18-Bromooctadeca-9,17-dien-5,7,15-triynoic acid

Details

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Internal ID 146a09c3-6e86-43ca-86b6-ebff76f75c7f
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name 18-bromooctadeca-9,17-dien-5,7,15-triynoic acid
SMILES (Canonical) C(CCC#CC=CBr)CC=CC#CC#CCCCC(=O)O
SMILES (Isomeric) C(CCC#CC=CBr)CC=CC#CC#CCCCC(=O)O
InChI InChI=1S/C18H19BrO2/c19-17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16-18(20)21/h1-2,15,17H,3,5,7,9,12,14,16H2,(H,20,21)
InChI Key FBQBLKRYQBDOAU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H19BrO2
Molecular Weight 347.20 g/mol
Exact Mass 346.05684 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 5.00
Atomic LogP (AlogP) 4.28
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 18-Bromooctadeca-9,17-dien-5,7,15-triynoic 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 - 0.6542 65.42%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.5676 56.76%
OATP2B1 inhibitior - 0.8563 85.63%
OATP1B1 inhibitior + 0.7892 78.92%
OATP1B3 inhibitior + 0.8985 89.85%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9194 91.94%
P-glycoprotein inhibitior - 0.8317 83.17%
P-glycoprotein substrate - 0.8975 89.75%
CYP3A4 substrate + 0.5060 50.60%
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 - 0.6578 65.78%
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 - 0.7179 71.79%
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 - 0.5000 50.00%
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 - 0.6276 62.76%
Acute Oral Toxicity (c) III 0.4427 44.27%
Estrogen receptor binding + 0.7635 76.35%
Androgen receptor binding - 0.6498 64.98%
Thyroid receptor binding + 0.6779 67.79%
Glucocorticoid receptor binding + 0.5930 59.30%
Aromatase binding - 0.5754 57.54%
PPAR gamma + 0.7667 76.67%
Honey bee toxicity - 0.8533 85.33%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.5200 52.00%
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 94.90% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.43% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.09% 96.09%
CHEMBL1781 P11387 DNA topoisomerase I 88.84% 97.00%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 88.53% 96.38%
CHEMBL2581 P07339 Cathepsin D 86.64% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.34% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.89% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.42% 94.45%

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 73831926
LOTUS LTS0227529
wikiData Q104992828