(1R,4R,5R,8R,10S,13S,14R,17R,18R,19R)-4,5,9,9,13,20,20-heptamethyl-24-oxahexacyclo[17.3.2.01,18.04,17.05,14.08,13]tetracosan-10-ol
Internal ID | 5b7b1c33-7c36-452f-8c31-1ff3a43e64b1 |
Taxonomy | Lipids and lipid-like molecules > Prenol lipids > Triterpenoids |
IUPAC Name | (1R,4R,5R,8R,10S,13S,14R,17R,18R,19R)-4,5,9,9,13,20,20-heptamethyl-24-oxahexacyclo[17.3.2.01,18.04,17.05,14.08,13]tetracosan-10-ol |
SMILES (Canonical) | CC1(CCC23CCC4(C(C2C1OC3)CCC5C4(CCC6C5(CCC(C6(C)C)O)C)C)C)C |
SMILES (Isomeric) | C[C@@]12CC[C@@]34CCC([C@@H]([C@@H]3[C@H]1CC[C@H]5[C@]2(CC[C@@H]6[C@]5(CC[C@@H](C6(C)C)O)C)C)OC4)(C)C |
InChI | InChI=1S/C30H50O2/c1-25(2)14-16-30-17-15-28(6)19(23(30)24(25)32-18-30)8-9-21-27(5)12-11-22(31)26(3,4)20(27)10-13-29(21,28)7/h19-24,31H,8-18H2,1-7H3/t19-,20+,21-,22+,23+,24-,27-,28-,29-,30-/m1/s1 |
InChI Key | BZNIIOGSANMIET-CQLGYBRPSA-N |
Popularity | 0 references in papers |
Molecular Formula | C30H50O2 |
Molecular Weight | 442.70 g/mol |
Exact Mass | 442.381080833 g/mol |
Topological Polar Surface Area (TPSA) | 29.50 Ų |
XlogP | 8.10 |
There are no found synonyms. |
![2D Structure of (1R,4R,5R,8R,10S,13S,14R,17R,18R,19R)-4,5,9,9,13,20,20-heptamethyl-24-oxahexacyclo[17.3.2.01,18.04,17.05,14.08,13]tetracosan-10-ol 2D Structure of (1R,4R,5R,8R,10S,13S,14R,17R,18R,19R)-4,5,9,9,13,20,20-heptamethyl-24-oxahexacyclo[17.3.2.01,18.04,17.05,14.08,13]tetracosan-10-ol](https://plantaedb.com/storage/docs/compounds/2023/11/02392e50-8592-11ee-b009-bb2bc205a2c2.jpg)
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 |
---|---|---|---|---|
CHEMBL204 | P00734 | Thrombin | 93.03% | 96.01% |
CHEMBL241 | Q14432 | Phosphodiesterase 3A | 91.35% | 92.94% |
CHEMBL1994 | P08235 | Mineralocorticoid receptor | 89.10% | 100.00% |
CHEMBL3137262 | O60341 | LSD1/CoREST complex | 88.74% | 97.09% |
CHEMBL3251 | P19838 | Nuclear factor NF-kappa-B p105 subunit | 88.62% | 96.09% |
CHEMBL253 | P34972 | Cannabinoid CB2 receptor | 88.25% | 97.25% |
CHEMBL226 | P30542 | Adenosine A1 receptor | 88.00% | 95.93% |
CHEMBL1937 | Q92769 | Histone deacetylase 2 | 86.65% | 94.75% |
CHEMBL4026 | P40763 | Signal transducer and activator of transcription 3 | 85.05% | 82.69% |
CHEMBL4681 | P42330 | Aldo-keto-reductase family 1 member C3 | 84.73% | 89.05% |
CHEMBL4203 | Q9HAZ1 | Dual specificity protein kinase CLK4 | 84.12% | 94.45% |
CHEMBL4302 | P08183 | P-glycoprotein 1 | 84.10% | 92.98% |
CHEMBL1907601 | P11802 | Cyclin-dependent kinase 4/cyclin D1 | 84.08% | 98.99% |
CHEMBL221 | P23219 | Cyclooxygenase-1 | 83.99% | 90.17% |
CHEMBL4685 | P14902 | Indoleamine 2,3-dioxygenase | 83.57% | 96.38% |
CHEMBL4303 | P08238 | Heat shock protein HSP 90-beta | 82.30% | 96.77% |
CHEMBL218 | P21554 | Cannabinoid CB1 receptor | 81.85% | 96.61% |
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.
Diospyros montana |
PubChem | 163002677 |
LOTUS | LTS0204646 |
wikiData | Q104950595 |