Sennidin B
Based on 1 Customer Validation
Sennidin B is an anthraquinone compound isolated from Cassia angustifolia. Sennidin B is a DPP-4 inhibitor with an IC50 of 39.39 μM. Sennidin B is an insect chitinase inhibitor with a Ki of 80 nM against OfChi-h. Sennidin B competitively inhibits chitinase activity by forming π-π stacking interactions with key tryptophan residues in the active site through a folded conformation. Sennidin B activates PI3K/Akt to promote glucose uptake in adipocytes. Sennidin B can be used for the development of biopesticides and research on type 2 diabetes and metabolism-related signaling pathways.
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- Pureté : 99.25%
- CAS No.: 517-44-2
- Formule: C30H18O10
- Masse moléculaire:538.46
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Stockage:
4°C, protect from light
* The compound is unstable in solutions, freshly prepared is recommended.
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
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Activité biologique
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Chemical Information
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Solvant et solubilité
- Protocole
- Pureté et documentation
- Références
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Help & FAQs
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Sennidin B (Standard)Reference Standard
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Activité biologique
Description
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DPP-4 39.39 μM (IC50) |
OfChi-h 80 nM (Ki) |
In Vitro
Sennidin B (300 μM; 30 min) stimulates glucose incorporation in rat adipocytes, although its potency is lower than that of Sennidin A[1].
Sennidin B is a potent competitive multi-target inhibitor of Ostrinia furnacalis chitinolytic enzymes (OfChtI, OfChtII, OfChi-h, and OfHex1), with the strongest inhibitory potency against OfChi-h (Ki = 80 nM)[4].
Sennidin B inhibits DPP-4 enzyme activity in a concentration-dependent manner in cell-free in vitro assays, with an IC50 of 39.39 μM[2].
Sennidin B (1000 nM; 2 h) binds to DPP-4 and enhances its thermal stability in Caco-2 cells[2].
Sennidin B (0.1-1000 nM; 4 days) downregulates DPP-4 mRNA expression in Caco-2 cells, but has no effect at high concentrations, and inhibits DPP-4 protein expression in a concentration-dependent manner[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:Caco-2
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Concentration:0.1, 1, 10, 100, 1000 nM
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Incubation Time:4 days
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Result:Significantly decreased DPP-4 mRNA expression only at 1 nM compared with the control group, whereas no consistent dose-dependent decrease was observed at higher concentrations.
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Cell Line:Caco-2
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Concentration:0.1, 1, 10, 100, 1000 nM
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Incubation Time:4 days
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Result:Showed an overall decreasing trend in DPP-4 protein expression with increasing concentrations.
In Vivo
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Ostrinia furnacalis (day-1 fifth-instar larvae)[4]
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Dosage:1 mM, 5 mM
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Administration:p.o.; ad libitum; 2, 4, 6, 8, 10 days
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Result:Achieved 50% mortality at 1 mM.
Achieved 100% mortality at 5 mM.
Suppressed larval growth at 1 mM, with surviving larvae developing to the fourth instar but weight remaining stagnant, comparable to that of the third instar.
Chemical Information
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CAS No. 517-44-2
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Appearance Solid
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Masse moléculaire 538.46
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Formule C30H18O10
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Color Yellow to brown
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SMILES
O=C1C2=C(O)C=C(C(O)=O)C=C2[C@@]([C@]3([H])C4=CC(C(O)=O)=CC(O)=C4C(C5=C(O)C=CC=C35)=O)([H])C6=CC=CC(O)=C16
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Structure Classification
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Initial Source
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Livraison
Room temperature in continental US; may vary elsewhere.
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Stockage
4°C, protect from light
* The compound is unstable in solutions, freshly prepared is recommended.
Solvant et solubilité
In Vitro:
DMSO : 50 mg/mL (92.86 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. The compound is unstable in solutions, freshly prepared is recommended.
Please refer to the solubility information to select the appropriate solvent. The compound is unstable in solutions, freshly prepared is recommended.
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Pureté et documentation
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Fiche technique (299 KB)
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SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 KB)
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Instruction de manipulation (2659 KB)
Références
Complete Stock Solution Preparation Table
Please refer to the solubility information to select the appropriate solvent. The compound is unstable in solutions, freshly prepared is recommended.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
|---|---|---|---|---|---|
| DMSO | 1 mM | 1.8571 mL | 9.2857 mL | 18.5715 mL | 46.4287 mL |
| 5 mM | 0.3714 mL | 1.8571 mL | 3.7143 mL | 9.2857 mL | |
| 10 mM | 0.1857 mL | 0.9286 mL | 1.8571 mL | 4.6429 mL | |
| 15 mM | 0.1238 mL | 0.6190 mL | 1.2381 mL | 3.0952 mL | |
| 20 mM | 0.0929 mL | 0.4643 mL | 0.9286 mL | 2.3214 mL | |
| 25 mM | 0.0743 mL | 0.3714 mL | 0.7429 mL | 1.8571 mL | |
| 30 mM | 0.0619 mL | 0.3095 mL | 0.6190 mL | 1.5476 mL | |
| 40 mM | 0.0464 mL | 0.2321 mL | 0.4643 mL | 1.1607 mL | |
| 50 mM | 0.0371 mL | 0.1857 mL | 0.3714 mL | 0.9286 mL | |
| 60 mM | 0.0310 mL | 0.1548 mL | 0.3095 mL | 0.7738 mL | |
| 80 mM | 0.0232 mL | 0.1161 mL | 0.2321 mL | 0.5804 mL |
Sennidin B Related Classifications
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