[(1S,3aR,5R,5aS,6S,8S,8aS,9aS)-1,8-dihydroxy-1-(hydroxymethyl)-5,8a-dimethyl-2-oxo-4,5,5a,6,7,8,9,9a-octahydro-3aH-azuleno[6,5-b]furan-6-yl] (E)-2-methylbut-2-enoate

Details

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Internal ID cd9a3d03-7673-48d4-a843-df25a9ff7162
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Sesquiterpene lactones > Ambrosanolides and secoambrosanolides
IUPAC Name [(1S,3aR,5R,5aS,6S,8S,8aS,9aS)-1,8-dihydroxy-1-(hydroxymethyl)-5,8a-dimethyl-2-oxo-4,5,5a,6,7,8,9,9a-octahydro-3aH-azuleno[6,5-b]furan-6-yl] (E)-2-methylbut-2-enoate
SMILES (Canonical) CC=C(C)C(=O)OC1CC(C2(C1C(CC3C(C2)C(C(=O)O3)(CO)O)C)C)O
SMILES (Isomeric) C/C=C(\C)/C(=O)O[C@H]1C[C@@H]([C@@]2([C@@H]1[C@@H](C[C@@H]3[C@H](C2)[C@@](C(=O)O3)(CO)O)C)C)O
InChI InChI=1S/C20H30O7/c1-5-10(2)17(23)26-14-7-15(22)19(4)8-12-13(6-11(3)16(14)19)27-18(24)20(12,25)9-21/h5,11-16,21-22,25H,6-9H2,1-4H3/b10-5+/t11-,12+,13-,14+,15+,16-,19-,20-/m1/s1
InChI Key GNFIFVXADUGFIS-HPXAHJFOSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H30O7
Molecular Weight 382.40 g/mol
Exact Mass 382.19915329 g/mol
Topological Polar Surface Area (TPSA) 113.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 0.95
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1S,3aR,5R,5aS,6S,8S,8aS,9aS)-1,8-dihydroxy-1-(hydroxymethyl)-5,8a-dimethyl-2-oxo-4,5,5a,6,7,8,9,9a-octahydro-3aH-azuleno[6,5-b]furan-6-yl] (E)-2-methylbut-2-enoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9548 95.48%
Caco-2 - 0.5509 55.09%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.6961 69.61%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9022 90.22%
OATP1B3 inhibitior + 0.9577 95.77%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.4931 49.31%
P-glycoprotein inhibitior - 0.7282 72.82%
P-glycoprotein substrate - 0.5872 58.72%
CYP3A4 substrate + 0.6796 67.96%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8872 88.72%
CYP3A4 inhibition + 0.5190 51.90%
CYP2C9 inhibition - 0.6789 67.89%
CYP2C19 inhibition - 0.7996 79.96%
CYP2D6 inhibition - 0.9521 95.21%
CYP1A2 inhibition - 0.6469 64.69%
CYP2C8 inhibition - 0.7289 72.89%
CYP inhibitory promiscuity - 0.9490 94.90%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6052 60.52%
Eye corrosion - 0.9886 98.86%
Eye irritation - 0.9681 96.81%
Skin irritation - 0.5657 56.57%
Skin corrosion - 0.9449 94.49%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5363 53.63%
Micronuclear - 0.7200 72.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation - 0.8935 89.35%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity + 0.6956 69.56%
Acute Oral Toxicity (c) III 0.4611 46.11%
Estrogen receptor binding + 0.7536 75.36%
Androgen receptor binding + 0.5499 54.99%
Thyroid receptor binding + 0.6941 69.41%
Glucocorticoid receptor binding + 0.7781 77.81%
Aromatase binding + 0.6756 67.56%
PPAR gamma - 0.5894 58.94%
Honey bee toxicity - 0.6051 60.51%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9721 97.21%

Targets

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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 95.43% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.43% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.27% 86.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.80% 97.25%
CHEMBL221 P23219 Cyclooxygenase-1 87.78% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.71% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.57% 94.45%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 86.60% 91.07%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.52% 89.00%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 86.14% 91.24%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.90% 100.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.18% 85.14%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.06% 96.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.10% 99.23%
CHEMBL340 P08684 Cytochrome P450 3A4 81.15% 91.19%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.41% 93.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 80.31% 96.77%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.27% 95.56%

Plants that contains it

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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.
Hymenoxys lemmonii

Cross-Links

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PubChem 14527107
LOTUS LTS0030133
wikiData Q105012366