Cystodione A

Details

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Internal ID 0339c3e9-8f6e-4a52-ae5b-81d00dd0116a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (1E,6Z,13E)-3,15-dihydroxy-1-(5-hydroxy-2-methoxy-3-methylphenyl)-3,7,11,15-tetramethylhexadeca-1,6,13-triene-5,12-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H40O6/c1-19(9-8-10-20(2)25(31)12-13-27(4,5)32)15-24(30)18-28(6,33)14-11-22-17-23(29)16-21(3)26(22)34-7/h11-17,20,29,32-33H,8-10,18H2,1-7H3/b13-12+,14-11+,19-15-
InChI Key KQMOBTZIZPBRGT-RZORCUHASA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C28H40O6
Molecular Weight 472.60 g/mol
Exact Mass 472.28248899 g/mol
Topological Polar Surface Area (TPSA) 104.00 Ų
XlogP 4.20
Atomic LogP (AlogP) 5.08
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 13

Synonyms

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CHEMBL2333075

2D Structure

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2D Structure of Cystodione A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9952 99.52%
Caco-2 - 0.6506 65.06%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8496 84.96%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8721 87.21%
OATP1B3 inhibitior + 0.9118 91.18%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.9821 98.21%
P-glycoprotein inhibitior + 0.7348 73.48%
P-glycoprotein substrate - 0.5000 50.00%
CYP3A4 substrate + 0.6412 64.12%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8472 84.72%
CYP3A4 inhibition - 0.6638 66.38%
CYP2C9 inhibition - 0.6001 60.01%
CYP2C19 inhibition + 0.5497 54.97%
CYP2D6 inhibition - 0.8899 88.99%
CYP1A2 inhibition + 0.5328 53.28%
CYP2C8 inhibition + 0.5819 58.19%
CYP inhibitory promiscuity - 0.8560 85.60%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7311 73.11%
Carcinogenicity (trinary) Non-required 0.6926 69.26%
Eye corrosion - 0.9883 98.83%
Eye irritation - 0.9049 90.49%
Skin irritation - 0.6981 69.81%
Skin corrosion - 0.9676 96.76%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6744 67.44%
Micronuclear - 0.7800 78.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.5759 57.59%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.6158 61.58%
Acute Oral Toxicity (c) III 0.5328 53.28%
Estrogen receptor binding + 0.7155 71.55%
Androgen receptor binding + 0.6122 61.22%
Thyroid receptor binding + 0.6602 66.02%
Glucocorticoid receptor binding + 0.6367 63.67%
Aromatase binding + 0.6455 64.55%
PPAR gamma + 0.6820 68.20%
Honey bee toxicity - 0.7903 79.03%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9882 98.82%

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 98.90% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.66% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 93.71% 96.00%
CHEMBL2581 P07339 Cathepsin D 93.67% 98.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 92.62% 93.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.90% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.85% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 90.46% 94.73%
CHEMBL236 P41143 Delta opioid receptor 89.85% 99.35%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.31% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.47% 86.33%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 87.17% 95.89%
CHEMBL5852 Q96P65 Pyroglutamylated RFamide peptide receptor 85.39% 85.00%
CHEMBL4581 P52732 Kinesin-like protein 1 84.95% 93.18%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.41% 91.07%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 82.54% 97.23%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 82.49% 100.00%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 81.39% 97.29%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.52% 97.21%
CHEMBL2535 P11166 Glucose transporter 80.50% 98.75%

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 71665621
LOTUS LTS0058930
wikiData Q105144620