(7E,13E,17E)-18-bromooctadeca-7,13,17-trien-5,15-diynoic acid

Details

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Internal ID eaee40f9-7031-49bc-b3d9-c1e0b8e1d43b
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name (7E,13E,17E)-18-bromooctadeca-7,13,17-trien-5,15-diynoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H21BrO2/c19-17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16-18(20)21/h4,6-7,9,15,17H,1-3,5,12,14,16H2,(H,20,21)/b6-4+,9-7+,17-15+
InChI Key XQBBTNXASWDRIQ-XEFVWHOUSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C18H21BrO2
Molecular Weight 349.30 g/mol
Exact Mass 348.07249 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 5.30
Atomic LogP (AlogP) 4.83
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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C18H21BrO2
BDBM50478567
(7e,13e,17e)-18-bromooctadeca-7,13,17-triene-5,15-diynoic acid

2D Structure

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2D Structure of (7E,13E,17E)-18-bromooctadeca-7,13,17-trien-5,15-diynoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9799 97.99%
Caco-2 - 0.6865 68.65%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.5676 56.76%
OATP2B1 inhibitior - 0.8566 85.66%
OATP1B1 inhibitior + 0.8049 80.49%
OATP1B3 inhibitior + 0.8985 89.85%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.6178 61.78%
P-glycoprotein inhibitior - 0.8093 80.93%
P-glycoprotein substrate - 0.9457 94.57%
CYP3A4 substrate - 0.5449 54.49%
CYP2C9 substrate - 0.5979 59.79%
CYP2D6 substrate - 0.8543 85.43%
CYP3A4 inhibition - 0.8135 81.35%
CYP2C9 inhibition - 0.7164 71.64%
CYP2C19 inhibition - 0.9208 92.08%
CYP2D6 inhibition - 0.9493 94.93%
CYP1A2 inhibition + 0.5655 56.55%
CYP2C8 inhibition - 0.7741 77.41%
CYP inhibitory promiscuity - 0.9325 93.25%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6114 61.14%
Carcinogenicity (trinary) Non-required 0.3801 38.01%
Eye corrosion + 0.9521 95.21%
Eye irritation - 0.5628 56.28%
Skin irritation + 0.7950 79.50%
Skin corrosion + 0.8931 89.31%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6583 65.83%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.6698 66.98%
skin sensitisation + 0.8818 88.18%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity - 0.7348 73.48%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.6861 68.61%
Acute Oral Toxicity (c) III 0.4427 44.27%
Estrogen receptor binding + 0.7489 74.89%
Androgen receptor binding - 0.7980 79.80%
Thyroid receptor binding + 0.6960 69.60%
Glucocorticoid receptor binding + 0.5622 56.22%
Aromatase binding - 0.4850 48.50%
PPAR gamma + 0.7873 78.73%
Honey bee toxicity - 0.8754 87.54%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.7198 71.98%

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 96.12% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.87% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.16% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.44% 96.09%
CHEMBL1781 P11387 DNA topoisomerase I 87.58% 97.00%
CHEMBL2581 P07339 Cathepsin D 84.53% 98.95%
CHEMBL4070 P19784 Casein kinase II alpha (prime) 81.11% 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 23427353
LOTUS LTS0118457
wikiData Q105339401