2-Desoxy-4-epi-pulchellin
Based on 1 Customer Validation
2-Desoxy-4-epi-pulchellin (compound 13) is a compound isolated from dichloromethane-soluble portion of Polygonum hydropiper.
For research use only. We do not sell to patients.
- Purity: 99.97%
- CAS No.: 122872-03-1
- Formula: C15H22O3
- Molecular Weight:250.33
-
Storage:
4°C, sealed storage, away from moisture and light
* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)
Biological Activity
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| A549 | IC50 |
6.2 μM
Compound: 4
|
Cytotoxicity against human A549 cells after 72 hrs by CCK8 assay
Cytotoxicity against human A549 cells after 72 hrs by CCK8 assay
|
[PMID: 26316467] |
| DU-145 | IC50 |
3.1 μM
Compound: 4
|
Cytotoxicity against human DU145 cells after 72 hrs by CCK8 assay
Cytotoxicity against human DU145 cells after 72 hrs by CCK8 assay
|
[PMID: 26316467] |
| HCT-116 | IC50 |
4.43 μM
Compound: 1; PCL
|
Cytotoxicity against human HCT116 cells assessed as reduction in cell viability after 72 hrs by MTT assay
Cytotoxicity against human HCT116 cells assessed as reduction in cell viability after 72 hrs by MTT assay
|
[PMID: 30711391] |
| HeLa | IC50 |
6 μM
Compound: 4
|
Cytotoxicity against human HeLa cells after 72 hrs by CCK8 assay
Cytotoxicity against human HeLa cells after 72 hrs by CCK8 assay
|
[PMID: 26316467] |
| HL-60 | IC50 |
2.4 μM
Compound: 4
|
Cytotoxicity against human HL60 cells after 72 hrs by CCK8 assay
Cytotoxicity against human HL60 cells after 72 hrs by CCK8 assay
|
[PMID: 26316467] |
| HT-29 | IC50 |
3.37 μM
Compound: 1; PCL
|
Cytotoxicity against human HT-29 cells assessed as reduction in cell viability after 72 hrs by MTT assay
Cytotoxicity against human HT-29 cells assessed as reduction in cell viability after 72 hrs by MTT assay
|
[PMID: 30711391] |
| K562 | IC50 |
17 μM
Compound: 4
|
Cytotoxicity against human K562 cells after 72 hrs by CCK8 assay
Cytotoxicity against human K562 cells after 72 hrs by CCK8 assay
|
[PMID: 26316467] |
| MCF7 | IC50 |
11 μM
Compound: 4
|
Cytotoxicity against human MCF7 cells after 72 hrs by CCK8 assay
Cytotoxicity against human MCF7 cells after 72 hrs by CCK8 assay
|
[PMID: 26316467] |
| MCF7 | IC50 |
9.8 μg/mL
Compound: 9, pseudoguaianolide
|
Antiproliferative activity against human MCF7 cells after 48 hrs by MTT assay
Antiproliferative activity against human MCF7 cells after 48 hrs by MTT assay
|
[PMID: 21109433] |
| MDCK | IC50 |
29.3 μM
Compound: 4
|
Antiviral activity against Influenza A virus H1N1 infected in MDCK cells assessed as protection against virus-induced cytopathic effect after 48 hrs by crystal violet staining
Antiviral activity against Influenza A virus H1N1 infected in MDCK cells assessed as protection against virus-induced cytopathic effect after 48 hrs by crystal violet staining
|
[PMID: 26316467] |
| MDCK | IC50 |
47.3 μM
Compound: 4
|
Antiviral activity against Influenza A virus H3N2 infected in MDCK cells assessed as protection against virus-induced cytopathic effect after 48 hrs by crystal violet staining
Antiviral activity against Influenza A virus H3N2 infected in MDCK cells assessed as protection against virus-induced cytopathic effect after 48 hrs by crystal violet staining
|
[PMID: 26316467] |
| MOLT-4 | IC50 |
5.5 μM
Compound: 4
|
Cytotoxicity against human MOLT4 cells after 72 hrs by CCK8 assay
Cytotoxicity against human MOLT4 cells after 72 hrs by CCK8 assay
|
[PMID: 26316467] |
| NCI-H1975 | IC50 |
13 μM
Compound: 4
|
Cytotoxicity against human NCI-H1975 cells after 72 hrs by CCK8 assay
Cytotoxicity against human NCI-H1975 cells after 72 hrs by CCK8 assay
|
[PMID: 26316467] |
| Neutrophil | IC50 |
>10 μg/mL
Compound: 5
|
Inhibition of FMLP/CB-induced elastase release in human neutrophils after 5 mins by spectrophotometry
Inhibition of FMLP/CB-induced elastase release in human neutrophils after 5 mins by spectrophotometry
|
[PMID: 24997688] |
| Neutrophil | IC50 |
>10 μg/mL
Compound: 5
|
Inhibition of FMLP/CB-induced superoxide anion generation in human neutrophils by ferricytochrome c reduction method
Inhibition of FMLP/CB-induced superoxide anion generation in human neutrophils by ferricytochrome c reduction method
|
[PMID: 24997688] |
| RAW264.7 | IC50 |
0.1 μM
Compound: 14
|
Inhibition of LPS-induced NO production in mouse RAW264.7 cells measured after 24 hrs
Inhibition of LPS-induced NO production in mouse RAW264.7 cells measured after 24 hrs
|
[PMID: 20515062] |
| RAW264.7 | IC50 |
14.9 μM
Compound: 5
|
Inhibition of NO production in LPS/IFN-gamma activated mouse RAW264.7 cells after 24 hrs by Griess assay
Inhibition of NO production in LPS/IFN-gamma activated mouse RAW264.7 cells after 24 hrs by Griess assay
|
[PMID: 24997688] |
| RAW264.7 | IC50 |
2.5 μM
Compound: 15
|
Inhibition of LPS-induced NO production in mouse RAW264.7 cells incubated for 24 hrs by Griess reagent based assay
Inhibition of LPS-induced NO production in mouse RAW264.7 cells incubated for 24 hrs by Griess reagent based assay
|
[PMID: 27276091] |
| RAW264.7 | IC50 |
9.89 μM
Compound: 19
|
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced NO production pretreated for 30 mins before LPS challenge measured 24 hrs after LPS challenge by Griess reaction method
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced NO production pretreated for 30 mins before LPS challenge measured 24 hrs after LPS challenge by Griess reaction method
|
[PMID: 21924800] |
| SGC-7901 | IC50 |
22 μM
Compound: 4
|
Cytotoxicity against human SGC7901 cells after 72 hrs by CCK8 assay
Cytotoxicity against human SGC7901 cells after 72 hrs by CCK8 assay
|
[PMID: 26316467] |
| U-937 | IC50 |
2.2 μM
Compound: 4
|
Cytotoxicity against human U937 cells after 72 hrs by CCK8 assay
Cytotoxicity against human U937 cells after 72 hrs by CCK8 assay
|
[PMID: 26316467] |
Chemical Information
-
CAS No. 122872-03-1
-
Appearance Solid
-
Molecular Weight 250.33
-
Formula C15H22O3
-
Color White to off-white
-
SMILES
O=C(O[C@]1([H])[C@]2([H])C[C@]3(C)[C@@H](O)CC[C@@]3([H])[C@H](C)C1)C2=C
-
Structure Classification
-
Initial Source
-
Shipping
Room temperature in continental US; may vary elsewhere.
-
Storage
4°C, sealed storage, away from moisture and light
* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)
Solvent & Solubility
DMSO : 25 mg/mL (99.87 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Purity & Documentation
-
Data Sheet (274 KB)
-
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)
-
Handling Instructions (2659 KB)
References
Complete Stock Solution Preparation Table
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
|---|---|---|---|---|---|
| DMSO | 1 mM | 3.9947 mL | 19.9736 mL | 39.9473 mL | 99.8682 mL |
| 5 mM | 0.7989 mL | 3.9947 mL | 7.9895 mL | 19.9736 mL | |
| 10 mM | 0.3995 mL | 1.9974 mL | 3.9947 mL | 9.9868 mL | |
| 15 mM | 0.2663 mL | 1.3316 mL | 2.6632 mL | 6.6579 mL | |
| 20 mM | 0.1997 mL | 0.9987 mL | 1.9974 mL | 4.9934 mL | |
| 25 mM | 0.1598 mL | 0.7989 mL | 1.5979 mL | 3.9947 mL | |
| 30 mM | 0.1332 mL | 0.6658 mL | 1.3316 mL | 3.3289 mL | |
| 40 mM | 0.0999 mL | 0.4993 mL | 0.9987 mL | 2.4967 mL | |
| 50 mM | 0.0799 mL | 0.3995 mL | 0.7989 mL | 1.9974 mL | |
| 60 mM | 0.0666 mL | 0.3329 mL | 0.6658 mL | 1.6645 mL | |
| 80 mM | 0.0499 mL | 0.2497 mL | 0.4993 mL | 1.2484 mL |