Procumbenoside A
Procumbenoside A is a lignan glycoside discovered in Justicia procumbens. Procumbenoside A inhibits HIV-1 replication with an IC50 of 4.95 μM. Procumbenoside A exerts cytotoxic effects on various cancer cells. Procumbenoside A induces Cu (II)-mediated strand breaks in supercoiled plasmid DNA, generating the relaxed circular DNA form, while no linear form is detected. Procumbenoside A is used in studies related to liver cancer, colon adenocarcinoma, and HIV-1 infection.
For research use only. We do not sell to patients.
- CAS No.: 408358-51-0
- Formula: C31H32O15
- Molecular Weight:644.58
-
Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Description
IC50 & Target
[1]|
HIV-1 4.95 μM (IC50) |
Cellular Effect
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| NIH3T3 | ED50 |
3.1 μg/mL
|
Cytotoxic activity against 212 cells measured by MTT assay after 6 days of incubation.
Cytotoxic activity against 212 cells measured by MTT assay after 6 days of incubation.
|
11908984 |
| Hep 3B2 | ED50 |
3.1 μg/mL
|
Cytotoxic activity against human Hep 3B cells measured by MTT assay after 6 days of incubation.
Cytotoxic activity against human Hep 3B cells measured by MTT assay after 6 days of incubation.
|
11908984 |
| HepG2 | ED50 |
3.9 μg/mL
|
Cytotoxic activity against human Hep G2 cells measured by MTT assay after 6 days of incubation.
Cytotoxic activity against human Hep G2 cells measured by MTT assay after 6 days of incubation.
|
11908984 |
| HT-29 | ED50 |
6.7 μg/mL
|
Cytotoxic activity against human HT-29 cells measured by MTT assay after 6 days of incubation.
Cytotoxic activity against human HT-29 cells measured by MTT assay after 6 days of incubation.
|
11908984 |
| A549 | CC50 |
> 31.0 μM
|
Cytotoxicity against human A549 lung epithelial cells assessed by MTS assay at 48 h after initial compound addition following 24 h incubation with procumbenoside A, with the CC50 value greater than 31.0 μM.
Cytotoxicity against human A549 lung epithelial cells assessed by MTS assay at 48 h after initial compound addition following 24 h incubation with procumbenoside A, with the CC50 value greater than 31.0 μM.
|
31882050 |
In Vitro
Procumbenoside A (6 days) exerts significant cytotoxic effects on 212, Hep 3B, Hep G2, and HT-29 cells, with ED50 values of 3.1, 3.1, 3.9, and 6.7 µg/mL, respectively[1].
Procumbenoside A (0.3125-10 μM; 24-48 h) inhibits the replication of HIV-1 pseudovirus in A549 human lung epithelial cells, with an IC50 of 4.95 μM. It exhibits low cytotoxicity (CC50 > 31.0 μM) and a selectivity index greater than 6.2[2].
Procumbenoside A significantly induces Cu (II)-mediated concentration-dependent strand breaks in supercoiled pBR322 plasmid DNA, resulting in the formation of relaxed open-circle DNA[3].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
-
Cell Line:A549 human lung epithelial cells
-
Concentration:0.3125, 0.625, 1.25, 2.5, 5 and 10 μM
-
Incubation Time:24 h
-
Result:Exhibited low cytotoxicity (CC50 > 31.0 μM).
Chemical Information
-
CAS No. 408358-51-0
-
Molecular Weight 644.58
-
Formula C31H32O15
-
SMILES
O=C1C2=C(C=3C(C(O[C@H]4[C@H](O[C@H]5[C@H](O)[C@@H](O)[C@@H](O)CO5)[C@](CO)(O)CO4)=C2CO1)=CC(OC)=C(OC)C3)C=6C=C7C(=CC6)OCO7
-
Structure Classification
-
Shipping
Room temperature in continental US; may vary elsewhere.
-
Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
[1]. Day SH, et al. Potent cytotoxic lignans from Justicia procumbens and their effects on nitric oxide and tumor necrosis factor-alpha production in mouse macrophages. Journal of natural products. 2002 Mar;65(3):379-81. [Content Brief]
[2]. Xu XY, et al. Anti-HIV lignans from Justicia procumbens. Chinese journal of natural medicines. 2019 Dec;17(12):945-952. [Content Brief]
[3]. Lu YH, et al. DNA strand-scission by phloroglucinols and lignans from heartwood of Garcinia subelliptica Merr. and Justicia plants. Phytochemistry. 2008 Jan;69(1):225-33. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)