2,5-Dihydroxy-3-farnesyl-1,4-benzoquinone

Details

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Internal ID 24e8d230-26b9-4aa9-b660-e61d61511ac9
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name 2,5-dihydroxy-3-(3,7,11-trimethyldodeca-2,6,10-trienyl)cyclohexa-2,5-diene-1,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H28O4/c1-14(2)7-5-8-15(3)9-6-10-16(4)11-12-17-20(24)18(22)13-19(23)21(17)25/h7,9,11,13,22,25H,5-6,8,10,12H2,1-4H3
InChI Key ADRVEZVEKSCRHP-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C21H28O4
Molecular Weight 344.40 g/mol
Exact Mass 344.19875937 g/mol
Topological Polar Surface Area (TPSA) 74.60 Ų
XlogP 5.40
Atomic LogP (AlogP) 5.20
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,5-Dihydroxy-3-farnesyl-1,4-benzoquinone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9718 97.18%
Caco-2 - 0.5472 54.72%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8654 86.54%
OATP2B1 inhibitior - 0.8586 85.86%
OATP1B1 inhibitior + 0.9239 92.39%
OATP1B3 inhibitior + 0.9110 91.10%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.6064 60.64%
BSEP inhibitior + 0.8080 80.80%
P-glycoprotein inhibitior - 0.6846 68.46%
P-glycoprotein substrate - 0.8842 88.42%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.7931 79.31%
CYP2D6 substrate - 0.8700 87.00%
CYP3A4 inhibition - 0.6966 69.66%
CYP2C9 inhibition - 0.7363 73.63%
CYP2C19 inhibition - 0.7546 75.46%
CYP2D6 inhibition - 0.6121 61.21%
CYP1A2 inhibition - 0.8292 82.92%
CYP2C8 inhibition - 0.9265 92.65%
CYP inhibitory promiscuity - 0.8820 88.20%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8550 85.50%
Carcinogenicity (trinary) Non-required 0.6875 68.75%
Eye corrosion - 0.9789 97.89%
Eye irritation - 0.7851 78.51%
Skin irritation - 0.5959 59.59%
Skin corrosion - 0.9563 95.63%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6456 64.56%
Micronuclear - 0.9100 91.00%
Hepatotoxicity - 0.5324 53.24%
skin sensitisation - 0.5368 53.68%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.7240 72.40%
Acute Oral Toxicity (c) III 0.5677 56.77%
Estrogen receptor binding + 0.7616 76.16%
Androgen receptor binding + 0.6110 61.10%
Thyroid receptor binding + 0.5489 54.89%
Glucocorticoid receptor binding + 0.7390 73.90%
Aromatase binding + 0.7419 74.19%
PPAR gamma + 0.9104 91.04%
Honey bee toxicity - 0.8478 84.78%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9958 99.58%

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 96.15% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.65% 92.08%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.74% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 87.45% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.76% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.10% 85.14%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 82.93% 92.68%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.71% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.39% 99.23%

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 71436999
LOTUS LTS0161061
wikiData Q104909759