Structure Info
- Chemspace ID
- CSSS09881015831 (In-Stock Screening Compounds)
- IUPAC Name
- (2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl (4aS,6aS,6bR,8aR,9R,10S,12aR,12bR,14bS)-10-{[(2S,3R,4S,5S)-3-{[(2S,3R,4R,5S,6S)-4-{[(2S,3R,4R,5R,6R)-5-{[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-{[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy}oxan-2-yl]oxy}-3-hydroxy-6-(hydroxymethyl)-4-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-3,5-dihydroxy-6-methyloxan-2-yl]oxy}-4,5-dihydroxyoxan-2-yl]oxy}-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylate
- Mol formula
- C76H124O40
- Mol weight
- 1678 Da
- Catalog Number(s)
- ArZ-UP483726, CFN95359, HY-N15220, TN7352, ZX-CY005502
- Copy structure to query editor
- SMILES
- INCHI
- INCHI key
- MOL
Properties
- LogP
- -6
- Heavy atoms count
- 116
- Rotatable bond count
- 22
- Number of rings
- 13
- Carbon bond saturation, Fsp3
- 0.96
- Polar surface area (Å)
- 630
- Hydrogen bond acceptors count
- 39
- Hydrogen bond donors count
- 23
- Zoom the structure
- CSSS09881015831
Items Overall 6 items from 2 suppliers
Supplier | Lead time | Ships from | Purity | Pack | Price, $ | Qty |
---|---|---|---|---|---|---|
ChemFaces | 12 days | China To: | 90 | 1 mg | 59 | |
Targetmol Chemicals Inc | 30 days | United States To: | 99 | 1 mg | 273 | |
Targetmol Chemicals Inc | 30 days | United States To: | 99 | 5 mg | 668 | |
Targetmol Chemicals Inc | 30 days | United States To: | 99 | 10 mg | 945 | |
Targetmol Chemicals Inc | 30 days | United States To: | 99 | 25 mg | 1,380 | |
Targetmol Chemicals Inc | 30 days | United States To: | 99 | 50 mg | 1,890 | |
Description: Dipsacus saponin X is a triterpenoid saponin derived from Dipsacus asper. It stimulates the proliferation of UMR106 cells and increases alkaline phosphatase(ALP) activity. Additionally, it exhibits anti-acetylcholinesterase(AChE) activity, suggesting potential neuroprotective effects.; CAS: 146100-01-8 |
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