Notoptol

Details

Top
Internal ID 6c6fa65b-9327-4333-a047-0a3c7af4da07
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Furanocoumarins > Psoralens
IUPAC Name 4-[(2E,5E)-7-hydroxy-3,7-dimethylocta-2,5-dienoxy]furo[3,2-g]chromen-7-one
SMILES (Canonical) CC(=CCOC1=C2C=CC(=O)OC2=CC3=C1C=CO3)CC=CC(C)(C)O
SMILES (Isomeric) C/C(=C\COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)/C/C=C/C(C)(C)O
InChI InChI=1S/C21H22O5/c1-14(5-4-10-21(2,3)23)8-11-25-20-15-6-7-19(22)26-18(15)13-17-16(20)9-12-24-17/h4,6-10,12-13,23H,5,11H2,1-3H3/b10-4+,14-8+
InChI Key WIEGIEBFVOUTDV-OVXNXNIRSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C21H22O5
Molecular Weight 354.40 g/mol
Exact Mass 354.14672380 g/mol
Topological Polar Surface Area (TPSA) 68.90 Ų
XlogP 4.10
Atomic LogP (AlogP) 4.58
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

Top
88206-49-9
AKOS040763474

2D Structure

Top
2D Structure of Notoptol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9826 98.26%
Caco-2 + 0.5547 55.47%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7807 78.07%
OATP2B1 inhibitior - 0.7198 71.98%
OATP1B1 inhibitior + 0.8772 87.72%
OATP1B3 inhibitior + 0.8352 83.52%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9717 97.17%
P-glycoprotein inhibitior + 0.7074 70.74%
P-glycoprotein substrate - 0.7497 74.97%
CYP3A4 substrate + 0.5757 57.57%
CYP2C9 substrate - 0.6340 63.40%
CYP2D6 substrate - 0.8186 81.86%
CYP3A4 inhibition + 0.6368 63.68%
CYP2C9 inhibition + 0.7758 77.58%
CYP2C19 inhibition + 0.7588 75.88%
CYP2D6 inhibition - 0.6654 66.54%
CYP1A2 inhibition + 0.7233 72.33%
CYP2C8 inhibition + 0.5575 55.75%
CYP inhibitory promiscuity + 0.7369 73.69%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5224 52.24%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.9190 91.90%
Skin irritation - 0.7261 72.61%
Skin corrosion - 0.9542 95.42%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8660 86.60%
Micronuclear - 0.6400 64.00%
Hepatotoxicity + 0.8000 80.00%
skin sensitisation - 0.7316 73.16%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.8746 87.46%
Acute Oral Toxicity (c) III 0.4022 40.22%
Estrogen receptor binding + 0.9156 91.56%
Androgen receptor binding + 0.7998 79.98%
Thyroid receptor binding + 0.6378 63.78%
Glucocorticoid receptor binding + 0.8101 81.01%
Aromatase binding + 0.7203 72.03%
PPAR gamma + 0.8467 84.67%
Honey bee toxicity - 0.8112 81.12%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 1.0000 100.00%

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 98.25% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 95.24% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.47% 89.00%
CHEMBL2581 P07339 Cathepsin D 94.27% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 92.24% 91.49%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.13% 99.17%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 90.33% 94.03%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.03% 95.56%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 87.35% 89.34%
CHEMBL1937 Q92769 Histone deacetylase 2 86.22% 94.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.33% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.92% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.72% 85.14%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.63% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.27% 86.33%

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.
Hansenia forbesii
Hansenia weberbaueriana
Tetradium daniellii

Cross-Links

Top
PubChem 5320228
NPASS NPC67936
LOTUS LTS0073060
wikiData Q105306173