Deca-4,6-diynoic Acid

Details

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Internal ID 57a358a4-59b9-4021-aa76-131e33aa2ba0
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Medium-chain fatty acids
IUPAC Name deca-4,6-diynoic acid
SMILES (Canonical) CCCC#CC#CCCC(=O)O
SMILES (Isomeric) CCCC#CC#CCCC(=O)O
InChI InChI=1S/C10H12O2/c1-2-3-4-5-6-7-8-9-10(11)12/h2-3,8-9H2,1H3,(H,11,12)
InChI Key XCPOOOWWRLQSDS-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C10H12O2
Molecular Weight 164.20 g/mol
Exact Mass 164.083729621 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 2.20
Atomic LogP (AlogP) 1.66
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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SCHEMBL5394804

2D Structure

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2D Structure of Deca-4,6-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 + 0.9919 99.19%
Caco-2 - 0.6268 62.68%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.5008 50.08%
OATP2B1 inhibitior - 0.8540 85.40%
OATP1B1 inhibitior + 0.9046 90.46%
OATP1B3 inhibitior + 0.8943 89.43%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8436 84.36%
P-glycoprotein inhibitior - 0.9728 97.28%
P-glycoprotein substrate - 0.9567 95.67%
CYP3A4 substrate - 0.6956 69.56%
CYP2C9 substrate - 0.5398 53.98%
CYP2D6 substrate - 0.8794 87.94%
CYP3A4 inhibition - 0.9414 94.14%
CYP2C9 inhibition - 0.8697 86.97%
CYP2C19 inhibition - 0.9404 94.04%
CYP2D6 inhibition - 0.9469 94.69%
CYP1A2 inhibition + 0.6148 61.48%
CYP2C8 inhibition - 0.9702 97.02%
CYP inhibitory promiscuity - 0.9717 97.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5435 54.35%
Carcinogenicity (trinary) Non-required 0.6376 63.76%
Eye corrosion + 0.9628 96.28%
Eye irritation + 0.9677 96.77%
Skin irritation + 0.8638 86.38%
Skin corrosion + 0.9926 99.26%
Ames mutagenesis - 0.9278 92.78%
Human Ether-a-go-go-Related Gene inhibition - 0.8052 80.52%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation + 0.6051 60.51%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.8667 86.67%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.6165 61.65%
Acute Oral Toxicity (c) III 0.4590 45.90%
Estrogen receptor binding - 0.8706 87.06%
Androgen receptor binding - 0.7804 78.04%
Thyroid receptor binding - 0.7819 78.19%
Glucocorticoid receptor binding - 0.8928 89.28%
Aromatase binding - 0.8301 83.01%
PPAR gamma + 0.5238 52.38%
Honey bee toxicity - 0.9772 97.72%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.7332 73.32%
Fish aquatic toxicity - 0.5887 58.87%

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 95.44% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.54% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.59% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.49% 99.17%

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.
Bellis perennis

Cross-Links

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PubChem 10352027
LOTUS LTS0220443
wikiData Q105325317