规格或纯度 | ≥97% |
---|---|
英文名称 | Veratridine |
英文别名 | 3-Veratroylveracevine;(3S,4S,4aS,6aS,6bS,8R,8aS,9S,9aS,12S,15aS,15bR,16aR,16bR)-4,6b,8,8a,9,15b-hexahydroxy-9,12,16b-trimethyldocosahydro-1H-4,16a-epoxybenzo[4,5]indeno[1,2-h]pyrido[1,2-b]isoquinolin-3-yl 3,4-dimethoxybenzoate |
生化机理 | 百合科植物中发现的生物碱毒素。导致电压门控的Na +通道持续打开,并降低其单通道电导。 |
储存温度 | -20°C储存,干燥 |
运输条件 | 超低温冰袋运输 |
备注 | 如果有可能,您尽量在使用的当天配置溶液,并在当天使用完它。但是,如果您需要预先配制储备溶液,我们建议您将溶液等份保存在-20°C的密封小瓶中。通常,它们最多可以使用一个月。在使用前和打开样品瓶之前,我们建议您让您的产品在室温下平衡至少1小时。需要更多关于溶解度,用法和处理的建议吗?请访问我们的常见问题(FAQ)页面以获取更多详细信息。 |
产品介绍 |
储存在-20℃。存放在干燥的条件下。该产品最多可存储12个月。 Store at -20°C. Store under desiccating conditions. The product can be stored for up to 12 months. Application: A Na+ channel opener. Increases intracellular Ca2+ levels without affecting Na+ - Ca2+ exchange. Acts at neurotoxin receptor site 2 and preferentially binds to activated Na+ channels causing persistent activation. Induces cell death in bovine chromaffin cells. A Na+ channel opener. Increases intracellular Ca2+ levels without affecting Na+-Ca2+ exchange. Acts at neurotoxin receptor site 2 and preferentially binds to activated Na+ channels causing persistent activation. Induces cell death in bovine chromaffin cells. |
IUPAC Name | [(1R,2S,6S,9S,10R,11S,12S,14R,15S,18S,19S,22S,23S,25R)-1,10,11,12,14,23-hexahydroxy-6,10,19-trimethyl-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-22-yl] 3,4-dimethoxybenzoate |
---|---|
INCHI | InChI=1S/C36H51NO11/c1-19-6-11-26-31(3,40)35(43)25(17-37(26)16-19)33(42)18-34-24(32(33,41)15-27(35)38)10-9-23-30(34,2)13-12-28(36(23,44)48-34)47-29(39)20-7-8-21(45-4)22(14-20)46-5/h7-8,14,19,23-28,38,40-44H,6,9-13,15-18H2,1-5H3/t19-,23-,24-,25-,26-,27-,28-,30-,31+,32+,33+,34+,35-,36-/m0/s1 |
InChi Key | FVECELJHCSPHKY-YFUMOZOISA-N |
Canonical SMILES | CC1CCC2C(C3(C(CC4(C5CCC6C7(C5(CC4(C3CN2C1)O)OC6(C(CC7)OC(=O)C8=CC(=C(C=C8)OC)OC)O)C)O)O)O)(C)O |
PubChem CID | 6280 |
分子量 | 673.8 |
PubChem CID | 6280 |
---|---|
Wikipedia | Veratridine |
ChEMBL Ligand | CHEMBL439496 |
BindingDB Ligand | 50158389 |
CAS Registry No. | 71-62-5 |
ChEBI | CHEBI:28051 |
溶解性 | Soluble in ethanol to 100 mM |
---|
象形图 |
Toxic Health Hazard Harmful |
---|---|
信号词 | Danger |
危险声明 |
H315: Causes skin irritation H319: Causes serious eye irritation H335: May cause respiratory irritation H300: Fatal if swallowed H310: Fatal in contact with skin H330: Fatal if inhaled H361: Suspected of damaging fertility or the unborn child |
预防措施声明 | P261,P305+P351+P338,P280,P302+P352,P321,P405,P501,P264,P260,P284,P271,P270,P304+P340,P403+P233,P362+P364,P330,P262,P320,P361+P364,P203,P264+P265,P301+P316,P318,P337+P317,P332+P317,P316,P319 |
Ligand ID | 2626 |
---|---|
名称 | veratridine |
别名 | veratrine |
类别 | Natural product |
学名 | 4-amino-N-(4,6-dimethylpyrimidin-2-yl)benzenesulfonamide |
生物活性评价 |
The sulfonamide class of antibacterial compounds are primarily bacteriostatic agents and have a broad spectrum of activity against both Gram-positive and Gram-negative species of bacteria (reviewed in |
评价 | Sulfadimidine (sulfamethazine) is a sulfonamide antibacterial compound. This class of compounds are competitive inhibitors of bacterial dihydropteroate synthase (DHPS), an enzyme in the pathway which generates the folic acid that is essential for bacterial growth. |
1. Wei XP et al.. (2022) A novel reticular node in the brainstem synchronizes neonatal mouse crying with breathing.. Neuron, 110 (4): (644-657.e6). [PMID:34998469] |
2. Mohammed ZA et al.. (2020) An unbiased and efficient assessment of excitability of sensory neurons for analgesic drug discovery.. Pain, 161 (5): (1100-1108). [PMID:31929383] |
3. Zimmermann K et al.. (2013) Analgesic treatment of ciguatoxin-induced cold allodynia.. Pain, 154 (10): (1999-2006). [PMID:23778293] |
4. Sousa SR et al.. (2017) Discovery and mode of action of a novel analgesic ?-toxin from the African spider Ceratogyrus darlingi.. PLoS One, 12 (9): (e0182848). [PMID:28880874] |
5. Henriques ST et al.. (2016) Interaction of Tarantula Venom Peptide ProTx-II with Lipid Membranes Is a Prerequisite for Its Inhibition of Human Voltage-gated Sodium Channel NaV1.7.. J Biol Chem, 291 (33): (17049-65). [PMID:27311819] |
6. Mohammed ZA et al.. (2017) Veratridine produces distinct calcium response profiles in mouse Dorsal Root Ganglia neurons.. Sci Rep, 7 (): (45221). [PMID:28338073] |