DPhPC
CAS No. 207131-40-6
DPhPC( —— )
Catalog No. M35830 CAS No. 207131-40-6
DPhPC is a synthetic liposome used to synthesize liposomes commonly used in artificial membrane matrices.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 29 | In Stock |
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| 5MG | 42 | In Stock |
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| 10MG | 65 | In Stock |
|
| 25MG | 106 | In Stock |
|
| 50MG | 152 | In Stock |
|
| 100MG | 226 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameDPhPC
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NoteResearch use only, not for human use.
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Brief DescriptionDPhPC is a synthetic liposome used to synthesize liposomes commonly used in artificial membrane matrices.
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DescriptionDPhPC is a phospholipid used to synthesize bilayer vesicles. DPhPC bilayers do not permit ions to leak in the absence of a pore/ion channel, which can be used for studies on channel proteins.
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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 Number207131-40-6
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Formula Weight846.25
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Molecular FormulaC48H96NO8P
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 3.57 mg/mL (4.22 mM; Ultrasonic (<60°C)
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SMILES[C@@H](OC(CC(CCCC(CCCC(CCCC(C)C)C)C)C)=O)(COC(CC(CCCC(CCCC(CCCC(C)C)C)C)C)=O)COP(OCC[N+](C)(C)C)(=O)[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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Peldesine
Peldesine is an effective, competitive, reversible, and orally active inhibitor of purine nucleoside phosphorylase.
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Multiflorin B
Multiflorin B (compound 5) is a kind of kaempferol glycoside. Multiflorin B can be isolated from the root of the fern Neocheiropteris palmatopedata. Multiflorin B inhibits nitric oxide production at a concentration of 20 μg/ml with an inhibition of 52%.
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TMN355
TMN355 is a potent chemical inhibitor of cyclophilin A and reduces foam cell formation and cytokine secretion,and is used for atherosclerosis. Silencing cyclophilin A in THP-1 cells and human monocytes using siRNA or chemical inhibitor, TMN355 resulted in decrease in lipid uptake by 65-75% even after exposure to oxidized LDL.
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