Toddalolactone 3'-O-methyl ether

Details

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Internal ID 807eba22-7d8d-4902-941c-a71a6ab1e58f
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 6-(2-hydroxy-3-methoxy-3-methylbutyl)-5,7-dimethoxychromen-2-one
SMILES (Canonical) CC(C)(C(CC1=C(C=C2C(=C1OC)C=CC(=O)O2)OC)O)OC
SMILES (Isomeric) CC(C)(C(CC1=C(C=C2C(=C1OC)C=CC(=O)O2)OC)O)OC
InChI InChI=1S/C17H22O6/c1-17(2,22-5)14(18)8-11-12(20-3)9-13-10(16(11)21-4)6-7-15(19)23-13/h6-7,9,14,18H,8H2,1-5H3
InChI Key OWHTXFVUUCBRRM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H22O6
Molecular Weight 322.40 g/mol
Exact Mass 322.14163842 g/mol
Topological Polar Surface Area (TPSA) 74.20 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.14
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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143614-35-1

2D Structure

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2D Structure of Toddalolactone 3'-O-methyl ether

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9806 98.06%
Caco-2 + 0.8663 86.63%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.6019 60.19%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8925 89.25%
OATP1B3 inhibitior + 0.9193 91.93%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.4766 47.66%
P-glycoprotein inhibitior - 0.7072 70.72%
P-glycoprotein substrate - 0.6012 60.12%
CYP3A4 substrate + 0.5282 52.82%
CYP2C9 substrate - 0.6435 64.35%
CYP2D6 substrate - 0.7811 78.11%
CYP3A4 inhibition - 0.8768 87.68%
CYP2C9 inhibition - 0.9234 92.34%
CYP2C19 inhibition - 0.8643 86.43%
CYP2D6 inhibition - 0.8900 89.00%
CYP1A2 inhibition - 0.5659 56.59%
CYP2C8 inhibition - 0.5710 57.10%
CYP inhibitory promiscuity - 0.9090 90.90%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6408 64.08%
Eye corrosion - 0.9892 98.92%
Eye irritation - 0.7155 71.55%
Skin irritation - 0.7500 75.00%
Skin corrosion - 0.9621 96.21%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6429 64.29%
Micronuclear - 0.6300 63.00%
Hepatotoxicity - 0.5569 55.69%
skin sensitisation - 0.8601 86.01%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.9236 92.36%
Acute Oral Toxicity (c) III 0.6180 61.80%
Estrogen receptor binding + 0.8107 81.07%
Androgen receptor binding + 0.6244 62.44%
Thyroid receptor binding + 0.6247 62.47%
Glucocorticoid receptor binding + 0.7658 76.58%
Aromatase binding + 0.5670 56.70%
PPAR gamma + 0.8676 86.76%
Honey bee toxicity - 0.8005 80.05%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9173 91.73%

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
CHEMBL2581 P07339 Cathepsin D 97.28% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.05% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.68% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.68% 94.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 91.00% 89.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.65% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.35% 85.14%
CHEMBL2535 P11166 Glucose transporter 89.68% 98.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.71% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.58% 99.17%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 86.77% 94.03%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.12% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.15% 93.99%
CHEMBL3401 O75469 Pregnane X receptor 84.15% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.22% 96.09%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.66% 97.14%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.24% 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.
Toddalia asiatica

Cross-Links

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PubChem 15071016
LOTUS LTS0078863
wikiData Q105202024