Dehydrochromolaenin

Details

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Internal ID d6ca5192-eb0c-407e-8ac6-c7a9dd917e40
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1,5,8-trimethylbenzo[e][1]benzofuran
SMILES (Canonical) CC1=CC2=C(C=C1)C(=CC3=C2C(=CO3)C)C
SMILES (Isomeric) CC1=CC2=C(C=C1)C(=CC3=C2C(=CO3)C)C
InChI InChI=1S/C15H14O/c1-9-4-5-12-10(2)7-14-15(13(12)6-9)11(3)8-16-14/h4-8H,1-3H3
InChI Key UYXJESJBZRIFPL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H14O
Molecular Weight 210.27 g/mol
Exact Mass 210.104465066 g/mol
Topological Polar Surface Area (TPSA) 13.10 Ų
XlogP 4.70
Atomic LogP (AlogP) 4.51
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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20013-76-7
1,5,8-trimethylbenzo[e][1]benzofuran
1,5,8-trimethyl-benzo[e]benzofuran
1,5,8-trimethylnaphtho[2,1-b]furan
AKOS032948992
FS-8729
Naphtho[2,1-b]furan, 1,5,8-trimethyl-

2D Structure

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2D Structure of Dehydrochromolaenin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9967 99.67%
Caco-2 + 0.8006 80.06%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Lysosomes 0.5319 53.19%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9322 93.22%
OATP1B3 inhibitior + 0.9644 96.44%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6568 65.68%
P-glycoprotein inhibitior - 0.8787 87.87%
P-glycoprotein substrate - 0.9211 92.11%
CYP3A4 substrate - 0.6020 60.20%
CYP2C9 substrate - 0.7965 79.65%
CYP2D6 substrate - 0.7092 70.92%
CYP3A4 inhibition - 0.8221 82.21%
CYP2C9 inhibition - 0.8838 88.38%
CYP2C19 inhibition + 0.5761 57.61%
CYP2D6 inhibition - 0.7983 79.83%
CYP1A2 inhibition + 0.8532 85.32%
CYP2C8 inhibition - 0.7054 70.54%
CYP inhibitory promiscuity + 0.7295 72.95%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Danger 0.4539 45.39%
Eye corrosion - 0.9136 91.36%
Eye irritation + 0.8668 86.68%
Skin irritation + 0.5255 52.55%
Skin corrosion - 0.9861 98.61%
Ames mutagenesis + 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4584 45.84%
Micronuclear - 0.5951 59.51%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation + 0.5801 58.01%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity - 0.5972 59.72%
Acute Oral Toxicity (c) III 0.7386 73.86%
Estrogen receptor binding + 0.7275 72.75%
Androgen receptor binding + 0.7141 71.41%
Thyroid receptor binding + 0.5286 52.86%
Glucocorticoid receptor binding + 0.6727 67.27%
Aromatase binding + 0.7177 71.77%
PPAR gamma - 0.6509 65.09%
Honey bee toxicity - 0.9320 93.20%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.7100 71.00%
Fish aquatic toxicity + 0.8226 82.26%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.70% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.31% 91.11%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 90.41% 93.65%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.98% 89.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 85.68% 89.62%
CHEMBL3401 O75469 Pregnane X receptor 84.72% 94.73%
CHEMBL4581 P52732 Kinesin-like protein 1 83.40% 93.18%
CHEMBL2581 P07339 Cathepsin D 83.35% 98.95%

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.
Chromolaena laevigata

Cross-Links

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PubChem 12309959
LOTUS LTS0029849
wikiData Q105282019