3-Methyl-2-buten-1-OL

Details

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Internal ID 09239a08-6b4f-4729-9727-28b9123b0626
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Primary alcohols
IUPAC Name 3-methylbut-2-en-1-ol
SMILES (Canonical) CC(=CCO)C
SMILES (Isomeric) CC(=CCO)C
InChI InChI=1S/C5H10O/c1-5(2)3-4-6/h3,6H,4H2,1-2H3
InChI Key ASUAYTHWZCLXAN-UHFFFAOYSA-N
Popularity 736 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 1.00
Atomic LogP (AlogP) 0.94
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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Prenol
556-82-1
3-Methylbut-2-en-1-ol
3,3-Dimethylallyl alcohol
2-Buten-1-ol, 3-methyl-
Prenyl alcohol
3-Methyl-2-butenol
Dimethylallyl alcohol
3-Methyl-2-butenyl alcohol
3-Methylcrotyl 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 3-Methyl-2-buten-1-OL

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9918 99.18%
Caco-2 + 0.8471 84.71%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.6205 62.05%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9502 95.02%
OATP1B3 inhibitior + 0.9520 95.20%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9278 92.78%
P-glycoprotein inhibitior - 0.9829 98.29%
P-glycoprotein substrate - 0.9863 98.63%
CYP3A4 substrate - 0.7710 77.10%
CYP2C9 substrate - 0.8453 84.53%
CYP2D6 substrate - 0.7851 78.51%
CYP3A4 inhibition - 0.9413 94.13%
CYP2C9 inhibition - 0.9148 91.48%
CYP2C19 inhibition - 0.8775 87.75%
CYP2D6 inhibition - 0.9245 92.45%
CYP1A2 inhibition - 0.8324 83.24%
CYP2C8 inhibition - 0.9942 99.42%
CYP inhibitory promiscuity - 0.8334 83.34%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) + 0.5283 52.83%
Carcinogenicity (trinary) Non-required 0.6836 68.36%
Eye corrosion + 0.8934 89.34%
Eye irritation + 0.9965 99.65%
Skin irritation + 0.8350 83.50%
Skin corrosion + 0.9671 96.71%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7216 72.16%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation + 0.6120 61.20%
Respiratory toxicity - 0.9556 95.56%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.6181 61.81%
Acute Oral Toxicity (c) III 0.8996 89.96%
Estrogen receptor binding - 0.9617 96.17%
Androgen receptor binding - 0.9319 93.19%
Thyroid receptor binding - 0.9186 91.86%
Glucocorticoid receptor binding - 0.9469 94.69%
Aromatase binding - 0.9327 93.27%
PPAR gamma - 0.8917 89.17%
Honey bee toxicity - 0.9606 96.06%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.9100 91.00%
Fish aquatic toxicity - 0.3743 37.43%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.54% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.15% 96.09%

Cross-Links

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PubChem 11173
NPASS NPC242117
LOTUS LTS0257971
wikiData Q425512