8-Methylnonan-2-ol

Details

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Internal ID 508e6d32-8bb5-49e5-9bda-68e3ce85bee7
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name 8-methylnonan-2-ol
SMILES (Canonical) CC(C)CCCCCC(C)O
SMILES (Isomeric) CC(C)CCCCCC(C)O
InChI InChI=1S/C10H22O/c1-9(2)7-5-4-6-8-10(3)11/h9-11H,4-8H2,1-3H3
InChI Key ZVZKLBCGIYWGOU-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H22O
Molecular Weight 158.28 g/mol
Exact Mass 158.167065321 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.70
Atomic LogP (AlogP) 2.97
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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2-Nonanol, 8-methyl-
14779-92-1
8-METHYL-2-NONANOL
SCHEMBL195982
DTXSID30591850
AKOS021491325

2D Structure

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2D Structure of 8-Methylnonan-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9891 98.91%
Caco-2 + 0.8419 84.19%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.5162 51.62%
OATP2B1 inhibitior - 0.8429 84.29%
OATP1B1 inhibitior + 0.9777 97.77%
OATP1B3 inhibitior + 0.9457 94.57%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9551 95.51%
P-glycoprotein inhibitior - 0.9781 97.81%
P-glycoprotein substrate - 0.9152 91.52%
CYP3A4 substrate - 0.6678 66.78%
CYP2C9 substrate - 0.8151 81.51%
CYP2D6 substrate - 0.6696 66.96%
CYP3A4 inhibition - 0.9644 96.44%
CYP2C9 inhibition - 0.8830 88.30%
CYP2C19 inhibition - 0.9149 91.49%
CYP2D6 inhibition - 0.9515 95.15%
CYP1A2 inhibition - 0.6013 60.13%
CYP2C8 inhibition - 0.9947 99.47%
CYP inhibitory promiscuity - 0.9107 91.07%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Non-required 0.7669 76.69%
Eye corrosion + 0.8491 84.91%
Eye irritation + 0.9737 97.37%
Skin irritation + 0.6523 65.23%
Skin corrosion - 0.9586 95.86%
Ames mutagenesis - 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7517 75.17%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation + 0.9485 94.85%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.7928 79.28%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity - 0.6264 62.64%
Acute Oral Toxicity (c) III 0.7496 74.96%
Estrogen receptor binding - 0.9353 93.53%
Androgen receptor binding - 0.9162 91.62%
Thyroid receptor binding - 0.6775 67.75%
Glucocorticoid receptor binding - 0.7461 74.61%
Aromatase binding - 0.8921 89.21%
PPAR gamma - 0.8769 87.69%
Honey bee toxicity - 0.9754 97.54%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.6938 69.38%
Fish aquatic toxicity + 0.7195 71.95%

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
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 93.12% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.74% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.76% 98.95%
CHEMBL2885 P07451 Carbonic anhydrase III 89.13% 87.45%
CHEMBL1907 P15144 Aminopeptidase N 82.00% 93.31%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 81.87% 92.86%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.54% 93.56%

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.
Capsicum annuum

Cross-Links

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PubChem 17975363
NPASS NPC306101