GLPBio

Finasteride

Catalog No.: GC16248Purity:>98.00%Synonyms: MK-906
فيناسترايد (MK-906) هو مثبط اختزال 5α قوي وتنافسي ، مع IC 50 من 4.2 نانومتر للنوع II 5α-reductaseيمتلك فيناسترايد تقاربًا أكبر بمقدار 100 ضعف تقريبًا للنوع الثاني من إنزيم اختزال 5α مقارنة بالنوع الأول من الإنزيميمكن استخدام الفيناسترايد في البحث عن تضخم البروستاتا الحميد (BPH) والثعلبة الأندروجينية

المنتجات مخصصة للاستخدام البحثي فقط، وليست للاستخدام البشري. نحن لا نبيع للمرضى.


Finasteride
Cas No.: 98319-26-7
10mM (in 1mL DMSO)In Stock
$40.00
1
100mgIn Stock
$39.00
1
200mgIn Stock
$59.00
1

المراجع (Citations)

لا تتوفر حاليًا مراجع لهذا المنتج. فيما يلي مجموعة مختارة من المنشورات التي تستشهد بمنتجات GlpBio.
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    Nature
    632, 686–694 (2024)
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    Nature
    618, 1017–1023 (2023)
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    Nature
    610, 366–372 (2022)
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    Cell
    187(9):2288-2304 (2024)
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    Cell
    183(7):1867-1883 (2020)
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    388(6745) (2025)
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    31, 1291–1307 (2021)

الوصف (Description)

Finasteride is a selective type II 5α-reductase inhibitor with an IC₅₀ value of 4.2nM [1]. Finasteride lowers dihydrotestosterone (DHT) levels and is used to treat male pattern hair loss (androgenetic alopecia)[2]. Additionally, Finasteride can be used to treat female pattern hair loss in patients who have failed local minoxidil treatment [3]. Finasteride has been shown to significantly reduce prostate volume and improve urinary symptoms [4].

In vitro, treatment of human dermal papilla cells (DPCs) with Finasteride (10–100μM) for 5 days significantly increased cell aggregation behavior, upregulated the expression of stem cell transcription factors Nanog and Sox-2, and activated the protein kinase B (AKT), β-catenin, and integrin β-1 signaling pathways, thereby enhancing stem cell properties[5]. Treatment of human prostate cell lines RWPE-1, LNCaP, PC3, and DU145 with Finasteride (10μM and 50μM) for 72 hours significantly downregulated the activities of MMP2 and MMP9, while upregulating the expression of TIMP-2. Moreover, 50μM Finasteride significantly inhibited the invasive potential of all cell lines and also significantly inhibited the migration of RWPE-1 and LNCaP cells [6].

In vivo, Ldlr−/− mice treated orally with Finasteride (1000mg/kg) for 12 weeks showed significant reductions in total cholesterol and triglyceride levels, decreased atherosclerotic plaque area in the aortic arch and root, and reduced macrophage content and necrotic core area in the plaques [7]. In a protein-overload nephropathy chronic kidney disease (CKD) mouse model fed a high-fat diet (HFD), treatment with Finasteride (1.5mg/30g) via gavage for 2 weeks significantly lowered plasma trimethylamine N-oxide (TMAO) levels, improved renal injury, and regulated the composition and distribution of gut microbiota[8].

References:
[1] Flores E, Bratoeff E, Cabeza M, et al. Steroid 5alpha-reductase inhibitors. Mini Rev Med Chem. 2003 May;3(3):225-37.
[2] Piraccini BM, Blume-Peytavi U, Scarci F, et al. Topical Finasteride Study Group. Efficacy and safety of topical finasteride spray solution for male androgenetic alopecia: a phase III, randomized, controlled clinical trial. J Eur Acad Dermatol Venereol. 2022 Feb;36(2):286-294.
[3] Stout SM, Stumpf JL. Finasteride treatment of hair loss in women. Ann Pharmacother. 2010 Jun;44(6):1090-7.
[4] Tacklind J, Fink HA, Macdonald R, et al. Finasteride for benign prostatic hyperplasia. Cochrane Database Syst Rev. 2010 Oct 6;2010(10):CD006015.
[5] Rattanachitthawat N, Pinkhien T, Opanasopit P, et al. Finasteride Enhances Stem Cell Signals of Human Dermal Papilla Cells. In Vivo. 2019 Jul-Aug;33(4):1209-1220.
[6] Moroz A, Delella FK, Almeida R, et al. Felisbino SL. Finasteride inhibits human prostate cancer cell invasion through MMP2 and MMP9 downregulation. PLoS One. 2013 Dec 30;8(12):e84757.
[7] McQueen P, Molina D, Pinos I, et al. Finasteride delays atherosclerosis progression in mice and is associated with a reduction in plasma cholesterol in men. J Lipid Res. 2024 Mar;65(3):100507.
[8] Wang Z, You L, Ren Y, et al. Finasteride Alleviates High Fat Associated Protein-Overload Nephropathy by Inhibiting Trimethylamine N-Oxide Synthesis and Regulating Gut Microbiota. Front Physiol. 2022 Aug 15;13:900961.

البروتوكول (Protocol)

Cell experiment [1]:

Cell lines

RWPE-1, LNCaP, PC3, DU145 (human prostate cancer cell line)

Preparation Method

Cells were maintained in RPMI 1640 medium supplemented with 10% fetal bovine serum (FBS) at 37°C, 5% CO₂. Cells were treated with Finasteride at concentrations of 10μM and 50μM for 72 hours.

Reaction Conditions

10μM, 50μM; 72h

Applications

Finasteride significantly downregulated the activities of MMP2 and MMP9 in RWPE-1 and PC3 cells, and MMP2 in DU145 cells. Finasteride inhibited cell invasion in all tested cell lines.
Animal experiment [2]:

Animal models

Balb/c mice

Preparation Method

Chronic kidney disease (CKD) mouse models were generated by intraperitoneal injection of bovine serum albumin (BSA) at 30mg/30g body weight (with 15 and 25mg/30g BSA on the first 2 days). Mice were fed a high-fat diet (HFD) simultaneously with BSA injection for 4 weeks. In the last 2 weeks, mice were treated with Finasteride at 1.5mg/30g body weight via intragastric administration. Mice were sacrificed on Day 35 for evaluation of renal function and histological analysis.

Dosage form

1.5mg/30g body weight; i.g.

Applications

Finasteride significantly alleviated HFD-induced hyperlipidemia and renal injury in CKD mice, as evidenced by reduced levels of serum creatinine, blood urea nitrogen, and urinary protein.

References:
[1] Moroz A, Delella FK, Almeida R, et al. Felisbino SL. Finasteride inhibits human prostate cancer cell invasion through MMP2 and MMP9 downregulation. PLoS One. 2013 Dec 30;8(12):e84757.
[2] Wang Z, You L, Ren Y, et al. Finasteride Alleviates High Fat Associated Protein-Overload Nephropathy by Inhibiting Trimethylamine N-Oxide Synthesis and Regulating Gut Microbiota. Front Physiol. 2022 Aug 15;13:900961.

وثائق المنتج (Product Documents)

Purity:>98.00%Appearance:A solid

الخصائص الكيميائية (Chemical Properties)

رقم CAS
98319-26-7
المرادفات
MK-906
الاسم الكيميائي
(1S,3aS,3bS,5aR,9aR,9bS,11aS)-N-tert-butyl-9a,11a-dimethyl-7-oxo-1,2,3,3a,3b,4,5,5a,6,9b,10,11-dodecahydroindeno[5,4-f]quinoline-1-carboxamide
SMILES
CC12CCC3C(C1CCC2C(=O)NC(C)(C)C)CCC4C3(C=CC(=O)N4)C
الصيغة الجزيئية
C23H36N2O2
الوزن الجزيئي
372.54
الذوبانية
≥ 14.65 mg/mL in DMSO, ≥ 76.4 mg/mL in EtOH
التخزين
Store at -20°C
إرشادات عامة
اختر مذيبًا مناسبًا وفقًا لبيانات ذوبانية المنتج. بعد التحضير، قسّم المحلول المخزون إلى أجزاء لتجنب دورات التجميد والذوبان المتكررة.
استخدم المحاليل المخزونة خلال 6 أشهر عند حفظها في -80°C، أو خلال شهر واحد عند حفظها في -20°C.
لتحسين الذوبانية، سخّن الأنبوب إلى 37°C وعرّضه للموجات فوق الصوتية لمدة مناسبة.
شروط الشحن
تُشحن عينات التقييم مع عبوات تبريد. وتُشحن الأحجام الأخرى المتاحة في درجة حرارة الغرفة، أو مع عبوات تبريد عند الطلب.

الحاسبات (Calculators)المولارية / التخفيف / الوزن الجزيئي / تحويل الوحدات / تركيبة داخل الجسم الحي / الذوبانية

g/mol

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