Methyl santolinate

Details

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Internal ID 494da146-4d6e-406d-8229-40ff73253833
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name methyl 3-ethenyl-2,5-dimethylhex-4-enoate
SMILES (Canonical) CC(C(C=C)C=C(C)C)C(=O)OC
SMILES (Isomeric) CC(C(C=C)C=C(C)C)C(=O)OC
InChI InChI=1S/C11H18O2/c1-6-10(7-8(2)3)9(4)11(12)13-5/h6-7,9-10H,1H2,2-5H3
InChI Key QYFHCJWTWXQYQS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H18O2
Molecular Weight 182.26 g/mol
Exact Mass 182.130679813 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.56
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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QYFHCJWTWXQYQS-UHFFFAOYSA-N
Methyl 2,5-dimethyl-3-vinyl-4-hexenoate #

2D Structure

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2D Structure of Methyl santolinate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9930 99.30%
Caco-2 + 0.7448 74.48%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.6581 65.81%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9511 95.11%
OATP1B3 inhibitior + 0.9485 94.85%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9678 96.78%
P-glycoprotein inhibitior - 0.9436 94.36%
P-glycoprotein substrate - 0.9501 95.01%
CYP3A4 substrate - 0.5723 57.23%
CYP2C9 substrate - 0.6131 61.31%
CYP2D6 substrate - 0.8882 88.82%
CYP3A4 inhibition - 0.9300 93.00%
CYP2C9 inhibition - 0.9083 90.83%
CYP2C19 inhibition - 0.8828 88.28%
CYP2D6 inhibition - 0.9582 95.82%
CYP1A2 inhibition - 0.9322 93.22%
CYP2C8 inhibition - 0.9393 93.93%
CYP inhibitory promiscuity - 0.8187 81.87%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6657 66.57%
Carcinogenicity (trinary) Non-required 0.6507 65.07%
Eye corrosion + 0.9333 93.33%
Eye irritation + 0.9386 93.86%
Skin irritation + 0.5536 55.36%
Skin corrosion - 0.9870 98.70%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5897 58.97%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6650 66.50%
skin sensitisation + 0.8778 87.78%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity + 0.7668 76.68%
Acute Oral Toxicity (c) IV 0.7210 72.10%
Estrogen receptor binding - 0.8040 80.40%
Androgen receptor binding - 0.7686 76.86%
Thyroid receptor binding - 0.7399 73.99%
Glucocorticoid receptor binding - 0.8897 88.97%
Aromatase binding - 0.7098 70.98%
PPAR gamma - 0.9008 90.08%
Honey bee toxicity - 0.5756 57.56%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.8200 82.00%
Fish aquatic toxicity + 0.8999 89.99%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.23% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.87% 94.45%
CHEMBL340 P08684 Cytochrome P450 3A4 89.46% 91.19%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.24% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.55% 91.11%
CHEMBL2581 P07339 Cathepsin D 84.85% 98.95%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 84.00% 100.00%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 83.48% 95.71%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.71% 91.07%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.18% 94.33%
CHEMBL3437 Q16853 Amine oxidase, copper containing 80.71% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 80.09% 94.73%

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.
Artemisia arbuscula
Artemisia tridentata

Cross-Links

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PubChem 565394
LOTUS LTS0062180
wikiData Q104375916