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Anamorelin Fumarate Sale

(Synonyms: 富马酸阿拉莫林; ONO-7643 Fumarate; RC1291 Fumarate) 目录号 : GC35337

A small molecule agonist of GHS-R1a

Anamorelin Fumarate Chemical Structure

Cas No.:339539-92-3

规格 价格 库存 购买数量
5mg
¥900.00
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10mg
¥1,350.00
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50mg
¥4,410.00
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100mg
¥7,650.00
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Sample solution is provided at 25 µL, 10mM.

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Quality Control & SDS

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实验参考方法

Kinase experiment:

For the competition assay, Anamorelin (ANAM) concentrations (1 pM-10 μM) are added to the membranes together with 35S-MK-677. Nonspecific binding is determined by adding 10 μM nonlabeled MK-677. The mixture is incubated at 30°C for 60 min, followed by application of the samples to GF/B filters, which has been pretreated with 0.5 % PEI for 60 min. The filters are subsequently washed in 0.9 % NaCl and counted using an OptiPhase counter[1].

Animal experiment:

Rats[1] For the assessment of food intake and body weight, rats are divided into four groups: Anamorelin 3 mg/kg (n=7), 10 mg/kg (n=7), or 30 mg/kg (n=7), or vehicle control (n=8), and 100 μL blood samples are collected before and 0.25, 0.5, 1, 2, 3, 4, 5, and 6 h after single dosing. Rats are anesthetized with sodium pentobarbital 64.8 mg/kg. A catheter filled with heparinized saline solution is inserted in the left femoral artery for blood collection and fitted with an extension tube, 1 mL sampling syringe, and a three-way cock to allow excess blood to return. Plasma levels of GH are measured immunochemically using a Rat Growth Hormone EIA kit and microplate reader. Measurements are performed in duplicate. Area under the GH concentration curve from 0 to 6 h (AUC0-6h) postdose and the time course of GH plasma concentrations are evaluated. Pig[1] In pigs (n=6 per group), Anamorelin is dosed directly into the gastric lumen via the dosing catheter. Blood samples are collected for the stimulation profile of GH at 30 and 15 min before, and 0, 5, 15, 30, 45, 60, and 120 min following dosing. Animals received either a single dose (3.5 mg/kg), or once-daily administration (1 mg/kg) for 7 days and stimulation profiles are taken after the first and seventh dose of Anamorelin. To assess IGF-1 levels, pigs receive either placebo or Anamorelin for 7 days (1 mg/kg/day), and the following 7 days the two treatments are crossed over. A single blood sample is taken once a day immediately before dosing.

References:

[1]. Pietra C, et al. Anamorelin HCl (ONO-7643), a novel ghrelin receptor agonist, for the treatment of cancer anorexia-cachexiasyndrome: preclinical profile. J Cachexia Sarcopenia Muscle. 2014 Dec;5(4):329-37.

产品描述

Anamorelin is a small molecule agonist of the growth hormone (GH) secretagogue receptor 1a (GHS-R1a) and a mimetic of ghrelin .1,2 It induces calcium mobilization in CHO cells expressing rat GHS-R1a in a concentration-dependent manner and GH release from rat pituitary cells (EC50 = 1.5 nM). In vivo, anamorelin stimulates GH release in sham and vagotomized rats in a dose-dependent manner.1 Anamorelin (3-30 mg/kg) also increases food intake in rats.2 Formulations containing anamorelin have been used to treat cancer anorexia and cachexia in patients with non-small cell lung cancer.

1.Morozumi, N., Hanada, T., Habara, H., et al.The role of C-terminal part of ghrelin in pharmacokinetic profile and biological activity in ratsPeptides32(5)1001-1007(2011) 2.Zhang, H., and Garcia, J.M.Anamorelin hydrochloride for the treatment of cancer-anorexia-cachexia in NSCLCExpert Opin. Pharmacother.16(8)1245-1253(2015)

Chemical Properties

Cas No. 339539-92-3 SDF
别名 富马酸阿拉莫林; ONO-7643 Fumarate; RC1291 Fumarate
Canonical SMILES [H][C@](CC1=CNC2=CC=CC=C21)(NC(C(C)(C)N)=O)C(N3CCC[C@@](C(N(C)N(C)C)=O)(CC4=CC=CC=C4)C3)=O.O=C(O)/C=C/C(O)=O
分子式 C35H46N6O7 分子量 662.78
溶解度 Soluble in DMSO 储存条件 Store at -20°C
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溶解性数据

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1 mg 5 mg 10 mg
1 mM 1.5088 mL 7.544 mL 15.088 mL
5 mM 0.3018 mL 1.5088 mL 3.0176 mL
10 mM 0.1509 mL 0.7544 mL 1.5088 mL
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