3-Pentanol

Details

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Internal ID 1db22875-c33d-4f57-89d7-2d4f4f615db6
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name pentan-3-ol
SMILES (Canonical) CCC(CC)O
SMILES (Isomeric) CCC(CC)O
InChI InChI=1S/C5H12O/c1-3-5(6)4-2/h5-6H,3-4H2,1-2H3
InChI Key AQIXEPGDORPWBJ-UHFFFAOYSA-N
Popularity 480 references in papers

Physical and Chemical Properties

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Molecular Formula C5H12O
Molecular Weight 88.15 g/mol
Exact Mass 88.088815002 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.17
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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584-02-1
Pentan-3-ol
Diethyl carbinol
Pentanol-3
3-Pentyl alcohol
1-Ethyl-1-propanol
NSC 8654
EINECS 209-526-7
BRN 1730964
UNII-X4ELC182I5
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-Pentanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9942 99.42%
Caco-2 + 0.8735 87.35%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Lysosomes 0.4743 47.43%
OATP2B1 inhibitior - 0.8549 85.49%
OATP1B1 inhibitior + 0.9496 94.96%
OATP1B3 inhibitior + 0.9499 94.99%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9367 93.67%
P-glycoprotein inhibitior - 0.9874 98.74%
P-glycoprotein substrate - 0.9793 97.93%
CYP3A4 substrate - 0.8374 83.74%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6625 66.25%
CYP3A4 inhibition - 0.9669 96.69%
CYP2C9 inhibition - 0.9254 92.54%
CYP2C19 inhibition - 0.8484 84.84%
CYP2D6 inhibition - 0.9278 92.78%
CYP1A2 inhibition - 0.6815 68.15%
CYP2C8 inhibition - 0.9944 99.44%
CYP inhibitory promiscuity - 0.9280 92.80%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) + 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.7591 75.91%
Eye corrosion + 0.8642 86.42%
Eye irritation + 0.9909 99.09%
Skin irritation + 0.7668 76.68%
Skin corrosion - 0.8496 84.96%
Ames mutagenesis - 0.9800 98.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7180 71.80%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6322 63.22%
skin sensitisation + 0.6527 65.27%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.8243 82.43%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity - 0.6170 61.70%
Acute Oral Toxicity (c) III 0.8447 84.47%
Estrogen receptor binding - 0.9166 91.66%
Androgen receptor binding - 0.8690 86.90%
Thyroid receptor binding - 0.8620 86.20%
Glucocorticoid receptor binding - 0.9109 91.09%
Aromatase binding - 0.9273 92.73%
PPAR gamma - 0.8876 88.76%
Honey bee toxicity - 0.9510 95.10%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.9300 93.00%
Fish aquatic toxicity - 0.8729 87.29%

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 93.53% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.69% 97.25%
CHEMBL2581 P07339 Cathepsin D 87.31% 98.95%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 80.00% 98.75%

Cross-Links

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PubChem 11428
NPASS NPC39977
LOTUS LTS0169578
wikiData Q590622