Chromolaenin

Details

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Internal ID d4b252fa-3d2e-4d23-9fc6-fc62a2947180
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (5R)-1,5,8-trimethyl-4,5-dihydrobenzo[e][1]benzofuran
SMILES (Canonical) CC1CC2=C(C(=CO2)C)C3=C1C=CC(=C3)C
SMILES (Isomeric) C[C@@H]1CC2=C(C(=CO2)C)C3=C1C=CC(=C3)C
InChI InChI=1S/C15H16O/c1-9-4-5-12-10(2)7-14-15(13(12)6-9)11(3)8-16-14/h4-6,8,10H,7H2,1-3H3/t10-/m1/s1
InChI Key CTILMUMVHPOCNU-SNVBAGLBSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H16O
Molecular Weight 212.29 g/mol
Exact Mass 212.120115130 g/mol
Topological Polar Surface Area (TPSA) 13.10 Ų
XlogP 4.00
Atomic LogP (AlogP) 4.22
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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Laevigatin
CTILMUMVHPOCNU-SNVBAGLBSA-N
DTXSID801318472
62502-10-7

2D Structure

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2D Structure of Chromolaenin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9964 99.64%
Caco-2 + 0.8417 84.17%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.4233 42.33%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9267 92.67%
OATP1B3 inhibitior + 0.9621 96.21%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.5856 58.56%
P-glycoprotein inhibitior - 0.9435 94.35%
P-glycoprotein substrate - 0.7887 78.87%
CYP3A4 substrate - 0.5209 52.09%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3729 37.29%
CYP3A4 inhibition - 0.8658 86.58%
CYP2C9 inhibition - 0.7655 76.55%
CYP2C19 inhibition + 0.5821 58.21%
CYP2D6 inhibition - 0.8286 82.86%
CYP1A2 inhibition + 0.7859 78.59%
CYP2C8 inhibition - 0.6280 62.80%
CYP inhibitory promiscuity + 0.6300 63.00%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7100 71.00%
Carcinogenicity (trinary) Danger 0.5032 50.32%
Eye corrosion - 0.9590 95.90%
Eye irritation - 0.9040 90.40%
Skin irritation - 0.6079 60.79%
Skin corrosion - 0.9787 97.87%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4031 40.31%
Micronuclear - 0.6567 65.67%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation + 0.6446 64.46%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity - 0.6075 60.75%
Acute Oral Toxicity (c) III 0.6799 67.99%
Estrogen receptor binding - 0.6503 65.03%
Androgen receptor binding + 0.6714 67.14%
Thyroid receptor binding + 0.5314 53.14%
Glucocorticoid receptor binding - 0.5337 53.37%
Aromatase binding + 0.6225 62.25%
PPAR gamma - 0.5405 54.05%
Honey bee toxicity - 0.9386 93.86%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6900 69.00%
Fish aquatic toxicity + 0.8791 87.91%

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
CHEMBL2581 P07339 Cathepsin D 95.09% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.08% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.76% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.23% 89.00%
CHEMBL4581 P52732 Kinesin-like protein 1 87.75% 93.18%
CHEMBL2073 P07947 Tyrosine-protein kinase YES 86.77% 83.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.76% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 85.78% 94.73%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 84.85% 96.21%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 84.18% 86.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.05% 86.33%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 83.26% 94.80%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.11% 95.89%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 82.26% 93.65%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 81.90% 96.09%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 81.32% 96.42%
CHEMBL3085 P43003 Excitatory amino acid transporter 1 81.08% 94.67%
CHEMBL5805 Q9NR97 Toll-like receptor 8 80.03% 96.25%

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.
Baccharis ulicina
Chromolaena laevigata
Eutrochium fistulosum

Cross-Links

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PubChem 11745938
LOTUS LTS0091155
wikiData Q104397120