(Z)-dec-8-en-4,6-diyn-1-ol

Details

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Internal ID 1fd3c539-d72c-46c8-bdc5-034aecff69f2
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (Z)-dec-8-en-4,6-diyn-1-ol
SMILES (Canonical) CC=CC#CC#CCCCO
SMILES (Isomeric) C/C=C\C#CC#CCCCO
InChI InChI=1S/C10H12O/c1-2-3-4-5-6-7-8-9-10-11/h2-3,11H,8-10H2,1H3/b3-2-
InChI Key MOCQCNVQYOZNTO-IHWYPQMZSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H12O
Molecular Weight 148.20 g/mol
Exact Mass 148.088815002 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.34
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (Z)-dec-8-en-4,6-diyn-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9869 98.69%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.5286 52.86%
OATP2B1 inhibitior - 0.8636 86.36%
OATP1B1 inhibitior + 0.8355 83.55%
OATP1B3 inhibitior + 0.9444 94.44%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9097 90.97%
P-glycoprotein inhibitior - 0.9840 98.40%
P-glycoprotein substrate - 0.8963 89.63%
CYP3A4 substrate - 0.5941 59.41%
CYP2C9 substrate - 0.8016 80.16%
CYP2D6 substrate - 0.7877 78.77%
CYP3A4 inhibition - 0.8683 86.83%
CYP2C9 inhibition - 0.8803 88.03%
CYP2C19 inhibition - 0.9008 90.08%
CYP2D6 inhibition - 0.9548 95.48%
CYP1A2 inhibition - 0.5772 57.72%
CYP2C8 inhibition - 0.8844 88.44%
CYP inhibitory promiscuity - 0.8522 85.22%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6300 63.00%
Carcinogenicity (trinary) Non-required 0.6335 63.35%
Eye corrosion + 0.9049 90.49%
Eye irritation + 0.6814 68.14%
Skin irritation + 0.8430 84.30%
Skin corrosion + 0.6262 62.62%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5872 58.72%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5340 53.40%
skin sensitisation + 0.6035 60.35%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.7003 70.03%
Acute Oral Toxicity (c) III 0.6021 60.21%
Estrogen receptor binding - 0.8948 89.48%
Androgen receptor binding - 0.7739 77.39%
Thyroid receptor binding - 0.6666 66.66%
Glucocorticoid receptor binding - 0.7382 73.82%
Aromatase binding - 0.7069 70.69%
PPAR gamma - 0.6776 67.76%
Honey bee toxicity - 0.9235 92.35%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.8855 88.55%
Fish aquatic toxicity - 0.9119 91.19%

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 90.75% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 86.98% 87.45%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 84.62% 83.57%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.58% 99.17%
CHEMBL2581 P07339 Cathepsin D 81.47% 98.95%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 80.28% 92.86%
CHEMBL226 P30542 Adenosine A1 receptor 80.25% 95.93%

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.
Leucanthemum maximum

Cross-Links

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PubChem 102317277
LOTUS LTS0164913
wikiData Q105168778