10-Undecyn-1-ol

Details

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Internal ID 28856300-65d4-40f8-b2c3-61de6d803986
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name undec-10-yn-1-ol
SMILES (Canonical) C#CCCCCCCCCCO
SMILES (Isomeric) C#CCCCCCCCCCO
InChI InChI=1S/C11H20O/c1-2-3-4-5-6-7-8-9-10-11-12/h1,12H,3-11H2
InChI Key YUQZOUNRPZBQJK-UHFFFAOYSA-N
Popularity 29 references in papers

Physical and Chemical Properties

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Molecular Formula C11H20O
Molecular Weight 168.28 g/mol
Exact Mass 168.151415257 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.30
Atomic LogP (AlogP) 2.73
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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undec-10-yn-1-ol
2774-84-7
MFCD00041675
10-undecynol
11-hydroxyundecyne
10-undecyne-1-ol
SCHEMBL128978
DTXSID0062638
AMY25626
AKOS005137924
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 10-Undecyn-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 + 0.9714 97.14%
Caco-2 + 0.7666 76.66%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Lysosomes 0.4739 47.39%
OATP2B1 inhibitior - 0.8549 85.49%
OATP1B1 inhibitior + 0.9426 94.26%
OATP1B3 inhibitior + 0.9436 94.36%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.7990 79.90%
P-glycoprotein inhibitior - 0.9720 97.20%
P-glycoprotein substrate - 0.9821 98.21%
CYP3A4 substrate - 0.6950 69.50%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7159 71.59%
CYP3A4 inhibition - 0.9264 92.64%
CYP2C9 inhibition - 0.7260 72.60%
CYP2C19 inhibition - 0.9179 91.79%
CYP2D6 inhibition - 0.9524 95.24%
CYP1A2 inhibition - 0.6127 61.27%
CYP2C8 inhibition - 0.9375 93.75%
CYP inhibitory promiscuity - 0.8665 86.65%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6900 69.00%
Carcinogenicity (trinary) Non-required 0.6279 62.79%
Eye corrosion + 0.9083 90.83%
Eye irritation + 0.8767 87.67%
Skin irritation + 0.7511 75.11%
Skin corrosion - 0.6663 66.63%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4697 46.97%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5571 55.71%
skin sensitisation + 0.7097 70.97%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.6203 62.03%
Acute Oral Toxicity (c) II 0.4939 49.39%
Estrogen receptor binding - 0.9237 92.37%
Androgen receptor binding - 0.8724 87.24%
Thyroid receptor binding - 0.7372 73.72%
Glucocorticoid receptor binding - 0.8232 82.32%
Aromatase binding - 0.8741 87.41%
PPAR gamma - 0.7783 77.83%
Honey bee toxicity - 0.9480 94.80%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity - 0.7221 72.21%
Fish aquatic toxicity - 0.8063 80.63%

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
CHEMBL2885 P07451 Carbonic anhydrase III 89.26% 87.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.17% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 84.69% 89.63%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.66% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.14% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 80.05% 97.29%

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.
Azadirachta indica
Kaempferia galanga
Perilla frutescens

Cross-Links

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PubChem 76015
NPASS NPC141134
LOTUS LTS0115069
wikiData Q18571289