9-Decynoic acid

Details

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Internal ID 941b4d66-4116-44a2-857f-71030c96aa69
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Medium-chain fatty acids
IUPAC Name dec-9-ynoic acid
SMILES (Canonical) C#CCCCCCCCC(=O)O
SMILES (Isomeric) C#CCCCCCCCC(=O)O
InChI InChI=1S/C10H16O2/c1-2-3-4-5-6-7-8-9-10(11)12/h1H,3-9H2,(H,11,12)
InChI Key KHOZXYSECXUORA-UHFFFAOYSA-N
Popularity 14 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O2
Molecular Weight 168.23 g/mol
Exact Mass 168.115029749 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.43
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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dec-9-ynoic acid
1642-49-5
MFCD08064029
SCHEMBL740489
LCZC1162
DTXSID70415566
CHEBI:195807
BAA64249
GEO-03731
LMFA01030463
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 9-Decynoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9759 97.59%
Caco-2 + 0.5346 53.46%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6887 68.87%
OATP2B1 inhibitior - 0.8465 84.65%
OATP1B1 inhibitior + 0.9387 93.87%
OATP1B3 inhibitior + 0.8994 89.94%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8703 87.03%
P-glycoprotein inhibitior - 0.9824 98.24%
P-glycoprotein substrate - 0.9851 98.51%
CYP3A4 substrate - 0.6923 69.23%
CYP2C9 substrate + 0.6406 64.06%
CYP2D6 substrate - 0.8617 86.17%
CYP3A4 inhibition - 0.9512 95.12%
CYP2C9 inhibition - 0.6104 61.04%
CYP2C19 inhibition - 0.9560 95.60%
CYP2D6 inhibition - 0.9685 96.85%
CYP1A2 inhibition + 0.6481 64.81%
CYP2C8 inhibition - 0.9555 95.55%
CYP inhibitory promiscuity - 0.9619 96.19%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6635 66.35%
Carcinogenicity (trinary) Non-required 0.6478 64.78%
Eye corrosion + 0.9721 97.21%
Eye irritation + 0.7404 74.04%
Skin irritation + 0.7422 74.22%
Skin corrosion + 0.6779 67.79%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7051 70.51%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.6571 65.71%
skin sensitisation + 0.7288 72.88%
Respiratory toxicity + 0.9556 95.56%
Reproductive toxicity - 0.6929 69.29%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.5959 59.59%
Acute Oral Toxicity (c) III 0.5082 50.82%
Estrogen receptor binding - 0.9067 90.67%
Androgen receptor binding - 0.9438 94.38%
Thyroid receptor binding - 0.8457 84.57%
Glucocorticoid receptor binding - 0.7851 78.51%
Aromatase binding - 0.8460 84.60%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.9711 97.11%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity - 0.4739 47.39%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.43% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.11% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 91.78% 90.17%
CHEMBL2581 P07339 Cathepsin D 85.98% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 85.35% 89.63%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.40% 91.11%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 82.75% 92.26%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Hibiscus rosa-sinensis

Cross-Links

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PubChem 5312603
LOTUS LTS0128650
wikiData Q82224500