5,7-dimethoxy-8-[(2R,3R,5S,6S)-2,3,5-trihydroxy-6-(3-hydroxy-2,2,3-trimethylbutoxy)-7-(7-methoxy-2-oxochromen-8-yl)-3,5-dimethylheptyl]chromen-2-one

Details

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Internal ID 90f8d651-fe32-46dd-9c5f-1c4ea4a95334
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 5,7-dimethoxy-8-[(2R,3R,5S,6S)-2,3,5-trihydroxy-6-(3-hydroxy-2,2,3-trimethylbutoxy)-7-(7-methoxy-2-oxochromen-8-yl)-3,5-dimethylheptyl]chromen-2-one
SMILES (Canonical) CC(C)(COC(CC1=C(C=CC2=C1OC(=O)C=C2)OC)C(C)(CC(C)(C(CC3=C(C=C(C4=C3OC(=O)C=C4)OC)OC)O)O)O)C(C)(C)O
SMILES (Isomeric) C[C@@](C[C@@](C)([C@H](CC1=C(C=CC2=C1OC(=O)C=C2)OC)OCC(C)(C)C(C)(C)O)O)([C@@H](CC3=C(C=C(C4=C3OC(=O)C=C4)OC)OC)O)O
InChI InChI=1S/C37H48O12/c1-34(2,35(3,4)41)20-47-29(17-24-25(44-7)13-10-21-11-14-30(39)48-32(21)24)37(6,43)19-36(5,42)28(38)16-23-27(46-9)18-26(45-8)22-12-15-31(40)49-33(22)23/h10-15,18,28-29,38,41-43H,16-17,19-20H2,1-9H3/t28-,29+,36-,37+/m1/s1
InChI Key YZLBEVMSWOPZDJ-DQBLALCNSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C37H48O12
Molecular Weight 684.80 g/mol
Exact Mass 684.31457696 g/mol
Topological Polar Surface Area (TPSA) 170.00 Ų
XlogP 3.90
Atomic LogP (AlogP) 4.15
H-Bond Acceptor 12
H-Bond Donor 4
Rotatable Bonds 15

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5,7-dimethoxy-8-[(2R,3R,5S,6S)-2,3,5-trihydroxy-6-(3-hydroxy-2,2,3-trimethylbutoxy)-7-(7-methoxy-2-oxochromen-8-yl)-3,5-dimethylheptyl]chromen-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 + 0.7772 77.72%
Caco-2 - 0.8201 82.01%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.6516 65.16%
OATP2B1 inhibitior + 0.5678 56.78%
OATP1B1 inhibitior + 0.8843 88.43%
OATP1B3 inhibitior + 0.8744 87.44%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9884 98.84%
P-glycoprotein inhibitior + 0.7923 79.23%
P-glycoprotein substrate + 0.5730 57.30%
CYP3A4 substrate + 0.6099 60.99%
CYP2C9 substrate - 0.8153 81.53%
CYP2D6 substrate - 0.8173 81.73%
CYP3A4 inhibition - 0.7442 74.42%
CYP2C9 inhibition - 0.9091 90.91%
CYP2C19 inhibition - 0.9084 90.84%
CYP2D6 inhibition - 0.9347 93.47%
CYP1A2 inhibition - 0.6172 61.72%
CYP2C8 inhibition + 0.7188 71.88%
CYP inhibitory promiscuity - 0.9717 97.17%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6887 68.87%
Eye corrosion - 0.9909 99.09%
Eye irritation - 0.9102 91.02%
Skin irritation - 0.8097 80.97%
Skin corrosion - 0.9531 95.31%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8805 88.05%
Micronuclear - 0.6300 63.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.9071 90.71%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.7736 77.36%
Acute Oral Toxicity (c) III 0.5301 53.01%
Estrogen receptor binding + 0.7844 78.44%
Androgen receptor binding + 0.7926 79.26%
Thyroid receptor binding + 0.6305 63.05%
Glucocorticoid receptor binding + 0.8085 80.85%
Aromatase binding + 0.7002 70.02%
PPAR gamma + 0.7134 71.34%
Honey bee toxicity - 0.7483 74.83%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9906 99.06%

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
CHEMBL2581 P07339 Cathepsin D 97.35% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.28% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.78% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.26% 94.00%
CHEMBL2535 P11166 Glucose transporter 91.76% 98.75%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 90.73% 89.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.88% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 87.52% 94.73%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 87.19% 96.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.89% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.22% 89.00%
CHEMBL1255126 O15151 Protein Mdm4 85.07% 90.20%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.58% 92.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.05% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.60% 96.09%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.98% 97.21%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.84% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.30% 99.23%
CHEMBL4581 P52732 Kinesin-like protein 1 80.13% 93.18%

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.
Triphasia trifolia

Cross-Links

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PubChem 163188658
LOTUS LTS0053473
wikiData Q105369303