[(3aR,4S,5R,5aS,8aR,8bR)-5-(hydroxymethyl)-5,8-dimethyl-3-methylidene-2-oxo-3a,4,5a,6,8a,8b-hexahydrocyclopenta[g][1]benzofuran-4-yl] (E)-2-methylbut-2-enoate

Details

Top
Internal ID 8397aca8-4e84-4264-8a82-ff2b17ae3e77
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name [(3aR,4S,5R,5aS,8aR,8bR)-5-(hydroxymethyl)-5,8-dimethyl-3-methylidene-2-oxo-3a,4,5a,6,8a,8b-hexahydrocyclopenta[g][1]benzofuran-4-yl] (E)-2-methylbut-2-enoate
SMILES (Canonical) CC=C(C)C(=O)OC1C2C(C3C(C1(C)CO)CC=C3C)OC(=O)C2=C
SMILES (Isomeric) C/C=C(\C)/C(=O)O[C@H]1[C@H]2[C@@H]([C@@H]3[C@@H]([C@]1(C)CO)CC=C3C)OC(=O)C2=C
InChI InChI=1S/C20H26O5/c1-6-10(2)18(22)25-17-15-12(4)19(23)24-16(15)14-11(3)7-8-13(14)20(17,5)9-21/h6-7,13-17,21H,4,8-9H2,1-3,5H3/b10-6+/t13-,14-,15+,16+,17-,20-/m0/s1
InChI Key HEABIUDLCLYYFN-YUFHJKRISA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C20H26O5
Molecular Weight 346.40 g/mol
Exact Mass 346.17802393 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.56
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of [(3aR,4S,5R,5aS,8aR,8bR)-5-(hydroxymethyl)-5,8-dimethyl-3-methylidene-2-oxo-3a,4,5a,6,8a,8b-hexahydrocyclopenta[g][1]benzofuran-4-yl] (E)-2-methylbut-2-enoate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9762 97.62%
Caco-2 + 0.6195 61.95%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.6268 62.68%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8539 85.39%
OATP1B3 inhibitior + 0.9196 91.96%
MATE1 inhibitior - 0.7812 78.12%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7579 75.79%
P-glycoprotein inhibitior - 0.5949 59.49%
P-glycoprotein substrate - 0.7428 74.28%
CYP3A4 substrate + 0.6345 63.45%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8921 89.21%
CYP3A4 inhibition + 0.6191 61.91%
CYP2C9 inhibition - 0.7498 74.98%
CYP2C19 inhibition - 0.7992 79.92%
CYP2D6 inhibition - 0.9487 94.87%
CYP1A2 inhibition + 0.5172 51.72%
CYP2C8 inhibition - 0.6773 67.73%
CYP inhibitory promiscuity - 0.6659 66.59%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5654 56.54%
Eye corrosion - 0.9794 97.94%
Eye irritation - 0.8639 86.39%
Skin irritation - 0.5306 53.06%
Skin corrosion - 0.9355 93.55%
Ames mutagenesis - 0.6678 66.78%
Human Ether-a-go-go-Related Gene inhibition - 0.5631 56.31%
Micronuclear - 0.7400 74.00%
Hepatotoxicity + 0.6178 61.78%
skin sensitisation - 0.7885 78.85%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.7372 73.72%
Acute Oral Toxicity (c) III 0.5350 53.50%
Estrogen receptor binding + 0.6758 67.58%
Androgen receptor binding + 0.6445 64.45%
Thyroid receptor binding - 0.5426 54.26%
Glucocorticoid receptor binding - 0.5149 51.49%
Aromatase binding - 0.6095 60.95%
PPAR gamma - 0.5799 57.99%
Honey bee toxicity - 0.6833 68.33%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9946 99.46%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.76% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.51% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.66% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.61% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.60% 97.25%
CHEMBL221 P23219 Cyclooxygenase-1 90.30% 90.17%
CHEMBL3401 O75469 Pregnane X receptor 88.99% 94.73%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 88.25% 91.07%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 86.47% 91.24%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.14% 95.50%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.82% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.37% 89.00%
CHEMBL3714130 P46095 G-protein coupled receptor 6 84.50% 97.36%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.03% 96.09%
CHEMBL2581 P07339 Cathepsin D 81.98% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.88% 99.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.44% 95.89%
CHEMBL2996 Q05655 Protein kinase C delta 80.73% 97.79%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.30% 100.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.24% 93.00%

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.
Lasiolaena santosii

Cross-Links

Top
PubChem 162953601
LOTUS LTS0263958
wikiData Q105026693