4'57-Trimethoxyflavone
CAS No. 5631-70-9
4'57-Trimethoxyflavone( —— )
Catalog No. M21520 CAS No. 5631-70-9
574'-Trimethoxyflavone is isolated from Kaempferia parviflora (KP) which is a medicinal plant from Thailand.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 42 | In Stock |
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| 5MG | 38 | In Stock |
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| 10MG | 61 | In Stock |
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| 25MG | 128 | In Stock |
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| 50MG | 184 | In Stock |
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| 100MG | 276 | In Stock |
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| 200MG | 431 | In Stock |
|
| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
|
Biological Information
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Product Name4'57-Trimethoxyflavone
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NoteResearch use only, not for human use.
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Brief Description574'-Trimethoxyflavone is isolated from Kaempferia parviflora (KP) which is a medicinal plant from Thailand.
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Description574'-Trimethoxyflavone is isolated from Kaempferia parviflora (KP) which is a medicinal plant from Thailand.
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In VitroCell Viability Assay Cell Line:AGS, SNU-1, SNU-16Concentration:12.5 ,25, 50, 100, 200 μM Incubation Time:24 and 48 h Result:Showed the highest cytotoxicity in SNU-16 cells.Apoptosis Analysis Cell Line: SNU-16 Concentration:12.5 ,25, 37.5, 50 μM Incubation Time:24 h Result:Increased the percentage of annexin V-positive SNU-16 cells from 7.2% to 58.0% and the expression of GRP78、IRE1a、ATF-4 and CHOP.Western Blot Analysis Cell Line:HDFs Concentration:6.25, 12.5 μM Incubation Time:24 h Result:Inhibited matrix metalloproteinase-1 ( MMP-1) expression and stimulated collagen, type I,and alpha 1 (COLIA1) expression.
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In Vivo——
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Synonyms——
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PathwayApoptosis
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TargetCaspase
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RecptorCaspase-3| PARP
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Research Area——
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Indication——
Chemical Information
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CAS Number5631-70-9
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Formula Weight312.3
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Molecular FormulaC18H16O5
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (320.18 mM)
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SMILESCOc(cc1)ccc1C(Oc1c2c(OC)cc(OC)c1)=CC2=O
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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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Abrine
Abrine exhibits inhibition of rabbit small intestine indoleamine 2, 3-dioxygenase, competitive inhibition of IDO.
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Ac-FLTD-CMK
Ac-FLTD-CMK is an inhibitor derived from abscisicin D (GSDMDD) with specific inhibitory effects on inflammatory caspases. ac-FLTD-CMK showed inhibitory effects on caspases-1, caspases-4 and caspases-11 with IC50s of 46.7 nM, 1.49 μM and 329 nM, respectively. Ac-FLTD-CMK showed potency against caspases-1, caspases-4 and caspases-11, but not against apoptosis-associated caspase-3.
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VX-765
VX-765 (Belnacasan) is an orally absorbed prodrug of VRT-043198, which is a potent and selective inhibitor of interleukin-converting enzyme/caspase-1 with Ki of 0.8 nM.
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