[(1R,2Z,4R,8R,9R,11S,13S)-1-hydroxy-13-methoxy-2,11-dimethyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.04,8]tetradec-2-en-9-yl] 2-methylpropanoate

Details

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Internal ID bf5e7df1-8e30-404a-8eb2-893718a9035c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones
IUPAC Name [(1R,2Z,4R,8R,9R,11S,13S)-1-hydroxy-13-methoxy-2,11-dimethyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.04,8]tetradec-2-en-9-yl] 2-methylpropanoate
SMILES (Canonical) CC1=CC2C(C(CC3(CC(C1(O3)O)OC)C)OC(=O)C(C)C)C(=C)C(=O)O2
SMILES (Isomeric) C/C/1=C/[C@@H]2[C@@H]([C@@H](C[C@]3(C[C@@H]([C@@]1(O3)O)OC)C)OC(=O)C(C)C)C(=C)C(=O)O2
InChI InChI=1S/C20H28O7/c1-10(2)17(21)26-14-8-19(5)9-15(24-6)20(23,27-19)11(3)7-13-16(14)12(4)18(22)25-13/h7,10,13-16,23H,4,8-9H2,1-3,5-6H3/b11-7-/t13-,14-,15+,16+,19+,20-/m1/s1
InChI Key OIZDLBIQXNXOLL-CQFNNYNPSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H28O7
Molecular Weight 380.40 g/mol
Exact Mass 380.18350323 g/mol
Topological Polar Surface Area (TPSA) 91.30 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.88
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1R,2Z,4R,8R,9R,11S,13S)-1-hydroxy-13-methoxy-2,11-dimethyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.04,8]tetradec-2-en-9-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 + 0.9756 97.56%
Caco-2 + 0.5312 53.12%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6066 60.66%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8998 89.98%
OATP1B3 inhibitior - 0.3191 31.91%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8604 86.04%
P-glycoprotein inhibitior - 0.5453 54.53%
P-glycoprotein substrate - 0.7108 71.08%
CYP3A4 substrate + 0.6673 66.73%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8871 88.71%
CYP3A4 inhibition - 0.5249 52.49%
CYP2C9 inhibition - 0.7916 79.16%
CYP2C19 inhibition - 0.8184 81.84%
CYP2D6 inhibition - 0.9388 93.88%
CYP1A2 inhibition - 0.7241 72.41%
CYP2C8 inhibition - 0.6974 69.74%
CYP inhibitory promiscuity - 0.9175 91.75%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.4575 45.75%
Eye corrosion - 0.9789 97.89%
Eye irritation - 0.8906 89.06%
Skin irritation - 0.6455 64.55%
Skin corrosion - 0.9023 90.23%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5943 59.43%
Micronuclear - 0.7100 71.00%
Hepatotoxicity + 0.5302 53.02%
skin sensitisation - 0.7142 71.42%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.6083 60.83%
Acute Oral Toxicity (c) III 0.4039 40.39%
Estrogen receptor binding + 0.8629 86.29%
Androgen receptor binding + 0.6191 61.91%
Thyroid receptor binding + 0.6453 64.53%
Glucocorticoid receptor binding + 0.7593 75.93%
Aromatase binding + 0.6023 60.23%
PPAR gamma + 0.7542 75.42%
Honey bee toxicity - 0.6672 66.72%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9557 95.57%

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 96.90% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.41% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.77% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.35% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.06% 94.45%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 88.15% 91.07%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.02% 85.14%
CHEMBL3714130 P46095 G-protein coupled receptor 6 87.10% 97.36%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.22% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.18% 89.00%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 86.17% 97.33%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.20% 95.50%
CHEMBL221 P23219 Cyclooxygenase-1 84.32% 90.17%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.28% 92.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.15% 94.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.06% 97.14%
CHEMBL340 P08684 Cytochrome P450 3A4 82.32% 91.19%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.85% 96.47%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 81.12% 85.30%

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.
Tithonia diversifolia

Cross-Links

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PubChem 163189111
LOTUS LTS0028927
wikiData Q105192927