3,5-Dimethyl-8-methoxy-3,4-dihydroisocoumarin

Details

Top
Internal ID 53b59a34-2f5b-4560-93bd-25b04f36fa94
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name 8-methoxy-3,5-dimethyl-3,4-dihydroisochromen-1-one
SMILES (Canonical) CC1CC2=C(C=CC(=C2C(=O)O1)OC)C
SMILES (Isomeric) CC1CC2=C(C=CC(=C2C(=O)O1)OC)C
InChI InChI=1S/C12H14O3/c1-7-4-5-10(14-3)11-9(7)6-8(2)15-12(11)13/h4-5,8H,6H2,1-3H3
InChI Key PUHAIJJCXSKQQD-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

Top
Molecular Formula C12H14O3
Molecular Weight 206.24 g/mol
Exact Mass 206.094294304 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.11
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
CHEMBL226463
BDBM50208251
3-5-dimethyl-8-methoxy-3,4-dihydroisocoumarin

2D Structure

Top
2D Structure of 3,5-Dimethyl-8-methoxy-3,4-dihydroisocoumarin

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.8598 85.98%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.5927 59.27%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9601 96.01%
OATP1B3 inhibitior + 0.9795 97.95%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8335 83.35%
P-glycoprotein inhibitior - 0.9352 93.52%
P-glycoprotein substrate - 0.8840 88.40%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.8135 81.35%
CYP3A4 inhibition - 0.9638 96.38%
CYP2C9 inhibition - 0.8795 87.95%
CYP2C19 inhibition - 0.7161 71.61%
CYP2D6 inhibition - 0.8975 89.75%
CYP1A2 inhibition + 0.9412 94.12%
CYP2C8 inhibition - 0.8510 85.10%
CYP inhibitory promiscuity - 0.7662 76.62%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9313 93.13%
Carcinogenicity (trinary) Non-required 0.5895 58.95%
Eye corrosion - 0.9107 91.07%
Eye irritation + 0.8196 81.96%
Skin irritation - 0.7119 71.19%
Skin corrosion - 0.9782 97.82%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5216 52.16%
Micronuclear - 0.6000 60.00%
Hepatotoxicity + 0.8282 82.82%
skin sensitisation - 0.8184 81.84%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.5153 51.53%
Acute Oral Toxicity (c) III 0.5815 58.15%
Estrogen receptor binding - 0.8039 80.39%
Androgen receptor binding - 0.5286 52.86%
Thyroid receptor binding - 0.6972 69.72%
Glucocorticoid receptor binding - 0.8295 82.95%
Aromatase binding - 0.9224 92.24%
PPAR gamma - 0.7077 70.77%
Honey bee toxicity - 0.9138 91.38%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.8886 88.86%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.35% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.74% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.83% 94.00%
CHEMBL2581 P07339 Cathepsin D 86.24% 98.95%
CHEMBL2535 P11166 Glucose transporter 84.86% 98.75%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.16% 97.14%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.63% 96.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.58% 85.14%
CHEMBL1951 P21397 Monoamine oxidase A 82.01% 91.49%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.60% 99.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.45% 95.89%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.20% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.81% 89.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.75% 93.65%

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 568998
LOTUS LTS0233881
wikiData Q77568725