1-Cyclopentyl-1-propanol

Details

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Internal ID 04758a59-1ed0-4aa7-aa10-c261d7891229
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name 1-cyclopentylpropan-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H16O/c1-2-8(9)7-5-3-4-6-7/h7-9H,2-6H2,1H3
InChI Key JXLATLGQNUUYCG-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C8H16O
Molecular Weight 128.21 g/mol
Exact Mass 128.120115130 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.30
Atomic LogP (AlogP) 1.95
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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Aethylcyclopentylcarbinol
SCHEMBL128333
JXLATLGQNUUYCG-UHFFFAOYSA-N
AKOS010015993

2D Structure

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2D Structure of 1-Cyclopentyl-1-propanol

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 + 0.7238 72.38%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.4409 44.09%
OATP2B1 inhibitior - 0.8266 82.66%
OATP1B1 inhibitior + 0.9388 93.88%
OATP1B3 inhibitior + 0.9268 92.68%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9499 94.99%
P-glycoprotein inhibitior - 0.9837 98.37%
P-glycoprotein substrate - 0.9360 93.60%
CYP3A4 substrate - 0.7378 73.78%
CYP2C9 substrate - 0.8151 81.51%
CYP2D6 substrate - 0.6696 66.96%
CYP3A4 inhibition - 0.9780 97.80%
CYP2C9 inhibition - 0.8675 86.75%
CYP2C19 inhibition - 0.8835 88.35%
CYP2D6 inhibition - 0.9387 93.87%
CYP1A2 inhibition - 0.6109 61.09%
CYP2C8 inhibition - 0.9720 97.20%
CYP inhibitory promiscuity - 0.8358 83.58%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.5755 57.55%
Eye corrosion + 0.7126 71.26%
Eye irritation + 0.9825 98.25%
Skin irritation + 0.7480 74.80%
Skin corrosion - 0.7881 78.81%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5528 55.28%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.5628 56.28%
skin sensitisation + 0.8112 81.12%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.5027 50.27%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity - 0.8147 81.47%
Acute Oral Toxicity (c) III 0.7362 73.62%
Estrogen receptor binding - 0.9258 92.58%
Androgen receptor binding - 0.7765 77.65%
Thyroid receptor binding - 0.8628 86.28%
Glucocorticoid receptor binding - 0.8779 87.79%
Aromatase binding - 0.8764 87.64%
PPAR gamma - 0.8987 89.87%
Honey bee toxicity - 0.9782 97.82%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity - 0.6178 61.78%

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 95.56% 96.09%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 93.40% 96.38%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.56% 97.25%
CHEMBL2581 P07339 Cathepsin D 88.77% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.74% 97.09%
CHEMBL5203 P33316 dUTP pyrophosphatase 83.12% 99.18%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.70% 85.14%
CHEMBL226 P30542 Adenosine A1 receptor 82.64% 95.93%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 82.06% 95.58%
CHEMBL1968 P07099 Epoxide hydrolase 1 81.90% 98.57%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.18% 95.89%

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.
Monosis parishii

Cross-Links

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PubChem 536851
LOTUS LTS0218619
wikiData Q105136620