6,7,21-Trihydroxy-17,17,20-trimethyl-8-(3-methylbut-2-enyl)-10,12,18-trioxapentacyclo[11.8.0.03,11.04,9.014,19]henicosa-1(13),3(11),4,6,8,14(19),15,20-octaen-2-one

Details

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Internal ID 179e6ce1-da8d-4f07-abcc-92711cf0587f
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflav-2-enes > Isoflavones
IUPAC Name 6,7,21-trihydroxy-17,17,20-trimethyl-8-(3-methylbut-2-enyl)-10,12,18-trioxapentacyclo[11.8.0.03,11.04,9.014,19]henicosa-1(13),3(11),4,6,8,14(19),15,20-octaen-2-one
SMILES (Canonical) CC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC4=C(C2=O)C5=CC(=C(C(=C5O4)CC=C(C)C)O)O)O
SMILES (Isomeric) CC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC4=C(C2=O)C5=CC(=C(C(=C5O4)CC=C(C)C)O)O)O
InChI InChI=1S/C26H24O7/c1-11(2)6-7-13-20(29)16(27)10-15-17-21(30)18-19(28)12(3)22-14(8-9-26(4,5)33-22)24(18)32-25(17)31-23(13)15/h6,8-10,27-29H,7H2,1-5H3
InChI Key UAZJALAPKMYVEE-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C26H24O7
Molecular Weight 448.50 g/mol
Exact Mass 448.15220310 g/mol
Topological Polar Surface Area (TPSA) 109.00 Ų
XlogP 6.40
Atomic LogP (AlogP) 5.81
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6,7,21-Trihydroxy-17,17,20-trimethyl-8-(3-methylbut-2-enyl)-10,12,18-trioxapentacyclo[11.8.0.03,11.04,9.014,19]henicosa-1(13),3(11),4,6,8,14(19),15,20-octaen-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9701 97.01%
Caco-2 - 0.6921 69.21%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7451 74.51%
OATP2B1 inhibitior - 0.5623 56.23%
OATP1B1 inhibitior + 0.8087 80.87%
OATP1B3 inhibitior + 0.9052 90.52%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.7755 77.55%
P-glycoprotein inhibitior + 0.6122 61.22%
P-glycoprotein substrate + 0.5203 52.03%
CYP3A4 substrate + 0.6167 61.67%
CYP2C9 substrate - 0.6077 60.77%
CYP2D6 substrate - 0.8218 82.18%
CYP3A4 inhibition - 0.8580 85.80%
CYP2C9 inhibition + 0.7464 74.64%
CYP2C19 inhibition + 0.7723 77.23%
CYP2D6 inhibition - 0.8184 81.84%
CYP1A2 inhibition - 0.6077 60.77%
CYP2C8 inhibition + 0.6381 63.81%
CYP inhibitory promiscuity + 0.6378 63.78%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5062 50.62%
Eye corrosion - 0.9912 99.12%
Eye irritation - 0.7335 73.35%
Skin irritation - 0.6679 66.79%
Skin corrosion - 0.9117 91.17%
Ames mutagenesis + 0.5736 57.36%
Human Ether-a-go-go-Related Gene inhibition + 0.6577 65.77%
Micronuclear - 0.5200 52.00%
Hepatotoxicity - 0.5824 58.24%
skin sensitisation - 0.7242 72.42%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.7802 78.02%
Acute Oral Toxicity (c) III 0.4733 47.33%
Estrogen receptor binding + 0.9186 91.86%
Androgen receptor binding + 0.7716 77.16%
Thyroid receptor binding + 0.7061 70.61%
Glucocorticoid receptor binding + 0.8668 86.68%
Aromatase binding + 0.6985 69.85%
PPAR gamma + 0.8777 87.77%
Honey bee toxicity - 0.7749 77.49%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9966 99.66%

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 99.71% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.15% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.14% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 95.14% 94.73%
CHEMBL1951 P21397 Monoamine oxidase A 94.90% 91.49%
CHEMBL2581 P07339 Cathepsin D 92.27% 98.95%
CHEMBL3038469 P24941 CDK2/Cyclin A 91.53% 91.38%
CHEMBL1937 Q92769 Histone deacetylase 2 91.15% 94.75%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 89.40% 89.34%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.71% 94.00%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 87.26% 80.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.05% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.63% 99.15%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.95% 99.23%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 82.21% 85.30%
CHEMBL4581 P52732 Kinesin-like protein 1 81.57% 93.18%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.06% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.71% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.70% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.40% 96.95%

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.
Tadehagi triquetrum

Cross-Links

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PubChem 102216287
LOTUS LTS0227934
wikiData Q105269145