3-Nonanol

Details

Top
Internal ID 240abcfc-d3f2-4479-af60-18802df494e6
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name nonan-3-ol
SMILES (Canonical) CCCCCCC(CC)O
SMILES (Isomeric) CCCCCCC(CC)O
InChI InChI=1S/C9H20O/c1-3-5-6-7-8-9(10)4-2/h9-10H,3-8H2,1-2H3
InChI Key GYSCXPVAKHVAAY-UHFFFAOYSA-N
Popularity 54 references in papers

Physical and Chemical Properties

Top
Molecular Formula C9H20O
Molecular Weight 144.25 g/mol
Exact Mass 144.151415257 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.30
Atomic LogP (AlogP) 2.73
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

Top
nonan-3-ol
624-51-1
Hexylethylcarbinol
(s)-nonan-3-ol
Ethylhexylcarbinol
(R)-1-Ethyl-1-heptanol
EINECS 210-850-6
UNII-047779Z489
AI3-37211
047779Z489
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of 3-Nonanol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9922 99.22%
Caco-2 + 0.9187 91.87%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.4494 44.94%
OATP2B1 inhibitior - 0.8394 83.94%
OATP1B1 inhibitior + 0.9502 95.02%
OATP1B3 inhibitior + 0.9044 90.44%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9271 92.71%
P-glycoprotein inhibitior - 0.9819 98.19%
P-glycoprotein substrate - 0.8820 88.20%
CYP3A4 substrate - 0.6926 69.26%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6625 66.25%
CYP3A4 inhibition - 0.9496 94.96%
CYP2C9 inhibition - 0.8890 88.90%
CYP2C19 inhibition - 0.9274 92.74%
CYP2D6 inhibition - 0.9254 92.54%
CYP1A2 inhibition + 0.6301 63.01%
CYP2C8 inhibition - 0.9712 97.12%
CYP inhibitory promiscuity - 0.8578 85.78%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.7457 74.57%
Eye corrosion + 0.8508 85.08%
Eye irritation + 0.9798 97.98%
Skin irritation + 0.5439 54.39%
Skin corrosion - 0.9046 90.46%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5665 56.65%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6135 61.35%
skin sensitisation + 0.9584 95.84%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.8409 84.09%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.5436 54.36%
Acute Oral Toxicity (c) III 0.8149 81.49%
Estrogen receptor binding - 0.8752 87.52%
Androgen receptor binding - 0.7948 79.48%
Thyroid receptor binding - 0.7219 72.19%
Glucocorticoid receptor binding - 0.8468 84.68%
Aromatase binding - 0.9170 91.70%
PPAR gamma - 0.8452 84.52%
Honey bee toxicity - 0.9882 98.82%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity + 0.5705 57.05%
Fish aquatic toxicity + 0.7676 76.76%

Targets

Top

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
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 96.16% 92.86%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 95.12% 97.29%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 95.11% 85.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.50% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.38% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.98% 97.25%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.35% 92.08%
CHEMBL230 P35354 Cyclooxygenase-2 89.42% 89.63%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.12% 99.17%
CHEMBL2885 P07451 Carbonic anhydrase III 88.37% 87.45%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 87.89% 91.81%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 86.08% 100.00%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 85.84% 90.24%
CHEMBL1907 P15144 Aminopeptidase N 85.28% 93.31%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 80.67% 98.75%

Plants that contains it

Top
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.
Achillea fragrantissima
Mentha arvensis
Mentha canadensis
Thymus zygioides

Cross-Links

Top
PubChem 12216
NPASS NPC66124
LOTUS LTS0160598
wikiData Q22668733