7-methoxy-3-methyl-5-(3-methylbut-2-en-1-yl)-1H-isochromen-6-ol

Details

Top
Internal ID 39c0d1b3-37d8-4615-8594-574afef2a76d
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name 7-methoxy-3-methyl-5-(3-methylbut-2-enyl)-1H-isochromen-6-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H20O3/c1-10(2)5-6-13-14-7-11(3)19-9-12(14)8-15(18-4)16(13)17/h5,7-8,17H,6,9H2,1-4H3
InChI Key UAIHQVFJEFNIKK-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C16H20O3
Molecular Weight 260.33 g/mol
Exact Mass 260.14124450 g/mol
Topological Polar Surface Area (TPSA) 38.70 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.80
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 7-methoxy-3-methyl-5-(3-methylbut-2-en-1-yl)-1H-isochromen-6-ol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.8386 83.86%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.7913 79.13%
OATP2B1 inhibitior - 0.8604 86.04%
OATP1B1 inhibitior + 0.8687 86.87%
OATP1B3 inhibitior + 0.9539 95.39%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.6315 63.15%
P-glycoprotein inhibitior - 0.8342 83.42%
P-glycoprotein substrate - 0.5969 59.69%
CYP3A4 substrate + 0.5306 53.06%
CYP2C9 substrate - 0.5853 58.53%
CYP2D6 substrate + 0.3937 39.37%
CYP3A4 inhibition - 0.6462 64.62%
CYP2C9 inhibition + 0.6777 67.77%
CYP2C19 inhibition + 0.8855 88.55%
CYP2D6 inhibition - 0.6036 60.36%
CYP1A2 inhibition + 0.8809 88.09%
CYP2C8 inhibition - 0.6115 61.15%
CYP inhibitory promiscuity + 0.7940 79.40%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.7696 76.96%
Eye corrosion - 0.9836 98.36%
Eye irritation + 0.9142 91.42%
Skin irritation - 0.7725 77.25%
Skin corrosion - 0.9499 94.99%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4756 47.56%
Micronuclear - 0.6900 69.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.6978 69.78%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.8259 82.59%
Acute Oral Toxicity (c) III 0.7234 72.34%
Estrogen receptor binding + 0.9157 91.57%
Androgen receptor binding + 0.5924 59.24%
Thyroid receptor binding - 0.4882 48.82%
Glucocorticoid receptor binding + 0.6742 67.42%
Aromatase binding + 0.7874 78.74%
PPAR gamma + 0.7474 74.74%
Honey bee toxicity - 0.8150 81.50%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9692 96.92%

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 98.90% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.82% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.79% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.06% 94.45%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 89.96% 97.21%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.34% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.19% 92.94%
CHEMBL3401 O75469 Pregnane X receptor 87.79% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.41% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.59% 96.95%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 85.37% 89.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.47% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.83% 95.89%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.77% 95.50%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.32% 92.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.13% 94.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.92% 100.00%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 81.85% 98.21%
CHEMBL2413 P32246 C-C chemokine receptor type 1 80.75% 89.50%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 80.19% 92.68%

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 132522673
LOTUS LTS0185809
wikiData Q77567329