Dehydropodophyllotoxin

Details

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Internal ID c06dc795-1d21-4539-bc13-61a0a34a4793
Taxonomy Lignans, neolignans and related compounds > Arylnaphthalene lignans
IUPAC Name 5-hydroxy-9-(3,4,5-trimethoxyphenyl)-6H-[2]benzofuro[5,6-f][1,3]benzodioxol-8-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H18O8/c1-25-16-4-10(5-17(26-2)21(16)27-3)18-11-6-14-15(30-9-29-14)7-12(11)20(23)13-8-28-22(24)19(13)18/h4-7,23H,8-9H2,1-3H3
InChI Key HSSDVCMYTACNSM-UHFFFAOYSA-N
Popularity 34 references in papers

Physical and Chemical Properties

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Molecular Formula C22H18O8
Molecular Weight 410.40 g/mol
Exact Mass 410.10016753 g/mol
Topological Polar Surface Area (TPSA) 92.70 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.64
H-Bond Acceptor 8
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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42123-27-3
5-hydroxy-9-(3,4,5-trimethoxyphenyl)-6H-[2]benzofuro[5,6-f][1,3]benzodioxol-8-one
5-hydroxy-9-(3,4,5-trimethoxyphenyl)-6H-(2)benzofuro(5,6-f)(1,3)benzodioxol-8-one
RefChem:131552
Tetradehydropodophyllotoxin
Podophyllotoxin Impurity N2
CHEMBL487214
orb1297160
HY-N2502
MFCD22586530
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Dehydropodophyllotoxin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9873 98.73%
Caco-2 + 0.7954 79.54%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7743 77.43%
OATP2B1 inhibitior - 0.8697 86.97%
OATP1B1 inhibitior + 0.9322 93.22%
OATP1B3 inhibitior + 0.9603 96.03%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.8787 87.87%
P-glycoprotein inhibitior - 0.4297 42.97%
P-glycoprotein substrate - 0.8963 89.63%
CYP3A4 substrate + 0.5674 56.74%
CYP2C9 substrate - 0.8012 80.12%
CYP2D6 substrate - 0.8332 83.32%
CYP3A4 inhibition + 0.7959 79.59%
CYP2C9 inhibition + 0.8948 89.48%
CYP2C19 inhibition + 0.8994 89.94%
CYP2D6 inhibition - 0.9231 92.31%
CYP1A2 inhibition - 0.9046 90.46%
CYP2C8 inhibition + 0.5411 54.11%
CYP inhibitory promiscuity + 0.7468 74.68%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.4302 43.02%
Eye corrosion - 0.9886 98.86%
Eye irritation - 0.6481 64.81%
Skin irritation - 0.8127 81.27%
Skin corrosion - 0.9705 97.05%
Ames mutagenesis + 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear + 0.8674 86.74%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation - 0.7800 78.00%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.4533 45.33%
Acute Oral Toxicity (c) III 0.5663 56.63%
Estrogen receptor binding + 0.9148 91.48%
Androgen receptor binding + 0.5719 57.19%
Thyroid receptor binding + 0.7532 75.32%
Glucocorticoid receptor binding + 0.9008 90.08%
Aromatase binding - 0.4891 48.91%
PPAR gamma + 0.7399 73.99%
Honey bee toxicity - 0.8367 83.67%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5749 57.49%
Fish aquatic toxicity + 0.9578 95.78%

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 99.22% 91.11%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 97.05% 98.21%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 96.64% 96.77%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.02% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.66% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.56% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.42% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.49% 85.14%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 91.06% 92.62%
CHEMBL2581 P07339 Cathepsin D 89.61% 98.95%
CHEMBL4302 P08183 P-glycoprotein 1 87.67% 92.98%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.65% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.84% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.42% 99.17%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 84.99% 94.80%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 84.77% 80.96%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.18% 99.23%
CHEMBL2717 Q9HCR9 Phosphodiesterase 11A 81.88% 85.00%
CHEMBL1951 P21397 Monoamine oxidase A 81.42% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 80.35% 94.73%

Plants that contains it

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Cross-Links

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PubChem 5316463
NPASS NPC174734
ChEMBL CHEMBL487214
LOTUS LTS0173342
wikiData Q104397704