2-Methyl-1-butanol

Details

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Internal ID 3f4275a6-eca5-42c7-bf4c-80cd3db01582
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Primary alcohols
IUPAC Name 2-methylbutan-1-ol
SMILES (Canonical) CCC(C)CO
SMILES (Isomeric) CCC(C)CO
InChI InChI=1S/C5H12O/c1-3-5(2)4-6/h5-6H,3-4H2,1-2H3
InChI Key QPRQEDXDYOZYLA-UHFFFAOYSA-N
Popularity 1,073 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) 1.02
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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2-Methylbutan-1-ol
137-32-6
Active amyl alcohol
2-Methylbutanol
sec-Butylcarbinol
1-Butanol, 2-methyl-
DL-2-Methyl-1-butanol
2-Methyl-n-butanol
2-Methylbutyl alcohol
Primary active amyl alcohol
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-Methyl-1-butanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9936 99.36%
Caco-2 + 0.7304 73.04%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.6816 68.16%
OATP2B1 inhibitior - 0.8544 85.44%
OATP1B1 inhibitior + 0.9382 93.82%
OATP1B3 inhibitior + 0.9403 94.03%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9220 92.20%
P-glycoprotein inhibitior - 0.9861 98.61%
P-glycoprotein substrate - 0.9723 97.23%
CYP3A4 substrate - 0.8131 81.31%
CYP2C9 substrate - 0.8468 84.68%
CYP2D6 substrate - 0.7359 73.59%
CYP3A4 inhibition - 0.9584 95.84%
CYP2C9 inhibition - 0.9094 90.94%
CYP2C19 inhibition - 0.9111 91.11%
CYP2D6 inhibition - 0.9201 92.01%
CYP1A2 inhibition - 0.7168 71.68%
CYP2C8 inhibition - 0.9957 99.57%
CYP inhibitory promiscuity - 0.9377 93.77%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.5200 52.00%
Carcinogenicity (trinary) Non-required 0.6895 68.95%
Eye corrosion + 0.9502 95.02%
Eye irritation + 0.9716 97.16%
Skin irritation - 0.5398 53.98%
Skin corrosion - 0.9370 93.70%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7304 73.04%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation + 0.5370 53.70%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity - 0.5671 56.71%
Acute Oral Toxicity (c) III 0.8568 85.68%
Estrogen receptor binding - 0.9339 93.39%
Androgen receptor binding - 0.9178 91.78%
Thyroid receptor binding - 0.8708 87.08%
Glucocorticoid receptor binding - 0.9199 91.99%
Aromatase binding - 0.8754 87.54%
PPAR gamma - 0.9320 93.20%
Honey bee toxicity - 0.9907 99.07%
Biodegradation + 0.8750 87.50%
Crustacea aquatic toxicity - 0.9600 96.00%
Fish aquatic toxicity - 0.4430 44.30%

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 90.30% 96.09%
CHEMBL2581 P07339 Cathepsin D 87.97% 98.95%
CHEMBL2885 P07451 Carbonic anhydrase III 87.93% 87.45%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.81% 97.29%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.77% 97.25%

Cross-Links

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PubChem 8723
NPASS NPC23071
LOTUS LTS0029080
wikiData Q209425