3-Methyl-3-buten-2-ol

Details

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Internal ID 99a3b8b2-24a8-455f-a4e4-f7d328c840b4
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols
IUPAC Name 3-methylbut-3-en-2-ol
SMILES (Canonical) CC(C(=C)C)O
SMILES (Isomeric) CC(C(=C)C)O
InChI InChI=1S/C5H10O/c1-4(2)5(3)6/h5-6H,1H2,2-3H3
InChI Key JEYLKNVLTAPJAF-UHFFFAOYSA-N
Popularity 36 references in papers

Physical and Chemical Properties

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Molecular Formula C5H10O
Molecular Weight 86.13 g/mol
Exact Mass 86.073164938 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 1.20
Atomic LogP (AlogP) 0.94
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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3-methylbut-3-en-2-ol
10473-14-0
3-Buten-2-ol, 3-methyl-
Methyl isopropenyl carbinol
xi-3-Methyl-3-buten-2-ol
KG8M3UNR9E
2-methyl-1-buten-3-ol
EINECS 233-964-8
AI3-28605
UNII-KG8M3UNR9E
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-3-buten-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9885 98.85%
Caco-2 - 0.6809 68.09%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.3936 39.36%
OATP2B1 inhibitior - 0.8688 86.88%
OATP1B1 inhibitior + 0.9600 96.00%
OATP1B3 inhibitior + 0.9667 96.67%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9420 94.20%
P-glycoprotein inhibitior - 0.9833 98.33%
P-glycoprotein substrate - 0.9822 98.22%
CYP3A4 substrate - 0.7852 78.52%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7392 73.92%
CYP3A4 inhibition - 0.7896 78.96%
CYP2C9 inhibition - 0.9228 92.28%
CYP2C19 inhibition - 0.6463 64.63%
CYP2D6 inhibition - 0.9441 94.41%
CYP1A2 inhibition - 0.8310 83.10%
CYP2C8 inhibition - 0.9973 99.73%
CYP inhibitory promiscuity - 0.8032 80.32%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) + 0.7083 70.83%
Carcinogenicity (trinary) Non-required 0.6659 66.59%
Eye corrosion + 0.9161 91.61%
Eye irritation + 0.9680 96.80%
Skin irritation + 0.7643 76.43%
Skin corrosion + 0.6023 60.23%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8114 81.14%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation + 0.7366 73.66%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity - 0.9667 96.67%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.6091 60.91%
Acute Oral Toxicity (c) III 0.4677 46.77%
Estrogen receptor binding - 0.8913 89.13%
Androgen receptor binding - 0.9112 91.12%
Thyroid receptor binding - 0.8075 80.75%
Glucocorticoid receptor binding - 0.9083 90.83%
Aromatase binding - 0.8686 86.86%
PPAR gamma - 0.8167 81.67%
Honey bee toxicity - 0.8771 87.71%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.8700 87.00%
Fish aquatic toxicity - 0.3853 38.53%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.53% 85.14%
CHEMBL2581 P07339 Cathepsin D 86.75% 98.95%
CHEMBL4040 P28482 MAP kinase ERK2 86.54% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.47% 96.09%

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 argyi
Artemisia montana
Artemisia princeps
Dactylanthus taylorii
Vaccinium macrocarpon

Cross-Links

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PubChem 66329
NPASS NPC68919
LOTUS LTS0160676
wikiData Q27282241