6,8-Dihydroxy-17,17-dimethyl-20-(3-methylbut-2-enoxy)-5-(2-methylbut-3-en-2-yl)-3,12,18-trioxapentacyclo[11.8.0.02,11.04,9.014,19]henicosa-1(21),2(11),4(9),5,7,13,15,19-octaen-10-one

Details

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Internal ID 26fabcf8-02af-46c1-9417-ba0cea76a47d
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > 2,2-dimethyl-1-benzopyrans
IUPAC Name 6,8-dihydroxy-17,17-dimethyl-20-(3-methylbut-2-enoxy)-5-(2-methylbut-3-en-2-yl)-3,12,18-trioxapentacyclo[11.8.0.02,11.04,9.014,19]henicosa-1(21),2(11),4(9),5,7,13,15,19-octaen-10-one
SMILES (Canonical) CC(=CCOC1=C2C(=C3C(=C1)C4=C(O3)C(=O)C5=C(O4)C(=C(C=C5O)O)C(C)(C)C=C)C=CC(O2)(C)C)C
SMILES (Isomeric) CC(=CCOC1=C2C(=C3C(=C1)C4=C(O3)C(=O)C5=C(O4)C(=C(C=C5O)O)C(C)(C)C=C)C=CC(O2)(C)C)C
InChI InChI=1S/C30H30O7/c1-8-29(4,5)22-19(32)14-18(31)21-23(33)28-26(36-27(21)22)17-13-20(34-12-10-15(2)3)25-16(24(17)35-28)9-11-30(6,7)37-25/h8-11,13-14,31-32H,1,12H2,2-7H3
InChI Key TVLDODQYCCAAQZ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C30H30O7
Molecular Weight 502.60 g/mol
Exact Mass 502.19915329 g/mol
Topological Polar Surface Area (TPSA) 98.40 Ų
XlogP 7.90
Atomic LogP (AlogP) 7.10
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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BDBM50486899

2D Structure

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2D Structure of 6,8-Dihydroxy-17,17-dimethyl-20-(3-methylbut-2-enoxy)-5-(2-methylbut-3-en-2-yl)-3,12,18-trioxapentacyclo[11.8.0.02,11.04,9.014,19]henicosa-1(21),2(11),4(9),5,7,13,15,19-octaen-10-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9777 97.77%
Caco-2 - 0.7458 74.58%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7389 73.89%
OATP2B1 inhibitior - 0.8570 85.70%
OATP1B1 inhibitior + 0.8922 89.22%
OATP1B3 inhibitior + 0.9088 90.88%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.7901 79.01%
P-glycoprotein inhibitior + 0.8162 81.62%
P-glycoprotein substrate + 0.6139 61.39%
CYP3A4 substrate + 0.6733 67.33%
CYP2C9 substrate - 0.6166 61.66%
CYP2D6 substrate - 0.8418 84.18%
CYP3A4 inhibition - 0.5295 52.95%
CYP2C9 inhibition + 0.6900 69.00%
CYP2C19 inhibition + 0.8214 82.14%
CYP2D6 inhibition - 0.7612 76.12%
CYP1A2 inhibition + 0.7967 79.67%
CYP2C8 inhibition + 0.7031 70.31%
CYP inhibitory promiscuity + 0.8903 89.03%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6845 68.45%
Eye corrosion - 0.9887 98.87%
Eye irritation - 0.7804 78.04%
Skin irritation - 0.7439 74.39%
Skin corrosion - 0.9266 92.66%
Ames mutagenesis + 0.5036 50.36%
Human Ether-a-go-go-Related Gene inhibition - 0.4232 42.32%
Micronuclear - 0.5200 52.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.6464 64.64%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.5792 57.92%
Acute Oral Toxicity (c) III 0.6291 62.91%
Estrogen receptor binding + 0.8673 86.73%
Androgen receptor binding + 0.6641 66.41%
Thyroid receptor binding + 0.7477 74.77%
Glucocorticoid receptor binding + 0.8060 80.60%
Aromatase binding + 0.6873 68.73%
PPAR gamma + 0.7801 78.01%
Honey bee toxicity - 0.7077 70.77%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9948 99.48%

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 99.32% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 98.20% 91.49%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.50% 94.45%
CHEMBL1937 Q92769 Histone deacetylase 2 95.51% 94.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.26% 89.00%
CHEMBL2581 P07339 Cathepsin D 94.43% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 93.03% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.80% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.04% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.89% 95.56%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 89.75% 95.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.95% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.54% 95.89%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.49% 89.34%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.56% 100.00%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 82.43% 91.24%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 81.95% 89.62%
CHEMBL4208 P20618 Proteasome component C5 81.79% 90.00%

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.
Broussonetia papyrifera

Cross-Links

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PubChem 44612850
LOTUS LTS0175375
wikiData Q105265379