(5R,6R,8R,9S,10R,13S,14R)-5,6,14-trihydroxy-10,13-dimethyl-6,7,8,9,11,12,15,16-octahydro-4H-cyclopenta[a]phenanthrene-1,17-dione
| Internal ID | fc21bf0e-fcd6-4f42-ae15-18ff22fedfb0 |
| Taxonomy | Lipids and lipid-like molecules > Steroids and steroid derivatives > Androstane steroids |
| IUPAC Name | (5R,6R,8R,9S,10R,13S,14R)-5,6,14-trihydroxy-10,13-dimethyl-6,7,8,9,11,12,15,16-octahydro-4H-cyclopenta[a]phenanthrene-1,17-dione |
| SMILES (Canonical) | CC12CCC3C(C1(CCC2=O)O)CC(C4(C3(C(=O)C=CC4)C)O)O |
| SMILES (Isomeric) | C[C@]12CC[C@H]3[C@H]([C@@]1(CCC2=O)O)C[C@H]([C@@]4([C@@]3(C(=O)C=CC4)C)O)O |
| InChI | InChI=1S/C19H26O5/c1-16-8-5-11-12(18(16,23)9-6-13(16)20)10-15(22)19(24)7-3-4-14(21)17(11,19)2/h3-4,11-12,15,22-24H,5-10H2,1-2H3/t11-,12+,15+,16+,17-,18+,19-/m0/s1 |
| InChI Key | GYJNAHSPSGNXIF-LSOYPGBFSA-N |
| Popularity | 0 references in papers |
| Molecular Formula | C19H26O5 |
| Molecular Weight | 334.40 g/mol |
| Exact Mass | 334.17802393 g/mol |
| Topological Polar Surface Area (TPSA) | 94.80 Ų |
| XlogP | 0.20 |
| There are no found synonyms. |
![2D Structure of (5R,6R,8R,9S,10R,13S,14R)-5,6,14-trihydroxy-10,13-dimethyl-6,7,8,9,11,12,15,16-octahydro-4H-cyclopenta[a]phenanthrene-1,17-dione](https://plantaedb.com/storage/docs/compounds/2023/11/c9a71be0-8577-11ee-8c39-432c0fb6af68.jpg "2D Structure of (5R,6R,8R,9S,10R,13S,14R)-5,6,14-trihydroxy-10,13-dimethyl-6,7,8,9,11,12,15,16-octahydro-4H-cyclopenta[a]phenanthrene-1,17-dione")
| Target | Value | Probability (raw) | Probability (%) |
|---|---|---|---|
| No predicted properties yet! | |||
Proven Targets:
| CHEMBL ID | UniProt ID | Name | Min activity | Assay type | Source |
|---|---|---|---|---|---|
| No proven targets yet! | |||||
Predicted Targets (via Super-PRED):
| CHEMBL ID | UniProt ID | Name | Probability | Model accuracy |
|---|---|---|---|---|
| CHEMBL253 | P34972 | Cannabinoid CB2 receptor | 96.90% | 97.25% |
| CHEMBL1994 | P08235 | Mineralocorticoid receptor | 93.92% | 100.00% |
| CHEMBL5619 | P27695 | DNA-(apurinic or apyrimidinic site) lyase | 93.39% | 91.11% |
| CHEMBL4261 | Q16665 | Hypoxia-inducible factor 1 alpha | 91.44% | 85.14% |
| CHEMBL3251 | P19838 | Nuclear factor NF-kappa-B p105 subunit | 90.18% | 96.09% |
| CHEMBL3108638 | O15164 | Transcription intermediary factor 1-alpha | 89.22% | 95.56% |
| CHEMBL3137262 | O60341 | LSD1/CoREST complex | 88.23% | 97.09% |
| CHEMBL1871 | P10275 | Androgen Receptor | 87.81% | 96.43% |
| CHEMBL226 | P30542 | Adenosine A1 receptor | 86.87% | 95.93% |
| CHEMBL4040 | P28482 | MAP kinase ERK2 | 86.43% | 83.82% |
| CHEMBL1937 | Q92769 | Histone deacetylase 2 | 85.62% | 94.75% |
| CHEMBL3038477 | P67870 | Casein kinase II alpha/beta | 84.93% | 99.23% |
| CHEMBL2581 | P07339 | Cathepsin D | 84.88% | 98.95% |
| CHEMBL3351 | Q13085 | Acetyl-CoA carboxylase 1 | 82.39% | 93.04% |
Below are displayed all the plants proven (via scientific papers) to contain this
compound!
To see more specific details click the taxa you are interested in.
To see more specific details click the taxa you are interested in.
| Physalis cinerascens |
| PubChem | 163082758 |
| LOTUS | LTS0162826 |
| wikiData | Q105023840 |