3,6-Nonadien-1-ol

Details

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Internal ID cea6f69f-53f8-4213-97ae-aac011fe2385
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name nona-3,6-dien-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H16O/c1-2-3-4-5-6-7-8-9-10/h3-4,6-7,10H,2,5,8-9H2,1H3
InChI Key PICGPEBVZGCYBV-UHFFFAOYSA-N
Popularity 13 references in papers

Physical and Chemical Properties

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Molecular Formula C9H16O
Molecular Weight 140.22 g/mol
Exact Mass 140.120115130 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.28
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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76649-25-7
NONA-3,6-DIEN-1-OL
EINECS 278-518-3
DTXSID6072843
RefChem:91795
DTXCID4047911
278-518-3
3,6-nonadienol
MFCD01632150
SCHEMBL88350
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3,6-Nonadien-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 + 0.9925 99.25%
Caco-2 + 0.9078 90.78%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.5616 56.16%
OATP2B1 inhibitior - 0.8641 86.41%
OATP1B1 inhibitior + 0.7276 72.76%
OATP1B3 inhibitior + 0.9201 92.01%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8509 85.09%
P-glycoprotein inhibitior - 0.9863 98.63%
P-glycoprotein substrate - 0.9654 96.54%
CYP3A4 substrate - 0.7380 73.80%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7528 75.28%
CYP3A4 inhibition - 0.9347 93.47%
CYP2C9 inhibition - 0.9230 92.30%
CYP2C19 inhibition - 0.9376 93.76%
CYP2D6 inhibition - 0.9509 95.09%
CYP1A2 inhibition - 0.6532 65.32%
CYP2C8 inhibition - 0.9710 97.10%
CYP inhibitory promiscuity - 0.8282 82.82%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.6300 63.00%
Carcinogenicity (trinary) Non-required 0.6885 68.85%
Eye corrosion + 0.9058 90.58%
Eye irritation + 0.9720 97.20%
Skin irritation + 0.7930 79.30%
Skin corrosion - 0.9828 98.28%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7511 75.11%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.6370 63.70%
skin sensitisation + 0.8353 83.53%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity - 0.6416 64.16%
Acute Oral Toxicity (c) III 0.8693 86.93%
Estrogen receptor binding - 0.9280 92.80%
Androgen receptor binding - 0.9390 93.90%
Thyroid receptor binding - 0.8249 82.49%
Glucocorticoid receptor binding - 0.7010 70.10%
Aromatase binding - 0.8913 89.13%
PPAR gamma - 0.6508 65.08%
Honey bee toxicity - 0.9832 98.32%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.8600 86.00%
Fish aquatic toxicity - 0.6435 64.35%

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 86.52% 96.09%
CHEMBL239 Q07869 Peroxisome proliferator-activated receptor alpha 84.55% 90.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.27% 99.17%
CHEMBL2581 P07339 Cathepsin D 81.73% 98.95%
CHEMBL2885 P07451 Carbonic anhydrase III 80.77% 87.45%

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.
Cucumis melo

Cross-Links

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PubChem 42011
LOTUS LTS0104921
wikiData Q82001091