4'-Demethyldehydropodophyllotoxin

Details

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Internal ID 929597e3-de25-4872-b7d4-772270e5e4fa
Taxonomy Lignans, neolignans and related compounds > Arylnaphthalene lignans
IUPAC Name 5-hydroxy-9-(4-hydroxy-3,5-dimethoxyphenyl)-6H-[2]benzofuro[5,6-f][1,3]benzodioxol-8-one
SMILES (Canonical) COC1=CC(=CC(=C1O)OC)C2=C3C(=C(C4=CC5=C(C=C42)OCO5)O)COC3=O
SMILES (Isomeric) COC1=CC(=CC(=C1O)OC)C2=C3C(=C(C4=CC5=C(C=C42)OCO5)O)COC3=O
InChI InChI=1S/C21H16O8/c1-25-15-3-9(4-16(26-2)20(15)23)17-10-5-13-14(29-8-28-13)6-11(10)19(22)12-7-27-21(24)18(12)17/h3-6,22-23H,7-8H2,1-2H3
InChI Key BBMUNWUDCBRTKC-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H16O8
Molecular Weight 396.30 g/mol
Exact Mass 396.08451746 g/mol
Topological Polar Surface Area (TPSA) 104.00 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.33
H-Bond Acceptor 8
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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117669-31-5
4 inverted exclamation mark -Demethyldehydropodophyllotoxin
5-hydroxy-9-(4-hydroxy-3,5-dimethoxyphenyl)-6H-[2]benzofuro[5,6-f][1,3]benzodioxol-8-one
CHEMBL521394
4-Demethyl-Dehydropodophyllotoxin
HY-N9318
CS-0159381
9-Hydroxy-5-(4-hydroxy-3,5-dimethoxyphenyl)furo[3',4':6,7]naphtho[2,3-d][1,3]dioxol-6(8H)-one

2D Structure

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2D Structure of 4'-Demethyldehydropodophyllotoxin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9809 98.09%
Caco-2 + 0.6162 61.62%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8045 80.45%
OATP2B1 inhibitior - 0.8620 86.20%
OATP1B1 inhibitior + 0.9078 90.78%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.8701 87.01%
P-glycoprotein inhibitior - 0.6220 62.20%
P-glycoprotein substrate - 0.8698 86.98%
CYP3A4 substrate + 0.5418 54.18%
CYP2C9 substrate - 0.8012 80.12%
CYP2D6 substrate - 0.8332 83.32%
CYP3A4 inhibition + 0.7959 79.59%
CYP2C9 inhibition + 0.9233 92.33%
CYP2C19 inhibition + 0.9051 90.51%
CYP2D6 inhibition - 0.7512 75.12%
CYP1A2 inhibition - 0.8690 86.90%
CYP2C8 inhibition - 0.6182 61.82%
CYP inhibitory promiscuity + 0.8147 81.47%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.4699 46.99%
Eye corrosion - 0.9887 98.87%
Eye irritation - 0.5087 50.87%
Skin irritation - 0.7982 79.82%
Skin corrosion - 0.9593 95.93%
Ames mutagenesis + 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6236 62.36%
Micronuclear + 0.8874 88.74%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation - 0.7824 78.24%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.5442 54.42%
Acute Oral Toxicity (c) III 0.7055 70.55%
Estrogen receptor binding + 0.9253 92.53%
Androgen receptor binding + 0.5983 59.83%
Thyroid receptor binding + 0.7170 71.70%
Glucocorticoid receptor binding + 0.9180 91.80%
Aromatase binding + 0.5295 52.95%
PPAR gamma + 0.7493 74.93%
Honey bee toxicity - 0.8671 86.71%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5549 55.49%
Fish aquatic toxicity + 0.9583 95.83%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.31% 91.11%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 97.47% 98.21%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 96.07% 96.77%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.02% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.44% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.45% 86.33%
CHEMBL2581 P07339 Cathepsin D 93.19% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.29% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.17% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 91.08% 91.49%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 90.04% 92.62%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.25% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.09% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.60% 99.23%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 83.55% 94.80%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.25% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.78% 99.17%
CHEMBL2717 Q9HCR9 Phosphodiesterase 11A 81.49% 85.00%
CHEMBL3401 O75469 Pregnane X receptor 81.13% 94.73%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 80.85% 80.96%

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.
Campsis grandiflora
Chrysosplenium tetrandrum
Dimorphotheca sinuata
Galega officinalis
Heptapleurum capitatum
Podophyllum hexandrum
Podophyllum pleianthum
Podophyllum versipelle
Roldana mexicana
Tacca plantaginea

Cross-Links

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PubChem 15232507
NPASS NPC117911
LOTUS LTS0068677
wikiData Q104888480