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EDANS
CAS No. 50402-56-7
EDANS( EDANS acid [5-((2-Aminoethyl)amino)napht | 1,5-EDANS )
Catalog No. M24462 CAS No. 50402-56-7
EDANS is a novel and quenched fluorogenic substrate for assaying retroviral protease by resonance energy transfer (RET).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 41 | In Stock |
|
| 50MG | 28 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameEDANS
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NoteResearch use only, not for human use.
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Brief DescriptionEDANS is a novel and quenched fluorogenic substrate for assaying retroviral protease by resonance energy transfer (RET).
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DescriptionEDANS is a novel and quenched fluorogenic substrate for assaying retroviral protease by resonance energy transfer (RET).
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In Vitro——
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In Vivo——
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SynonymsEDANS acid [5-((2-Aminoethyl)amino)napht | 1,5-EDANS
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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 Number50402-56-7
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Formula Weight266.32
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Molecular FormulaC12H14N2O3S
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Purity>98% (HPLC)
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SolubilityDMSO:13.89 mg/mL (52.16 mM; Need ultrasonic)
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SMILESNCCNc1c(cccc2S(O)(=O)=O)c2ccc1
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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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Apelin-12 (human, bo...
Apelin-12 is one of the most potent C-terminal fragments of the polypeptide that possesses a high affinity to orphan receptor APJ receptor. Apelin-12 is involved in the regulation of body fluid homeostasis and in the central control of feeding. Apelin-12 blocks HIV-1 entry through APJ receptor. Apelin-12 exerts neuroprotective effect.
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Divalproex Sodium
Divalproex Sodium binds to and inhibits gamma-aminobutyric acid (GABA) transaminase and its anticonvulsant activity may be exerted by increasing brain concentration of GABA and by inhibiting enzymes that catabolize GABA or block the reuptake of GABA into glia and nerve endings.
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A-196
A-196 is a potent and selective inhibitor of SUV420 h1 and SUV420 h2 with IC50 values of 0.025 and 0.144 μM, respectively.
