2-Hexyl-5-hydroxy-7-methoxychromen-4-one

Details

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Internal ID 372eeb95-6f4b-4edb-b287-a1eada5a3b6b
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromones
IUPAC Name 2-hexyl-5-hydroxy-7-methoxychromen-4-one
SMILES (Canonical) CCCCCCC1=CC(=O)C2=C(C=C(C=C2O1)OC)O
SMILES (Isomeric) CCCCCCC1=CC(=O)C2=C(C=C(C=C2O1)OC)O
InChI InChI=1S/C16H20O4/c1-3-4-5-6-7-11-8-13(17)16-14(18)9-12(19-2)10-15(16)20-11/h8-10,18H,3-7H2,1-2H3
InChI Key JNHVWACAXZPGJO-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H20O4
Molecular Weight 276.33 g/mol
Exact Mass 276.13615911 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.63
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Hexyl-5-hydroxy-7-methoxychromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9904 99.04%
Caco-2 + 0.9103 91.03%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Plasma membrane 0.5368 53.68%
OATP2B1 inhibitior - 0.8547 85.47%
OATP1B1 inhibitior + 0.9096 90.96%
OATP1B3 inhibitior + 0.9510 95.10%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5761 57.61%
P-glycoprotein inhibitior - 0.7231 72.31%
P-glycoprotein substrate - 0.7536 75.36%
CYP3A4 substrate + 0.5221 52.21%
CYP2C9 substrate - 0.5914 59.14%
CYP2D6 substrate - 0.8089 80.89%
CYP3A4 inhibition + 0.5527 55.27%
CYP2C9 inhibition - 0.8583 85.83%
CYP2C19 inhibition - 0.5538 55.38%
CYP2D6 inhibition - 0.8693 86.93%
CYP1A2 inhibition + 0.6668 66.68%
CYP2C8 inhibition + 0.5480 54.80%
CYP inhibitory promiscuity - 0.6543 65.43%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.7426 74.26%
Eye corrosion - 0.9812 98.12%
Eye irritation + 0.5722 57.22%
Skin irritation - 0.7837 78.37%
Skin corrosion - 0.9369 93.69%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4896 48.96%
Micronuclear - 0.7800 78.00%
Hepatotoxicity - 0.7143 71.43%
skin sensitisation - 0.9074 90.74%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.6393 63.93%
Acute Oral Toxicity (c) III 0.7270 72.70%
Estrogen receptor binding + 0.7509 75.09%
Androgen receptor binding + 0.8220 82.20%
Thyroid receptor binding + 0.5245 52.45%
Glucocorticoid receptor binding + 0.7452 74.52%
Aromatase binding + 0.7477 74.77%
PPAR gamma + 0.9257 92.57%
Honey bee toxicity - 0.9527 95.27%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6662 66.62%
Fish aquatic toxicity + 0.9726 97.26%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.13% 91.11%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 96.68% 92.08%
CHEMBL2581 P07339 Cathepsin D 95.92% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.73% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.57% 94.45%
CHEMBL230 P35354 Cyclooxygenase-2 92.60% 89.63%
CHEMBL3401 O75469 Pregnane X receptor 92.23% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.92% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.48% 93.99%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.81% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.69% 94.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.37% 90.71%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 83.90% 100.00%
CHEMBL3194 P02766 Transthyretin 83.58% 90.71%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.40% 96.95%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.53% 93.65%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.06% 96.09%
CHEMBL1907 P15144 Aminopeptidase N 80.85% 93.31%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.79% 99.23%

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.
Christiana africana

Cross-Links

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PubChem 163074689
LOTUS LTS0241613
wikiData Q105131915