Isodaphneticin

Details

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Internal ID fe63cacb-6d26-4378-9b43-08f876fa5864
Taxonomy Lignans, neolignans and related compounds > Coumarinolignans
IUPAC Name (2S,3S)-3-(4-hydroxy-3-methoxyphenyl)-2-(hydroxymethyl)-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one
SMILES (Canonical) COC1=C(C=CC(=C1)C2C(OC3=C(O2)C=CC4=C3OC(=O)C=C4)CO)O
SMILES (Isomeric) COC1=C(C=CC(=C1)[C@H]2[C@@H](OC3=C(O2)C=CC4=C3OC(=O)C=C4)CO)O
InChI InChI=1S/C19H16O7/c1-23-14-8-11(2-5-12(14)21)17-15(9-20)25-19-13(24-17)6-3-10-4-7-16(22)26-18(10)19/h2-8,15,17,20-21H,9H2,1H3/t15-,17-/m0/s1
InChI Key SPQBUENVXULSQS-RDJZCZTQSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C19H16O7
Molecular Weight 356.30 g/mol
Exact Mass 356.08960285 g/mol
Topological Polar Surface Area (TPSA) 94.40 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.38
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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CHEMBL574038

2D Structure

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2D Structure of Isodaphneticin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9303 93.03%
Caco-2 - 0.5578 55.78%
Blood Brain Barrier - 0.9250 92.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.8096 80.96%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8710 87.10%
OATP1B3 inhibitior + 0.8475 84.75%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.7107 71.07%
P-glycoprotein inhibitior + 0.6473 64.73%
P-glycoprotein substrate - 0.8815 88.15%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.8212 82.12%
CYP2D6 substrate - 0.8135 81.35%
CYP3A4 inhibition - 0.8665 86.65%
CYP2C9 inhibition + 0.5498 54.98%
CYP2C19 inhibition - 0.7163 71.63%
CYP2D6 inhibition - 0.9246 92.46%
CYP1A2 inhibition - 0.8900 89.00%
CYP2C8 inhibition - 0.6022 60.22%
CYP inhibitory promiscuity + 0.5677 56.77%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6441 64.41%
Eye corrosion - 0.9830 98.30%
Eye irritation - 0.7750 77.50%
Skin irritation - 0.8063 80.63%
Skin corrosion - 0.9718 97.18%
Ames mutagenesis - 0.5370 53.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4950 49.50%
Micronuclear + 0.7033 70.33%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.9162 91.62%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.6438 64.38%
Acute Oral Toxicity (c) III 0.7307 73.07%
Estrogen receptor binding + 0.8437 84.37%
Androgen receptor binding + 0.8102 81.02%
Thyroid receptor binding - 0.5892 58.92%
Glucocorticoid receptor binding + 0.8213 82.13%
Aromatase binding - 0.5561 55.61%
PPAR gamma + 0.7858 78.58%
Honey bee toxicity - 0.8153 81.53%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.6838 68.38%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL284 P27487 Dipeptidyl peptidase IV 14130 nM
IC50
PMID: 17417907

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.51% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.42% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.97% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.16% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.58% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.03% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.24% 99.23%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.97% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.46% 94.45%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 86.44% 86.92%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.85% 99.17%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.64% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.49% 86.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.43% 92.62%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.71% 96.95%
CHEMBL3401 O75469 Pregnane X receptor 80.09% 94.73%

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.
Daphne feddei

Cross-Links

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PubChem 45482320
NPASS NPC476347
ChEMBL CHEMBL574038
LOTUS LTS0117134
wikiData Q104401530