AC-262536|cas:870888-46-3|西域试剂

AC-262536,99.97%

产品编号：Bellancom-122025| CAS NO：870888-46-3| 分子式：C₁₈H₁₈N₂O| 分子量：278.35

本网站销售的所有产品仅用于工业应用或者科学研究等非医疗目的,不可用于人类或动物的临床诊断或者治疗,非药用,非食用，

货号	价格	库存与货期
Bellancom-122025	￥800.00	杭州北京（现货）
Bellancom-122025	￥1400.00	杭州北京（现货）
Bellancom-122025	￥3000.00	杭州北京（现货）
Bellancom-122025	￥5100.00	杭州北京（现货）
Bellancom-122025	￥8900.00	杭州北京（现货）

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AC-262536

产品介绍

AC-262536 是一种选择性的非甾体雄激素受体调节剂 (SARM)，具有有益的合成代谢作用。AC-262536 对雄激素受体具有强效激动剂活性，亲和力在低纳摩尔范围 (1-10 nM)。

生物活性

AC-262536 is a selective and non-steroidal androgen receptor modulators (SARMs) with beneficial anabolic effects. AC-262536 exhibits potent agonist activity at the androgen receptor, with an affinity in the low nanomolar range (1-10 nM).

体外研究

AC-262536 dose-dependently inhibits dihydroxytestosterone (DHT)-induced proliferation of LNCaP. The effects are significant with 100 nM AC-262536 (%inhibition 47.2±12.2), and reaches a plateau with 1 μM treatment (%inhibition 50.7±7.6). Thus, AC-262536 can act as a functional antagonist in prostate cells.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究

AC-262536 (3, 10, 30 mg/kg) reverses the luteinizing hormone (LH) spike in castrated rats.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model:	Male Sprague-Dawley rats (200-225 g)
Dosage:	3, 10 and 30 mg/kg
Administration:	Administered subcutaneously; once daily for 14 consecutive days
Result:	Significantly decreased LH levels by about 40% at the 3 mg/kg dose. The ED₅₀ was determined to be 2.8 mg/kg. At the 10 and 30 mg/kg doses, the effects of AC-262536 were significantly stronger than Testosterone Propionate (TP) : 1.91±0.32 ng/mL and 1.53±0.34 ng/mL vs. 3.12±0.69 ng/mL, respectively.

体内研究

AC-262536 (3, 10, 30 mg/kg) reverses the luteinizing hormone (LH) spike in castrated rats.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model:	Male Sprague-Dawley rats (200-225 g)
Dosage:	3, 10 and 30 mg/kg
Administration:	Administered subcutaneously; once daily for 14 consecutive days
Result:	Significantly decreased LH levels by about 40% at the 3 mg/kg dose. The ED₅₀ was determined to be 2.8 mg/kg. At the 10 and 30 mg/kg doses, the effects of AC-262536 were significantly stronger than Testosterone Propionate (TP) : 1.91±0.32 ng/mL and 1.53±0.34 ng/mL vs. 3.12±0.69 ng/mL, respectively.

性状

Solid

溶解性数据

In Vitro:

DMSO : 50 mg/mL (179.63 mM; ultrasonic and warming and heat to 60°C)

配制储备液

浓度溶剂体积质量	1 mg	5 mg	10 mg

1 mM	3.5926 mL	17.9630 mL	35.9260 mL
5 mM	0.7185 mL	3.5926 mL	7.1852 mL
10 mM	0.3593 mL	1.7963 mL	3.5926 mL

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液；一旦配成溶液，请分装保存，避免反复冻融造成的产品失效。
储备液的保存方式和期限：-80°C, 6 months; -20°C, 1 month。-80°C 储存时，请在 6 个月内使用，-20°C 储存时，请在 1 个月内使用。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液，再依次添加助溶剂：

——为保证实验结果的可靠性，澄清的储备液可以根据储存条件，适当保存；体内实验的工作液，建议您现用现配，当天使用；以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比；如在配制过程中出现沉淀、析出现象，可以通过加热和/或超声的方式助溶

1.

请依序添加每种溶剂： 10% DMSO 90% (20% SBE-β-CD in saline)
Solubility: ≥ 2.5 mg/mL (8.98 mM); Clear solution

此方案可获得 ≥ 2.5 mg/mL (8.98 mM，饱和度未知) 的澄清溶液。
以 1 mL 工作液为例，取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 900 μL 20% 的 SBE-β-CD 生理盐水水溶液中，混合均匀。
将 2 g 磺丁基醚 β-环糊精加入 5 mL 生理盐水中，再用生理盐水定容至 10 mL，完全溶解，澄清透明
2.

请依序添加每种溶剂： 10% DMSO 90% corn oil
Solubility: ≥ 2.5 mg/mL (8.98 mM); Clear solution

此方案可获得 ≥ 2.5 mg/mL (8.98 mM，饱和度未知) 的澄清溶液，此方案不适用于实验周期在半个月以上的实验。
以 1 mL 工作液为例，取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 900 μL玉米油中，混合均匀。
3.

请依序添加每种溶剂： 10% DMSO 40% PEG300 5% Tween-80 45% saline
Solubility: ≥ 0.56 mg/mL (2.01 mM); Clear solution

此方案可获得 ≥ 0.56 mg/mL (2.01 mM，饱和度未知) 的澄清溶液。
以 1 mL 工作液为例，取 100 μL 5.6 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中，混合均匀；向上述体系中加入50 μL Tween-80，混合均匀；然后继续加入 450 μL生理盐水定容至 1 mL。
将 0.9 g 氯化钠，完全溶解于 100 mL ddH₂O 中，得到澄清透明的生理盐水溶液