Deoxyartemisinin
CAS No. 72826-63-2
Deoxyartemisinin( —— )
Catalog No. M37735 CAS No. 72826-63-2
Deoxyartemisinin (2-deoxyartemisinin), a compound derived from Artemisia annua, has anti-inflammatory and anti-ulcer effects and is used in the study of malaria.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 504 | In Stock |
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| 5MG | 135 | In Stock |
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| 10MG | 198 | In Stock |
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| 25MG | 338 | In Stock |
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| 50MG | 490 | In Stock |
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| 100MG | Get Quote | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameDeoxyartemisinin
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NoteResearch use only, not for human use.
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Brief DescriptionDeoxyartemisinin (2-deoxyartemisinin), a compound derived from Artemisia annua, has anti-inflammatory and anti-ulcer effects and is used in the study of malaria.
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DescriptionDeoxy artemisinin, a orally bioavailable compound separated from Artemisinin annua L., shows anti-inflammatory and antiulcer activities.
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In Vitro——
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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 Number72826-63-2
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Formula Weight266.33
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Molecular FormulaC15H22O4
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Purity>98% (HPLC)
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Solubility——
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SMILESC[C@@H]1[C@]2([C@]34[C@@](O[C@](C)(O3)CC[C@]4([C@H](C)CC2)[H])(OC1=O)[H])[H]
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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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Biotin-MBP Derivatiz...
Biotin-MBP Derivatized Peptide
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Tachyplesin I
Tachyplesin I is a β-hairpin antimicrobial peptide that contains 17 amino acid residues. Tachyplesin I exhibits cytotoxic properties against various human tumor cell lines acting primarily by impairing the integrity of the outer cell membrane.
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Emoxipine
Emoxipine is an antidepressant agent.The influence of emoxipine (2-ethyl-6-methyl-3-hydroxypyridine hydrochloride) and mexidol (2-ethyl-6-methyl-3-hydroxypyridine succinate) on the content of lipid peroxidation products in peripheral blood and the dynamics of clinical symptoms of gastrointestinal tract pathology has been studied in patients of middle and senile age with atherosclerosis in the abdominal aorta.
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