Orexin B amide (human) (trifluoroacetate salt)
(Synonyms: Hypocretin 2, OXB) 目录号 : GC49553A hypothalamic neuropeptide
Sample solution is provided at 25 µL, 10mM.
Quality Control & SDS
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- Purity: >95.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
Orexin B amide is a hypothalamic neuropeptide that regulates feeding behavior, wakefulness, and behavior under situations of high motivational relevance.1 It is an agonist of orexin (OX) receptors with IC50 values of 420 and 36 nM for human recombinant OX1 and OX2 receptors, respectively, expressed in CHO cells.2 It induces transient increases in intracellular calcium in CHO cells stably expressing OX1 and OX2 (EC50s = 2,500 and 60 nM, respectively) and in primary rat ventral tegmental area (VTA) dopaminergic neurons.2,3 Orexin B amide stimulates arachidonic acid release from CHO cells expressing human recombinant OX1 (EC50 = 4.17 nM).4 It also stimulates food intake in freely feeding mice and goldfish when administered at intracerebroventricular doses of 30 nmol and 10 ng/g, respectively.2,5
1.Mahler, S.V., Moorman, D.E., Smith, R.J., et al.Motivational activation: A unifying hypothesis of orexin/hypocretin functionNat. Neurosci.17(10)1298-1303(2014) 2.Sakurai, T., Amemiya, A., Ishii, M., et al.Orexins and orexin receptors: A family of hypothalamic neuropeptides and G protein-coupled receptors that regulate feeding behaviorCell92(4)573-585(1998) 3.Nakamura, T., Uramura, K., Nambu, T., et al.Orexin-induced hyperlocomotion and stereotypy are mediated by the dopaminergic systemBrain Res.873(1)181-187(2000) 4.Turunen, P.M., Ekholm, M.E., Somerharju, P., et al.Arachidonic acid release mediated by OX1 orexin receptorsBr. J. Pharmacol.159(1)212-221(2010) 5.Volkoff, H., Bjorklund, J.M., and Peter, R.E.Stimulation of feeding behavior and food consumption in the goldfish, Carassius auratus, by orexin-A and orexin-BBrain Res.846(2)204-209(1999)
Cas No. | N/A | SDF | Download SDF |
别名 | Hypocretin 2, OXB | ||
Canonical SMILES | NC([C@@H](NC([C@@]([C@@H](C)O)([H])NC([C@H](CC(C)C)NC([C@@]([C@H](CC)C)([H])NC(CNC([C@@H](NC([C@@H](NC([C@@H](NC([C@H](CC(N)=O)NC(CNC([C@H](CO)NC([C@@H](NC([C@H](CCC(N)=O)NC([C@H](CC(C)C)NC([C@H](CC(C)C)NC([C@H](CCCNC(N)=N)NC([C@H](CCC(N)=O)NC([C@H](CC(C)C)NC([C@H](CCCNC(N)=N)NC(CNC([C@H](CCC(N)=O)NC([C@H](CC(C)C)NC(CNC([C@@H]1CCCN1C([C@@H]2CCCN2C(CNC([C@H](CO)NC([C@H](CCCNC(N)=N)N[H])=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)C)=O)=O)=O)=O)CC3=CN=CN3)=O)C)=O)C)=O)=O)=O)=O)=O)CCSC)=O.FC(F)(C(O)=O)F | ||
分子式 | C123H212N44O35S • XCF3COOH | 分子量 | 2899.3 |
溶解度 | Water: 1 mg/ml | 储存条件 | -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 | 0.3449 mL | 1.7246 mL | 3.4491 mL |
5 mM | 0.069 mL | 0.3449 mL | 0.6898 mL |
10 mM | 0.0345 mL | 0.1725 mL | 0.3449 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。
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