Islandicin 4-methyl ether

Details

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Internal ID eb8ca529-0481-48ba-8f7b-f2f10249e458
Taxonomy Benzenoids > Anthracenes > Anthraquinones
IUPAC Name 4,5-dihydroxy-1-methoxy-2-methylanthracene-9,10-dione
SMILES (Canonical) CC1=CC(=C2C(=C1OC)C(=O)C3=C(C2=O)C(=CC=C3)O)O
SMILES (Isomeric) CC1=CC(=C2C(=C1OC)C(=O)C3=C(C2=O)C(=CC=C3)O)O
InChI InChI=1S/C16H12O5/c1-7-6-10(18)12-13(16(7)21-2)14(19)8-4-3-5-9(17)11(8)15(12)20/h3-6,17-18H,1-2H3
InChI Key NNCFIAAUBKRACV-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H12O5
Molecular Weight 284.26 g/mol
Exact Mass 284.06847348 g/mol
Topological Polar Surface Area (TPSA) 83.80 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.19
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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CHEMBL478711

2D Structure

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2D Structure of Islandicin 4-methyl ether

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9911 99.11%
Caco-2 + 0.7684 76.84%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.8853 88.53%
OATP2B1 inhibitior - 0.7195 71.95%
OATP1B1 inhibitior + 0.9531 95.31%
OATP1B3 inhibitior + 0.9603 96.03%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.7442 74.42%
P-glycoprotein inhibitior - 0.7792 77.92%
P-glycoprotein substrate - 0.9146 91.46%
CYP3A4 substrate - 0.5050 50.50%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7976 79.76%
CYP3A4 inhibition - 0.8400 84.00%
CYP2C9 inhibition + 0.5439 54.39%
CYP2C19 inhibition - 0.6249 62.49%
CYP2D6 inhibition - 0.7517 75.17%
CYP1A2 inhibition + 0.9340 93.40%
CYP2C8 inhibition - 0.7567 75.67%
CYP inhibitory promiscuity - 0.5909 59.09%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7829 78.29%
Carcinogenicity (trinary) Non-required 0.5706 57.06%
Eye corrosion - 0.9859 98.59%
Eye irritation + 0.9098 90.98%
Skin irritation - 0.6149 61.49%
Skin corrosion - 0.9569 95.69%
Ames mutagenesis + 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6945 69.45%
Micronuclear + 0.8300 83.00%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation - 0.9491 94.91%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity + 0.6597 65.97%
Acute Oral Toxicity (c) II 0.6613 66.13%
Estrogen receptor binding + 0.8633 86.33%
Androgen receptor binding - 0.4829 48.29%
Thyroid receptor binding - 0.5757 57.57%
Glucocorticoid receptor binding + 0.9172 91.72%
Aromatase binding + 0.6596 65.96%
PPAR gamma + 0.6741 67.41%
Honey bee toxicity - 0.9247 92.47%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9835 98.35%

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
CHEMBL2581 P07339 Cathepsin D 97.44% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.13% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.70% 99.15%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.11% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.05% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 91.02% 94.73%
CHEMBL2535 P11166 Glucose transporter 90.72% 98.75%
CHEMBL1951 P21397 Monoamine oxidase A 90.28% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.06% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.48% 94.00%
CHEMBL3492 P49721 Proteasome Macropain subunit 88.08% 90.24%
CHEMBL1937 Q92769 Histone deacetylase 2 86.56% 94.75%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 86.33% 93.03%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 86.14% 93.40%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 84.84% 96.67%
CHEMBL4208 P20618 Proteasome component C5 84.53% 90.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.18% 96.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.41% 89.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 81.37% 97.21%
CHEMBL2056 P21728 Dopamine D1 receptor 81.15% 91.00%

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.
Ventilago leiocarpa

Cross-Links

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PubChem 11119613
NPASS NPC124365
LOTUS LTS0256956
wikiData Q105182061