Thurberogenone

Details

Top
Internal ID f4af38aa-bf17-4b58-a3d6-fcf16e0b1bbc
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name 4,5,9,9,13-pentamethyl-19-prop-1-en-2-yl-21-oxahexacyclo[18.2.1.01,18.04,17.05,14.08,13]tricosane-10,22-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H44O3/c1-17(2)23-19-16-30(25(32)33-19)15-14-28(6)18(24(23)30)8-9-21-27(5)12-11-22(31)26(3,4)20(27)10-13-29(21,28)7/h18-21,23-24H,1,8-16H2,2-7H3
InChI Key FBKSKAJRUZAKSW-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C30H44O3
Molecular Weight 452.70 g/mol
Exact Mass 452.32904526 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 7.50
Atomic LogP (AlogP) 6.75
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
FBKSKAJRUZAKSW-UHFFFAOYSA-N
Lup-20(30)-en-28-oic acid, 19.beta.-hydroxy-3-oxo-, .gamma.-lactone

2D Structure

Top
2D Structure of Thurberogenone

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9931 99.31%
Caco-2 - 0.5691 56.91%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7557 75.57%
OATP2B1 inhibitior - 0.7221 72.21%
OATP1B1 inhibitior + 0.8714 87.14%
OATP1B3 inhibitior - 0.2236 22.36%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior + 0.6250 62.50%
BSEP inhibitior + 0.6716 67.16%
P-glycoprotein inhibitior - 0.5105 51.05%
P-glycoprotein substrate - 0.7116 71.16%
CYP3A4 substrate + 0.6802 68.02%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8424 84.24%
CYP3A4 inhibition - 0.5825 58.25%
CYP2C9 inhibition - 0.8991 89.91%
CYP2C19 inhibition - 0.5979 59.79%
CYP2D6 inhibition - 0.9374 93.74%
CYP1A2 inhibition - 0.6010 60.10%
CYP2C8 inhibition + 0.4450 44.50%
CYP inhibitory promiscuity - 0.8745 87.45%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6222 62.22%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.8828 88.28%
Skin irritation + 0.5085 50.85%
Skin corrosion - 0.8639 86.39%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3883 38.83%
Micronuclear - 0.7800 78.00%
Hepatotoxicity - 0.5893 58.93%
skin sensitisation - 0.5394 53.94%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity + 0.6413 64.13%
Acute Oral Toxicity (c) III 0.7173 71.73%
Estrogen receptor binding + 0.8202 82.02%
Androgen receptor binding + 0.7446 74.46%
Thyroid receptor binding + 0.6533 65.33%
Glucocorticoid receptor binding + 0.8221 82.21%
Aromatase binding + 0.7246 72.46%
PPAR gamma + 0.7024 70.24%
Honey bee toxicity - 0.7141 71.41%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.9970 99.70%

Targets

Top

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
CHEMBL241 Q14432 Phosphodiesterase 3A 90.97% 92.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.95% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.77% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.09% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.74% 91.11%
CHEMBL259 P32245 Melanocortin receptor 4 84.78% 95.38%
CHEMBL1937 Q92769 Histone deacetylase 2 84.54% 94.75%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.23% 93.04%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.88% 99.23%
CHEMBL5408 Q9UHD2 Serine/threonine-protein kinase TBK1 81.66% 90.48%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.46% 82.69%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.41% 94.00%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 81.30% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.00% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.76% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.41% 97.09%

Plants that contains it

Top
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.
Perrottetia arisanensis

Cross-Links

Top
PubChem 572464
LOTUS LTS0246874
wikiData Q105104782