3-Butenoic acid, 3-methyl-, (3-methyl-3-butenyl) ester

Details

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Internal ID 2d51c5e2-81aa-4b46-87b3-6969cc43baa7
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name 3-methylbut-3-enyl 3-methylbut-3-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H16O2/c1-8(2)5-6-12-10(11)7-9(3)4/h1,3,5-7H2,2,4H3
InChI Key AYKGECXGINYBJE-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O2
Molecular Weight 168.23 g/mol
Exact Mass 168.115029749 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.46
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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3-Butenoic acid, 3-methyl-, (3-methyl-3-butenyl) ester
AYKGECXGINYBJE-UHFFFAOYSA-N
3-Methyl-3-butenyl 3-methyl-3-butenoate #

2D Structure

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2D Structure of 3-Butenoic acid, 3-methyl-, (3-methyl-3-butenyl) ester

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9947 99.47%
Caco-2 + 0.8217 82.17%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.5840 58.40%
OATP2B1 inhibitior - 0.8524 85.24%
OATP1B1 inhibitior + 0.9351 93.51%
OATP1B3 inhibitior + 0.9153 91.53%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9399 93.99%
P-glycoprotein inhibitior - 0.9684 96.84%
P-glycoprotein substrate - 0.9465 94.65%
CYP3A4 substrate - 0.5754 57.54%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8708 87.08%
CYP3A4 inhibition - 0.8941 89.41%
CYP2C9 inhibition - 0.9266 92.66%
CYP2C19 inhibition - 0.8834 88.34%
CYP2D6 inhibition - 0.9409 94.09%
CYP1A2 inhibition - 0.6485 64.85%
CYP2C8 inhibition - 0.9398 93.98%
CYP inhibitory promiscuity - 0.7745 77.45%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Non-required 0.5873 58.73%
Eye corrosion + 0.9202 92.02%
Eye irritation + 0.9949 99.49%
Skin irritation + 0.6135 61.35%
Skin corrosion - 0.9911 99.11%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7299 72.99%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation + 0.6461 64.61%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity + 0.7215 72.15%
Acute Oral Toxicity (c) III 0.6483 64.83%
Estrogen receptor binding - 0.9704 97.04%
Androgen receptor binding - 0.9312 93.12%
Thyroid receptor binding - 0.8242 82.42%
Glucocorticoid receptor binding - 0.8972 89.72%
Aromatase binding - 0.8355 83.55%
PPAR gamma - 0.8983 89.83%
Honey bee toxicity - 0.8812 88.12%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity + 0.9878 98.78%

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
CHEMBL4040 P28482 MAP kinase ERK2 96.06% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.84% 96.09%
CHEMBL3437 Q16853 Amine oxidase, copper containing 92.00% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.98% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.14% 91.11%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 86.01% 94.33%
CHEMBL2581 P07339 Cathepsin D 81.39% 98.95%

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.
Callitropsis nootkatensis

Cross-Links

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PubChem 549289
LOTUS LTS0000655
wikiData Q105100321