4-Hydroxybutanenitrile

Details

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Internal ID 0d6b29bd-c11c-4326-a88c-a78c25638a53
Taxonomy Organic nitrogen compounds > Organonitrogen compounds > Organic cyanides > Nitriles
IUPAC Name 4-hydroxybutanenitrile
SMILES (Canonical) C(CC#N)CO
SMILES (Isomeric) C(CC#N)CO
InChI InChI=1S/C4H7NO/c5-3-1-2-4-6/h6H,1-2,4H2
InChI Key BAQQRABCRRQRSR-UHFFFAOYSA-N
Popularity 27 references in papers

Physical and Chemical Properties

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Molecular Formula C4H7NO
Molecular Weight 85.10 g/mol
Exact Mass 85.052763847 g/mol
Topological Polar Surface Area (TPSA) 44.00 Ų
XlogP -0.40
Atomic LogP (AlogP) 0.28
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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628-22-8
4-HYDROXY-BUTYRONITRILE
3-cyano-1-propanol
4-hydroxybutyronitrile
3-cyanopropanol
NSC3805
4-hydroxybutylnitrile
3-hydroxypropyl cyanide
3-cyano-1-n-propanol
1-cyano-3-hydroxypropane
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-Hydroxybutanenitrile

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9876 98.76%
Caco-2 + 0.6784 67.84%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.6117 61.17%
OATP2B1 inhibitior - 0.8657 86.57%
OATP1B1 inhibitior + 0.9488 94.88%
OATP1B3 inhibitior + 0.9493 94.93%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9384 93.84%
P-glycoprotein inhibitior - 0.9854 98.54%
P-glycoprotein substrate - 0.9842 98.42%
CYP3A4 substrate - 0.7251 72.51%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7149 71.49%
CYP3A4 inhibition - 0.9039 90.39%
CYP2C9 inhibition - 0.8966 89.66%
CYP2C19 inhibition - 0.9046 90.46%
CYP2D6 inhibition - 0.9548 95.48%
CYP1A2 inhibition - 0.7006 70.06%
CYP2C8 inhibition - 0.9837 98.37%
CYP inhibitory promiscuity - 0.9073 90.73%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.7651 76.51%
Eye corrosion + 0.9812 98.12%
Eye irritation + 0.9873 98.73%
Skin irritation + 0.8088 80.88%
Skin corrosion + 0.8118 81.18%
Ames mutagenesis - 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6912 69.12%
Micronuclear - 0.9000 90.00%
Hepatotoxicity + 0.5719 57.19%
skin sensitisation - 0.8840 88.40%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.8222 82.22%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity + 0.6926 69.26%
Acute Oral Toxicity (c) III 0.7617 76.17%
Estrogen receptor binding - 0.9158 91.58%
Androgen receptor binding - 0.8890 88.90%
Thyroid receptor binding - 0.8383 83.83%
Glucocorticoid receptor binding - 0.7393 73.93%
Aromatase binding - 0.8743 87.43%
PPAR gamma - 0.9107 91.07%
Honey bee toxicity - 0.7121 71.21%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity - 0.8300 83.00%
Fish aquatic toxicity - 0.9924 99.24%

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 89.28% 96.09%
CHEMBL226 P30542 Adenosine A1 receptor 87.12% 95.93%
CHEMBL2885 P07451 Carbonic anhydrase III 85.63% 87.45%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 83.52% 86.92%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.30% 91.11%
CHEMBL2835 P23458 Tyrosine-protein kinase JAK1 81.16% 98.79%

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.
Arabidopsis thaliana

Cross-Links

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PubChem 220705
LOTUS LTS0272406
wikiData Q82009110