6-(3-Methoxyprop-1-enyl)-2,2-dimethyl-3,4-dihydrochromen-3-ol

Details

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Internal ID 1eaddd11-afc5-4ff5-b7a5-2d3b145e7603
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > 2,2-dimethyl-1-benzopyrans
IUPAC Name 6-(3-methoxyprop-1-enyl)-2,2-dimethyl-3,4-dihydrochromen-3-ol
SMILES (Canonical) CC1(C(CC2=C(O1)C=CC(=C2)C=CCOC)O)C
SMILES (Isomeric) CC1(C(CC2=C(O1)C=CC(=C2)C=CCOC)O)C
InChI InChI=1S/C15H20O3/c1-15(2)14(16)10-12-9-11(5-4-8-17-3)6-7-13(12)18-15/h4-7,9,14,16H,8,10H2,1-3H3
InChI Key VMLZITRLQHOQKZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H20O3
Molecular Weight 248.32 g/mol
Exact Mass 248.14124450 g/mol
Topological Polar Surface Area (TPSA) 38.70 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.42
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-(3-Methoxyprop-1-enyl)-2,2-dimethyl-3,4-dihydrochromen-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9946 99.46%
Caco-2 + 0.8670 86.70%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6939 69.39%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8467 84.67%
OATP1B3 inhibitior + 0.9507 95.07%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.5841 58.41%
P-glycoprotein inhibitior - 0.9613 96.13%
P-glycoprotein substrate - 0.8559 85.59%
CYP3A4 substrate + 0.5583 55.83%
CYP2C9 substrate - 0.8111 81.11%
CYP2D6 substrate + 0.3938 39.38%
CYP3A4 inhibition - 0.6156 61.56%
CYP2C9 inhibition - 0.7472 74.72%
CYP2C19 inhibition + 0.5116 51.16%
CYP2D6 inhibition - 0.6748 67.48%
CYP1A2 inhibition + 0.6325 63.25%
CYP2C8 inhibition - 0.5586 55.86%
CYP inhibitory promiscuity - 0.7270 72.70%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6625 66.25%
Eye corrosion - 0.9870 98.70%
Eye irritation - 0.8469 84.69%
Skin irritation - 0.7766 77.66%
Skin corrosion - 0.9391 93.91%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6456 64.56%
Micronuclear - 0.7500 75.00%
Hepatotoxicity - 0.6575 65.75%
skin sensitisation - 0.6396 63.96%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.5748 57.48%
Acute Oral Toxicity (c) III 0.5337 53.37%
Estrogen receptor binding + 0.6949 69.49%
Androgen receptor binding + 0.5234 52.34%
Thyroid receptor binding - 0.6158 61.58%
Glucocorticoid receptor binding + 0.5774 57.74%
Aromatase binding + 0.5759 57.59%
PPAR gamma - 0.6467 64.67%
Honey bee toxicity - 0.8418 84.18%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.8319 83.19%

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 99.15% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.30% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.48% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.98% 94.45%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.37% 96.00%
CHEMBL2581 P07339 Cathepsin D 88.88% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.88% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.65% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.09% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.58% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.04% 93.99%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.94% 96.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.83% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 81.96% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.87% 89.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.66% 92.62%

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.
Zanthoxylum wutaiense

Cross-Links

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PubChem 163001566
LOTUS LTS0055144
wikiData Q105289063