Vogelin F

Details

Top
Internal ID 0e44bd47-2e1b-405c-8868-4c19ef371ae8
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflav-2-enes > Isoflavones
IUPAC Name 5,7-dihydroxy-3-[4-hydroxy-2-methoxy-5-(3-methylbut-2-enyl)phenyl]chromen-4-one
SMILES (Canonical) CC(=CCC1=CC(=C(C=C1O)OC)C2=COC3=CC(=CC(=C3C2=O)O)O)C
SMILES (Isomeric) CC(=CCC1=CC(=C(C=C1O)OC)C2=COC3=CC(=CC(=C3C2=O)O)O)C
InChI InChI=1S/C21H20O6/c1-11(2)4-5-12-6-14(18(26-3)9-16(12)23)15-10-27-19-8-13(22)7-17(24)20(19)21(15)25/h4,6-10,22-24H,5H2,1-3H3
InChI Key TXSJLKKSBFSNIH-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C21H20O6
Molecular Weight 368.40 g/mol
Exact Mass 368.12598835 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.09
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

Top
CHEMBL461270

2D Structure

Top
2D Structure of Vogelin F

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9897 98.97%
Caco-2 + 0.7621 76.21%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7048 70.48%
OATP2B1 inhibitior + 0.5714 57.14%
OATP1B1 inhibitior + 0.9205 92.05%
OATP1B3 inhibitior + 0.8466 84.66%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.7705 77.05%
P-glycoprotein inhibitior + 0.6331 63.31%
P-glycoprotein substrate - 0.7120 71.20%
CYP3A4 substrate + 0.5826 58.26%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8145 81.45%
CYP3A4 inhibition - 0.6395 63.95%
CYP2C9 inhibition + 0.8833 88.33%
CYP2C19 inhibition + 0.9477 94.77%
CYP2D6 inhibition - 0.5417 54.17%
CYP1A2 inhibition + 0.8808 88.08%
CYP2C8 inhibition + 0.5296 52.96%
CYP inhibitory promiscuity + 0.9500 95.00%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6792 67.92%
Eye corrosion - 0.9881 98.81%
Eye irritation + 0.5650 56.50%
Skin irritation - 0.7722 77.22%
Skin corrosion - 0.9507 95.07%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6728 67.28%
Micronuclear + 0.5400 54.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation - 0.8343 83.43%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity + 0.7303 73.03%
Acute Oral Toxicity (c) III 0.6798 67.98%
Estrogen receptor binding + 0.9228 92.28%
Androgen receptor binding + 0.7127 71.27%
Thyroid receptor binding + 0.6588 65.88%
Glucocorticoid receptor binding + 0.9291 92.91%
Aromatase binding + 0.7624 76.24%
PPAR gamma + 0.8077 80.77%
Honey bee toxicity - 0.8121 81.21%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9903 99.03%

Targets

Top

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 99.42% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.75% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.67% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.10% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.70% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.38% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.39% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 87.98% 94.73%
CHEMBL1929 P47989 Xanthine dehydrogenase 87.69% 96.12%
CHEMBL2535 P11166 Glucose transporter 87.67% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.84% 94.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.06% 96.00%
CHEMBL3194 P02766 Transthyretin 84.99% 90.71%
CHEMBL4208 P20618 Proteasome component C5 83.15% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.87% 96.09%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.29% 92.62%
CHEMBL1937 Q92769 Histone deacetylase 2 81.36% 94.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.38% 99.23%

Plants that contains it

Top
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

Top
PubChem 11143123
NPASS NPC299634
LOTUS LTS0108343
wikiData Q105266979