14,16-Dibromohexadeca-7,13,15-trien-5-ynoic acid

Details

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Internal ID a4936abe-5096-4a2c-b0e8-0b3669d5d172
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name 14,16-dibromohexadeca-7,13,15-trien-5-ynoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H20Br2O2/c17-14-13-15(18)11-9-7-5-3-1-2-4-6-8-10-12-16(19)20/h1-2,11,13-14H,3,5,7-10,12H2,(H,19,20)
InChI Key VDRFUGQYPWWVGI-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C16H20Br2O2
Molecular Weight 404.14 g/mol
Exact Mass 403.98096 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 5.40
Atomic LogP (AlogP) 5.55
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 14,16-Dibromohexadeca-7,13,15-trien-5-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 + 0.9804 98.04%
Caco-2 + 0.5988 59.88%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6475 64.75%
OATP2B1 inhibitior - 0.8561 85.61%
OATP1B1 inhibitior + 0.8095 80.95%
OATP1B3 inhibitior + 0.9105 91.05%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5401 54.01%
P-glycoprotein inhibitior - 0.8701 87.01%
P-glycoprotein substrate - 0.8956 89.56%
CYP3A4 substrate + 0.5097 50.97%
CYP2C9 substrate - 0.5979 59.79%
CYP2D6 substrate - 0.8543 85.43%
CYP3A4 inhibition - 0.8383 83.83%
CYP2C9 inhibition - 0.6886 68.86%
CYP2C19 inhibition - 0.8921 89.21%
CYP2D6 inhibition - 0.9415 94.15%
CYP1A2 inhibition - 0.5720 57.20%
CYP2C8 inhibition - 0.6570 65.70%
CYP inhibitory promiscuity - 0.9014 90.14%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6149 61.49%
Carcinogenicity (trinary) Non-required 0.4054 40.54%
Eye corrosion + 0.8755 87.55%
Eye irritation - 0.6099 60.99%
Skin irritation + 0.6473 64.73%
Skin corrosion + 0.7228 72.28%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6453 64.53%
Micronuclear - 0.9100 91.00%
Hepatotoxicity - 0.7073 70.73%
skin sensitisation + 0.7990 79.90%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity - 0.7215 72.15%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.6446 64.46%
Acute Oral Toxicity (c) III 0.4473 44.73%
Estrogen receptor binding + 0.7021 70.21%
Androgen receptor binding - 0.8474 84.74%
Thyroid receptor binding + 0.6469 64.69%
Glucocorticoid receptor binding - 0.6146 61.46%
Aromatase binding + 0.5807 58.07%
PPAR gamma + 0.9044 90.44%
Honey bee toxicity - 0.8502 85.02%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.8338 83.38%

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 98.01% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.59% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.76% 96.09%
CHEMBL1781 P11387 DNA topoisomerase I 86.67% 97.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.67% 91.11%
CHEMBL4070 P19784 Casein kinase II alpha (prime) 85.11% 91.67%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 84.45% 96.38%
CHEMBL2581 P07339 Cathepsin D 83.73% 98.95%

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 327029
LOTUS LTS0111605
wikiData Q105284335