Phomosine G

Details

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Internal ID 0bad8ec9-8bc4-4b95-9130-c68cbac550b1
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Diarylethers
IUPAC Name methyl 3,7-dihydroxy-1,4,9-trimethyl-6H-benzo[b][1,4]benzodioxepine-2-carboxylate
SMILES (Canonical) CC1=CC(=C2COC3=C(C(=C(C(=C3C)O)C(=O)OC)C)OC2=C1)O
SMILES (Isomeric) CC1=CC(=C2COC3=C(C(=C(C(=C3C)O)C(=O)OC)C)OC2=C1)O
InChI InChI=1S/C18H18O6/c1-8-5-12(19)11-7-23-16-10(3)15(20)14(18(21)22-4)9(2)17(16)24-13(11)6-8/h5-6,19-20H,7H2,1-4H3
InChI Key FUDMGOSDBJQZJV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H18O6
Molecular Weight 330.30 g/mol
Exact Mass 330.11033829 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.49
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Phomosine G

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9577 95.77%
Caco-2 + 0.8395 83.95%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6694 66.94%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8204 82.04%
OATP1B3 inhibitior - 0.2607 26.07%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.6521 65.21%
P-glycoprotein inhibitior - 0.7749 77.49%
P-glycoprotein substrate - 0.8280 82.80%
CYP3A4 substrate + 0.5340 53.40%
CYP2C9 substrate - 0.8024 80.24%
CYP2D6 substrate - 0.8507 85.07%
CYP3A4 inhibition - 0.7871 78.71%
CYP2C9 inhibition - 0.7560 75.60%
CYP2C19 inhibition - 0.6951 69.51%
CYP2D6 inhibition - 0.9270 92.70%
CYP1A2 inhibition - 0.6536 65.36%
CYP2C8 inhibition + 0.5281 52.81%
CYP inhibitory promiscuity - 0.7170 71.70%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6199 61.99%
Eye corrosion - 0.9868 98.68%
Eye irritation + 0.6950 69.50%
Skin irritation - 0.7960 79.60%
Skin corrosion - 0.9734 97.34%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3832 38.32%
Micronuclear + 0.7300 73.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.8620 86.20%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.6813 68.13%
Acute Oral Toxicity (c) III 0.4480 44.80%
Estrogen receptor binding + 0.8381 83.81%
Androgen receptor binding + 0.6125 61.25%
Thyroid receptor binding - 0.5116 51.16%
Glucocorticoid receptor binding + 0.6795 67.95%
Aromatase binding + 0.5905 59.05%
PPAR gamma + 0.7652 76.52%
Honey bee toxicity - 0.8797 87.97%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9554 95.54%

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 98.38% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.00% 94.45%
CHEMBL1951 P21397 Monoamine oxidase A 94.54% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.64% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.44% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.54% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 88.21% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.47% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.31% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.44% 89.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 86.12% 94.80%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.19% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 81.48% 97.21%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.42% 86.33%
CHEMBL4208 P20618 Proteasome component C5 81.31% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.28% 99.17%
CHEMBL340 P08684 Cytochrome P450 3A4 80.79% 91.19%
CHEMBL2535 P11166 Glucose transporter 80.55% 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.
Adenocarpus foliolosus

Cross-Links

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PubChem 11674333
LOTUS LTS0108444
wikiData Q77384165