6-Hydroxy-7-(3,7,11-trimethyldodeca-2,6,10-trienoxy)chromen-2-one

Details

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Internal ID 43184bee-df3c-40ca-992f-3a1126e34310
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones
IUPAC Name 6-hydroxy-7-(3,7,11-trimethyldodeca-2,6,10-trienoxy)chromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H30O4/c1-17(2)7-5-8-18(3)9-6-10-19(4)13-14-27-23-16-22-20(15-21(23)25)11-12-24(26)28-22/h7,9,11-13,15-16,25H,5-6,8,10,14H2,1-4H3
InChI Key KRJOBTPWAFTOGJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H30O4
Molecular Weight 382.50 g/mol
Exact Mass 382.21440943 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 6.70
Atomic LogP (AlogP) 6.30
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-Hydroxy-7-(3,7,11-trimethyldodeca-2,6,10-trienoxy)chromen-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9601 96.01%
Caco-2 + 0.6036 60.36%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8280 82.80%
OATP2B1 inhibitior - 0.8576 85.76%
OATP1B1 inhibitior + 0.9223 92.23%
OATP1B3 inhibitior + 0.8784 87.84%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.8811 88.11%
P-glycoprotein inhibitior + 0.8021 80.21%
P-glycoprotein substrate - 0.8136 81.36%
CYP3A4 substrate + 0.5000 50.00%
CYP2C9 substrate - 0.6172 61.72%
CYP2D6 substrate - 0.8048 80.48%
CYP3A4 inhibition - 0.7193 71.93%
CYP2C9 inhibition + 0.6962 69.62%
CYP2C19 inhibition + 0.8896 88.96%
CYP2D6 inhibition - 0.6520 65.20%
CYP1A2 inhibition + 0.9548 95.48%
CYP2C8 inhibition - 0.6511 65.11%
CYP inhibitory promiscuity + 0.5828 58.28%
UGT catelyzed - 0.6638 66.38%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7442 74.42%
Eye corrosion - 0.9919 99.19%
Eye irritation - 0.9141 91.41%
Skin irritation - 0.7710 77.10%
Skin corrosion - 0.9623 96.23%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8231 82.31%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.8121 81.21%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.5570 55.70%
Acute Oral Toxicity (c) III 0.5343 53.43%
Estrogen receptor binding + 0.8313 83.13%
Androgen receptor binding + 0.6509 65.09%
Thyroid receptor binding + 0.6608 66.08%
Glucocorticoid receptor binding + 0.6056 60.56%
Aromatase binding + 0.6044 60.44%
PPAR gamma + 0.8526 85.26%
Honey bee toxicity - 0.8789 87.89%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 1.0000 100.00%

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 98.10% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 94.81% 94.73%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.58% 92.08%
CHEMBL2581 P07339 Cathepsin D 94.24% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.29% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.96% 94.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.68% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.23% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.64% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.18% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 82.18% 94.75%
CHEMBL4208 P20618 Proteasome component C5 82.15% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.71% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.30% 89.00%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 81.17% 83.57%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 80.77% 93.10%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.55% 96.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.12% 96.09%

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 163037064
LOTUS LTS0269351
wikiData Q105145050