Nonan-1-ol

Details

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Internal ID 7ad5e86e-adf0-49ab-a143-c58f6387dcb4
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name nonan-1-ol
SMILES (Canonical) CCCCCCCCCO
SMILES (Isomeric) CCCCCCCCCO
InChI InChI=1S/C9H20O/c1-2-3-4-5-6-7-8-9-10/h10H,2-9H2,1H3
InChI Key ZWRUINPWMLAQRD-UHFFFAOYSA-N
Popularity 2,255 references 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 4.30
Atomic LogP (AlogP) 2.73
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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1-Nonanol
Nonanol
143-08-8
NONYL ALCOHOL
n-Nonyl alcohol
Pelargonic alcohol
1-Hydroxynonane
Nonalol
Octyl carbinol
n-Nonanol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Nonan-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 + 0.9911 99.11%
Caco-2 + 0.9120 91.20%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.8429 84.29%
Subcellular localzation Lysosomes 0.7017 70.17%
OATP2B1 inhibitior - 0.8498 84.98%
OATP1B1 inhibitior + 0.9187 91.87%
OATP1B3 inhibitior + 0.8824 88.24%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.8965 89.65%
P-glycoprotein inhibitior - 0.9803 98.03%
P-glycoprotein substrate - 0.9503 95.03%
CYP3A4 substrate - 0.7564 75.64%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7296 72.96%
CYP3A4 inhibition - 0.9142 91.42%
CYP2C9 inhibition - 0.8798 87.98%
CYP2C19 inhibition - 0.9330 93.30%
CYP2D6 inhibition - 0.9262 92.62%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition - 0.9552 95.52%
CYP inhibitory promiscuity - 0.8928 89.28%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.7292 72.92%
Eye corrosion + 0.7309 73.09%
Eye irritation + 0.9934 99.34%
Skin irritation + 0.7609 76.09%
Skin corrosion - 0.9639 96.39%
Ames mutagenesis - 1.0000 100.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6241 62.41%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5312 53.12%
skin sensitisation + 0.8750 87.50%
Respiratory toxicity - 0.9556 95.56%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.6444 64.44%
Acute Oral Toxicity (c) III 0.8548 85.48%
Estrogen receptor binding - 0.9534 95.34%
Androgen receptor binding - 0.8512 85.12%
Thyroid receptor binding - 0.7825 78.25%
Glucocorticoid receptor binding - 0.8918 89.18%
Aromatase binding - 0.9130 91.30%
PPAR gamma - 0.8640 86.40%
Honey bee toxicity - 0.9967 99.67%
Biodegradation + 1.0000 100.00%
Crustacea aquatic toxicity - 0.5057 50.57%
Fish aquatic toxicity + 0.7179 71.79%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL1293235 P02545 Prelamin-A/C 2.5 nM
354.8 nM
Potency
Potency
via Super-PRED
via Super-PRED
CHEMBL1963 P16473 Thyroid stimulating hormone receptor 12.6 nM
Potency
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL2885 P07451 Carbonic anhydrase III 94.65% 87.45%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 93.94% 97.29%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 93.31% 92.86%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.30% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.12% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 90.28% 89.63%
CHEMBL2581 P07339 Cathepsin D 89.31% 98.95%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 88.08% 91.81%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.66% 99.17%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 82.08% 85.94%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.66% 96.95%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.40% 100.00%
CHEMBL2996 Q05655 Protein kinase C delta 80.02% 97.79%

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.
Abies sachalinensis
Aizoon africanum
Alangium premnifolium
Angelica tarokoensis
Anthemis aciphylla
Avena sativa
Bidens andicola
Bombax ceiba
Bunium paucifolium
Bupleurum chinense
Cannabis sativa
Castanopsis cuspidata
Chaenomeles sinensis
Citrullus lanatus
Citrus × aurantium
Citrus deliciosa
Citrus trifoliata
Codonopsis pilosula
Cucumis melo
Diospyros ferrea
Epimedium davidii
Erysimum odoratum
Frullania tamarisci
Globba variabilis
Hamamelis virginiana
Heterotheca inuloides
Hordeum vulgare
Houttuynia cordata
Humulus lupulus
Ilex amara
Isodon japonicus
Knightia excelsa
Lasiosiphon lampranthus
Leonurus glaucescens
Lepidium draba
Ligularia hodgsonii
Micromeria pineolens
Ophrys sphegodes
Opuntia ficus-indica
Origanum vulgare subsp. gracile
Panax ginseng
Panax quinquefolius
Pelargonium endlicherianum
Phaseolus vulgaris
Phyllanthus emblica
Pimenta racemosa
Prunus dulcis
Quercus petraea subsp. petraea
Rehmannia glutinosa
Rhodiola rosea
Rosa gallica
Salacia madagascariensis
Satureja montana
Saussurea lyrata
Senna alexandrina
Sideritis lyciae
Solanum acaule
Swertia delavayi
Thymus quinquecostatus
Thymus vulgaris
Trichosanthes kirilowii
Trichosanthes rosthornii
Trigonotis peduncularis
Triticum aestivum
Vaccinium macrocarpon
Vaccinium vitis-idaea
Vepris hiernii
Vismia jefensis
Vitex negundo
Vitis vinifera
Zanthoxylum bungeanum
Zanthoxylum schinifolium
Zea mays
Zingiber officinale

Cross-Links

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PubChem 8914
NPASS NPC225783
LOTUS LTS0157379
wikiData Q161662