6-(4-Hydroxy-4-methylpent-2-enyl)-7-methoxychromen-2-one

Details

Top
Internal ID 18c49688-01d7-433a-aa60-c1ae734552a8
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 6-(4-hydroxy-4-methylpent-2-enyl)-7-methoxychromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H18O4/c1-16(2,18)8-4-5-11-9-12-6-7-15(17)20-14(12)10-13(11)19-3/h4,6-10,18H,5H2,1-3H3
InChI Key BWNRXRQSFMRLCZ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C16H18O4
Molecular Weight 274.31 g/mol
Exact Mass 274.12050905 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.67
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 6-(4-Hydroxy-4-methylpent-2-enyl)-7-methoxychromen-2-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9564 95.64%
Caco-2 + 0.8686 86.86%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.7248 72.48%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8454 84.54%
OATP1B3 inhibitior + 0.9546 95.46%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.7931 79.31%
P-glycoprotein inhibitior - 0.7786 77.86%
P-glycoprotein substrate - 0.8083 80.83%
CYP3A4 substrate - 0.5456 54.56%
CYP2C9 substrate - 0.6340 63.40%
CYP2D6 substrate - 0.8186 81.86%
CYP3A4 inhibition - 0.6498 64.98%
CYP2C9 inhibition + 0.6095 60.95%
CYP2C19 inhibition + 0.6162 61.62%
CYP2D6 inhibition - 0.8473 84.73%
CYP1A2 inhibition + 0.5784 57.84%
CYP2C8 inhibition - 0.6562 65.62%
CYP inhibitory promiscuity + 0.6564 65.64%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9513 95.13%
Carcinogenicity (trinary) Non-required 0.4930 49.30%
Eye corrosion - 0.9873 98.73%
Eye irritation - 0.7119 71.19%
Skin irritation - 0.7851 78.51%
Skin corrosion - 0.9665 96.65%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7447 74.47%
Micronuclear - 0.5100 51.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.8656 86.56%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.6191 61.91%
Acute Oral Toxicity (c) II 0.3909 39.09%
Estrogen receptor binding + 0.9106 91.06%
Androgen receptor binding - 0.5688 56.88%
Thyroid receptor binding + 0.6067 60.67%
Glucocorticoid receptor binding + 0.6793 67.93%
Aromatase binding + 0.7847 78.47%
PPAR gamma + 0.7970 79.70%
Honey bee toxicity - 0.9151 91.51%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9850 98.50%

Targets

Top

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 97.08% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.93% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.94% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 90.34% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.90% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.34% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.20% 94.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 85.10% 89.62%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.34% 96.00%
CHEMBL4208 P20618 Proteasome component C5 82.80% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.72% 96.09%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 162910199
LOTUS LTS0268554
wikiData Q104947404