(+)-Camphor (D-(+)-Camphor)
(Synonyms: (+)-樟脑; D-(+)-Camphor; (1R)-(+)-Camphor) 目录号 : GC33515A terpene with diverse biological activities
Cas No.:464-49-3
Sample solution is provided at 25 µL, 10mM.
(1R)-(+)-Camphor is a terpene that has been found in C. sativa, C. indica, and C. sativa/C. indica hybrid strains as well as the essential oils from a variety of herbs including rosemary, lavender, and sage and has diverse biological activities.1,2,3,4,5,6 It inhibits norepinephrine secretion and cytosolic calcium and sodium increases induced by the nicotinic acetylcholine receptor (nAChR) agonist 1,1-dimethyl-4-phenylpiperazinium iodide (DMPP) in chromaffin cells (IC50s = 70, 88, and 19 μM, respectively).2 (1R)-(+)-Camphor (65-260 μM) induces proliferation of and increases expression of collagen IA, collagen IIIA, collagen IVA, and elastin in human primary dermal fibroblasts.3 In vivo, (1R)-(+)-camphor increases expression of collagen IA, collagen IIIA, collagen IVA, and elastin in skin in UV-exposed mice when administered at doses of 26 and 55 mM in drinking water post UV-exposure. It reduces cough frequency in citric acid-challenged guinea pigs.4 (1R)-(+)-Camphor is insecticidal, reducing digging activity and inducing mortality of fire ant workers.5 It has also been used as a building block in the synthesis of cannabinergic ligands.6
1.Elzinga, S., Fischedick, J., Podkolinski, R., et al.Cannabinoids and terpenes as chemotaxonomic markers in CannabisNat. Prod. Chem. Res.3(4)181(2015) 2.Park, T.-J., Seo, H.-K., Kang, B.-J., et al.Noncompetitive inhibition by camphor of nicotinic acetylcholine receptorsBiochem. Pharmacol.61(7)787-793(2001) 3.Tran, T.A., Ho, M.T., Song, Y.W., et al.Camphor induces proliferative and anti-senescence activities in human primary dermal fibroblasts and inhibits UV-induced wrinkle formation in mouse skinPhytother. Res.29(12)1917-1925(2015) 4.Laude, E.A., Morice, A.H., and Grattan, T.J.The antitussive effects of menthol, camphor and cineole in conscious guinea-pigsPulm. Pharmacol.7(3)179-184(1994) 5.Zhang, N., Tang, L., Hu, W., et al.Insecticidal, fumigant, and repellent activities of sweet wormwood oil and its individual components against red imported fire ant workers (Hymenoptera: Formicidae)J. Insect Sci.14(1)pii:241(2014) 6.Lu, D., Guo, J., Duclos, R.I., Jr., et al.Bornyl- and isobornyl-Δ8-tetrahydrocannabinols: A novel class of cannabinergic ligandsJ. Med. Chem.51(20)6393-6399(2008)
Cas No. | 464-49-3 | SDF | |
别名 | (+)-樟脑; D-(+)-Camphor; (1R)-(+)-Camphor | ||
Canonical SMILES | CC1(C)[C@@]2(C)CC[C@@H]1CC2=O | ||
分子式 | C10H16O | 分子量 | 152.23 |
溶解度 | DMSO : ≥ 50 mg/mL (328.45 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 | |||
1 mg | 5 mg | 10 mg | |
1 mM | 6.569 mL | 32.845 mL | 65.6901 mL |
5 mM | 1.3138 mL | 6.569 mL | 13.138 mL |
10 mM | 0.6569 mL | 3.2845 mL | 6.569 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
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- Purity: >99.50%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet