CGRP receptor ( Ki = 0.027 nM )
Rimegepant hemisulfate (BMS-927711, BHV-3000) is a potent, competitive, and selective antagonist of the human calcitonin gene-related peptide (CGRP) receptor with ki of 0.027 nM.

Rimegepant hemisulfate (BMS-927711, BHV-3000) 是一种有效的、竞争性的、选择性的人降钙素基因相关肽 (CGRP) 受体拮抗剂，ki 为 0.027 nM。

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BMS-927711 对人CGRP受体表现出强效的结合亲和力，Ki为0.027 ± 0.009 nM，该数据通过抑制¹²⁵I-CGRP与内源性表达该受体的SK-N-MC细胞膜的结合来测定。[1]
在使用SK-N-MC细胞的功能性实验中，BMS-927711 抑制CGRP刺激的cAMP产生，IC50为0.14 ± 0.01 nM，表现为完全、竞争性拮抗剂。[1]
该化合物对一组八种重组人CYP亚型显示出低水平的抑制，除CYP3A4 (IC50 = 17 μM)外，其余所有亚型的IC50值均≥20 μM。[1]
BMS-927711 在一组包含45个受体、离子通道结合和酶活性实验中，未显示出显著的脱靶风险。[1]
体外心血管安全性评估显示，在10和30 μM浓度下，BMS-927711 对HEK-293细胞中表达的hERG钾通道α亚单位的抑制小于30%，并且对这些细胞中表达的L型钠通道或钙通道没有显著影响。[1]
该化合物在探索性Ames试验中无致突变性。[1]
BMS-927711 在平行人工膜渗透性测定 (PAMPA) 中表现出良好的渗透性，在pH 5.5和7.4下的值分别为190和320 nm/sec。[1]
BMS-927711 的结晶溶解度为50 μg/mL。[1]
BMS-927711 的人血浆蛋白未结合分数 (fu) 为6.9%。[1]
BMS-927711 的人肝微粒体稳定性半衰期 (HLM T1/2) 为83分钟。[1]

体内疗效[1]
开发了一种新的无创绒猴恢复模型，用于评估CGRP受体拮抗剂的体内疗效，该模型利用激光多普勒面部血流作为颅内动脉直径的替代指标。简而言之，对狨猴进行麻醉，并通过四次静脉注射hαCGRP（10μg/kg）来增加面部血流量，每45分钟（-30、15、60和105分钟）一次。通过激光多普勒血流仪测量0分钟皮下注射（SC）拮抗剂对hαCGRP诱导的面部血流变化的影响。在该模型中，化合物8（Rimegapant，也称为BMS-927711）抑制了皮下（SC）给药时hαCGRP诱导的狨猴面部血流量的增加。与给药前hCGRP对照组（-30分钟）相比，在给药后15、60和105分钟，以7mg/kg的剂量皮下注射化合物8，观察到对CGRP诱导的面部血流作用的强烈（>50%）抑制（图2）。比较给药后15分钟的活性与暴露量，约400 nM的血浆水平与强烈的体内疗效（>65%的抑制率）相关。相比之下，在该模型中，需要5 nM以上的血浆水平才能达到类似的疗效。在给药后60和105分钟，8的峰值抑制在75-80%时非常强烈，相应的血浆水平略低于800 nM（图3）

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体内PK[1]
化合物8在大鼠（FPO=45%）和食蟹猴（溶液FPO=67%）中表现出良好的口服生物利用度。当以晶体材料的游离碱悬浮液给药时，8在猴子体内的口服生物利用度保持在48%。

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在一个用于评估CGRP受体拮抗剂疗效的新型无创狨猴恢复模型中，皮下 (SC) 注射 BMS-927711 (7 mg/kg) 强烈抑制了人αCGRP (hαCGRP) 诱导的面部血流增加。与给药前的CGRP对照相比，在给药后15、60和105分钟观察到强效 (>50%) 抑制。在给药后60和105分钟达到75-80%的峰值抑制。给药后15分钟时，约400 nM的血浆浓度与强效的体内活性 (>65%抑制) 相关。[1]

[125I]CGRP结合试验的竞争：[1]
使用放射性配体竞争分析法测量8抑制放射性标记的人α-CGRP（[125I]CGRP）与人CGRP受体结合的能力。内源性表达CGRP受体的人神经母细胞瘤SK-N-MC细胞被用作CGRP受体来源（Aiyar等人，2001）。首先将8溶解并连续稀释在100%DMSO中。将化合物进一步稀释25倍到测定缓冲液（50 mM Tris-Cl pH 7.5，5 mM MgCl2，0.005%Triton X-100）中，并转移（50µl）到96孔测定板中。[125I]在测定缓冲液中将CGRP稀释至72 pM，并向每个孔中加入50µl（测定中的最终浓度为18 pM，Kd=27.7 pM）。将SK-N-MC膜颗粒解冻，用新鲜的0.1%哺乳动物蛋白酶抑制剂混合物在测定缓冲液中稀释，并均质化。然后向每个孔中加入100µl的匀浆（5至10µg蛋白质）。将测定板在室温（25°C）下孵育两小时。通过立即加入过量的冷洗涤缓冲液（50mM Tris-Cl pH 7.5，0.1%BSA）终止测定，然后用预浸在0.5%PEI中的玻璃纤维过滤器过滤。非特异性结合被定义为在1µMβ-CGRP存在下的结合。使用伽马闪烁计数器测量蛋白质结合放射性。IC50定义为抑制50%放射性配体结合所需的化合物浓度。

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其他物种中的CGRP受体结合[1]
对S6 8在绒猴（普通绒猴（Callithrix jacchus））CGRP受体上的效力进行了测试。放射性配体结合分析用于评估活性：使用每种物种的50µg脑匀浆作为受体来源，15pM[125I]CGRP作为放射性配体。

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使用人重组酶抑制CYP[1]
使用3-氰基-7-乙氧基香豆素（CYP1A2和CYP2C19）、7-甲氧基-4-三氟甲基香豆素（CYP2C9）或3-[2-（N，N-二乙基-N-甲基氨基）乙基]-7-甲氧基-4-甲基香豆素（CY2D6）作为模型底物，测量测试化合物抑制由杆状病毒感染的昆虫细胞制备的微粒体中cDNA衍生的CYP酶的能力。CYP3A4用两种底物7-苄氧基-4-三氟甲基香豆素（BFC）和苯甲酰间苯二酚进行了测试。对每种酶测定试验化合物的50%抑制浓度（IC50）。将每种模型底物的单一浓度（约为表观Km，BFC除外）与10种浓度的2 nM至40µM的感兴趣化合物在0.2%v/v DMSO中孵育。通过产生7-羟基-3-氰基香豆素、3-[2-（N，N-二乙氨基）乙基]-7-羟基-4-甲基香豆素、7-羟基-4-三氟甲基香豆素或间苯二酚代谢物来测定模型底物的代谢，并通过荧光检测进行测量。在总体积为30µl的384孔微孔板中进行了检测。用由杆状病毒感染的昆虫细胞制备的微粒体孵育45分钟（CYP3A4 BFC测定为20分钟），微粒体含有cDNA衍生的CYP酶，并使用NADPH生成系统。

SK-N-MC CGRP细胞/功能测定[1]
CGRP受体复合物与Gαs类G蛋白偶联。CGRP与这种复合物的结合导致通过Gαs依赖性激活腺苷酸环化酶产生环AMP（腺苷3'5'-环磷酸）。通过测量化合物抑制附着的SK-N-S5 MC细胞中CGRP刺激的环AMP形成的能力，将8评估为人CGRP受体信号传导的抑制剂。SK-N-MC细胞与不同浓度的8或载体预孵育15分钟。加入激动剂（300 pMαCGRP，EC50=26.7+2.7 pM n=3），将样品在室温下孵育30分钟。使用基于HTRF的cAMP检测试剂盒裂解细胞并进行评估。IC50值定义为抑制300pM CGRP刺激的cAMP产生的50%所需的化合物浓度。

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渗透性和P-糖蛋白相互作用[1]
通过基于非细胞的平行人工膜渗透性测定（PAMPA）以及基于细胞的Caco-2细胞模型评估8的渗透性。PAMPA渗透性研究使用pION©脂质溶液在室温下在pH 5.5和7.4下用100µM 8进行4小时。这些研究一式三份（即每种化合物3个孔），平均值以nm/秒为单位报告。对培养约21天的单层进行Caco-2细胞研究。在浓度为3.7至100µM、pH 7.4的条件下，对8个样本进行了双向渗透性研究。在P-gp抑制剂（酮康唑20µM和环孢素20µM两侧）存在的情况下，对8（3µM，pH 7.4）进行了随访双向研究。研究了[3H]-地高辛（初始浓度5µM）（P-gp底物）通过Caco-2细胞膜的转运抑制8（初始浓度10µM），以评估该化合物对P-gp的潜在抑制作用。

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人CGRP受体的结合亲和力通过测量 BMS-927711 对¹²⁵I-CGRP与内源性表达该受体的SK-N-MC细胞制备的膜结合的抑制来测定。[1]
功能性受体拮抗作用通过测量 BMS-927711 对SK-N-MC细胞中CGRP刺激的cAMP产生的抑制来测定。[1]

In Vivo Efficacy of 8 [Rimegepant hemisulfate (BMS927711 hemisulfate)] in Marmoset Facial Blood Flow[1]
To assess in vivo efficacy and duration of action, a control increase in facial blood flow is induced by administration of hαCGRP (10 µg/kg, IV) 30 min prior (-0.5 hr) to drug delivery. The CGRP antagonist compound under study is administered at time zero (0 min) and three additional hαCGRP challenges are delivered at 45 min intervals for ~2 hr (data collected at 0.25, 1 and 1.75 hrs post-dose). Plasma samples are obtained just before each of the three post-dose hαCGRP administrations, to define the antagonist levels on board at the time of hαCGRP agonist challenge. Each antagonist is administered across a range of doses to define the no-effect, first significant effect and maximal peak effect dose. In the present study, 8 [Rimegepant hemisulfate (BMS927711 hemisulfate)] is dosed from 0.3 to 7 mg/kg, SC. The highest dose (7 mg/kg for 8 [Rimegepant hemisulfate (BMS927711 hemisulfate)]) represents the maximum dose deliverable within solubility limits and constrained by vehicle volumes that do not disrupt baseline facial blood flow. Following testing, animals are returned to the transport cage and placed on a temperature controlled surface that keeps the animals warm until fully awake and ambulatory. Animals may be tested again after a 14-21 day rest and washout period.

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In Vivo Methods – Pharmacokinetics in Rat and Cynomolgus Monkey [1]
In the rat and monkey studies described below, 8 [Rimegepant hemisulfate (BMS927711 hemisulfate)] was administered IV as a solution in a polyethylene glycol 400 (PEG-400)/ethanol (90:10, v/v). Rat Male Sprague-Dawley rats (250-350 g) were used in the PK studies of 8 [Rimegepant hemisulfate (BMS927711 hemisulfate)]. Blood samples (~0.3 mL) were collected from the jugular vein into K3EDTA-containing tubes and then centrifuged at 4°C (1500-2000 x g) to obtain plasma, which was stored at -20°C until analysis by LC/MS/MS. In an oral bioavailability study with 8 [Rimegepant hemisulfate (BMS927711 hemisulfate)], 2 groups of animals (N = 3 per group) received the compound as an intra-venous (IV) bolus (1 mg/kg) via a jugular vein cannula or as a solution by oral gavage (10 mg/kg to fasted rats). The oral solution contained 8 [Rimegepant hemisulfate (BMS927711 hemisulfate)] dissolved in PEG-400/water (90:10, v/v). Serial blood samples were obtained predose and at 0.03 and 0.17 (IV only), 0.25, 0.5, 0.75, 1, 2, 4, 6, 8, and 24 S9 hours post dose. Plasma samples, obtained by centrifugation at 4°C (1500-2000 x g), were stored at -20°C until analysis.

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Cynomolgus Monkey [1]
The PK of 8 was evaluated in a crossover-design study in male cynomolgus monkeys. Following an overnight fast (oral only), 3 animals (5.4 to 6.3 kg) received 8 [Rimegepant hemisulfate (BMS927711 hemisulfate)] by IV infusion (1 mg/kg over 5 minutes) via a femoral vein and by oral gavage as either a solution (10 mg/kg dissolved in 79.8% PEG400; 20% N-methylpyrrolidone; 0.2% Tween 80) or suspension of crystalline free base (10 mg/kg suspended in 98.95% water;1% povidone K-30; 0.05% docusate sodium), with at least a 2- week washout between treatments. Serial blood samples (~0.3 mL) were collected from a femoral artery predose and at 0.083, 0.17 (IV only), 0.25, 0.5, 0.75, 1, 2, 4, 6, 8, and 24 hours post dose, and centrifuged at 4°C (1500-2000 x g) to obtain plasma. Samples were stored at -20°C until analysis by LC/MS/MS.

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For the in vivo efficacy assessment in marmosets, a novel non-invasive recovery model was used. Marmosets were anesthetized. Facial blood flow was increased by four intravenous (IV) administrations of hαCGRP (10 µg/kg) delivered at 45-minute intervals (at -30, 15, 60, and 105 minutes relative to antagonist dosing). The test antagonist, BMS-927711, was administered subcutaneously (SC) at time 0 minutes. The effect of the antagonist on the hαCGRP-induced changes in facial blood flow was measured using laser Doppler flowmetry.[1]

Absorption, Distribution and Excretion
The absolute oral bioavailability of Rimegepant hemisulfate is approximately 64%. Following oral administration of the orally disintegrating tablet, maximum plasma concentrations were achieved at 1.5 hours (Tmax). When administered with a high-fat meal, Tmax is delayed by 1 hour, Cmax is decreased by 42-53%, and AUC is decreased by 32-38%. The clinical significance of this difference in pharmacokinetics is unknown.
Following oral administration of radiolabeled Rimegepant hemisulfate in healthy subjects, 78% of the administered radioactivity was recovered in feces and 24% in urine. Unchanged parent drug was the major component in each, comprising 42% and 51% of the recovered doses, respectively.
At steady state, the volume of distribution is approximately 120 L.

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Metabolism / Metabolites
Rimegepant hemisulfate is metabolized by CYP3A4 and, to a lesser extent, CYP2C9. Specific metabolites of Rimegepant hemisulfate have not been characterized and no major metabolites have been detected in plasma. Approximately 77% of an administered dose is eliminated unchanged, suggesting metabolism is likely to be a minor means of drug elimination.

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Biological Half-Life
The elimination half-life in healthy subjects is approximately 11 hours.

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BMS-927711 exhibited good oral bioavailability in rats (Fpo = 45%) and in cynomolgus monkeys (Fpo = 67% when dosed as a solution).[1]
When dosed as a free base suspension of crystalline material, the oral bioavailability in monkeys remained good at 48%.[1]
In the marmoset efficacy model, subcutaneous administration of 7 mg/kg BMS-927711 resulted in plasma levels of approximately 400 nM at 15 minutes post-dose and just below 800 nM at 60 and 105 minutes post-dose.[1]
Initial Phase I human pharmacokinetic results were in good agreement with preclinical human PK projections, with exposures at a 75 mg dose expected to be efficacious.[1]

Hepatotoxicity
In preregistration controlled trials of Rimegepant hemisulfate in several thousand patients, mild-to-moderate serum aminotransferase elevations arose in a small percentage of patients (1% to 2%) and overall rates were not different from those in placebo recipients. In the controlled trials and subsequently with general use, there have been no reports of clinically apparent liver injury attributed to ubrogepant. In contrast, telcagepant, the initial oral CGRP receptor antagonist evaluated as therapy for migraine headaches, was abandoned during development because of several instances of clinically apparent liver injury in recipients that was characterized by marked elevations in serum aminotransferase levels and symptoms of fatigue, nausea and abdominal discomfort arising within 2 to 4 weeks of starting therapy which rapidly resolved with stopping therapy. Similar episodes have not been reported with Rimegepant hemisulfate.
Likelihood score: E (unlikely cause of clinically apparent acute liver injury).

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Effects During Pregnancy and Lactation
◉ Summary of Use during Lactation
No information is available on the clinical use of Rimegepant hemisulfate during breastfeeding. However, amounts in breastmilk are low and would not be expected to cause any adverse effects in breastfed infants. If Rimegepant hemisulfate is required by the mother of an older infant, it is not a reason to discontinue breastfeeding, but until more data become available, an alternate drug may be preferred while nursing a newborn or preterm infant.
◉ Effects in Breastfed Infants
Relevant published information was not found as of the revision date.
◉ Effects on Lactation and Breastmilk
Relevant published information was not found as of the revision date.

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Protein Binding
Rimegepant hemisulfate is approximately 96% plasma protein-bound. The specific proteins to which Rimegepant hemisulfate binds have not been elucidated.

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In pre-nomination and pre-IND toxicological studies, BMS-927711 demonstrated a favorable predictive toxicological profile, which supported its selection for clinical development.[1]
In initial Phase I human studies, no significant adverse effects were encountered at doses up to 600 mg.[1]

[1]. J Med Chem . 2012 Dec 13;55(23):10644-51.

Rimegepant hemisulfate is an oral antagonist of the CGRP receptor developed by Biohaven Pharmaceuticals. It received FDA approval on February 27, 2020 for the acute treatment migraine headache, and was subsequently approved by the European Commission in April 2022 for both the treatment and prevention of migraines. While several parenteral antagonists of CGRP and its receptor have been approved for migraine therapy (e.g. [erenumab], [fremanezumab], [galcanezumab]), Rimegepant hemisulfate and [ubrogepant] were the only CGRP antagonists that possessed oral bioavailability until the approval of [atogepant] in 2021. The current standard of migraine therapy involves abortive treatment with \\\"triptans\\\", such as [sumatriptan], but these medications are contraindicated in patients with pre-existing cerebrovascular and cardiovascular disease due to their vasoconstrictive properties. Antagonism of the CGRP pathway has become an attractive target for migraine therapy as, unlike the triptans, oral CGRP antagonists have no observed vasoconstrictive properties and are therefore safer for use in patients with contraindications to standard therapy.
Rimegepant hemisulfate is a Calcitonin Gene-related Peptide Receptor Antagonist. The mechanism of action of Rimegepant hemisulfate is as a Calcitonin Gene-related Peptide Receptor Antagonist.
Rimegepant hemisulfate is a small molecule inhibitor of the calcitonin gene-related peptide (CGRP) receptor that blocks the action of CGRP, a potent vasodilator believed to play a role in migraine headaches. Rimegepant hemisulfate is approved for treatment of acute migraine attacks. In clinical trials, Rimegepant hemisulfate was generally well tolerated with only rare instances of transient serum aminotransferase elevations during therapy and with no reported instances of clinically apparent liver injury.
See also: Rimegepant hemisulfate Sulfate (active moiety of).

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Drug Indication
Rimegepant hemisulfate is indicated for the acute treatment of migraine with or without aura in adults. Rimegepant hemisulfate is also indicated for the prevention of episodic migraine in adults.
Vydura is indicated for theAcute treatment of migraine with or without aura in adults; Preventative treatment of episodic migraine in adults who have at least 4 migraine attacks per month.
Treatment of migraine headaches
Prevention of migraine headaches

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Mechanism of Action
The currently accepted theory of migraine pathophysiology considers dysfunction of the central nervous system, in particular the trigeminal ganglion, to be the root cause behind the condition. Activation of the trigeminal ganglion triggers the stimulation of trigeminal afferents that project to the spinal cord and synapse on various pain-sensing intra- and extracranial structures, such as the dura mater. Pain signals are then further transmitted via second-order ascending neurons to the brainstem, hypothalamus, and thalamic nuclei, and from there to several cortical regions (e.g. auditory, visual, motor cortices). The trigeminal ganglion appears to amplify and perpetuate the migraine headache pain through the activation of perivascular fibers and the release of molecules involved in pain generation, such as calcitonin gene-related peptide (CGRP). The α-isoform of CGRP, expressed in primary sensory neurons, is a potent vasodilator and has been implicated in migraine pathogenesis - CGRP levels are acutely elevated during migraine attacks, return to normal following treatment with triptan medications, and intravenous infusions of CGRP have been shown to trigger migraine-like headaches in migraine patients. In addition to its vasodilatory properties, CGRP appears to be a pronociceptive factor that modulates neuronal excitability to facilitate pain responses. Rimegepant hemisulfate is an antagonist of the calcitonin gene-related peptide receptor - it competes with CGRP for occupancy at these receptors, preventing the actions of CGRP and its ability to amplify and perpetuate migraine headache pain, ultimately terminating the headache.

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Pharmacodynamics
Rimegepant hemisulfate helps to abort migraine headaches by preventing the activity of a pronociceptive molecule that has been implicated in migraine pathophysiology. It is intended for use as an abortive migraine therapy and therefore has a relatively rapid onset of effect, with most efficacy trials evaluating for effect at the 2 hour mark. Rimegepant hemisulfate does not require dose adjustment in patients with mild, moderate, or severe renal impairment, nor does it require dose adjustment in patients with mild or moderate hepatic impairment. In clinical trials, plasma concentrations of Rimegepant hemisulfate were significantly higher in patients with severe (i.e. Child-Pugh C) hepatic impairment - it should therefore be avoided in this population. Hypersensitivity reactions have occurred during clinical studies and patients should be made aware of this possibility. Rimegepant hemisulfate should be discontinued immediately if hypersensitivity reaction occurs.

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\nBMS-927711 (also referred to as compound 8 in the literature) is a highly potent, oral, small-molecule antagonist of the calcitonin gene-related peptide (CGRP) receptor discovered for the treatment of acute migraine.[1]
\nIt was designed from a lead compound (BMS-846372) by incorporating a primary amine group to improve aqueous solubility while maintaining potency and permeability.[1]
\nThe presence of the primary amino group greatly improved aqueous solubility (50 µg/mL) without compromising bilayer permeability, resulting in enhanced ADME properties.[1]
\nThe compound has very good metabolic stability, an acceptable CYP inhibition profile, and good animal PK.[1]
\nBMS-927711 was in Phase II clinical trials for migraine at the time of publication.[1]

C28H28F2N6O3

583.607

1642783-82-1

1642783-82-1; 1642783-82-1 (0.5 sulfate); 1374024-48-2 (0.5 sulfate 1.5 hydrate); 2377164-85-5 (0.5 sulfate 3 hydrate); 1289023-67-1Rimegepant (BMS927711)

Typically exists as solids at room temperature

KRNAOFGYEFKHPB-ANJVHQHFSA-N

InChI=1S/C28H28F2N6O3/c29-20-6-1-4-17(23(20)30)18-8-9-22(25-19(24(18)31)5-2-12-32-25)39-28(38)35-14-10-16(11-15-35)36-21-7-3-13-33-26(21)34-27(36)37/h1-7,12-13,16,18,22,24H,8-11,14-15,31H2,(H,33,34,37)/t18-,22+,24-/m0/s1

[(5S,6S,9R)-5-amino-6-(2,3-difluorophenyl)-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-9-yl] 4-(2-oxo-3H-imidazo[4,5-b]pyridin-1-yl)piperidine-1-carboxylate

2934.99.9001

Powder      -20°C    3 years

                     4°C     2 years

In solvent   -80°C    6 months

                  -20°C    1 month

Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)

5%DMSO + Corn oil: 5.0mg/ml (9.35mM) 请根据您的实验动物和给药方式选择适当的溶解配方/方案：
1、请先配制澄清的储备液(如：用DMSO配置50 或 100 mg/mL母液(储备液));
2、取适量母液，按从左到右的顺序依次添加助溶剂，澄清后再加入下一助溶剂。以 下列配方为例说明 (注意此配方只用于说明，并不一定代表此产品 的实际溶解配方):
10% DMSO → 40% PEG300 → 5% Tween-80 → 45% ddH2O (或 saline);
假设最终工作液的体积为 1 mL, 浓度为5 mg/mL: 取 100 μL 50 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中，混合均匀/澄清；向上述体系中加入50 μL Tween-80，混合均匀/澄清；然后继续加入450 μL ddH2O (或 saline)定容至 1 mL；
3、溶剂前显示的百分比是指该溶剂在最终溶液/工作液中的体积所占比例;
4、 如产品在配制过程中出现沉淀/析出，可通过加热(≤50℃)或超声的方式助溶;
5、为保证最佳实验结果，工作液请现配现用！
6、如不确定怎么将母液配置成体内动物实验的工作液，请查看说明书或联系我们;
7、 以上所有助溶剂都可在 Invivochem.cn网站购买。