Fusaraisochromanone

Details

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Internal ID b4c9c4cb-b6fd-4b40-a624-c58b29895c6a
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name (3S,4R)-4,8-dihydroxy-6-methoxy-3,4,5-trimethyl-3H-isochromen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H16O5/c1-6-9(17-4)5-8(14)10-11(6)13(3,16)7(2)18-12(10)15/h5,7,14,16H,1-4H3/t7-,13-/m0/s1
InChI Key QIWHCAJJZMZSLM-CPFSXVBKSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H16O5
Molecular Weight 252.26 g/mol
Exact Mass 252.09977361 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.48
H-Bond Acceptor 5
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 Fusaraisochromanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9464 94.64%
Caco-2 + 0.5189 51.89%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.6885 68.85%
OATP2B1 inhibitior - 0.8596 85.96%
OATP1B1 inhibitior + 0.9064 90.64%
OATP1B3 inhibitior + 0.9440 94.40%
MATE1 inhibitior - 0.6600 66.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9060 90.60%
P-glycoprotein inhibitior - 0.8720 87.20%
P-glycoprotein substrate - 0.9012 90.12%
CYP3A4 substrate + 0.5790 57.90%
CYP2C9 substrate - 0.5773 57.73%
CYP2D6 substrate - 0.8512 85.12%
CYP3A4 inhibition - 0.8423 84.23%
CYP2C9 inhibition - 0.9784 97.84%
CYP2C19 inhibition - 0.8840 88.40%
CYP2D6 inhibition - 0.9058 90.58%
CYP1A2 inhibition + 0.5096 50.96%
CYP2C8 inhibition - 0.8722 87.22%
CYP inhibitory promiscuity - 0.7460 74.60%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5298 52.98%
Eye corrosion - 0.9711 97.11%
Eye irritation + 0.6255 62.55%
Skin irritation - 0.6640 66.40%
Skin corrosion - 0.9602 96.02%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7383 73.83%
Micronuclear + 0.7300 73.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation - 0.9160 91.60%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.5273 52.73%
Acute Oral Toxicity (c) III 0.5003 50.03%
Estrogen receptor binding - 0.5755 57.55%
Androgen receptor binding - 0.6493 64.93%
Thyroid receptor binding - 0.5788 57.88%
Glucocorticoid receptor binding - 0.6009 60.09%
Aromatase binding - 0.6941 69.41%
PPAR gamma + 0.5733 57.33%
Honey bee toxicity - 0.8411 84.11%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.8489 84.89%

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 97.02% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.38% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.05% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.16% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.36% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.54% 94.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 87.14% 92.94%
CHEMBL2581 P07339 Cathepsin D 86.75% 98.95%
CHEMBL1255126 O15151 Protein Mdm4 86.59% 90.20%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.34% 89.00%
CHEMBL2535 P11166 Glucose transporter 84.97% 98.75%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.52% 99.15%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.85% 91.07%
CHEMBL340 P08684 Cytochrome P450 3A4 83.77% 91.19%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.38% 97.14%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 83.26% 82.38%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.77% 94.45%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 81.73% 96.21%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 80.93% 93.03%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.14% 95.50%

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 132566877
LOTUS LTS0045095
wikiData Q105222438