(5E,17E)-18-bromo-octadeca-5,17-diene-15-ynoic acid

Details

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Internal ID 87438b65-df35-4897-8d85-2d0d5f38a288
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name (5E,17E)-18-bromooctadeca-5,17-dien-15-ynoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H27BrO2/c19-17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16-18(20)21/h8,10,15,17H,1-7,9,12,14,16H2,(H,20,21)/b10-8+,17-15+
InChI Key GLVCRWQIQQDOLB-ARBZGMGISA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C18H27BrO2
Molecular Weight 355.30 g/mol
Exact Mass 354.11944 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 6.40
Atomic LogP (AlogP) 5.83
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 12

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (5E,17E)-18-bromo-octadeca-5,17-diene-15-ynoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9844 98.44%
Caco-2 - 0.5937 59.37%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.5312 53.12%
OATP2B1 inhibitior - 0.8556 85.56%
OATP1B1 inhibitior + 0.7637 76.37%
OATP1B3 inhibitior + 0.8820 88.20%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.5601 56.01%
P-glycoprotein inhibitior - 0.8120 81.20%
P-glycoprotein substrate - 0.9499 94.99%
CYP3A4 substrate - 0.5358 53.58%
CYP2C9 substrate - 0.5979 59.79%
CYP2D6 substrate - 0.8543 85.43%
CYP3A4 inhibition - 0.8500 85.00%
CYP2C9 inhibition - 0.6592 65.92%
CYP2C19 inhibition - 0.9225 92.25%
CYP2D6 inhibition - 0.9546 95.46%
CYP1A2 inhibition + 0.5930 59.30%
CYP2C8 inhibition - 0.7636 76.36%
CYP inhibitory promiscuity - 0.9424 94.24%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6214 62.14%
Carcinogenicity (trinary) Non-required 0.4377 43.77%
Eye corrosion + 0.9367 93.67%
Eye irritation + 0.6548 65.48%
Skin irritation + 0.7092 70.92%
Skin corrosion - 0.5321 53.21%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7847 78.47%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.7250 72.50%
skin sensitisation + 0.9139 91.39%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity - 0.7641 76.41%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.6662 66.62%
Acute Oral Toxicity (c) III 0.5693 56.93%
Estrogen receptor binding + 0.5749 57.49%
Androgen receptor binding - 0.8441 84.41%
Thyroid receptor binding + 0.6752 67.52%
Glucocorticoid receptor binding - 0.5880 58.80%
Aromatase binding - 0.7234 72.34%
PPAR gamma + 0.7819 78.19%
Honey bee toxicity - 0.8946 89.46%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.8459 84.59%

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
CHEMBL221 P23219 Cyclooxygenase-1 96.00% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.53% 99.17%
CHEMBL1781 P11387 DNA topoisomerase I 92.01% 97.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.33% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.87% 96.09%
CHEMBL2581 P07339 Cathepsin D 86.73% 98.95%
CHEMBL4070 P19784 Casein kinase II alpha (prime) 83.49% 91.67%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 129861882
LOTUS LTS0112618
wikiData Q77509689