Isopongachromene

Details

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Internal ID 80e2d163-e6b9-4e28-a2cc-2b8345973086
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Pyranoflavonoids
IUPAC Name 2-(1,3-benzodioxol-5-yl)-6-methoxy-8,8-dimethylpyrano[2,3-h]chromen-4-one
SMILES (Canonical) CC1(C=CC2=C3C(=CC(=C2O1)OC)C(=O)C=C(O3)C4=CC5=C(C=C4)OCO5)C
SMILES (Isomeric) CC1(C=CC2=C3C(=CC(=C2O1)OC)C(=O)C=C(O3)C4=CC5=C(C=C4)OCO5)C
InChI InChI=1S/C22H18O6/c1-22(2)7-6-13-20-14(9-19(24-3)21(13)28-22)15(23)10-17(27-20)12-4-5-16-18(8-12)26-11-25-16/h4-10H,11H2,1-3H3
InChI Key CKTFYXPCWPPHAT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H18O6
Molecular Weight 378.40 g/mol
Exact Mass 378.11033829 g/mol
Topological Polar Surface Area (TPSA) 63.20 Ų
XlogP 3.90
Atomic LogP (AlogP) 4.38
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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LMPK12110065

2D Structure

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2D Structure of Isopongachromene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9906 99.06%
Caco-2 + 0.6352 63.52%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7814 78.14%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9339 93.39%
OATP1B3 inhibitior + 0.9330 93.30%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.9235 92.35%
P-glycoprotein inhibitior + 0.9380 93.80%
P-glycoprotein substrate - 0.6384 63.84%
CYP3A4 substrate + 0.6323 63.23%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8223 82.23%
CYP3A4 inhibition + 0.9564 95.64%
CYP2C9 inhibition + 0.7167 71.67%
CYP2C19 inhibition + 0.9157 91.57%
CYP2D6 inhibition + 0.6355 63.55%
CYP1A2 inhibition - 0.6426 64.26%
CYP2C8 inhibition + 0.5234 52.34%
CYP inhibitory promiscuity + 0.9180 91.80%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Danger 0.3861 38.61%
Eye corrosion - 0.9838 98.38%
Eye irritation - 0.7737 77.37%
Skin irritation - 0.8094 80.94%
Skin corrosion - 0.9612 96.12%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7234 72.34%
Micronuclear + 0.6674 66.74%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.7098 70.98%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.5298 52.98%
Acute Oral Toxicity (c) III 0.4975 49.75%
Estrogen receptor binding + 0.9443 94.43%
Androgen receptor binding + 0.8522 85.22%
Thyroid receptor binding + 0.7782 77.82%
Glucocorticoid receptor binding + 0.9342 93.42%
Aromatase binding + 0.5939 59.39%
PPAR gamma + 0.8850 88.50%
Honey bee toxicity - 0.6498 64.98%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9768 97.68%

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
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 98.93% 96.77%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.86% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.55% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.61% 85.14%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 95.93% 85.30%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.62% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.38% 94.00%
CHEMBL2581 P07339 Cathepsin D 94.34% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 91.38% 93.99%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.15% 95.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 90.37% 92.62%
CHEMBL1907 P15144 Aminopeptidase N 89.42% 93.31%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 88.88% 80.96%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.02% 95.89%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 87.51% 94.80%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 87.38% 97.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.28% 86.33%
CHEMBL1937 Q92769 Histone deacetylase 2 86.40% 94.75%
CHEMBL4895 P30530 Tyrosine-protein kinase receptor UFO 84.51% 90.95%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 83.80% 96.00%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 83.19% 95.78%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.12% 96.09%
CHEMBL3922 P50579 Methionine aminopeptidase 2 82.89% 97.28%
CHEMBL2535 P11166 Glucose transporter 82.69% 98.75%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.13% 100.00%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 81.94% 95.71%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 81.83% 82.67%
CHEMBL2717 Q9HCR9 Phosphodiesterase 11A 81.50% 85.00%

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.
Pongamia pinnata

Cross-Links

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PubChem 44257584
LOTUS LTS0013897
wikiData Q104962767