(4R)-nonan-4-ol

Details

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Internal ID 12a0d39c-84c3-4117-a112-ae4c79665a8f
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (4R)-nonan-4-ol
SMILES (Canonical) CCCCCC(CCC)O
SMILES (Isomeric) CCCCC[C@@H](CCC)O
InChI InChI=1S/C9H20O/c1-3-5-6-8-9(10)7-4-2/h9-10H,3-8H2,1-2H3/t9-/m1/s1
InChI Key IXUOEGRSQCCEHB-SECBINFHSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C9H20O
Molecular Weight 144.25 g/mol
Exact Mass 144.151415257 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.73
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4R)-nonan-4-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9922 99.22%
Caco-2 + 0.9552 95.52%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.4494 44.94%
OATP2B1 inhibitior - 0.8312 83.12%
OATP1B1 inhibitior + 0.9461 94.61%
OATP1B3 inhibitior + 0.9044 90.44%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8988 89.88%
P-glycoprotein inhibitior - 0.9744 97.44%
P-glycoprotein substrate - 0.8937 89.37%
CYP3A4 substrate - 0.7083 70.83%
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 - 0.9806 98.06%
CYP inhibitory promiscuity - 0.8578 85.78%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.7457 74.57%
Eye corrosion + 0.8508 85.08%
Eye irritation + 0.9759 97.59%
Skin irritation + 0.5439 54.39%
Skin corrosion - 0.9046 90.46%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6133 61.33%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5424 54.24%
skin sensitisation + 0.9584 95.84%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.8409 84.09%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.6046 60.46%
Acute Oral Toxicity (c) III 0.8149 81.49%
Estrogen receptor binding - 0.8734 87.34%
Androgen receptor binding - 0.8782 87.82%
Thyroid receptor binding - 0.7723 77.23%
Glucocorticoid receptor binding - 0.8731 87.31%
Aromatase binding - 0.9202 92.02%
PPAR gamma - 0.8867 88.67%
Honey bee toxicity - 0.9891 98.91%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.5739 57.39%
Fish aquatic toxicity + 0.7676 76.76%

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
CHEMBL2581 P07339 Cathepsin D 94.70% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 94.37% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.36% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.85% 97.25%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 91.69% 92.86%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 86.60% 85.94%
CHEMBL2885 P07451 Carbonic anhydrase III 86.18% 87.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.80% 99.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.50% 92.08%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.68% 93.56%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 84.07% 91.81%
CHEMBL230 P35354 Cyclooxygenase-2 83.08% 89.63%
CHEMBL1907 P15144 Aminopeptidase N 81.90% 93.31%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.13% 100.00%
CHEMBL4105838 Q96GG9 DCN1-like protein 1 80.77% 95.00%

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.
Capillipedium parviflorum

Cross-Links

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PubChem 7004864
LOTUS LTS0089884
wikiData Q105122493