(Z)-2-Methyl-2-buten-1-ol

Details

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Internal ID 16c6fcd2-1701-450b-ac7f-b0ea103898f1
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Primary alcohols
IUPAC Name (Z)-2-methylbut-2-en-1-ol
SMILES (Canonical) CC=C(C)CO
SMILES (Isomeric) C/C=C(/C)\CO
InChI InChI=1S/C5H10O/c1-3-5(2)4-6/h3,6H,4H2,1-2H3/b5-3-
InChI Key NEJDKFPXHQRVMV-HYXAFXHYSA-N
Popularity 5 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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(Z)-2-Methyl-2-butenol
2-Methylbut-2-en-1-ol, (2Z)-
cis-2-Methyl-2-buten-1-ol
2-Buten-1-ol, 2-methyl-, (Z)-
19319-26-7
UNII-204DWM50MS
204DWM50MS
2-Buten-1-ol, 2-methyl-, (2Z)-
2-Buten-1-ol, 2-methyl-
2-Methyl-2-butenol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (Z)-2-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 + 0.9908 99.08%
Caco-2 + 0.8591 85.91%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.6551 65.51%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9278 92.78%
OATP1B3 inhibitior + 0.9488 94.88%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9055 90.55%
P-glycoprotein inhibitior - 0.9855 98.55%
P-glycoprotein substrate - 0.9739 97.39%
CYP3A4 substrate - 0.7604 76.04%
CYP2C9 substrate - 0.8453 84.53%
CYP2D6 substrate - 0.7851 78.51%
CYP3A4 inhibition - 0.9254 92.54%
CYP2C9 inhibition - 0.9352 93.52%
CYP2C19 inhibition - 0.8793 87.93%
CYP2D6 inhibition - 0.9150 91.50%
CYP1A2 inhibition - 0.7962 79.62%
CYP2C8 inhibition - 0.9927 99.27%
CYP inhibitory promiscuity - 0.8552 85.52%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) + 0.5383 53.83%
Carcinogenicity (trinary) Non-required 0.6508 65.08%
Eye corrosion + 0.8655 86.55%
Eye irritation + 0.9591 95.91%
Skin irritation + 0.6872 68.72%
Skin corrosion + 0.6557 65.57%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8149 81.49%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5426 54.26%
skin sensitisation + 0.6065 60.65%
Respiratory toxicity - 0.9111 91.11%
Reproductive toxicity - 0.9222 92.22%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity + 0.6458 64.58%
Acute Oral Toxicity (c) III 0.9115 91.15%
Estrogen receptor binding - 0.9321 93.21%
Androgen receptor binding - 0.9276 92.76%
Thyroid receptor binding - 0.9023 90.23%
Glucocorticoid receptor binding - 0.8743 87.43%
Aromatase binding - 0.8742 87.42%
PPAR gamma - 0.8962 89.62%
Honey bee toxicity - 0.9599 95.99%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.9000 90.00%
Fish aquatic toxicity + 0.7231 72.31%

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 85.16% 96.09%
CHEMBL2581 P07339 Cathepsin D 81.58% 98.95%

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

Cross-Links

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PubChem 5366266
NPASS NPC96953