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Cyaonoside B
CAS No. 51161-58-1
Cyaonoside B( —— )
Catalog No. M24476 CAS No. 51161-58-1
Cyaonoside B is isolated from S. simplex as a saponin and has a glucuronic acid attached to carbon C-3.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 221 | In Stock |
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| 5MG | 132 | In Stock |
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| 10MG | 202 | In Stock |
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| 25MG | 339 | In Stock |
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| 50MG | 491 | In Stock |
|
| 100MG | 706 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameCyaonoside B
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NoteResearch use only, not for human use.
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Brief DescriptionCyaonoside B is isolated from S. simplex as a saponin and has a glucuronic acid attached to carbon C-3.
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DescriptionCyaonoside B is isolated from S. simplex as a saponin and has a glucuronic acid attached to carbon C-3.
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In Vitroβ-D-glucopyranosyl-[α-L-rhamnopyranosyl-(1→3)-βD-glucuronopyranosyl-(1→3)]-3β-hydroxyolean-12-ene28-oate has a glucuronic acid attached to carbon C-3 and is isolated from S. simplex.
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In Vivo——
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number51161-58-1
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Formula Weight941.11
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Molecular FormulaC48H76O18
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (106.26 mM)
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SMILESO[C@H]([C@H]([C@@H]([C@@H](C(O)=O)O1)O)O[C@H]2[C@@H]([C@@H]([C@H]([C@H](C)O2)O)O)O)[C@@H]1O[C@@H]3CC[C@]4(C)[C@@]5([H])CC=C6[C@]7([H])CC(C)(C)CC[C@@](C(O[C@H]8[C@@H]([C@H]([C@@H]([C@@H](CO)O8)O)O)O)=O)7CC[C@](C)6[C@@](C)5CC[C@]([H])4C3(C)C
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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OD1
Potent rat Nav1.7, human Nav1.4 and rat Nav1.6 channel activator (EC50 values are 7, 10 and 47 nM, respectively). Exhibits minimal activation at mammalian Nav1.2, Nav1.3 and Nav1.5 (EC50 values >3 μM). Inhibits fast inactivation on all channels. Increases peak currents at all voltages and stimulates a persistent Na+ current at hNav1.7 channel. Increases hyperpolarization at Nav1.4 and Nav1.6 channels. Induces spontaneous pain in vivo.
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Epaminurad HCl
Epaminurad HCl is a URAT1 inhibitor with partial inhibition of OAT1 and OAT3 (organic anion transporters).Epaminurad HCl is a pro-uric acid excretory agent used for the prevention and treatment of gout and hyperuricemia.
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MSC 2032964A
MSC 2032964A is a potent selective ASK1 inhibitor (IC50 = 93 nM) that is oral bioavailable and brain permeable. It inhibited neuroinflammation in mouse EAE models and blocked LPS-induced phosphorylation of ASK1 and p38 in cultured mouse astrocytes.
