(5S,8R)-8-ethyl-5-(4-hydroxy-5,6-dimethyl-2-oxopyran-3-yl)-6-(hydroxymethyl)-2,3,8-trimethyl-5,6-dihydrochromene-4,7-dione

Details

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Internal ID 48443b1b-65c8-453d-a770-7408c51d29a7
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name (5S,8R)-8-ethyl-5-(4-hydroxy-5,6-dimethyl-2-oxopyran-3-yl)-6-(hydroxymethyl)-2,3,8-trimethyl-5,6-dihydrochromene-4,7-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H26O7/c1-7-22(6)19(26)13(8-23)14(15-17(24)9(2)11(4)28-20(15)22)16-18(25)10(3)12(5)29-21(16)27/h13-14,23,25H,7-8H2,1-6H3/t13?,14-,22-/m0/s1
InChI Key BENLGGSSMMCRCK-AZQKXBOTSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C22H26O7
Molecular Weight 402.40 g/mol
Exact Mass 402.16785316 g/mol
Topological Polar Surface Area (TPSA) 110.00 Ų
XlogP 1.70
Atomic LogP (AlogP) 2.52
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (5S,8R)-8-ethyl-5-(4-hydroxy-5,6-dimethyl-2-oxopyran-3-yl)-6-(hydroxymethyl)-2,3,8-trimethyl-5,6-dihydrochromene-4,7-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9446 94.46%
Caco-2 + 0.5857 58.57%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.8026 80.26%
OATP2B1 inhibitior - 0.7159 71.59%
OATP1B1 inhibitior + 0.7772 77.72%
OATP1B3 inhibitior + 0.8541 85.41%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.4496 44.96%
P-glycoprotein inhibitior - 0.6936 69.36%
P-glycoprotein substrate - 0.6943 69.43%
CYP3A4 substrate + 0.5870 58.70%
CYP2C9 substrate + 0.8488 84.88%
CYP2D6 substrate - 0.8660 86.60%
CYP3A4 inhibition - 0.8513 85.13%
CYP2C9 inhibition - 0.5268 52.68%
CYP2C19 inhibition - 0.6653 66.53%
CYP2D6 inhibition - 0.9711 97.11%
CYP1A2 inhibition - 0.6953 69.53%
CYP2C8 inhibition - 0.5880 58.80%
CYP inhibitory promiscuity - 0.7434 74.34%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8913 89.13%
Carcinogenicity (trinary) Non-required 0.6610 66.10%
Eye corrosion - 0.9906 99.06%
Eye irritation - 0.8001 80.01%
Skin irritation - 0.8270 82.70%
Skin corrosion - 0.9608 96.08%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7158 71.58%
Micronuclear - 0.5000 50.00%
Hepatotoxicity - 0.5231 52.31%
skin sensitisation - 0.9040 90.40%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.4714 47.14%
Acute Oral Toxicity (c) III 0.5499 54.99%
Estrogen receptor binding + 0.7556 75.56%
Androgen receptor binding + 0.7492 74.92%
Thyroid receptor binding + 0.5843 58.43%
Glucocorticoid receptor binding + 0.6932 69.32%
Aromatase binding - 0.4835 48.35%
PPAR gamma + 0.6743 67.43%
Honey bee toxicity - 0.9242 92.42%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5044 50.44%
Fish aquatic toxicity + 0.9901 99.01%

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 94.36% 91.11%
CHEMBL2581 P07339 Cathepsin D 89.20% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.82% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.99% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 86.04% 94.75%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.22% 89.34%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.74% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.33% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.33% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.58% 86.33%
CHEMBL5103 Q969S8 Histone deacetylase 10 80.27% 90.08%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 162818707
LOTUS LTS0118833
wikiData Q104933231