Flexibilisolide A

Details

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Internal ID b783ca9d-c013-4d7a-9c41-6a41aa21baee
Taxonomy Organoheterocyclic compounds > Lactones
IUPAC Name [(1R,3S,5S,7E,9R,12S,13R)-9-hydroxy-5,9,13-trimethyl-16-methylidene-15-oxo-4,14-dioxatricyclo[11.3.2.03,5]octadec-7-en-12-yl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H32O6/c1-14-16-7-12-22(5,28-19(14)24)17(26-15(2)23)8-11-20(3,25)9-6-10-21(4)18(13-16)27-21/h6,9,16-18,25H,1,7-8,10-13H2,2-5H3/b9-6+/t16-,17+,18+,20+,21+,22-/m1/s1
InChI Key SXSOYTHMKCYVOO-QSEBMAHISA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C22H32O6
Molecular Weight 392.50 g/mol
Exact Mass 392.21988874 g/mol
Topological Polar Surface Area (TPSA) 85.40 Ų
XlogP 2.70
Atomic LogP (AlogP) 3.22
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Flexibilisolide A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9604 96.04%
Caco-2 + 0.5944 59.44%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.6339 63.39%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8917 89.17%
OATP1B3 inhibitior + 0.8996 89.96%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6342 63.42%
BSEP inhibitior + 0.9015 90.15%
P-glycoprotein inhibitior + 0.6055 60.55%
P-glycoprotein substrate - 0.7281 72.81%
CYP3A4 substrate + 0.6865 68.65%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8923 89.23%
CYP3A4 inhibition - 0.5113 51.13%
CYP2C9 inhibition - 0.7016 70.16%
CYP2C19 inhibition - 0.7140 71.40%
CYP2D6 inhibition - 0.9342 93.42%
CYP1A2 inhibition - 0.5257 52.57%
CYP2C8 inhibition + 0.4776 47.76%
CYP inhibitory promiscuity - 0.9787 97.87%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8843 88.43%
Carcinogenicity (trinary) Non-required 0.6410 64.10%
Eye corrosion - 0.9837 98.37%
Eye irritation - 0.9193 91.93%
Skin irritation - 0.5289 52.89%
Skin corrosion - 0.9258 92.58%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7232 72.32%
Micronuclear - 0.6800 68.00%
Hepatotoxicity + 0.5357 53.57%
skin sensitisation - 0.7524 75.24%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity + 0.7686 76.86%
Acute Oral Toxicity (c) III 0.5791 57.91%
Estrogen receptor binding + 0.9196 91.96%
Androgen receptor binding + 0.5443 54.43%
Thyroid receptor binding + 0.6920 69.20%
Glucocorticoid receptor binding + 0.8494 84.94%
Aromatase binding + 0.6744 67.44%
PPAR gamma + 0.5931 59.31%
Honey bee toxicity - 0.8050 80.50%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9834 98.34%

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 98.70% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.08% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.44% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.71% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.29% 94.45%
CHEMBL2581 P07339 Cathepsin D 89.33% 98.95%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 88.59% 97.14%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.92% 92.94%
CHEMBL340 P08684 Cytochrome P450 3A4 86.91% 91.19%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.28% 97.25%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.42% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.57% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.74% 97.09%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.50% 93.04%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.12% 92.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.07% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.97% 86.33%
CHEMBL5028 O14672 ADAM10 81.96% 97.50%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.93% 91.07%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.38% 100.00%

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.
There are no matching plants.

Cross-Links

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PubChem 102483003
LOTUS LTS0172468
wikiData Q105263306