Graphostrin F

Details

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Internal ID 994bc9ba-0677-4437-9946-faa09736ac97
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Hydroxybenzoic acid derivatives
IUPAC Name 4-hydroxy-3-[(E)-4-hydroxy-3-methylbut-2-enyl]benzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H14O4/c1-8(7-13)2-3-9-6-10(12(15)16)4-5-11(9)14/h2,4-6,13-14H,3,7H2,1H3,(H,15,16)/b8-2+
InChI Key HOSRDVYFIODRKS-KRXBUXKQSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H14O4
Molecular Weight 222.24 g/mol
Exact Mass 222.08920892 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.57
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Graphostrin F

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9910 99.10%
Caco-2 - 0.5124 51.24%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.8991 89.91%
OATP2B1 inhibitior - 0.8599 85.99%
OATP1B1 inhibitior + 0.9519 95.19%
OATP1B3 inhibitior + 0.9497 94.97%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8852 88.52%
P-glycoprotein inhibitior - 0.9908 99.08%
P-glycoprotein substrate - 0.9224 92.24%
CYP3A4 substrate - 0.7043 70.43%
CYP2C9 substrate - 0.8100 81.00%
CYP2D6 substrate - 0.8665 86.65%
CYP3A4 inhibition - 0.7161 71.61%
CYP2C9 inhibition - 0.5643 56.43%
CYP2C19 inhibition - 0.5292 52.92%
CYP2D6 inhibition - 0.7348 73.48%
CYP1A2 inhibition + 0.6790 67.90%
CYP2C8 inhibition - 0.6999 69.99%
CYP inhibitory promiscuity - 0.5504 55.04%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7170 71.70%
Carcinogenicity (trinary) Non-required 0.7254 72.54%
Eye corrosion - 0.9783 97.83%
Eye irritation + 0.8117 81.17%
Skin irritation - 0.6591 65.91%
Skin corrosion - 0.9354 93.54%
Ames mutagenesis - 0.7823 78.23%
Human Ether-a-go-go-Related Gene inhibition - 0.7630 76.30%
Micronuclear - 0.7600 76.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation + 0.5000 50.00%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.4621 46.21%
Acute Oral Toxicity (c) III 0.5920 59.20%
Estrogen receptor binding - 0.6236 62.36%
Androgen receptor binding - 0.5717 57.17%
Thyroid receptor binding - 0.7201 72.01%
Glucocorticoid receptor binding + 0.7545 75.45%
Aromatase binding - 0.5976 59.76%
PPAR gamma + 0.5737 57.37%
Honey bee toxicity - 0.9731 97.31%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.8500 85.00%
Fish aquatic toxicity + 1.0000 100.00%

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 94.77% 91.11%
CHEMBL3194 P02766 Transthyretin 92.20% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.43% 86.33%
CHEMBL2581 P07339 Cathepsin D 89.68% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.91% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.49% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 87.99% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 86.92% 94.73%
CHEMBL4208 P20618 Proteasome component C5 81.96% 90.00%

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 131839381
LOTUS LTS0137701
wikiData Q105031512