2-Propyl-1-pentanol

Details

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Internal ID 1c10e30b-fb7e-4a8b-88f3-42e9cd5e4c6f
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Primary alcohols
IUPAC Name 2-propylpentan-1-ol
SMILES (Canonical) CCCC(CCC)CO
SMILES (Isomeric) CCCC(CCC)CO
InChI InChI=1S/C8H18O/c1-3-5-8(7-9)6-4-2/h8-9H,3-7H2,1-2H3
InChI Key LASHFHLFDRTERB-UHFFFAOYSA-N
Popularity 20 references in papers

Physical and Chemical Properties

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Molecular Formula C8H18O
Molecular Weight 130.23 g/mol
Exact Mass 130.135765193 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.20
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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58175-57-8
2-propylpentan-1-ol
1-Pentanol, 2-propyl-
2-Propylpentanol
2-n-propyl-1-pentanol
BRN 1697442
SCHEMBL282622
2-Propyl-1-pentanol, 99%
DTXSID0074716
MFCD00010260
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-Propyl-1-pentanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9860 98.60%
Caco-2 + 0.9429 94.29%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.6184 61.84%
OATP2B1 inhibitior - 0.7844 78.44%
OATP1B1 inhibitior + 0.9601 96.01%
OATP1B3 inhibitior + 0.9240 92.40%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9410 94.10%
P-glycoprotein inhibitior - 0.9848 98.48%
P-glycoprotein substrate - 0.9550 95.50%
CYP3A4 substrate - 0.7663 76.63%
CYP2C9 substrate - 0.8468 84.68%
CYP2D6 substrate - 0.7359 73.59%
CYP3A4 inhibition - 0.9326 93.26%
CYP2C9 inhibition - 0.8505 85.05%
CYP2C19 inhibition - 0.9197 91.97%
CYP2D6 inhibition - 0.9027 90.27%
CYP1A2 inhibition - 0.6895 68.95%
CYP2C8 inhibition - 0.9948 99.48%
CYP inhibitory promiscuity - 0.8393 83.93%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.6159 61.59%
Eye corrosion + 0.8489 84.89%
Eye irritation + 0.9882 98.82%
Skin irritation - 0.8761 87.61%
Skin corrosion - 0.9951 99.51%
Ames mutagenesis - 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5734 57.34%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5494 54.94%
skin sensitisation + 0.9130 91.30%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.9444 94.44%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.5597 55.97%
Acute Oral Toxicity (c) III 0.7975 79.75%
Estrogen receptor binding - 0.9278 92.78%
Androgen receptor binding - 0.9482 94.82%
Thyroid receptor binding - 0.8599 85.99%
Glucocorticoid receptor binding - 0.8877 88.77%
Aromatase binding - 0.8478 84.78%
PPAR gamma - 0.9108 91.08%
Honey bee toxicity - 0.9822 98.22%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.8734 87.34%
Fish aquatic toxicity + 0.7929 79.29%

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 92.34% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.75% 98.95%
CHEMBL4040 P28482 MAP kinase ERK2 89.10% 83.82%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.39% 97.25%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 83.45% 97.29%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 81.29% 92.86%
CHEMBL1907 P15144 Aminopeptidase N 80.75% 93.31%

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.
Lobelia chinensis

Cross-Links

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PubChem 123543
NPASS NPC293353