(3aR,4R,9R,9aR)-4,6,7-trihydroxy-9-(3,4,5-trimethoxyphenyl)-3a,4,9,9a-tetrahydro-3H-benzo[f]isobenzofuran-1-one

Details

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Internal ID 8727e5af-611c-43c1-bd18-f0e12021281b
Taxonomy Lignans, neolignans and related compounds > Lignan lactones
IUPAC Name (3aR,4R,9R,9aR)-4,6,7-trihydroxy-9-(3,4,5-trimethoxyphenyl)-3a,4,9,9a-tetrahydro-3H-benzo[f][2]benzofuran-1-one
SMILES (Canonical) COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC(=C(C=C24)O)O)O
SMILES (Isomeric) COC1=CC(=CC(=C1OC)OC)[C@H]2[C@@H]3[C@H](COC3=O)[C@H](C4=CC(=C(C=C24)O)O)O
InChI InChI=1S/C21H22O8/c1-26-15-4-9(5-16(27-2)20(15)28-3)17-10-6-13(22)14(23)7-11(10)19(24)12-8-29-21(25)18(12)17/h4-7,12,17-19,22-24H,8H2,1-3H3/t12-,17+,18-,19-/m0/s1
InChI Key AIEQNTGIFXFNRB-BTINSWFASA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C21H22O8
Molecular Weight 402.40 g/mol
Exact Mass 402.13146766 g/mol
Topological Polar Surface Area (TPSA) 115.00 Ų
XlogP 1.50
Atomic LogP (AlogP) 2.09
H-Bond Acceptor 8
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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SCHEMBL14214781
3',4'-Demethylene-Podophyllotoxin
(3aR,4R,9R,9aR)-4,6,7-trihydroxy-9-(3,4,5-trimethoxyphenyl)-3a,4,9,9a-tetrahydro-3H-benzo[f]isobenzofuran-1-one
4beta,6,7-Trihydroxy-9beta-(3,4,5-trimethoxyphenyl)-3abeta,4,9,9aalpha-tetrahydronaphtho[2,3-c]furan-1(3H)-one
Naphtho[2,3-c]furan-1(3H)-one, 3a,4,9,9a-tetrahydro-4,6,7-trihydroxy-9-(3,4,5-trimethoxyphenyl)-, (3aR,4R,9R,9aR)-

2D Structure

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2D Structure of (3aR,4R,9R,9aR)-4,6,7-trihydroxy-9-(3,4,5-trimethoxyphenyl)-3a,4,9,9a-tetrahydro-3H-benzo[f]isobenzofuran-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9756 97.56%
Caco-2 + 0.4947 49.47%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.8066 80.66%
OATP2B1 inhibitior - 0.8640 86.40%
OATP1B1 inhibitior + 0.8161 81.61%
OATP1B3 inhibitior + 0.8349 83.49%
MATE1 inhibitior - 0.6600 66.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.4510 45.10%
P-glycoprotein inhibitior - 0.6214 62.14%
P-glycoprotein substrate - 0.8770 87.70%
CYP3A4 substrate + 0.5811 58.11%
CYP2C9 substrate - 0.6043 60.43%
CYP2D6 substrate - 0.7454 74.54%
CYP3A4 inhibition - 0.7237 72.37%
CYP2C9 inhibition + 0.5988 59.88%
CYP2C19 inhibition - 0.5309 53.09%
CYP2D6 inhibition - 0.9495 94.95%
CYP1A2 inhibition - 0.5502 55.02%
CYP2C8 inhibition - 0.6209 62.09%
CYP inhibitory promiscuity + 0.5148 51.48%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5374 53.74%
Eye corrosion - 0.9888 98.88%
Eye irritation - 0.8237 82.37%
Skin irritation - 0.8171 81.71%
Skin corrosion - 0.9685 96.85%
Ames mutagenesis - 0.7737 77.37%
Human Ether-a-go-go-Related Gene inhibition - 0.6490 64.90%
Micronuclear + 0.8074 80.74%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.8884 88.84%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.6590 65.90%
Acute Oral Toxicity (c) III 0.5725 57.25%
Estrogen receptor binding + 0.8020 80.20%
Androgen receptor binding + 0.8290 82.90%
Thyroid receptor binding + 0.7787 77.87%
Glucocorticoid receptor binding + 0.8722 87.22%
Aromatase binding - 0.7870 78.70%
PPAR gamma + 0.5391 53.91%
Honey bee toxicity - 0.7030 70.30%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9790 97.90%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.90% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.96% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.31% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.76% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.85% 95.56%
CHEMBL4040 P28482 MAP kinase ERK2 91.38% 83.82%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.83% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.06% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.04% 94.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.79% 97.09%
CHEMBL2581 P07339 Cathepsin D 84.66% 98.95%
CHEMBL213 P08588 Beta-1 adrenergic receptor 83.80% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.45% 99.17%
CHEMBL2535 P11166 Glucose transporter 83.41% 98.75%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.29% 92.62%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.35% 97.14%

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.
Dimorphotheca sinuata
Heptapleurum capitatum
Podophyllum hexandrum
Roldana mexicana

Cross-Links

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PubChem 3010625
NPASS NPC178574
LOTUS LTS0156960
wikiData Q104912689