Kuwanon U
Based on 1 Customer Validation
Kuwanon U is a potent cholinesterase inhibitor with IC50s of 19.69, 10.11 µM and Kis of 6.48, 9.59 µM for acetylcholinesterase (AChE) and butyrylcholinesterase (BChE), respectively. Kuwanon U has the potential for the research of Alzheimer’s disease (AD).
Para uso exclusivo en investigación. No vendemos a pacientes.
- Pureza : 97.30%
- No. CAS: 123702-95-4
- Fòrmula: C26H30O6
- Peso molecular:438.51
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Almacenamiento:
4°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
Actividad biológica
Descripciòn
IC50 & Target
[1]|
AChE 19.69 μM (IC50) |
AChE 6.48 μM (IC50) |
BChE 10.11 μM (Ki) |
BChE 9.59 μM (Ki) |
Cellular Effect
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Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| BJ | EC50 |
>10 μM
Compound: 14
|
Cytotoxicity against human BJ cells assessed as viable cells after 72 hrs by calcein AM assay
Cytotoxicity against human BJ cells assessed as viable cells after 72 hrs by calcein AM assay
|
[PMID: 20192247] |
| CCRF-CEM | EC50 |
>10 μM
Compound: 14
|
Cytotoxicity against human CEM cells assessed as viable cells after 72 hrs by calcein AM assay
Cytotoxicity against human CEM cells assessed as viable cells after 72 hrs by calcein AM assay
|
[PMID: 20192247] |
| HeLa | EC50 |
>10 μM
Compound: 14
|
Cytotoxicity against human HeLa cells assessed as viable cells after 72 hrs by calcein AM assay
Cytotoxicity against human HeLa cells assessed as viable cells after 72 hrs by calcein AM assay
|
[PMID: 20192247] |
| MCF7 | EC50 |
>10 μM
Compound: 14
|
Cytotoxicity against human MCF7 cells assessed as viable cells after 72 hrs by calcein AM assay
Cytotoxicity against human MCF7 cells assessed as viable cells after 72 hrs by calcein AM assay
|
[PMID: 20192247] |
| RPMI-8226 | EC50 |
>10 μM
Compound: 14
|
Cytotoxicity against human RPMI8226 cells assessed as viable cells after 72 hrs by calcein AM assay
Cytotoxicity against human RPMI8226 cells assessed as viable cells after 72 hrs by calcein AM assay
|
[PMID: 20192247] |
| SR | IC50 |
35.62 μM
Compound: Kuwanon U
|
Inhibition of SERCA1 in NewZealand rabbit skeletal muscle SR vesicles using ATP as substrate incubated for 2 mins followed by Ca2+ addition by NADH coupled enzyme assay
Inhibition of SERCA1 in NewZealand rabbit skeletal muscle SR vesicles using ATP as substrate incubated for 2 mins followed by Ca2+ addition by NADH coupled enzyme assay
|
[PMID: 32435418] |
| THP-1 | EC50 |
>10 μM
Compound: 14
|
Cytotoxicity against human THP1 cells after 72 hrs by erythosin B staining method
Cytotoxicity against human THP1 cells after 72 hrs by erythosin B staining method
|
[PMID: 20192247] |
| U-266 | EC50 |
>10 μM
Compound: 14
|
Cytotoxicity against human U266 cells assessed as viable cells after 72 hrs by calcein AM assay
Cytotoxicity against human U266 cells assessed as viable cells after 72 hrs by calcein AM assay
|
[PMID: 20192247] |
Chemical Information
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No. CAS 123702-95-4
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Appearance Solid
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Peso molecular 438.51
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Fòrmula C26H30O6
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Color Off-white to light yellow
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SMILES
O=C1C2=C(O)C=C(O)C=C2O[C@H](C3=CC(C/C=C(C)/CC/C=C(C)\C)=C(C=C3O)OC)C1
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Structure Classification
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Initial Source
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Envío
Room temperature in continental US; may vary elsewhere.
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Almacenamiento
4°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
Pureza y Documentación
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Ficha de datos (265 KB)
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SDS (252 KB)
- English - EN (252 KB)
- Français - FR (252 KB)
- Deutsch - DE (252 KB)
- Norwegian - NO (252 KB)
- Español - ES (252 KB)
- Swedish - SV (252 KB)
- Italian - IT (252 KB)
- Korean - KR (252 KB)
- Portuguese - PT (252 KB)
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Instrucciones de manejo (2659 KB)
Referencias
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)