3-Methyl-1-pentanol

Details

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Internal ID 185848ff-b8a1-4492-a57e-c1b5be455e55
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Primary alcohols
IUPAC Name 3-methylpentan-1-ol
SMILES (Canonical) CCC(C)CCO
SMILES (Isomeric) CCC(C)CCO
InChI InChI=1S/C6H14O/c1-3-6(2)4-5-7/h6-7H,3-5H2,1-2H3
InChI Key IWTBVKIGCDZRPL-UHFFFAOYSA-N
Popularity 102 references in papers

Physical and Chemical Properties

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Molecular Formula C6H14O
Molecular Weight 102.17 g/mol
Exact Mass 102.104465066 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.41
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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3-Methylpentan-1-ol
589-35-5
3-Methylpentanol
2-Ethyl-4-butanol
3-Ethyl-1-butanol
1-Pentanol, 3-methyl-
FEMA No. 3762
UNII-N8W93SI0FS
N8W93SI0FS
(+/-)-3-methyl-1-pentanol
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-Methyl-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 + 0.9862 98.62%
Caco-2 + 0.9062 90.62%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.7423 74.23%
OATP2B1 inhibitior - 0.8454 84.54%
OATP1B1 inhibitior + 0.9265 92.65%
OATP1B3 inhibitior + 0.9166 91.66%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9548 95.48%
P-glycoprotein inhibitior - 0.9871 98.71%
P-glycoprotein substrate - 0.9266 92.66%
CYP3A4 substrate - 0.7824 78.24%
CYP2C9 substrate - 0.8468 84.68%
CYP2D6 substrate - 0.7359 73.59%
CYP3A4 inhibition - 0.9139 91.39%
CYP2C9 inhibition - 0.9109 91.09%
CYP2C19 inhibition - 0.9244 92.44%
CYP2D6 inhibition - 0.9274 92.74%
CYP1A2 inhibition - 0.6598 65.98%
CYP2C8 inhibition - 0.9958 99.58%
CYP inhibitory promiscuity - 0.8800 88.00%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.7440 74.40%
Eye corrosion + 0.8653 86.53%
Eye irritation + 0.9834 98.34%
Skin irritation + 0.7943 79.43%
Skin corrosion - 0.9593 95.93%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5983 59.83%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6259 62.59%
skin sensitisation + 0.8664 86.64%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.5093 50.93%
Acute Oral Toxicity (c) III 0.8816 88.16%
Estrogen receptor binding - 0.9366 93.66%
Androgen receptor binding - 0.9111 91.11%
Thyroid receptor binding - 0.8650 86.50%
Glucocorticoid receptor binding - 0.9278 92.78%
Aromatase binding - 0.8696 86.96%
PPAR gamma - 0.9514 95.14%
Honey bee toxicity - 0.9807 98.07%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity - 0.9900 99.00%
Fish aquatic toxicity - 0.5357 53.57%

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 92.62% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 90.28% 87.45%
CHEMBL2581 P07339 Cathepsin D 88.72% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.11% 97.25%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.33% 97.29%

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.
Artemisia capillaris
Pelargonium graveolens
Vitis vinifera

Cross-Links

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PubChem 11508
NPASS NPC206143
LOTUS LTS0205837
wikiData Q3278324