Citreoviripyrone A

Details

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Internal ID 670a539d-aa14-4376-8da7-6c6ef62982f2
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 4-methoxy-5-methyl-6-[(1E,3E)-4-[(1R,6S,7S,8S)-1,3,5,8-tetramethyl-7-bicyclo[4.2.0]octa-2,4-dienyl]buta-1,3-dienyl]pyran-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H28O3/c1-14-11-15(2)22-18(17(4)23(22,5)13-14)9-7-8-10-19-16(3)20(25-6)12-21(24)26-19/h7-13,17-18,22H,1-6H3/b9-7+,10-8+/t17-,18-,22+,23-/m0/s1
InChI Key AFLXFQMVMOJBCC-PNWRMOOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H28O3
Molecular Weight 352.50 g/mol
Exact Mass 352.20384475 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 4.20
Atomic LogP (AlogP) 5.32
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Citreoviripyrone A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9956 99.56%
Caco-2 + 0.6250 62.50%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7044 70.44%
OATP2B1 inhibitior - 0.8595 85.95%
OATP1B1 inhibitior + 0.8506 85.06%
OATP1B3 inhibitior + 0.9772 97.72%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9752 97.52%
P-glycoprotein inhibitior + 0.7424 74.24%
P-glycoprotein substrate - 0.5606 56.06%
CYP3A4 substrate + 0.6254 62.54%
CYP2C9 substrate - 0.6044 60.44%
CYP2D6 substrate - 0.8686 86.86%
CYP3A4 inhibition + 0.5000 50.00%
CYP2C9 inhibition - 0.8180 81.80%
CYP2C19 inhibition + 0.8285 82.85%
CYP2D6 inhibition - 0.9166 91.66%
CYP1A2 inhibition + 0.8016 80.16%
CYP2C8 inhibition + 0.5709 57.09%
CYP inhibitory promiscuity + 0.8043 80.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9331 93.31%
Carcinogenicity (trinary) Danger 0.4109 41.09%
Eye corrosion - 0.9635 96.35%
Eye irritation - 0.9256 92.56%
Skin irritation - 0.6439 64.39%
Skin corrosion - 0.9717 97.17%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8743 87.43%
Micronuclear + 0.5959 59.59%
Hepatotoxicity + 0.5302 53.02%
skin sensitisation - 0.7400 74.00%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.6637 66.37%
Acute Oral Toxicity (c) III 0.5480 54.80%
Estrogen receptor binding + 0.8531 85.31%
Androgen receptor binding + 0.6939 69.39%
Thyroid receptor binding + 0.7638 76.38%
Glucocorticoid receptor binding + 0.6824 68.24%
Aromatase binding + 0.7698 76.98%
PPAR gamma + 0.8170 81.70%
Honey bee toxicity - 0.6862 68.62%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9696 96.96%

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 96.28% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.25% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.91% 86.33%
CHEMBL1937 Q92769 Histone deacetylase 2 90.43% 94.75%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.67% 92.94%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.79% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.32% 94.00%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 86.24% 82.38%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.19% 96.00%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 85.67% 85.30%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.73% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.20% 96.09%
CHEMBL2581 P07339 Cathepsin D 82.12% 98.95%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.74% 91.07%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 80.66% 93.40%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.09% 94.45%

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 139587237
LOTUS LTS0249175
wikiData Q77560871