2-Butenoic acid, 3-methyl-, 3-methylbutyl ester

Details

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Internal ID 831fb5f7-f080-4401-890f-9e316ec00392
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name 3-methylbutyl 3-methylbut-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H18O2/c1-8(2)5-6-12-10(11)7-9(3)4/h7-8H,5-6H2,1-4H3
InChI Key DBGLRAHCYJTYEH-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C10H18O2
Molecular Weight 170.25 g/mol
Exact Mass 170.130679813 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.54
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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Isopentyl 3-methyl-2-butenoate
56922-73-7
3-methylbutyl 3-methylbut-2-enoate
2-Butenoic acid, 3-methyl-, 3-methylbutyl ester
EINECS 260-438-5
AI3-33688
DTXSID3069142
RefChem:468034
DTXCID7042140
260-438-5
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-Butenoic acid, 3-methyl-, 3-methylbutyl ester

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9953 99.53%
Caco-2 + 0.8737 87.37%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6359 63.59%
OATP2B1 inhibitior - 0.8547 85.47%
OATP1B1 inhibitior + 0.9623 96.23%
OATP1B3 inhibitior + 0.8988 89.88%
MATE1 inhibitior - 0.6600 66.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9013 90.13%
P-glycoprotein inhibitior - 0.9767 97.67%
P-glycoprotein substrate - 0.9212 92.12%
CYP3A4 substrate - 0.5823 58.23%
CYP2C9 substrate + 0.6298 62.98%
CYP2D6 substrate - 0.9134 91.34%
CYP3A4 inhibition - 0.9611 96.11%
CYP2C9 inhibition - 0.9316 93.16%
CYP2C19 inhibition - 0.8725 87.25%
CYP2D6 inhibition - 0.9358 93.58%
CYP1A2 inhibition - 0.7651 76.51%
CYP2C8 inhibition - 0.9891 98.91%
CYP inhibitory promiscuity - 0.7881 78.81%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.4973 49.73%
Eye corrosion + 0.8962 89.62%
Eye irritation + 0.9713 97.13%
Skin irritation + 0.8507 85.07%
Skin corrosion - 0.8839 88.39%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6616 66.16%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation + 0.7146 71.46%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity - 0.9444 94.44%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.5253 52.53%
Acute Oral Toxicity (c) III 0.7965 79.65%
Estrogen receptor binding - 0.8643 86.43%
Androgen receptor binding - 0.6487 64.87%
Thyroid receptor binding - 0.8067 80.67%
Glucocorticoid receptor binding - 0.8394 83.94%
Aromatase binding - 0.8833 88.33%
PPAR gamma - 0.9229 92.29%
Honey bee toxicity - 0.9260 92.60%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.8200 82.00%
Fish aquatic toxicity + 0.8779 87.79%

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 95.26% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.53% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.03% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.79% 99.17%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.42% 89.34%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.41% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 81.46% 94.73%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.24% 96.47%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.64% 93.56%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 80.57% 97.29%

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.
Hippophae rhamnoides

Cross-Links

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PubChem 92570
NPASS NPC190515