(9R,10R)-14,16-dibromo-9,10-dihydroxyhexadeca-7,13,15-trien-5-ynoic acid

Details

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Internal ID 887f1c89-098f-4535-b3cd-183c80e29fad
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name (9R,10R)-14,16-dibromo-9,10-dihydroxyhexadeca-7,13,15-trien-5-ynoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H20Br2O4/c17-12-11-13(18)7-6-9-15(20)14(19)8-4-2-1-3-5-10-16(21)22/h4,7-8,11-12,14-15,19-20H,3,5-6,9-10H2,(H,21,22)/t14-,15-/m1/s1
InChI Key OGYZPLNGMUVBNX-HUUCEWRRSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H20Br2O4
Molecular Weight 436.10 g/mol
Exact Mass 435.97078 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.49
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (9R,10R)-14,16-dibromo-9,10-dihydroxyhexadeca-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 + 0.7975 79.75%
Caco-2 - 0.7113 71.13%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.7458 74.58%
OATP2B1 inhibitior - 0.8559 85.59%
OATP1B1 inhibitior + 0.8706 87.06%
OATP1B3 inhibitior + 0.9425 94.25%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.6021 60.21%
P-glycoprotein inhibitior - 0.8853 88.53%
P-glycoprotein substrate - 0.8071 80.71%
CYP3A4 substrate + 0.5554 55.54%
CYP2C9 substrate - 0.7929 79.29%
CYP2D6 substrate - 0.8471 84.71%
CYP3A4 inhibition - 0.8348 83.48%
CYP2C9 inhibition - 0.8426 84.26%
CYP2C19 inhibition - 0.8831 88.31%
CYP2D6 inhibition - 0.9212 92.12%
CYP1A2 inhibition - 0.7453 74.53%
CYP2C8 inhibition - 0.7539 75.39%
CYP inhibitory promiscuity - 0.9397 93.97%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7231 72.31%
Carcinogenicity (trinary) Non-required 0.4319 43.19%
Eye corrosion - 0.6791 67.91%
Eye irritation - 0.9039 90.39%
Skin irritation - 0.5966 59.66%
Skin corrosion + 0.5328 53.28%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5955 59.55%
Micronuclear - 0.7100 71.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.5907 59.07%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity - 0.7444 74.44%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.5547 55.47%
Estrogen receptor binding + 0.6375 63.75%
Androgen receptor binding - 0.8654 86.54%
Thyroid receptor binding + 0.6478 64.78%
Glucocorticoid receptor binding - 0.5404 54.04%
Aromatase binding + 0.5616 56.16%
PPAR gamma + 0.7709 77.09%
Honey bee toxicity - 0.8300 83.00%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.6694 66.94%

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 97.33% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.76% 99.17%
CHEMBL2581 P07339 Cathepsin D 92.41% 98.95%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 92.11% 96.38%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.72% 96.09%
CHEMBL4227 P25090 Lipoxin A4 receptor 86.47% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.15% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.58% 96.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.32% 93.56%

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 162942966
LOTUS LTS0236124
wikiData Q105191951