3,4-dihydrofusidienol A

Details

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Internal ID e1ee724b-2183-4893-8074-2c4e1c15e89f
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name methyl 7-hydroxy-9-methyl-6-oxo-2,3-dihydrooxepino[2,3-b]chromene-5-carboxylate
SMILES (Canonical) CC1=CC(=C2C(=C1)OC3=C(C2=O)C(=CCCO3)C(=O)OC)O
SMILES (Isomeric) CC1=CC(=C2C(=C1)OC3=C(C2=O)C(=CCCO3)C(=O)OC)O
InChI InChI=1S/C16H14O6/c1-8-6-10(17)13-11(7-8)22-16-12(14(13)18)9(15(19)20-2)4-3-5-21-16/h4,6-7,17H,3,5H2,1-2H3
InChI Key FCSZMXPBNNJHCE-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H14O6
Molecular Weight 302.28 g/mol
Exact Mass 302.07903816 g/mol
Topological Polar Surface Area (TPSA) 82.10 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.15
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,4-dihydrofusidienol A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9750 97.50%
Caco-2 + 0.8471 84.71%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8454 84.54%
OATP2B1 inhibitior - 0.8613 86.13%
OATP1B1 inhibitior + 0.9059 90.59%
OATP1B3 inhibitior + 0.9467 94.67%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.6337 63.37%
P-glycoprotein inhibitior - 0.6345 63.45%
P-glycoprotein substrate - 0.8128 81.28%
CYP3A4 substrate + 0.5984 59.84%
CYP2C9 substrate - 0.5603 56.03%
CYP2D6 substrate - 0.8600 86.00%
CYP3A4 inhibition - 0.5617 56.17%
CYP2C9 inhibition - 0.6222 62.22%
CYP2C19 inhibition + 0.5696 56.96%
CYP2D6 inhibition - 0.6854 68.54%
CYP1A2 inhibition + 0.5840 58.40%
CYP2C8 inhibition + 0.5525 55.25%
CYP inhibitory promiscuity - 0.6429 64.29%
UGT catelyzed + 0.5362 53.62%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6664 66.64%
Eye corrosion - 0.9814 98.14%
Eye irritation + 0.8002 80.02%
Skin irritation - 0.8093 80.93%
Skin corrosion - 0.9655 96.55%
Ames mutagenesis + 0.6354 63.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5154 51.54%
Micronuclear - 0.5267 52.67%
Hepatotoxicity + 0.6285 62.85%
skin sensitisation - 0.7745 77.45%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.5282 52.82%
Acute Oral Toxicity (c) II 0.4825 48.25%
Estrogen receptor binding + 0.8249 82.49%
Androgen receptor binding + 0.8028 80.28%
Thyroid receptor binding - 0.6902 69.02%
Glucocorticoid receptor binding + 0.8060 80.60%
Aromatase binding + 0.5794 57.94%
PPAR gamma + 0.7994 79.94%
Honey bee toxicity - 0.9103 91.03%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity + 0.9137 91.37%

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 98.56% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 91.67% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.95% 89.00%
CHEMBL2581 P07339 Cathepsin D 90.31% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.18% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.19% 94.00%
CHEMBL4208 P20618 Proteasome component C5 87.94% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.34% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.86% 86.33%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 85.32% 94.80%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 85.17% 96.77%
CHEMBL4040 P28482 MAP kinase ERK2 84.48% 83.82%
CHEMBL340 P08684 Cytochrome P450 3A4 84.45% 91.19%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 84.09% 96.21%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.52% 96.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.39% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.09% 99.23%
CHEMBL1951 P21397 Monoamine oxidase A 82.07% 91.49%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.48% 99.17%

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 102300481
LOTUS LTS0037343
wikiData Q77520434