Azelaic acid (Nonanedioic acid)
(Synonyms: 壬二酸; Nonanedioic acid) 目录号 : GC30219
A dicarboxylic acid with diverse biological activities
Cas No.:123-99-9
Sample solution is provided at 25 µL, 10mM.
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Azelaic acid is a naturally occurring and saturated dicarboxylic acid with diverse biological activities.1,2,3,4,5 It is a competitive inhibitor of tyrosinase, NADH dehydrogenase, succinic dehydrogenase, and reduced ubiquitinone:cytochrome C oxidoreductase in vitro.1,2 Azelaic acid inhibits the growth and colony formation of B16 murine as well as HMB2 and SK32 human melanoma cells in a concentration-dependent manner but has no effect on CHO cells.3 It decreases DNA synthesis, induces mitochondrial damage and dilation of the rough endoplasmic reticulum (RER), and reduces growth of mouse keratinocytes in a dose- and time-dependent manner.4 Azelaic acid is bacteriostatic against S. epidermidis, S. aureus, S. capitis, P. acnes, P. avidum, P. mirabilis, and C. albicans in vitro (MICs = 0.03-0.25 M).5 Formulations containing azelaic acid have been used in the treatment of acne and hyperpigmentation disorders.
1.Nazzaro-Porro, M., and Passi, S.Identification of tyrosinase inhibitors in cultures of PityrosporumJ. Invest. Dermatol.71(3)205-208(1978) 2.Passi, S., Picardo, M., Nazzaro-Porro, M., et al.Antimitochondrial effect of saturated medium chain length (C8-C13) dicarboxylic acidsBiochem. Pharmacol.33(1)103-108(1984) 3.Lemic-Stojcevic, L., Nias, A.H., and Breathnach, A.S.Effect of azelaic acid on melanoma cells in cultureExp. Dermatol.4(2)79-81(1995) 4.Detmar, M., Mayer-da-Silva, A., Stadler, R., et al.Effects of azelaic acid on proliferation and ultrastructure of mouse keratinocytes in vitroJ. Invest. Dermatol.93(1)70-74(1989) 5.Nguyen, Q.H., and Bui, T.P.Azelaic acid: Pharmacokinetic and pharmacodynamic properties and its therapeutic role in hyperpigmentary disorders and acneInt. J. Dermatol.34(2)75-84(1995)
| Cas No. | 123-99-9 | SDF | |
| 别名 | 壬二酸; Nonanedioic acid | ||
| Canonical SMILES | OC(CCCCCCCC(O)=O)=O | ||
| 分子式 | C9H16O4 | 分子量 | 188.22 |
| 溶解度 | DMSO : ≥ 100 mg/mL (531.29 mM);Water : 2 mg/mL (10.63 mM) | 储存条件 | Store at -20°C |
| General tips | 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 储存时，请在 6 个月内使用，-20°C 储存时，请在 1 个月内使用。 为了提高溶解度，请将管子加热至37℃，然后在超声波浴中震荡一段时间。 |
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| Shipping Condition | 评估样品解决方案：配备蓝冰进行发货。所有其他可用尺寸：配备RT，或根据请求配备蓝冰。 | ||
| 制备储备液 | |||
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1 mg | 5 mg | 10 mg |
| 1 mM | 5.3129 mL | 26.5647 mL | 53.1293 mL |
| 5 mM | 1.0626 mL | 5.3129 mL | 10.6259 mL |
| 10 mM | 0.5313 mL | 2.6565 mL | 5.3129 mL |
| 第一步：请输入基本实验信息（考虑到实验过程中的损耗，建议多配一只动物的药量） | ||||||||||
| 给药剂量 | mg/kg |  |
动物平均体重 | g | |
每只动物给药体积 | ul | |
动物数量 | 只 |
| 第二步：请输入动物体内配方组成（配方适用于不溶于水的药物；不同批次药物配方比例不同，请联系GLPBIO为您提供正确的澄清溶液配方） | ||||||||||
| % DMSO % % Tween 80 % saline | ||||||||||
| 计算重置 | ||||||||||
计算结果:
工作液浓度： mg/ml；
DMSO母液配制方法： mg 药物溶于 μL DMSO溶液（母液浓度 mg/mL，
体内配方配制方法：取 μL DMSO母液，加入 μL PEG300，混匀澄清后加入μL Tween 80，混匀澄清后加入 μL saline，混匀澄清。
1. 首先保证母液是澄清的；
2.
一定要按照顺序依次将溶剂加入，进行下一步操作之前必须保证上一步操作得到的是澄清的溶液，可采用涡旋、超声或水浴加热等物理方法助溶。
3. 以上所有助溶剂都可在 GlpBio 网站选购。
Quality Control & SDS
- View current batch:
- Purity: >98.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet