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Kaempferol 3,7,4-trimethyl ether
CAS No. 15486-34-7
Kaempferol 3,7,4-trimethyl ether( Kaempferol 3,7,4'-trimethylether )
Catalog No. M29174 CAS No. 15486-34-7
Kaempferol 3,7,4'-trimethylether shows selective cyctoxic activities against the nine tested cancer cell lines.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 267 | Get Quote |
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| 10MG | 473 | Get Quote |
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| 25MG | 754 | Get Quote |
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| 50MG | 1017 | Get Quote |
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| 100MG | 1368 | Get Quote |
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| 200MG | Get Quote | 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 NameKaempferol 3,7,4-trimethyl ether
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NoteResearch use only, not for human use.
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Brief DescriptionKaempferol 3,7,4'-trimethylether shows selective cyctoxic activities against the nine tested cancer cell lines.
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DescriptionKaempferol 3,7,4'-trimethylether shows selective cyctoxic activities against the nine tested cancer cell lines.(In Vitro):The IC50 values below or around 30 μg/mL were recorded with A. arundinaceum extract against eight of the nine tested cancer cell lines. This extract displayed IC50 values below 40 μg/mL towards the nine tested cancer cell lines whilst A. polyanthum extract, Kaempferol 3,7,4'-trimethylether showed selective activities. Collateral sensitivity (hypersensitivity) was observed with A. arundinaceum extract towards leukemia CEM/ADR5000 cells and glioblastoma U87MG.ΔEGFR compared to their respective sensitive counterparts CEM/CEM and U87MG.
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In Vitro——
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In Vivo——
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SynonymsKaempferol 3,7,4'-trimethylether
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PathwayImmunology/Inflammation
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TargetNOS
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RecptorNO Synthase
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Research Area——
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Indication——
Chemical Information
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CAS Number15486-34-7
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Formula Weight328.32
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Molecular FormulaC18H16O6
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Purity>98% (HPLC)
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Solubility——
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SMILESCOc1ccc(cc1)-c1oc2cc(OC)cc(O)c2c(=O)c1OC
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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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AR-C102222
AR-C102222 is a potent, selective iNOS inhibitor with IC50 of 35 nM, dislapys 3,000-fold and 20-fold selectivity over eNOS and nNOS respectively; reduces inflammation produced by the application of arachidonic acid to the ear, attenuates FCA-induced mechanical hyperalgesia, and attenuates acetic acid-induced writhing in mice.Rheumatoid ArthritisDiscontinued
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ZLc002
ZLc002 (ZLc-002) is a putative small-molecule inhibitor of nNOS interaction with NOS1AP.
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S-Nitroso-N-acetyl-D...
S-Nitroso-N-acetyl-DL-penicillamine acts as a stable inhibitor of platelet aggregation, is a nitric oxide donor and . S-Nitroso-N-acetyl-DL-penicillamine (10 mM; 8 hours) after 6 hours under normoxic conditions by releasing nitric oxide (NO)induces toxicity of about 80% .
