3-Methyl-2-butanol

Details

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Internal ID 65f3bcaf-8526-4062-aec7-0e89e57ee84a
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name 3-methylbutan-2-ol
SMILES (Canonical) CC(C)C(C)O
SMILES (Isomeric) CC(C)C(C)O
InChI InChI=1S/C5H12O/c1-4(2)5(3)6/h4-6H,1-3H3
InChI Key MXLMTQWGSQIYOW-UHFFFAOYSA-N
Popularity 239 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 1.30
Atomic LogP (AlogP) 1.02
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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3-Methylbutan-2-ol
598-75-4
sec-Isoamyl alcohol
2-Methyl-3-butanol
2-Butanol, 3-methyl-
Methylisopropylcarbinol
Isopropylmethylcarbinol
1,2-Dimethylpropanol
1,2-Dimethyl-1-propanol
DL-3-Methyl-2-butanol
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-2-butanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9874 98.74%
Caco-2 - 0.6313 63.13%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.5388 53.88%
OATP2B1 inhibitior - 0.8665 86.65%
OATP1B1 inhibitior + 0.9688 96.88%
OATP1B3 inhibitior + 0.9662 96.62%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9209 92.09%
P-glycoprotein inhibitior - 0.9856 98.56%
P-glycoprotein substrate - 0.9921 99.21%
CYP3A4 substrate - 0.8380 83.80%
CYP2C9 substrate - 0.7877 78.77%
CYP2D6 substrate - 0.7247 72.47%
CYP3A4 inhibition - 0.9674 96.74%
CYP2C9 inhibition - 0.9503 95.03%
CYP2C19 inhibition - 0.9394 93.94%
CYP2D6 inhibition - 0.9569 95.69%
CYP1A2 inhibition - 0.8836 88.36%
CYP2C8 inhibition - 0.9991 99.91%
CYP inhibitory promiscuity - 0.9394 93.94%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) + 0.6283 62.83%
Carcinogenicity (trinary) Non-required 0.6586 65.86%
Eye corrosion + 0.9902 99.02%
Eye irritation + 0.9544 95.44%
Skin irritation + 0.7756 77.56%
Skin corrosion - 0.5424 54.24%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7932 79.32%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation - 0.9590 95.90%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.6143 61.43%
Acute Oral Toxicity (c) IV 0.4710 47.10%
Estrogen receptor binding - 0.9551 95.51%
Androgen receptor binding - 0.9108 91.08%
Thyroid receptor binding - 0.8360 83.60%
Glucocorticoid receptor binding - 0.9040 90.40%
Aromatase binding - 0.9114 91.14%
PPAR gamma - 0.8851 88.51%
Honey bee toxicity - 0.9258 92.58%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.8800 88.00%
Fish aquatic toxicity - 0.8201 82.01%

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 86.26% 96.09%
CHEMBL2581 P07339 Cathepsin D 86.21% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.95% 85.14%

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.
Camellia saluenensis
Campanula glomerata subsp. speciosa
Campanula rapunculus subsp. rapunculus
Croton cortesianus
Dactylanthus taylorii
Quercus salicina
Vitis rotundifolia
Vitis vinifera

Cross-Links

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PubChem 11732
NPASS NPC190797
LOTUS LTS0257088
wikiData Q3205874