Prenylcandidusin C

Details

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Internal ID 86f1722b-211a-4339-9dee-bbfcd8ebc921
Taxonomy Organoheterocyclic compounds > Benzofurans > Phenylbenzofurans
IUPAC Name 7-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-3,6,9-trimethoxydibenzofuran-2-ol
SMILES (Canonical) CC(=CCC1=C(C=CC(=C1)C2=CC(=C3C4=CC(=C(C=C4OC3=C2OC)OC)O)OC)O)C
SMILES (Isomeric) CC(=CCC1=C(C=CC(=C1)C2=CC(=C3C4=CC(=C(C=C4OC3=C2OC)OC)O)OC)O)C
InChI InChI=1S/C26H26O6/c1-14(2)6-7-16-10-15(8-9-19(16)27)17-12-23(30-4)24-18-11-20(28)22(29-3)13-21(18)32-26(24)25(17)31-5/h6,8-13,27-28H,7H2,1-5H3
InChI Key HWBQSNYBSJLMIS-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C26H26O6
Molecular Weight 434.50 g/mol
Exact Mass 434.17293854 g/mol
Topological Polar Surface Area (TPSA) 81.30 Ų
XlogP 6.40
Atomic LogP (AlogP) 6.20
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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CHEBI:67532
CHEMBL1795463
DTXSID301315811
Q27136001
7-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]-3,6,9-trimethoxydibenzo[b,d]furan-2-ol
1297472-20-8

2D Structure

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2D Structure of Prenylcandidusin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9959 99.59%
Caco-2 + 0.7295 72.95%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.6582 65.82%
OATP2B1 inhibitior - 0.7222 72.22%
OATP1B1 inhibitior + 0.9127 91.27%
OATP1B3 inhibitior + 0.8836 88.36%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9358 93.58%
P-glycoprotein inhibitior + 0.8684 86.84%
P-glycoprotein substrate - 0.5075 50.75%
CYP3A4 substrate + 0.5776 57.76%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4182 41.82%
CYP3A4 inhibition - 0.6078 60.78%
CYP2C9 inhibition + 0.8893 88.93%
CYP2C19 inhibition + 0.9330 93.30%
CYP2D6 inhibition - 0.6434 64.34%
CYP1A2 inhibition + 0.8067 80.67%
CYP2C8 inhibition + 0.7919 79.19%
CYP inhibitory promiscuity + 0.9688 96.88%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4843 48.43%
Eye corrosion - 0.9900 99.00%
Eye irritation - 0.6029 60.29%
Skin irritation - 0.7954 79.54%
Skin corrosion - 0.9463 94.63%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7268 72.68%
Micronuclear + 0.5800 58.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.7800 78.00%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.8683 86.83%
Acute Oral Toxicity (c) III 0.5856 58.56%
Estrogen receptor binding + 0.9503 95.03%
Androgen receptor binding + 0.8233 82.33%
Thyroid receptor binding + 0.7584 75.84%
Glucocorticoid receptor binding + 0.9244 92.44%
Aromatase binding + 0.7537 75.37%
PPAR gamma + 0.7947 79.47%
Honey bee toxicity - 0.7679 76.79%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9944 99.44%

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 99.52% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.55% 98.95%
CHEMBL5747 Q92793 CREB-binding protein 94.83% 95.12%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.10% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.17% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.79% 94.00%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 91.30% 98.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.82% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.21% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.14% 99.15%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.71% 96.00%
CHEMBL3438 Q05513 Protein kinase C zeta 88.96% 88.48%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.74% 92.62%
CHEMBL3401 O75469 Pregnane X receptor 87.03% 94.73%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 85.95% 94.03%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 85.78% 89.62%
CHEMBL3194 P02766 Transthyretin 85.38% 90.71%
CHEMBL3922 P50579 Methionine aminopeptidase 2 85.03% 97.28%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.20% 95.56%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 82.77% 95.17%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 82.39% 83.57%
CHEMBL2535 P11166 Glucose transporter 81.21% 98.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.57% 94.45%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.44% 92.94%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.08% 96.95%

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.
Acrostichum aureum
Anthocleista procera
Crepidiastrum denticulatum subsp. denticulatum
Pseudognaphalium oligandrum
Sideritis hirsuta
Wulfenia orientalis

Cross-Links

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PubChem 53354807
NPASS NPC8127
ChEMBL CHEMBL1795463
LOTUS LTS0054693
wikiData Q27136001