Fumigatin

Details

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Internal ID 17b309a3-3443-49d3-b592-ed50c6a55e60
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Quinone and hydroquinone lipids > Prenylquinones > Ubiquinones
IUPAC Name 3-hydroxy-2-methoxy-5-methylcyclohexa-2,5-diene-1,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H8O4/c1-4-3-5(9)8(12-2)7(11)6(4)10/h3,11H,1-2H3
InChI Key GSNBWTFAGXSQCO-UHFFFAOYSA-N
Popularity 60 references in papers

Physical and Chemical Properties

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Molecular Formula C8H8O4
Molecular Weight 168.15 g/mol
Exact Mass 168.04225873 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 0.50
Atomic LogP (AlogP) 0.50
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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484-89-9
3-hydroxy-2-methoxy-5-methylcyclohexa-2,5-diene-1,4-dione
D4Y1CD8EH8
3-Hydroxy-2-methoxy-5-methyl-2,5-cyclohexadiene-1,4-dione
6-hydroxy-5-methoxy-p-toluquinone
UNII-D4Y1CD8EH8
3-demethylubiquinone 0
FUMIGATIN [MI]
3-hydroxy-2-methoxy-5-methyl-p-benzoquinone
SCHEMBL1915628
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Fumigatin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9782 97.82%
Caco-2 + 0.5739 57.39%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Mitochondria 0.8524 85.24%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9395 93.95%
OATP1B3 inhibitior + 0.9753 97.53%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9035 90.35%
P-glycoprotein inhibitior - 0.9561 95.61%
P-glycoprotein substrate - 0.9836 98.36%
CYP3A4 substrate - 0.6170 61.70%
CYP2C9 substrate - 0.7962 79.62%
CYP2D6 substrate - 0.8816 88.16%
CYP3A4 inhibition - 0.9179 91.79%
CYP2C9 inhibition - 0.9400 94.00%
CYP2C19 inhibition - 0.7591 75.91%
CYP2D6 inhibition - 0.8716 87.16%
CYP1A2 inhibition - 0.8658 86.58%
CYP2C8 inhibition - 0.9756 97.56%
CYP inhibitory promiscuity - 0.8781 87.81%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7168 71.68%
Carcinogenicity (trinary) Non-required 0.6712 67.12%
Eye corrosion - 0.8369 83.69%
Eye irritation + 0.8891 88.91%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9572 95.72%
Ames mutagenesis - 0.7170 71.70%
Human Ether-a-go-go-Related Gene inhibition - 0.7402 74.02%
Micronuclear + 0.6100 61.00%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation - 0.5804 58.04%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.7282 72.82%
Acute Oral Toxicity (c) III 0.3884 38.84%
Estrogen receptor binding - 0.7691 76.91%
Androgen receptor binding - 0.6970 69.70%
Thyroid receptor binding - 0.7124 71.24%
Glucocorticoid receptor binding - 0.8425 84.25%
Aromatase binding - 0.8191 81.91%
PPAR gamma - 0.8272 82.72%
Honey bee toxicity - 0.8993 89.93%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.8116 81.16%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.69% 95.56%
CHEMBL2581 P07339 Cathepsin D 91.51% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.57% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.00% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.19% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.47% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 82.74% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.04% 94.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 119035
LOTUS LTS0060348
wikiData Q27276098