Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C57H92O28 |
| Molecular Weight | 1225.3236 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 31 / 31 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@@H](O)CO[C@H]2OC(=O)[C@]34CCC(C)(C)C[C@H]3C5=CC[C@@H]6[C@@]7(C)C[C@H](O)[C@H](O[C@@H]8O[C@H](CO)[C@@H](O)[C@H](O)[C@H]8O)C(CO)(CO)[C@@H]7CC[C@@]6(C)[C@]5(C)C[C@H]4O)[C@H](O)[C@H](O)[C@H]1O[C@@H]9OC[C@@H](O)[C@H](O[C@@H]%10OC[C@](O)(CO)[C@H]%10O)[C@H]9O
InChI
InChIKey=CYBWUNOAQPMRBA-NDTOZIJESA-N
InChI=1S/C57H92O28/c1-23-40(81-45-39(72)41(28(64)18-76-45)82-49-43(73)56(75,21-61)22-78-49)36(69)38(71)46(79-23)83-42-33(66)27(63)17-77-48(42)85-50(74)57-12-11-51(2,3)13-25(57)24-7-8-30-52(4)14-26(62)44(84-47-37(70)35(68)34(67)29(16-58)80-47)55(19-59,20-60)31(52)9-10-53(30,5)54(24,6)15-32(57)65/h7,23,25-49,58-73,75H,8-22H2,1-6H3/t23-,25-,26-,27-,28+,29+,30+,31+,32+,33-,34+,35-,36-,37+,38+,39+,40-,41-,42+,43-,44-,45-,46-,47-,48-,49-,52+,53+,54+,56+,57+/m0/s1
| Molecular Formula | C57H92O28 |
| Molecular Weight | 1225.3236 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 31 / 31 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/26648178Curator's Comment: The description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/21975926 | https://www.ncbi.nlm.nih.gov/pubmed/20939516
Sources: https://www.ncbi.nlm.nih.gov/pubmed/26648178
Curator's Comment: The description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/21975926 | https://www.ncbi.nlm.nih.gov/pubmed/20939516
Platycodin D, a triterpenoid saponin, is one the major active components of the roots of Platycodon grandiflorum and possesses multiple biological and pharmacological properties including, anti-nociceptive, anti-atherosclerosis, antiviral, anti-inflammatory, anti-obesity, immunoregulatory, hepatoprotective and anti-tumor activities.
Platycodin D has been shown to exert anti-tumor activity in various cancer cells without affecting normal cells in various in vitro and in vivo models. Platycodin D has been extensively investigated and found to exhibit significant anti-cancer activity against a wide range of human cancers types both in vitro and in vivo through multiple mechanisms which are considered to be crucial and central to cancer development and metastasis. Apart from in vitro anti-cancer activity of Platycodin D, various tumor models and drug administration routes have been tested for Platycodin D in vivo. Both intraperitoneal, as well as oral administration of Platycodin D, has been shown to exhibit significant anti-tumor activity. Intraperitoneal administration of Platycodin D at a dose of 5 mg/kg bodyweight significantly reduced the volume and size of MDA-MB-231 xenograft tumor.
Originator
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: map04370 Sources: https://www.ncbi.nlm.nih.gov/pubmed/25250884 |
|||
Target ID: WP1018 Sources: https://www.ncbi.nlm.nih.gov/pubmed/26648178 |
|||
Target ID: map04064 Sources: https://www.ncbi.nlm.nih.gov/pubmed/26648178 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | Unknown Approved UseUnknown |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Platycodin D inhibits migration, invasion, and growth of MDA-MB-231 human breast cancer cells via suppression of EGFR-mediated Akt and MAPK pathways. | 2013-10-05 |
|
| Saponins, especially platycodin D, from Platycodon grandiflorum modulate hepatic lipogenesis in high-fat diet-fed rats and high glucose-exposed HepG2 cells. | 2013-03-01 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/21975926
five healthy volunteers were orally treated with platycodi radix extract standardized to 414 mg of platycodin D
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/20939516
The cytotoxicity of the compounds against cultured human tumor cell lines was evaluated by the sulforhodamine B (SRB) method. Each tumor cell line (MES-SA, MES-SA/DX5, HCT, HCT15/CL02) was inoculated over standard 96-well flat-bottom microplates and then incubated for 24 h at 37 C in a humidified atmosphere of 5% CO2. The attached cells were then incubated with the serially diluted saponin samples. After continuous exposure to the compounds for 48 h, the culture medium was removed from each well and the cells were fixed with 10% cold trichloroacetic acid at 4 C for 1 h. After washing with tap water, the cells were stained with 0.4% SRB dye and incubated for 30 min at room temperature. The cells were washed again and then solubilized with 10 mM unbuffered Tris base solution (pH 10.5). The absorbance was measured spectrophotometrically at 520 nm with a microtiter plate reader.
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 20:51:46 GMT 2025
by
admin
on
Mon Mar 31 20:51:46 GMT 2025
|
| Record UNII |
CWJ06TA2GI
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
58479-68-8
Created by
admin on Mon Mar 31 20:51:46 GMT 2025 , Edited by admin on Mon Mar 31 20:51:46 GMT 2025
|
PRIMARY | |||
|
Platycodin D
Created by
admin on Mon Mar 31 20:51:46 GMT 2025 , Edited by admin on Mon Mar 31 20:51:46 GMT 2025
|
PRIMARY | |||
|
C108953
Created by
admin on Mon Mar 31 20:51:46 GMT 2025 , Edited by admin on Mon Mar 31 20:51:46 GMT 2025
|
PRIMARY | |||
|
DTXSID901021773
Created by
admin on Mon Mar 31 20:51:46 GMT 2025 , Edited by admin on Mon Mar 31 20:51:46 GMT 2025
|
PRIMARY | |||
|
CWJ06TA2GI
Created by
admin on Mon Mar 31 20:51:46 GMT 2025 , Edited by admin on Mon Mar 31 20:51:46 GMT 2025
|
PRIMARY | |||
|
162859
Created by
admin on Mon Mar 31 20:51:46 GMT 2025 , Edited by admin on Mon Mar 31 20:51:46 GMT 2025
|
PRIMARY |