LY 334370 hydrochloride |
| Catalog No.GC12657 |
5-HT1F receptor agonist
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 199673-74-0
Sample solution is provided at 25 µL, 10mM.
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LY334370 is a selective 5-HT1F receptor agonist with a Ki of 1.6 nM.
LY334370 has no vasoconstrictor effects on human cerebral arteries in vitro until a dose of 10-5 M, at which it produces a contraction of 8.5±5.7%; however, this is not significant[1].
Following intravenous administration of LY334370 at 3 mg/kg (n=3) or 10 mg/kg (n=6) electrical stimulation evokes an increase in dural blood vessel diameter of 135±6% and 106±11%, respectively, which is not significantly different from the respective control values. LY334370 has no effect on dural blood vessel diameter per se, since the actualdural blood vessel diameter is 43±4 arbitrary units before drug and 43±4 arbitrary units 15 min after injection of LY334370 (10 mg/kg)[1].
References:
[1]. Shepheard S, et al. Possible antimigraine mechanisms of action of the 5HT1F receptor agonist LY334370. Cephalalgia. 1999 Dec;19(10):851-8.
Cell experiment: | in vitro studies, LY334370 is dissolved in buffer solution.--> Human cerebral artery is used in this study. Segments are prepared as previously described, but briefly they are placed in a buffer solution containing (mM) NaCl 119, NaHCo3 15, KCl 4.6, CaCl2 1.5, NaH2PO4 1.2, MgCl2 1.2, and glucose 5.5. Sections of vessel about 0.5 mm in diameter and 1 to 2 mm in length are mounted in a temperature-controlled tissue bath (37°C) containing buffer solution bubbled with 95% O2 and 5% CO2. The vessel segments are given a tension of 4 mN and allowed to stabilize at this tension for 1 to 1.5 h. Vessel reactivity is tested by exposure to 60 mM KCl. This is done twice for each segment and only if the response is similar to the segment used for LY334370 testing. Responses to LY334370 is calculated as a percentage of the maximum KC1 response[1]. |
Animal experiment: | in vivo studies, LY334370 is dissolved in 0.9% saline and is administered at a volume of 1 mL/kg except for hyperalgesia studies where it is dissolved in distilled water and is administered at a volume of 2 mL/kg.--> Male Sprague-Dawley rats (300 to 400 g) are anesthetized with pentobarbitone sodium. Briefly, a femoral artery and both femoral veins are cannulated for blood pressure recording, intravenous injection of drugs and infusion of anesthetic, respectively. Rats are placed in a stereotaxic frame, the skull exposed and thinned by drilling to reveal a branch of the middle meningeal artery whose diameter is measured continuously through the intact skull using intravital microscopy and a video dimension analyser. Neurogenic vasodilation is evoked using a bipolar stimulating electrode placed on the surface of the cranial window approximately 200 μM from the vessel of interest. A control vasodilation response to electrical stimulation is produced and 5 min later LY334370 (3 or 10 mg/kg, iv.) is given and the electrical stimulation repeated after a further 15 min. The mean maximum percentage increase in dural vessel diameter relative to pre-stimulus baseline is calculated for each response and comparisons of vasodilation responses evoked in the presence or absence of LY334370 are made by analysis of variance (ANOVA) followed by paired t-tests[1]. |
References: [1]. Shepheard S, et al. Possible antimigraine mechanisms of action of the 5HT1F receptor agonist LY334370. Cephalalgia. 1999 Dec;19(10):851-8. | |
| Cas No. | 199673-74-0 | SDF | |
| Chemical Name | 4-fluoro-N-(3-(1-methylpiperidin-4-yl)-1H-indol-5-yl)benzamide hydrochloride | ||
| Canonical SMILES | CN1CCC(C2=CNC3=C2C=C(NC(C4=CC=C(F)C=C4)=O)C=C3)CC1.Cl | ||
| Formula | C21H22FN3O.HCl | M.Wt | 387.88 |
| Solubility | <9.7mg/ml in Water; <9.7mg/ml in DMSO | Storage | Store at -20°C |
| General tips | Please select the appropriate solvent to prepare the stock solution according to the
solubility of the product in different solvents; once the solution is prepared, please store it in
separate packages to avoid product failure caused by repeated freezing and thawing.Storage method
and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored
at -20°C, please use it within 1 month. To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time. |
||
| Shipping Condition | Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request. | ||
| Prepare stock solution | |||
|
1 mg | 5 mg | 10 mg |
| 1 mM | 2.5781 mL | 12.8906 mL | 25.7812 mL |
| 5 mM | 515.6 μL | 2.5781 mL | 5.1562 mL |
| 10 mM | 257.8 μL | 1.2891 mL | 2.5781 mL |
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Quality Control & SDS
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- Purity: >98.00%
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Average Rating: 5 (Based on Reviews and 13 reference(s) in Google Scholar.)
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