[(1S,2R,3R,4R,7S,8Z,10R,12S,13R,14S)-2,12,14-triacetyloxy-3-hydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.03,7]heptadeca-8,16-dien-10-yl] 2-methylpropanoate

Details

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Internal ID 061d702a-6543-46fa-8d5f-9cb7a26a101a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name [(1S,2R,3R,4R,7S,8Z,10R,12S,13R,14S)-2,12,14-triacetyloxy-3-hydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.03,7]heptadeca-8,16-dien-10-yl] 2-methylpropanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H42O11/c1-14(2)27(34)40-21-13-23(38-19(7)32)29(9)22(37-18(6)31)11-10-15(3)25(29)26(39-20(8)33)30(36)17(5)28(35)41-24(30)12-16(21)4/h10,12,14,17,21-26,36H,11,13H2,1-9H3/b16-12-/t17-,21+,22-,23-,24-,25+,26+,29+,30+/m0/s1
InChI Key KMUMKRPZIHFTIZ-NDGXWEOESA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C30H42O11
Molecular Weight 578.60 g/mol
Exact Mass 578.27271215 g/mol
Topological Polar Surface Area (TPSA) 152.00 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.96
H-Bond Acceptor 11
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1S,2R,3R,4R,7S,8Z,10R,12S,13R,14S)-2,12,14-triacetyloxy-3-hydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.03,7]heptadeca-8,16-dien-10-yl] 2-methylpropanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9883 98.83%
Caco-2 - 0.6852 68.52%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7481 74.81%
OATP2B1 inhibitior - 0.8602 86.02%
OATP1B1 inhibitior + 0.8757 87.57%
OATP1B3 inhibitior + 0.8122 81.22%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9579 95.79%
P-glycoprotein inhibitior + 0.8752 87.52%
P-glycoprotein substrate - 0.5845 58.45%
CYP3A4 substrate + 0.6857 68.57%
CYP2C9 substrate - 0.8135 81.35%
CYP2D6 substrate - 0.8794 87.94%
CYP3A4 inhibition - 0.8723 87.23%
CYP2C9 inhibition - 0.9016 90.16%
CYP2C19 inhibition - 0.8648 86.48%
CYP2D6 inhibition - 0.9561 95.61%
CYP1A2 inhibition - 0.7682 76.82%
CYP2C8 inhibition - 0.5802 58.02%
CYP inhibitory promiscuity - 0.9096 90.96%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5072 50.72%
Eye corrosion - 0.9795 97.95%
Eye irritation - 0.8647 86.47%
Skin irritation - 0.5528 55.28%
Skin corrosion - 0.8993 89.93%
Ames mutagenesis - 0.6037 60.37%
Human Ether-a-go-go-Related Gene inhibition - 0.6263 62.63%
Micronuclear - 0.6300 63.00%
Hepatotoxicity + 0.6232 62.32%
skin sensitisation - 0.6242 62.42%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.5105 51.05%
Acute Oral Toxicity (c) III 0.4728 47.28%
Estrogen receptor binding + 0.8045 80.45%
Androgen receptor binding + 0.6637 66.37%
Thyroid receptor binding + 0.5469 54.69%
Glucocorticoid receptor binding + 0.8269 82.69%
Aromatase binding + 0.5799 57.99%
PPAR gamma + 0.7789 77.89%
Honey bee toxicity - 0.6248 62.48%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9697 96.97%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.26% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.06% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.83% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.58% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.81% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.39% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.80% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.72% 89.00%
CHEMBL340 P08684 Cytochrome P450 3A4 89.62% 91.19%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.72% 97.09%
CHEMBL2581 P07339 Cathepsin D 87.76% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.62% 99.23%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 85.66% 85.30%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.68% 94.00%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 83.15% 95.71%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.86% 93.56%
CHEMBL1937 Q92769 Histone deacetylase 2 82.21% 94.75%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.67% 95.50%
CHEMBL3714130 P46095 G-protein coupled receptor 6 81.15% 97.36%
CHEMBL4208 P20618 Proteasome component C5 80.53% 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.
There are no matching plants.

Cross-Links

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PubChem 163104748
LOTUS LTS0256234
wikiData Q105143212