Methyl 5-hydroxypyridine-2-carboxylate
CAS No. 30766-12-2
Methyl 5-hydroxypyridine-2-carboxylate( —— )
Catalog No. M28296 CAS No. 30766-12-2
Methyl 5-hydroxypyridine-2-carboxylate is a phenolic acid that can found in the stems of Mahonia fortune . Methyl 5-hydroxypyridine-2-carboxylate exhibits NO inhibitory effects in vitro.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 100MG | 37 | Get Quote |
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| 500MG | Get Quote | Get Quote |
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| 1G | Get Quote | Get Quote |
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Biological Information
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Product NameMethyl 5-hydroxypyridine-2-carboxylate
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NoteResearch use only, not for human use.
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Brief DescriptionMethyl 5-hydroxypyridine-2-carboxylate is a phenolic acid that can found in the stems of Mahonia fortune . Methyl 5-hydroxypyridine-2-carboxylate exhibits NO inhibitory effects in vitro.
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DescriptionMethyl 5-hydroxypyridine-2-carboxylate is a phenolic acid that can found in the stems of Mahonia fortune . Methyl 5-hydroxypyridine-2-carboxylate exhibits NO inhibitory effects in vitro.(In Vitro):Methyl 5-hydroxypyridine-2-carboxylate (compound 2) inhibits NO in LPS-stimulated RAW264.7 and BV2 cells, with IC 50 s of 115.67 and 118.80 μM, respectively. Methyl 5-hydroxypyridine-2-carboxylate (6.25-200μM) does not exhibit any cytotoxic effect .
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In VitroMethyl 5-hydroxypyridine-2-carboxylate (compound 2) inhibits NO in LPS-stimulated RAW264.7 and BV2 cells, with IC50s of 115.67 and 118.80 μM, respectively.Methyl 5-hydroxypyridine-2-carboxylate (6.25-200?μM) does not exhibit any cytotoxic effect.
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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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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number30766-12-2
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Formula Weight153.137
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Molecular FormulaC7H7NO3
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 50 mg/mL (326.50 mM)
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SMILESCOC(=O)c1ccc(O)cn1
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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
1.NabinC. Barua, et al. Coumarins in artemisia caruifolia. Phytochemistry. 1980,19(10):2217-2218.
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