![Chemical structure of (2R,3R,4S,5R,6R)-2-[[(1R,4R,5R,8S,16S,19S,22R)-5,19-dimethyl-15,18,20-trioxahexacyclo[14.5.1.01,14.04,13.05,10.019,22]docosa-10,13-dien-8-yl]oxy]-4-methoxy-6-methyloxane-3,5-diol](/structures/PHY-NP-11354.webp)
Cynatratoside A
白薇苷A
PHY-NP-11369 · Natural product research catalog
| Catalog number | PHY-NP-11369 |
|---|---|
| CAS number | 97399-96-7 |
| Molecular formula | C28H40O8 |
| Molecular weight | 504.62 g/mol |
| Chemical class | Steroids |
| Main reported source | Agave cocui |
| Purity / assay | Min. 98% Other purity specifications available on inquiry. |
Chemical structure

Select a pack size
| Pack | Price (USD) | Availability | Lead time |
|---|---|---|---|
| 5 mg | Request quote | To be confirmed | Confirm in quotation |
| 10 mg | Request quote | To be confirmed | Confirm in quotation |
| 20 mg | Request quote | To be confirmed | Confirm in quotation |
| 50 mg | Request quote | To be confirmed | Confirm in quotation |
| 100 mg | Request quote | To be confirmed | Confirm in quotation |
Final specifications and availability are confirmed in your quotation. No purchase or reservation is made here.
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Product information
Cynatratoside A is listed in the Steroids section of the Phytide Bio research catalog. Standard pack sizes are 5, 10, 20, 50 and 100 mg.
For research use only. Not for human or veterinary use, diagnosis or treatment.
Names & identifiers
| IUPAC name | 8-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1(21),10-dien-14-one |
|---|---|
| SMILES | CC1C(C(CC(O1)OC2CCC3(C4CCC5=COC6(C5C(CO6)OC(=O)C4CC=C3C2)C)C)OC)O |
| InChIKey | QANVGLGBLJFUIP-UHFFFAOYSA-N |
| Subclass / scaffold | Pregnane steroids;皂苷/苷 |
| PubChem CID | 175701 |
Computed properties
| Exact mass (Da) | 504.2723 | Predicted LogP | 3.6174 |
|---|---|---|---|
| Predicted TPSA (Ų) | 92.68 | H-bond donors | 1 |
| H-bond acceptors | 8 | Rotatable bonds | 3 |
Calculated values from the supplied dataset; not measured batch specifications.
View additional properties & classification
| Ring count | 6 |
|---|---|
| Aromatic rings | 0 |
| Fraction Csp³ | 0.821 |
| Synthetic accessibility score | 5.77 |
| QED score | 0.46 |
| Lipinski rule violations | 1 |
| NPClassifier pathway | Terpenoids |
| NPClassifier superclass | Steroids |
| NPClassifier class | Pregnane steroids |
| Parent SMILES | COC1CC(OC2CCC3(C)C(=CCC4C(=O)OC5COC6(C)OC=C(CCC43)C56)C2)OC(C)C1O |
| Parent formula | C28H40O8 |
| Parent molecular weight | 504.62 |
| Specified stereocenters | 0 |
| Unspecified stereocenters | 11 |
Reported natural occurrence
| Main reported source | Agave cocui |
|---|
Reported natural occurrence does not establish the manufacturing origin of the supplied material.
View occurrence records & references
| LOTUS species records | 0 |
|---|---|
| LOTUS reference records | 0 |
| COCONUT occurrence records | Agave cocui; Alcyonium coralloides; Campanula hypopolia; Chasmanthera dependens; Corydalis pallida; Crepis czerepanovii; Cylindropuntia leptocaulis; Dendrobates auratus; Eupatoriastrum nelsonii; Huperzia selago; Hydroclathrus tenuis; Hymenoxys grandiflora; Kielmeyera rubriflora; Larix lyallii; Lethariella sinensis; Maackia floribunda; Meliosma wightii; Oroxylum indicum; Othonna tagetes; Pellina semitubulosa; Penicillium expansum; Phakellia flabellata; Philadelphus coronarius; Phragmatobia fuliginosa; Phyllosticta cirsii; Polygala fruticosa; Pteris pedata; Pterocarpus macrocarpus; Russula lepida; Scandix pecten-veneris |
| COCONUT organism records | 42 |
| COCONUT identifier | CNP0221402.1 |
Records are inherited from the supplied dataset and are not independently verified. Taxonomic names may include synonyms.
Documents & specifications
| Certificate of analysis (COA) | Batch-specific COA available on request; no PDF published yet |
|---|---|
| Safety data sheet (SDS) | Not yet published |
| Storage / solubility | Product-specific conditions to be confirmed |
| Shipping | Confirmed with the quotation |
Request applicable documentation and handling information before ordering or use.
![Chemical structure of (2R,3S,4R,6R)-6-[[(1R,4R,5R,8S,16S,19S,22R)-5,19-dimethyl-15,18,20-trioxahexacyclo[14.5.1.01,14.04,13.05,10.019,22]docosa-10,13-dien-8-yl]oxy]-2-methyloxane-3,4-diol](/structures/PHY-NP-11355.webp)
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![Chemical structure of [(3S,8S,9R,10R,12R,13S,14R,17S)-17-acetyl-8,14,17-trihydroxy-3-[(2R,4S,5R,6R)-5-[(2S,4S,5R,6R)-5-[(2S,4R,5R,6R)-5-[(2S,4R,5S,6S)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-1,2,3,4,7,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-12-yl] 4-hydroxybenzoate](/structures/PHY-NP-11411.webp)
![Chemical structure of [(3S,8S,9R,10R,12R,13S,14R,17S)-17-acetyl-8,14,17-trihydroxy-3-[(2R,4S,5S,6R)-4-hydroxy-5-[(2S,4S,5R,6R)-5-[(2S,4R,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-1,2,3,4,7,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-12-yl] 4-hydroxybenzoate](/structures/PHY-NP-11412.webp)