Eucomin

Details

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Internal ID 4c3d6a9f-aad9-44b8-8a0f-59df9a49d27a
Taxonomy Phenylpropanoids and polyketides > Homoisoflavonoids
IUPAC Name (3Z)-5,7-dihydroxy-3-[(4-methoxyphenyl)methylidene]chromen-4-one
SMILES (Canonical) COC1=CC=C(C=C1)C=C2COC3=CC(=CC(=C3C2=O)O)O
SMILES (Isomeric) COC1=CC=C(C=C1)/C=C\2/COC3=CC(=CC(=C3C2=O)O)O
InChI InChI=1S/C17H14O5/c1-21-13-4-2-10(3-5-13)6-11-9-22-15-8-12(18)7-14(19)16(15)17(11)20/h2-8,18-19H,9H2,1H3/b11-6-
InChI Key MNFFPBYXUIMSFC-WDZFZDKYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H14O5
Molecular Weight 298.29 g/mol
Exact Mass 298.08412354 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.77
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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61350-54-7
CHEMBL4451649
XE161742

2D Structure

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2D Structure of Eucomin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9805 98.05%
Caco-2 + 0.8576 85.76%
Blood Brain Barrier - 0.7879 78.79%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.7060 70.60%
OATP2B1 inhibitior - 0.5796 57.96%
OATP1B1 inhibitior + 0.9552 95.52%
OATP1B3 inhibitior + 0.9626 96.26%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.7113 71.13%
P-glycoprotein inhibitior - 0.7554 75.54%
P-glycoprotein substrate - 0.9630 96.30%
CYP3A4 substrate + 0.5117 51.17%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8124 81.24%
CYP3A4 inhibition + 0.6944 69.44%
CYP2C9 inhibition + 0.7618 76.18%
CYP2C19 inhibition + 0.9306 93.06%
CYP2D6 inhibition - 0.7207 72.07%
CYP1A2 inhibition + 0.9579 95.79%
CYP2C8 inhibition - 0.7442 74.42%
CYP inhibitory promiscuity + 0.9471 94.71%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6819 68.19%
Eye corrosion - 0.9819 98.19%
Eye irritation + 0.9463 94.63%
Skin irritation - 0.7060 70.60%
Skin corrosion - 0.9548 95.48%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6340 63.40%
Micronuclear + 0.8100 81.00%
Hepatotoxicity - 0.5141 51.41%
skin sensitisation - 0.8043 80.43%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.6511 65.11%
Acute Oral Toxicity (c) III 0.6177 61.77%
Estrogen receptor binding + 0.9100 91.00%
Androgen receptor binding + 0.9223 92.23%
Thyroid receptor binding + 0.6790 67.90%
Glucocorticoid receptor binding + 0.8117 81.17%
Aromatase binding + 0.8611 86.11%
PPAR gamma + 0.8767 87.67%
Honey bee toxicity - 0.9009 90.09%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9466 94.66%

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
CHEMBL1929 P47989 Xanthine dehydrogenase 98.98% 96.12%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.78% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 98.38% 95.56%
CHEMBL4208 P20618 Proteasome component C5 94.78% 90.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.77% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.17% 86.33%
CHEMBL2581 P07339 Cathepsin D 89.96% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.62% 89.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 89.45% 93.40%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.95% 99.15%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.68% 96.09%
CHEMBL2039 P27338 Monoamine oxidase B 87.54% 92.51%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.24% 99.23%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.25% 93.99%
CHEMBL3401 O75469 Pregnane X receptor 85.49% 94.73%
CHEMBL1951 P21397 Monoamine oxidase A 84.56% 91.49%
CHEMBL3194 P02766 Transthyretin 83.05% 90.71%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.00% 96.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.98% 95.89%

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.
Eucomis comosa
Microdesmis keayana

Cross-Links

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PubChem 21676268
LOTUS LTS0269296
wikiData Q105168331