Boletopsin 12

Details

Top
Internal ID 2e523826-2701-4b90-ae9d-d6cc9aa8cd97
Taxonomy Organoheterocyclic compounds > Benzofurans > Phenylbenzofurans
IUPAC Name [1-acetyloxy-3-(4-hydroxyphenyl)-4,7,8-trimethoxydibenzofuran-2-yl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H22O9/c1-12(26)32-23-20(14-6-8-15(28)9-7-14)22(31-5)24-21(25(23)33-13(2)27)16-10-18(29-3)19(30-4)11-17(16)34-24/h6-11,28H,1-5H3
InChI Key UZNUWUQLEBDKTH-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C25H22O9
Molecular Weight 466.40 g/mol
Exact Mass 466.12638228 g/mol
Topological Polar Surface Area (TPSA) 114.00 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.84
H-Bond Acceptor 9
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Boletopsin 12

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9862 98.62%
Caco-2 + 0.6218 62.18%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7583 75.83%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8942 89.42%
OATP1B3 inhibitior + 0.8046 80.46%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.9210 92.10%
P-glycoprotein inhibitior + 0.8913 89.13%
P-glycoprotein substrate - 0.5862 58.62%
CYP3A4 substrate + 0.5786 57.86%
CYP2C9 substrate + 0.6054 60.54%
CYP2D6 substrate - 0.7912 79.12%
CYP3A4 inhibition - 0.7808 78.08%
CYP2C9 inhibition - 0.5243 52.43%
CYP2C19 inhibition - 0.8479 84.79%
CYP2D6 inhibition - 0.9496 94.96%
CYP1A2 inhibition + 0.5922 59.22%
CYP2C8 inhibition + 0.8156 81.56%
CYP inhibitory promiscuity - 0.5362 53.62%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9543 95.43%
Carcinogenicity (trinary) Danger 0.3866 38.66%
Eye corrosion - 0.9885 98.85%
Eye irritation - 0.6491 64.91%
Skin irritation - 0.8124 81.24%
Skin corrosion - 0.9801 98.01%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear + 0.8259 82.59%
Hepatotoxicity - 0.6678 66.78%
skin sensitisation - 0.9207 92.07%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.7700 77.00%
Acute Oral Toxicity (c) II 0.5669 56.69%
Estrogen receptor binding + 0.9190 91.90%
Androgen receptor binding + 0.8778 87.78%
Thyroid receptor binding + 0.6139 61.39%
Glucocorticoid receptor binding + 0.8828 88.28%
Aromatase binding + 0.5978 59.78%
PPAR gamma + 0.7517 75.17%
Honey bee toxicity - 0.7190 71.90%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6304 63.04%
Fish aquatic toxicity + 0.9836 98.36%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.63% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.38% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.14% 89.00%
CHEMBL2581 P07339 Cathepsin D 95.60% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.77% 94.00%
CHEMBL242 Q92731 Estrogen receptor beta 91.48% 98.35%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.54% 99.17%
CHEMBL2535 P11166 Glucose transporter 87.35% 98.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.61% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.34% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.91% 86.33%
CHEMBL340 P08684 Cytochrome P450 3A4 85.23% 91.19%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.19% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.69% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 83.51% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.36% 96.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.78% 97.21%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.65% 95.89%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 80.28% 92.29%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.23% 97.14%

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.
There are no matching plants.

Cross-Links

Top
PubChem 75202403
LOTUS LTS0246582
wikiData Q75052678