(1S,9S,10S)-3,4-dimethoxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6,13-tetraene-8,12,15-trione

Details

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Internal ID 3c3ce83d-31d3-4ea6-bfc9-adb22ce60c83
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name (1S,9S,10S)-3,4-dimethoxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6,13-tetraene-8,12,15-trione
SMILES (Canonical) CC(C)C1=C(C(=C2C(=C1)C(=O)C3C4C2(C=CC(=O)C4(C)C)C(=O)O3)OC)OC
SMILES (Isomeric) CC(C)C1=C(C(=C2C(=C1)C(=O)[C@@H]3[C@@H]4[C@]2(C=CC(=O)C4(C)C)C(=O)O3)OC)OC
InChI InChI=1S/C22H24O6/c1-10(2)11-9-12-14(17(27-6)16(11)26-5)22-8-7-13(23)21(3,4)19(22)18(15(12)24)28-20(22)25/h7-10,18-19H,1-6H3/t18-,19+,22-/m1/s1
InChI Key DCGPWGGQZOPSKB-XQBPLPMBSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H24O6
Molecular Weight 384.40 g/mol
Exact Mass 384.15728848 g/mol
Topological Polar Surface Area (TPSA) 78.90 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.97
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,9S,10S)-3,4-dimethoxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6,13-tetraene-8,12,15-trione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9935 99.35%
Caco-2 + 0.7531 75.31%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.6765 67.65%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8833 88.33%
OATP1B3 inhibitior + 0.9338 93.38%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.5641 56.41%
P-glycoprotein inhibitior + 0.6434 64.34%
P-glycoprotein substrate - 0.6868 68.68%
CYP3A4 substrate + 0.6386 63.86%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8661 86.61%
CYP3A4 inhibition + 0.8316 83.16%
CYP2C9 inhibition - 0.6035 60.35%
CYP2C19 inhibition + 0.5621 56.21%
CYP2D6 inhibition - 0.8638 86.38%
CYP1A2 inhibition + 0.5342 53.42%
CYP2C8 inhibition - 0.6335 63.35%
CYP inhibitory promiscuity + 0.7273 72.73%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9443 94.43%
Carcinogenicity (trinary) Danger 0.4660 46.60%
Eye corrosion - 0.9784 97.84%
Eye irritation - 0.7812 78.12%
Skin irritation - 0.8032 80.32%
Skin corrosion - 0.9447 94.47%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5079 50.79%
Micronuclear + 0.5500 55.00%
Hepatotoxicity + 0.6324 63.24%
skin sensitisation - 0.7815 78.15%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.5456 54.56%
Acute Oral Toxicity (c) III 0.4891 48.91%
Estrogen receptor binding + 0.8721 87.21%
Androgen receptor binding + 0.5935 59.35%
Thyroid receptor binding + 0.6265 62.65%
Glucocorticoid receptor binding + 0.5890 58.90%
Aromatase binding - 0.5621 56.21%
PPAR gamma + 0.8180 81.80%
Honey bee toxicity - 0.8069 80.69%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9932 99.32%

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
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 96.48% 96.77%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.67% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.64% 95.56%
CHEMBL2535 P11166 Glucose transporter 91.09% 98.75%
CHEMBL1907 P15144 Aminopeptidase N 90.89% 93.31%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 89.49% 96.21%
CHEMBL2581 P07339 Cathepsin D 89.42% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.94% 96.09%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 88.75% 97.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.73% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.24% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.61% 99.15%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.54% 93.56%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.34% 91.07%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.82% 89.00%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 81.36% 92.88%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 81.36% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.00% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.59% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.47% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 80.10% 94.73%

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.
Taxus mairei

Cross-Links

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PubChem 163041234
LOTUS LTS0107192
wikiData Q104975366