3',4'-Dimethoxy-3',4'-desmethylenecubebin

Details

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Internal ID e8e9466c-6db0-41b1-851c-72eab90c3445
Taxonomy Lignans, neolignans and related compounds > Furanoid lignans > Tetrahydrofuran lignans > 9,9-epoxylignans > Dibenzylbutyrolactols
IUPAC Name 3-(1,3-benzodioxol-5-ylmethyl)-4-[(3,4-dimethoxyphenyl)methyl]oxolan-2-ol
SMILES (Canonical) COC1=C(C=C(C=C1)CC2COC(C2CC3=CC4=C(C=C3)OCO4)O)OC
SMILES (Isomeric) COC1=C(C=C(C=C1)CC2COC(C2CC3=CC4=C(C=C3)OCO4)O)OC
InChI InChI=1S/C21H24O6/c1-23-17-5-3-13(9-19(17)24-2)7-15-11-25-21(22)16(15)8-14-4-6-18-20(10-14)27-12-26-18/h3-6,9-10,15-16,21-22H,7-8,11-12H2,1-2H3
InChI Key VHLUROMCVXTWNM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H24O6
Molecular Weight 372.40 g/mol
Exact Mass 372.15728848 g/mol
Topological Polar Surface Area (TPSA) 66.40 Ų
XlogP 3.50
Atomic LogP (AlogP) 2.80
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3',4'-Dimethoxy-3',4'-desmethylenecubebin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9595 95.95%
Caco-2 + 0.7457 74.57%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8065 80.65%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9285 92.85%
OATP1B3 inhibitior + 0.9567 95.67%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.9266 92.66%
P-glycoprotein inhibitior + 0.7234 72.34%
P-glycoprotein substrate - 0.6060 60.60%
CYP3A4 substrate + 0.5694 56.94%
CYP2C9 substrate - 0.8071 80.71%
CYP2D6 substrate - 0.6587 65.87%
CYP3A4 inhibition + 0.9326 93.26%
CYP2C9 inhibition + 0.8557 85.57%
CYP2C19 inhibition + 0.9127 91.27%
CYP2D6 inhibition - 0.5057 50.57%
CYP1A2 inhibition + 0.6535 65.35%
CYP2C8 inhibition + 0.5230 52.30%
CYP inhibitory promiscuity + 0.8668 86.68%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.4585 45.85%
Eye corrosion - 0.9892 98.92%
Eye irritation - 0.9059 90.59%
Skin irritation - 0.7950 79.50%
Skin corrosion - 0.9563 95.63%
Ames mutagenesis + 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8530 85.30%
Micronuclear + 0.5900 59.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.7508 75.08%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.8147 81.47%
Acute Oral Toxicity (c) III 0.5875 58.75%
Estrogen receptor binding + 0.7895 78.95%
Androgen receptor binding + 0.6961 69.61%
Thyroid receptor binding + 0.5351 53.51%
Glucocorticoid receptor binding + 0.5770 57.70%
Aromatase binding - 0.5903 59.03%
PPAR gamma + 0.6107 61.07%
Honey bee toxicity - 0.8438 84.38%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5449 54.49%
Fish aquatic toxicity + 0.9830 98.30%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.57% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.31% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.15% 91.11%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 94.01% 92.62%
CHEMBL2581 P07339 Cathepsin D 93.12% 98.95%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 92.61% 96.77%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.38% 86.33%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 89.67% 94.80%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.99% 95.89%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.87% 85.14%
CHEMBL261 P00915 Carbonic anhydrase I 88.77% 96.76%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.76% 99.17%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.28% 95.89%
CHEMBL4208 P20618 Proteasome component C5 84.60% 90.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 83.83% 89.62%
CHEMBL5555 O00767 Acyl-CoA desaturase 82.90% 97.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.27% 97.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.69% 92.94%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 81.34% 85.49%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.23% 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.
Piper nigrum
Virola venosa

Cross-Links

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PubChem 14137606
LOTUS LTS0044643
wikiData Q105286487