suggest that a placebo controlled study assessing its clinical usefulness would be worthwhile.
    Arch Ital Urol Androl. 2014 Jun 30;86(2):103-7.
    Medical expulsive therapy for distal ureteric stones: tamsulosin versus silodosin.[Pubmed: 25017589]
    To compare the efficacy and safety of tamsulosin and Silodosin in the context of medical expulsive therapy (MET) of distal ureteric stones.
    METHODS AND RESULTS:
    Observational data were collected retrospectively from patients who received Silodosin (N = 50) or tamsulosin (N = 50) as MET from January 2012 to January 2013. Inclusion criteria were: patients aged ≥ 18 years with a single, unilateral, symptomatic, radiopaque ureteric stone of 10 mm or smaller in the largest dimension located between the lower border of the sacroiliac joint and the vesico-ureteric junction. Stone expulsion rate, stone expulsion time, number of pain episodes, need for analgesics use, incidence of side effects were compared. Stone-expulsion rate in the Silodosin and in the tamsulosin groups were 88% and 82%, respectively (p not significant). Mean expulsion times were 6.7 and 6.5 days in the Silodosin and tamsulosin group, respectively (p not significant). Mean number of pain episodes were 1.6 and 1.7 in the Silodosin and tamsulosin group, respectively (p not significant). The mean number of analgesic requirement was 0.84 and 0.9 for the Silodosin and tamsulosin group, respectively (p not significant). Overall, incidence of side effects was similar in both groups. Patients taking Silodosin experienced an higher incidence of retrograde ejaculation but a lower incidence of side effects related to peripheral vasodilation when compared to patients taking tamsulosin. Subgroup analysis demonstrated significantly lower mean expulsion times and pain episodes in patients with stones ≤ 5 mm in both groups.
    CONCLUSIONS:
    Tamsulosin and Silodosin are equally effective as MET for distal ureteric stones sized 10 mm or smaller. MET with Silodosin is associatd with a lower incidence of side effects related to peripheral vasodilation but an higher incidence of retrograde ejaculation when compared to tamsulosin.
    Drugs. 2015 Feb;75(2):207-17.
    Silodosin: a review of its use in the treatment of the signs and symptoms of benign prostatic hyperplasia.[Pubmed: 25575983]
    Silodosin is a highly selective α1A-adrenoceptor antagonist indicated for the treatment of the signs and symptoms of benign prostatic hyperplasia (BPH).
    METHODS AND RESULTS:
    Oral Silodosin had a rapid onset of effect in men with lower urinary tract symptoms (LUTS) associated with BPH, with improvements seen in voiding and storage symptoms, maximum urinary flow rate and health-related quality of life in well-designed, 12-week trials. Silodosin was noninferior to tamsulosin in terms of improving LUTS associated with BPH. The efficacy of Silodosin was maintained in 9-month extension studies and was also seen in a phase IV study conducted in a real-world setting. Silodosin was generally well tolerated and was associated with a low risk of orthostatic hypotension. Abnormal ejaculation was the most commonly reported adverse event, although few patients discontinued treatment with Silodosin because of this adverse event.
    CONCLUSIONS:
    In conclusion, Silodosin is a useful option for the treatment of LUTS associated with BPH.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.018 mL 10.0902 mL 20.1804 mL 40.3608 mL 50.451 mL
    5 mM 0.4036 mL 2.018 mL 4.0361 mL 8.0722 mL 10.0902 mL
    10 mM 0.2018 mL 1.009 mL 2.018 mL 4.0361 mL 5.0451 mL
    50 mM 0.0404 mL 0.2018 mL 0.4036 mL 0.8072 mL 1.009 mL
    100 mM 0.0202 mL 0.1009 mL 0.2018 mL 0.4036 mL 0.5045 mL
    * Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
    部分图片展示
    产品名称 产品编号 CAS编号 分子式 = 分子量 位单 联系QQ
    西洛多辛; Silodosin CFN90002 160970-54-7 C25H32F3N3O4 = 495.53 5mg QQ客服:2159513211
    卡培他滨; Capecitabine CFN90006 154361-50-9 C15H22FN3O6 = 359.35 20mg QQ客服:3257982914
    卡奈替尼; 卡耐替尼; Canertinib CFN90010 267243-28-7 C24H25ClFN5O3 = 485.94 20mg QQ客服:3257982914
    吉非替尼; Gefitinib CFN90011 184475-35-2 C22H24ClFN4O3 = 446.9 20mg QQ客服:1413575084
    索拉非尼; Sorafenib CFN90012 284461-73-0 C21H16ClF3N4O3 = 464.83 20mg QQ客服:2056216494
    决奈达隆; Dronedarone CFN90014 141626-36-0 C31H44N2O5S = 556.76 20mg QQ客服:2056216494
    达沙替尼水合物; Dasatinib monohydrate CFN90015 863127-77-9 C22H28ClN7O3S = 506.02 5mg QQ客服:215959384

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