Acetic acid, (13-tetradecene-2,4-diynyloxy)-

Details

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Internal ID ffda7155-5bd4-48ce-a832-f643f4d037e2
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acids
IUPAC Name 2-tetradec-13-en-2,4-diynoxyacetic acid
SMILES (Canonical) C=CCCCCCCCC#CC#CCOCC(=O)O
SMILES (Isomeric) C=CCCCCCCCC#CC#CCOCC(=O)O
InChI InChI=1S/C16H22O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-19-15-16(17)18/h2H,1,3-9,14-15H2,(H,17,18)
InChI Key ODJULCBAODTNBX-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C16H22O3
Molecular Weight 262.34 g/mol
Exact Mass 262.15689456 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 4.40
Atomic LogP (AlogP) 3.01
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 10

Synonyms

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179600-05-6
2-tetradec-13-en-2,4-diynoxyacetic acid
Montiporic acid B
(13-Tetradecene-2,4-diynyloxy)acetic acid
MONOTIPORIC ACID B
CHEMBL453153
DTXSID10170844

2D Structure

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2D Structure of Acetic acid, (13-tetradecene-2,4-diynyloxy)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8918 89.18%
Caco-2 - 0.6127 61.27%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7124 71.24%
OATP2B1 inhibitior - 0.8567 85.67%
OATP1B1 inhibitior + 0.9083 90.83%
OATP1B3 inhibitior + 0.9416 94.16%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.6607 66.07%
P-glycoprotein inhibitior - 0.9053 90.53%
P-glycoprotein substrate - 0.9300 93.00%
CYP3A4 substrate - 0.5253 52.53%
CYP2C9 substrate + 0.6171 61.71%
CYP2D6 substrate - 0.8538 85.38%
CYP3A4 inhibition - 0.8572 85.72%
CYP2C9 inhibition - 0.8877 88.77%
CYP2C19 inhibition - 0.8747 87.47%
CYP2D6 inhibition - 0.9514 95.14%
CYP1A2 inhibition - 0.8787 87.87%
CYP2C8 inhibition - 0.7291 72.91%
CYP inhibitory promiscuity - 0.9503 95.03%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.6621 66.21%
Eye corrosion + 0.9685 96.85%
Eye irritation + 0.6923 69.23%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.8209 82.09%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4109 41.09%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation + 0.8688 86.88%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.9667 96.67%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.6832 68.32%
Acute Oral Toxicity (c) III 0.7824 78.24%
Estrogen receptor binding - 0.5848 58.48%
Androgen receptor binding - 0.7454 74.54%
Thyroid receptor binding + 0.5754 57.54%
Glucocorticoid receptor binding + 0.5585 55.85%
Aromatase binding - 0.5142 51.42%
PPAR gamma + 0.6998 69.98%
Honey bee toxicity - 0.8167 81.67%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.7741 77.41%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 93.74% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.62% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.23% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.46% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 86.04% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.46% 91.11%
CHEMBL4070 P19784 Casein kinase II alpha (prime) 80.25% 91.67%

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.
Stevia pilosa
Stevia porphyrea
Stevia serrata

Cross-Links

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PubChem 177349
LOTUS LTS0260725
wikiData Q105304660