2-Hydroxy-3-methyl-2-butenenitrile

Details

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Internal ID ab25d00e-efa6-44a8-9330-585f071329c0
Taxonomy Organic nitrogen compounds > Organonitrogen compounds > Organic cyanides > Nitriles > Cyanohydrins
IUPAC Name 2-hydroxy-3-methylbut-2-enenitrile
SMILES (Canonical) CC(=C(C#N)O)C
SMILES (Isomeric) CC(=C(C#N)O)C
InChI InChI=1S/C5H7NO/c1-4(2)5(7)3-6/h7H,1-2H3
InChI Key SEYPSMUGVMMWTC-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C5H7NO
Molecular Weight 97.12 g/mol
Exact Mass 97.052763847 g/mol
Topological Polar Surface Area (TPSA) 44.00 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.36
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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QNC9Z64Z5B
2-Butenenitrile, 2-hydroxy-3-methyl-
116130-35-9

2D Structure

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2D Structure of 2-Hydroxy-3-methyl-2-butenenitrile

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9890 98.90%
Caco-2 + 0.5550 55.50%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.4783 47.83%
OATP2B1 inhibitior - 0.8658 86.58%
OATP1B1 inhibitior + 0.9620 96.20%
OATP1B3 inhibitior + 0.9653 96.53%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8961 89.61%
P-glycoprotein inhibitior - 0.9832 98.32%
P-glycoprotein substrate - 0.9857 98.57%
CYP3A4 substrate - 0.7195 71.95%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8424 84.24%
CYP3A4 inhibition - 0.8796 87.96%
CYP2C9 inhibition - 0.8241 82.41%
CYP2C19 inhibition - 0.7317 73.17%
CYP2D6 inhibition - 0.8995 89.95%
CYP1A2 inhibition - 0.7056 70.56%
CYP2C8 inhibition - 0.9912 99.12%
CYP inhibitory promiscuity - 0.6657 66.57%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) + 0.5500 55.00%
Carcinogenicity (trinary) Non-required 0.7637 76.37%
Eye corrosion + 0.7548 75.48%
Eye irritation + 0.9966 99.66%
Skin irritation + 0.5778 57.78%
Skin corrosion + 0.7799 77.99%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7387 73.87%
Micronuclear - 0.7800 78.00%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation - 0.6246 62.46%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.7978 79.78%
Acute Oral Toxicity (c) II 0.4357 43.57%
Estrogen receptor binding - 0.9196 91.96%
Androgen receptor binding - 0.8172 81.72%
Thyroid receptor binding - 0.8032 80.32%
Glucocorticoid receptor binding - 0.8357 83.57%
Aromatase binding - 0.8087 80.87%
PPAR gamma - 0.8254 82.54%
Honey bee toxicity - 0.8194 81.94%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity - 0.7511 75.11%

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
CHEMBL2581 P07339 Cathepsin D 82.06% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.04% 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.
Vachellia sieberiana var. woodii

Cross-Links

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PubChem 14148809
LOTUS LTS0215644
wikiData Q105251611