6Alpha-Acetoxyisoinuviscolide

Details

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Internal ID 82870e28-9731-4a31-93ff-7209695ff27d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Sesquiterpene lactones > Guaianolides and derivatives
IUPAC Name [(3aS,5aS,8R,8aS,9S,9aR)-8-hydroxy-5,8-dimethyl-1-methylidene-2-oxo-5a,6,7,8a,9,9a-hexahydro-3aH-azuleno[6,5-b]furan-9-yl] acetate
SMILES (Canonical) CC1=CC2C(C(C3C1CCC3(C)O)OC(=O)C)C(=C)C(=O)O2
SMILES (Isomeric) CC1=C[C@H]2[C@H]([C@@H]([C@@H]3[C@@H]1CC[C@@]3(C)O)OC(=O)C)C(=C)C(=O)O2
InChI InChI=1S/C17H22O5/c1-8-7-12-13(9(2)16(19)22-12)15(21-10(3)18)14-11(8)5-6-17(14,4)20/h7,11-15,20H,2,5-6H2,1,3-4H3/t11-,12+,13-,14+,15+,17-/m1/s1
InChI Key PLSCGWSBZMOKAA-RURKYGKJSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H22O5
Molecular Weight 306.40 g/mol
Exact Mass 306.14672380 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.75
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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CHEBI:69341
(3aR,4S,4aS,5R,7aS,9aS)-5-hydroxy-5,8-dimethyl-3-methylidene-2-oxo-2,3,3a,4,4a,5,6,7,7a,9a-decahydroazuleno[6,5-b]furan-4-yl acetate
((3aS,5aS,8R,8aS,9S,9aR)-8-hydroxy-5,8-dimethyl-1-methylidene-2-oxo-5a,6,7,8a,9,9a-hexahydro-3aH-azuleno(6,5-b)furan-9-yl) acetate
(3aR,4S,4aS,5R,7aS,9aS)-5-hydroxy-5,8-dimethyl-3-methylidene-2-oxo-2,3,3a,4,4a,5,6,7,7a,9a-decahydroazuleno(6,5-b)furan-4-yl acetate
[(3aS,5aS,8R,8aS,9S,9aR)-8-hydroxy-5,8-dimethyl-1-methylidene-2-oxo-5a,6,7,8a,9,9a-hexahydro-3aH-azuleno[6,5-b]furan-9-yl] acetate
RefChem:105322
CHEMBL1911139
Q27137683

2D Structure

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2D Structure of 6Alpha-Acetoxyisoinuviscolide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9804 98.04%
Caco-2 + 0.5923 59.23%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.5493 54.93%
OATP2B1 inhibitior - 0.8580 85.80%
OATP1B1 inhibitior + 0.8645 86.45%
OATP1B3 inhibitior + 0.8370 83.70%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7842 78.42%
BSEP inhibitior - 0.9437 94.37%
P-glycoprotein inhibitior - 0.7878 78.78%
P-glycoprotein substrate - 0.7944 79.44%
CYP3A4 substrate + 0.6554 65.54%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8958 89.58%
CYP3A4 inhibition - 0.5759 57.59%
CYP2C9 inhibition - 0.7180 71.80%
CYP2C19 inhibition - 0.7773 77.73%
CYP2D6 inhibition - 0.9482 94.82%
CYP1A2 inhibition + 0.5856 58.56%
CYP2C8 inhibition - 0.6278 62.78%
CYP inhibitory promiscuity - 0.9389 93.89%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5516 55.16%
Eye corrosion - 0.9802 98.02%
Eye irritation - 0.7823 78.23%
Skin irritation + 0.5229 52.29%
Skin corrosion - 0.8204 82.04%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6790 67.90%
Micronuclear - 0.7700 77.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.7630 76.30%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity + 0.5671 56.71%
Acute Oral Toxicity (c) II 0.4619 46.19%
Estrogen receptor binding + 0.6064 60.64%
Androgen receptor binding + 0.5249 52.49%
Thyroid receptor binding - 0.5072 50.72%
Glucocorticoid receptor binding + 0.5955 59.55%
Aromatase binding - 0.6841 68.41%
PPAR gamma - 0.5063 50.63%
Honey bee toxicity - 0.7586 75.86%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9591 95.91%

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 94.04% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.80% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.87% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.65% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.97% 99.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.82% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.24% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.79% 89.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.65% 97.25%
CHEMBL2996 Q05655 Protein kinase C delta 83.81% 97.79%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.12% 95.89%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 82.19% 97.33%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.14% 93.03%
CHEMBL5255 O00206 Toll-like receptor 4 81.51% 92.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.36% 97.09%
CHEMBL340 P08684 Cytochrome P450 3A4 81.29% 91.19%
CHEMBL5028 O14672 ADAM10 81.05% 97.50%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.85% 92.94%
CHEMBL2581 P07339 Cathepsin D 80.25% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.23% 94.00%

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.
Inula hupehensis
Rhanteriopsis bombycina

Cross-Links

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PubChem 57399052
NPASS NPC67584
ChEMBL CHEMBL1911139
LOTUS LTS0059204
wikiData Q27137683