Vismiaguianin A

Details

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Internal ID 4e5853e6-eb07-4778-8f14-f77b4bbf7bc3
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Pyranocoumarins > Angular pyranocoumarins
IUPAC Name 12-hydroxy-14-methoxy-4,4,18-trimethyl-3,9-dioxatetracyclo[8.8.0.02,7.011,16]octadeca-1(10),2(7),5,11,13,15,17-heptaen-8-one
SMILES (Canonical) CC1=CC2=CC(=CC(=C2C3=C1C4=C(C=CC(O4)(C)C)C(=O)O3)O)OC
SMILES (Isomeric) CC1=CC2=CC(=CC(=C2C3=C1C4=C(C=CC(O4)(C)C)C(=O)O3)O)OC
InChI InChI=1S/C20H18O5/c1-10-7-11-8-12(23-4)9-14(21)16(11)18-15(10)17-13(19(22)24-18)5-6-20(2,3)25-17/h5-9,21H,1-4H3
InChI Key OGTVKOGEJPVHQE-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C20H18O5
Molecular Weight 338.40 g/mol
Exact Mass 338.11542367 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 3.80
Atomic LogP (AlogP) 4.15
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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10-Hydroxy-8-methoxy-3,3,5-trimethyl-3H-4,11-dioxa-chrysen-12-one
10-hydroxy-8-methoxy-3,3,5-trimethyl-3H,12H-benzo[h]pyrano[3,2-c]chromen-12-one
3H,12H-naphtho[1,2-b]pyrano[2,3-d]pyran-12-one, 10-hydroxy-8-methoxy-3,3,5-trimethyl-
InChI=1/C20H18O5/c1-10-7-11-8-12(23-4)9-14(21)16(11)18-15(10)17-13(19(22)24-18)5-6-20(2,3)25-17/h5-9,21H,1-4H

2D Structure

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2D Structure of Vismiaguianin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9826 98.26%
Caco-2 + 0.7685 76.85%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7587 75.87%
OATP2B1 inhibitior - 0.7149 71.49%
OATP1B1 inhibitior + 0.8892 88.92%
OATP1B3 inhibitior + 0.9570 95.70%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.6568 65.68%
P-glycoprotein inhibitior + 0.6698 66.98%
P-glycoprotein substrate - 0.6943 69.43%
CYP3A4 substrate + 0.5957 59.57%
CYP2C9 substrate - 0.6233 62.33%
CYP2D6 substrate - 0.8433 84.33%
CYP3A4 inhibition - 0.5900 59.00%
CYP2C9 inhibition - 0.7958 79.58%
CYP2C19 inhibition - 0.5768 57.68%
CYP2D6 inhibition - 0.7803 78.03%
CYP1A2 inhibition - 0.6871 68.71%
CYP2C8 inhibition + 0.5516 55.16%
CYP inhibitory promiscuity - 0.6492 64.92%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9313 93.13%
Carcinogenicity (trinary) Danger 0.5654 56.54%
Eye corrosion - 0.9809 98.09%
Eye irritation + 0.8535 85.35%
Skin irritation - 0.7702 77.02%
Skin corrosion - 0.9790 97.90%
Ames mutagenesis + 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4098 40.98%
Micronuclear + 0.6000 60.00%
Hepatotoxicity - 0.5698 56.98%
skin sensitisation - 0.8517 85.17%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.6420 64.20%
Acute Oral Toxicity (c) II 0.4903 49.03%
Estrogen receptor binding + 0.9106 91.06%
Androgen receptor binding + 0.7211 72.11%
Thyroid receptor binding + 0.7426 74.26%
Glucocorticoid receptor binding + 0.8574 85.74%
Aromatase binding + 0.8585 85.85%
PPAR gamma + 0.8224 82.24%
Honey bee toxicity - 0.8295 82.95%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9655 96.55%

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 99.01% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 96.31% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.46% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.17% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.72% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.06% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.86% 99.23%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.68% 93.99%
CHEMBL4208 P20618 Proteasome component C5 88.46% 90.00%
CHEMBL4581 P52732 Kinesin-like protein 1 87.92% 93.18%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 87.71% 91.07%
CHEMBL3401 O75469 Pregnane X receptor 86.08% 94.73%
CHEMBL2581 P07339 Cathepsin D 85.73% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.61% 86.33%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 85.32% 93.65%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.15% 89.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.63% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.44% 99.17%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 83.42% 94.42%
CHEMBL2535 P11166 Glucose transporter 82.04% 98.75%
CHEMBL204 P00734 Thrombin 81.93% 96.01%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Vismia guianensis

Cross-Links

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PubChem 5324262
LOTUS LTS0186902
wikiData Q105191850