Vogelin J

Details

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Internal ID b83c8762-2c06-49cb-a131-0eec82308904
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Pyranoflavonoids
IUPAC Name 5-hydroxy-8-(4-hydroxyphenyl)-2,2-dimethylpyrano[2,3-f]chromen-10-one
SMILES (Canonical) CC1(C=CC2=C(O1)C3=C(C=C2O)OC(=CC3=O)C4=CC=C(C=C4)O)C
SMILES (Isomeric) CC1(C=CC2=C(O1)C3=C(C=C2O)OC(=CC3=O)C4=CC=C(C=C4)O)C
InChI InChI=1S/C20H16O5/c1-20(2)8-7-13-14(22)9-17-18(19(13)25-20)15(23)10-16(24-17)11-3-5-12(21)6-4-11/h3-10,21-22H,1-2H3
InChI Key GHUQHFLVTXMEHU-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C20H16O5
Molecular Weight 336.30 g/mol
Exact Mass 336.09977361 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 3.40
Atomic LogP (AlogP) 4.06
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 Vogelin J

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9912 99.12%
Caco-2 - 0.5253 52.53%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.8750 87.50%
OATP2B1 inhibitior - 0.5791 57.91%
OATP1B1 inhibitior + 0.8994 89.94%
OATP1B3 inhibitior + 0.9759 97.59%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.6198 61.98%
P-glycoprotein inhibitior + 0.6035 60.35%
P-glycoprotein substrate - 0.7105 71.05%
CYP3A4 substrate + 0.5979 59.79%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7991 79.91%
CYP3A4 inhibition + 0.5918 59.18%
CYP2C9 inhibition + 0.9095 90.95%
CYP2C19 inhibition + 0.7446 74.46%
CYP2D6 inhibition - 0.8415 84.15%
CYP1A2 inhibition - 0.5815 58.15%
CYP2C8 inhibition + 0.7553 75.53%
CYP inhibitory promiscuity + 0.7125 71.25%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9713 97.13%
Carcinogenicity (trinary) Non-required 0.5443 54.43%
Eye corrosion - 0.9891 98.91%
Eye irritation + 0.5430 54.30%
Skin irritation - 0.7227 72.27%
Skin corrosion - 0.9562 95.62%
Ames mutagenesis - 0.5137 51.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5542 55.42%
Micronuclear + 0.7200 72.00%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation - 0.8193 81.93%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.6495 64.95%
Acute Oral Toxicity (c) III 0.7252 72.52%
Estrogen receptor binding + 0.9447 94.47%
Androgen receptor binding + 0.9084 90.84%
Thyroid receptor binding + 0.7618 76.18%
Glucocorticoid receptor binding + 0.9135 91.35%
Aromatase binding + 0.8087 80.87%
PPAR gamma + 0.8053 80.53%
Honey bee toxicity - 0.8239 82.39%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9704 97.04%

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 98.86% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.50% 85.14%
CHEMBL2581 P07339 Cathepsin D 95.86% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.66% 89.00%
CHEMBL242 Q92731 Estrogen receptor beta 94.88% 98.35%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.80% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.43% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.61% 99.15%
CHEMBL1951 P21397 Monoamine oxidase A 89.83% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.03% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.69% 90.71%
CHEMBL5284 Q96RR4 CaM-kinase kinase beta 86.05% 89.23%
CHEMBL3038469 P24941 CDK2/Cyclin A 85.80% 91.38%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.68% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 84.98% 94.73%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 83.98% 85.11%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 82.72% 93.10%
CHEMBL3194 P02766 Transthyretin 82.33% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.43% 99.23%

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.
Anthotroche myoporoides
Astragalus flexus
Erythrina vogelii
Helenium virginicum
Heliotropium digynum
Hypericum caprifoliatum
Nannoglottis ravida

Cross-Links

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PubChem 101396889
NPASS NPC244727
LOTUS LTS0009604
wikiData Q105008735