13-Heptadecyn-1-ol

Details

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Internal ID 65019b8c-6bd0-4900-b7bd-665ca5db4acf
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name heptadec-13-yn-1-ol
SMILES (Canonical) CCCC#CCCCCCCCCCCCCO
SMILES (Isomeric) CCCC#CCCCCCCCCCCCCO
InChI InChI=1S/C17H32O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18/h18H,2-3,6-17H2,1H3
InChI Key DZJZIJZUKAATIV-UHFFFAOYSA-N
Popularity 10 references in papers

Physical and Chemical Properties

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Molecular Formula C17H32O
Molecular Weight 252.40 g/mol
Exact Mass 252.245315640 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 6.70
Atomic LogP (AlogP) 5.07
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 12

Synonyms

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heptadec-13-yn-1-ol
SCHEMBL18614852
CHEBI:172494
DZJZIJZUKAATIV-UHFFFAOYSA-N
56554-77-9

2D Structure

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2D Structure of 13-Heptadecyn-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 + 0.9852 98.52%
Caco-2 + 0.7841 78.41%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Lysosomes 0.5554 55.54%
OATP2B1 inhibitior - 0.8556 85.56%
OATP1B1 inhibitior + 0.9233 92.33%
OATP1B3 inhibitior + 0.9183 91.83%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.6526 65.26%
P-glycoprotein inhibitior - 0.9192 91.92%
P-glycoprotein substrate - 0.9155 91.55%
CYP3A4 substrate - 0.6524 65.24%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7491 74.91%
CYP3A4 inhibition - 0.8566 85.66%
CYP2C9 inhibition - 0.7824 78.24%
CYP2C19 inhibition - 0.8924 89.24%
CYP2D6 inhibition - 0.9275 92.75%
CYP1A2 inhibition - 0.5069 50.69%
CYP2C8 inhibition - 0.9318 93.18%
CYP inhibitory promiscuity - 0.8339 83.39%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.6355 63.55%
Eye corrosion + 0.6693 66.93%
Eye irritation + 0.9754 97.54%
Skin irritation + 0.6336 63.36%
Skin corrosion - 0.9499 94.99%
Ames mutagenesis - 0.9900 99.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5874 58.74%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5257 52.57%
skin sensitisation + 0.7544 75.44%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity + 0.6836 68.36%
Acute Oral Toxicity (c) III 0.4179 41.79%
Estrogen receptor binding - 0.7652 76.52%
Androgen receptor binding - 0.7278 72.78%
Thyroid receptor binding + 0.5378 53.78%
Glucocorticoid receptor binding - 0.8168 81.68%
Aromatase binding - 0.8113 81.13%
PPAR gamma - 0.7899 78.99%
Honey bee toxicity - 0.9823 98.23%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.7135 71.35%
Fish aquatic toxicity - 0.4563 45.63%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.11% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 92.84% 87.45%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 90.40% 92.86%
CHEMBL2581 P07339 Cathepsin D 88.09% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 87.17% 89.63%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 85.09% 97.29%
CHEMBL221 P23219 Cyclooxygenase-1 84.36% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.02% 99.17%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 82.42% 91.81%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 81.59% 92.08%

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.
Citrus × aurantium
Citrus deliciosa

Cross-Links

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PubChem 557439
NPASS NPC180555