5-Decen-1-ol, (5Z)-

Details

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Internal ID 33c3f311-a570-433f-bd1a-8a60751a7a93
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (Z)-dec-5-en-1-ol
SMILES (Canonical) CCCCC=CCCCCO
SMILES (Isomeric) CCCC/C=C\CCCCO
InChI InChI=1S/C10H20O/c1-2-3-4-5-6-7-8-9-10-11/h5-6,11H,2-4,7-10H2,1H3/b6-5-
InChI Key WYPQHXVMNVEVEB-WAYWQWQTSA-N
Popularity 25 references in papers

Physical and Chemical Properties

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Molecular Formula C10H20O
Molecular Weight 156.26 g/mol
Exact Mass 156.151415257 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.90
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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51652-47-2
5-Decen-1-ol, (5Z)-
(Z)-dec-5-en-1-ol
5Z-Decen-1-ol
(Z)-5-DECEN-1-OL
5-Decen-1-ol, (Z)-
cis-5-decenol
(Z)-5-decenol
(5Z)-dec-5-en-1-ol
SCHEMBL1301211
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 5-Decen-1-ol, (5Z)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9926 99.26%
Caco-2 + 0.9100 91.00%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Lysosomes 0.5404 54.04%
OATP2B1 inhibitior - 0.8560 85.60%
OATP1B1 inhibitior + 0.7681 76.81%
OATP1B3 inhibitior + 0.8796 87.96%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8054 80.54%
P-glycoprotein inhibitior - 0.9798 97.98%
P-glycoprotein substrate - 0.9575 95.75%
CYP3A4 substrate - 0.7089 70.89%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7528 75.28%
CYP3A4 inhibition - 0.9065 90.65%
CYP2C9 inhibition - 0.8810 88.10%
CYP2C19 inhibition - 0.9136 91.36%
CYP2D6 inhibition - 0.9196 91.96%
CYP1A2 inhibition + 0.5542 55.42%
CYP2C8 inhibition - 0.9367 93.67%
CYP inhibitory promiscuity - 0.8235 82.35%
UGT catelyzed - 0.8000 80.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Non-required 0.7272 72.72%
Eye corrosion + 0.7375 73.75%
Eye irritation + 0.9828 98.28%
Skin irritation + 0.8261 82.61%
Skin corrosion - 0.9507 95.07%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5784 57.84%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5752 57.52%
skin sensitisation + 0.8671 86.71%
Respiratory toxicity - 0.9667 96.67%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.5438 54.38%
Acute Oral Toxicity (c) IV 0.6293 62.93%
Estrogen receptor binding - 0.9575 95.75%
Androgen receptor binding - 0.8358 83.58%
Thyroid receptor binding - 0.7638 76.38%
Glucocorticoid receptor binding - 0.7899 78.99%
Aromatase binding - 0.9270 92.70%
PPAR gamma - 0.7362 73.62%
Honey bee toxicity - 0.9934 99.34%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.7358 73.58%
Fish aquatic toxicity + 0.8334 83.34%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 92.60% 99.17%
CHEMBL2581 P07339 Cathepsin D 91.01% 98.95%
CHEMBL2885 P07451 Carbonic anhydrase III 90.53% 87.45%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.38% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.43% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.08% 92.08%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.74% 96.95%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 83.13% 92.86%
CHEMBL1781 P11387 DNA topoisomerase I 82.90% 97.00%
CHEMBL230 P35354 Cyclooxygenase-2 80.62% 89.63%

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.
Valeriana jatamansi

Cross-Links

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PubChem 5365622
NPASS NPC24822