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5-hydroxy-4-(hydroxymethyl)-8,8,11a-trimethyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6,7,7a,9,10,11-hexahydro-1H-naphtho[1,2-e][2]benzofuran-3-one

Table of Contents

Details
Physical and Chemical Properties
Synonyms
2D Structure
3D Structure
ADMET Properties
Targets (proven and/or predicted)
Plants that contains it
Cross-Links

Details

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Internal ID bab789f9-7a8f-4e77-9659-e9b6c0619374
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name 5-hydroxy-4-(hydroxymethyl)-8,8,11a-trimethyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6,7,7a,9,10,11-hexahydro-1H-naphtho[1,2-e][2]benzofuran-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H36O10/c1-25(2)7-4-8-26(3)14(25)6-5-11-17(26)16-15(12(9-27)18(11)29)22(33)35-23(16)36-24-21(32)20(31)19(30)13(10-28)34-24/h13-14,19-21,23-24,27-32H,4-10H2,1-3H3
InChI Key OHUWCLPFQBDELY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C26H36O10
Molecular Weight 508.60 g/mol
Exact Mass 508.23084734 g/mol
Topological Polar Surface Area (TPSA) 166.00 Ų
XlogP 2.50
Atomic LogP (AlogP) 0.90
H-Bond Acceptor 10
H-Bond Donor 6
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-hydroxy-4-(hydroxymethyl)-8,8,11a-trimethyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6,7,7a,9,10,11-hexahydro-1H-naphtho[1,2-e][2]benzofuran-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7767 77.67%
Caco-2 - 0.8121 81.21%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.8332 83.32%
OATP2B1 inhibitior - 0.7182 71.82%
OATP1B1 inhibitior + 0.8010 80.10%
OATP1B3 inhibitior + 0.8808 88.08%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.4669 46.69%
P-glycoprotein inhibitior - 0.5539 55.39%
P-glycoprotein substrate - 0.7169 71.69%
CYP3A4 substrate + 0.7030 70.30%
CYP2C9 substrate - 0.6043 60.43%
CYP2D6 substrate - 0.8620 86.20%
CYP3A4 inhibition - 0.8805 88.05%
CYP2C9 inhibition - 0.8375 83.75%
CYP2C19 inhibition - 0.8086 80.86%
CYP2D6 inhibition - 0.9307 93.07%
CYP1A2 inhibition - 0.7632 76.32%
CYP2C8 inhibition + 0.5841 58.41%
CYP inhibitory promiscuity - 0.8772 87.72%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6245 62.45%
Eye corrosion - 0.9917 99.17%
Eye irritation - 0.9094 90.94%
Skin irritation - 0.7648 76.48%
Skin corrosion - 0.9527 95.27%
Ames mutagenesis - 0.5418 54.18%
Human Ether-a-go-go-Related Gene inhibition - 0.4642 46.42%
Micronuclear - 0.8300 83.00%
Hepatotoxicity - 0.7226 72.26%
skin sensitisation - 0.9291 92.91%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.8153 81.53%
Acute Oral Toxicity (c) III 0.4353 43.53%
Estrogen receptor binding + 0.7336 73.36%
Androgen receptor binding + 0.6404 64.04%
Thyroid receptor binding - 0.5911 59.11%
Glucocorticoid receptor binding + 0.7687 76.87%
Aromatase binding + 0.7767 77.67%
PPAR gamma + 0.6617 66.17%
Honey bee toxicity - 0.7933 79.33%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9778 97.78%

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 99.16% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.71% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.86% 97.09%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 94.29% 86.92%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.03% 94.45%
CHEMBL220 P22303 Acetylcholinesterase 93.72% 94.45%
CHEMBL1937 Q92769 Histone deacetylase 2 92.21% 94.75%
CHEMBL237 P41145 Kappa opioid receptor 92.20% 98.10%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 91.21% 96.38%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.95% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.70% 89.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.53% 95.89%
CHEMBL233 P35372 Mu opioid receptor 88.65% 97.93%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.57% 99.23%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.44% 97.25%
CHEMBL226 P30542 Adenosine A1 receptor 88.06% 95.93%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.06% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.77% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.99% 96.09%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 85.69% 95.64%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.07% 94.00%
CHEMBL5103 Q969S8 Histone deacetylase 10 83.94% 90.08%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.64% 93.99%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 82.60% 96.21%
CHEMBL5555 O00767 Acyl-CoA desaturase 82.23% 97.50%
CHEMBL5255 O00206 Toll-like receptor 4 82.13% 92.50%
CHEMBL2083 P15090 Fatty acid binding protein adipocyte 81.10% 95.71%

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.
Betonica officinalis

Cross-Links

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PubChem 85163941
LOTUS LTS0088936
wikiData Q105192309