Loxodin

Details

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Internal ID 0fdb127d-0cdb-4288-911d-985cba77e063
Taxonomy Phenylpropanoids and polyketides > Depsides and depsidones
IUPAC Name methyl 3,9-dihydroxy-6-oxo-7-pentanoyl-1-pentylbenzo[b][1,4]benzodioxepine-2-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H28O8/c1-4-6-8-9-15-21(24(29)31-3)18(28)13-20-23(15)32-19-12-14(26)11-16(17(27)10-7-5-2)22(19)25(30)33-20/h11-13,26,28H,4-10H2,1-3H3
InChI Key KDGYIQJGCXRCIL-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C25H28O8
Molecular Weight 456.50 g/mol
Exact Mass 456.17841785 g/mol
Topological Polar Surface Area (TPSA) 119.00 Ų
XlogP 6.10
Atomic LogP (AlogP) 5.31
H-Bond Acceptor 8
H-Bond Donor 2
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Loxodin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9060 90.60%
Caco-2 - 0.5982 59.82%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.6905 69.05%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior - 0.5640 56.40%
OATP1B3 inhibitior - 0.5455 54.55%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.5601 56.01%
P-glycoprotein inhibitior + 0.5841 58.41%
P-glycoprotein substrate - 0.5698 56.98%
CYP3A4 substrate + 0.6470 64.70%
CYP2C9 substrate + 0.8166 81.66%
CYP2D6 substrate - 0.8654 86.54%
CYP3A4 inhibition - 0.8430 84.30%
CYP2C9 inhibition - 0.8057 80.57%
CYP2C19 inhibition - 0.7263 72.63%
CYP2D6 inhibition - 0.9073 90.73%
CYP1A2 inhibition - 0.5898 58.98%
CYP2C8 inhibition + 0.8611 86.11%
CYP inhibitory promiscuity - 0.8271 82.71%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6452 64.52%
Eye corrosion - 0.9912 99.12%
Eye irritation - 0.5934 59.34%
Skin irritation - 0.7865 78.65%
Skin corrosion - 0.9315 93.15%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4054 40.54%
Micronuclear - 0.7800 78.00%
Hepatotoxicity - 0.6010 60.10%
skin sensitisation - 0.9005 90.05%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.7825 78.25%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity + 0.5811 58.11%
Acute Oral Toxicity (c) III 0.4248 42.48%
Estrogen receptor binding + 0.6798 67.98%
Androgen receptor binding + 0.6163 61.63%
Thyroid receptor binding - 0.6621 66.21%
Glucocorticoid receptor binding + 0.7716 77.16%
Aromatase binding - 0.4843 48.43%
PPAR gamma + 0.7193 71.93%
Honey bee toxicity - 0.8814 88.14%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5750 57.50%
Fish aquatic toxicity + 0.9934 99.34%

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
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 99.65% 95.17%
CHEMBL2581 P07339 Cathepsin D 98.56% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.31% 91.11%
CHEMBL230 P35354 Cyclooxygenase-2 97.58% 89.63%
CHEMBL240 Q12809 HERG 96.96% 89.76%
CHEMBL3401 O75469 Pregnane X receptor 94.05% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.43% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.56% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.88% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.73% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.37% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.33% 95.56%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 84.73% 94.80%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 84.16% 82.38%
CHEMBL2535 P11166 Glucose transporter 83.42% 98.75%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.16% 93.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.47% 92.62%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 80.30% 92.67%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 101974134
LOTUS LTS0100343
wikiData Q77374388