4-Hydroxy-3-(hydroxymethyl)but-2-enenitrile

Details

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Internal ID 80f953e9-3cdb-4d73-adb3-76d96d616b97
IUPAC Name 4-hydroxy-3-(hydroxymethyl)but-2-enenitrile
SMILES (Canonical) C(C(=CC#N)CO)O
SMILES (Isomeric) C(C(=CC#N)CO)O
InChI InChI=1S/C5H7NO2/c6-2-1-5(3-7)4-8/h1,7-8H,3-4H2
InChI Key DIBCQZAAUOUKOX-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C5H7NO2
Molecular Weight 113.11 g/mol
Exact Mass 113.047678466 g/mol
Topological Polar Surface Area (TPSA) 64.20 Ų
XlogP -1.10
Atomic LogP (AlogP) -0.58
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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4-hydroxy-3-(hydroxymethyl)but-2-enenitrile
2-Butenenitrile, 4-hydroxy-3-(hydroxymethyl)-
29768-68-1
SCHEMBL10931353
DTXSID80415698
4-Hydroxy-3-hydroxymethyl-2-butenenitrile
4-hydroxy-3-(hydroxymethyl)-2-butenenitrile

2D Structure

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2D Structure of 4-Hydroxy-3-(hydroxymethyl)but-2-enenitrile

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9318 93.18%
Caco-2 + 0.5768 57.68%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Lysosomes 0.4784 47.84%
OATP2B1 inhibitior - 0.8647 86.47%
OATP1B1 inhibitior + 0.9473 94.73%
OATP1B3 inhibitior + 0.9517 95.17%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8838 88.38%
BSEP inhibitior - 0.9301 93.01%
P-glycoprotein inhibitior - 0.9805 98.05%
P-glycoprotein substrate - 0.9868 98.68%
CYP3A4 substrate - 0.7199 71.99%
CYP2C9 substrate - 0.8227 82.27%
CYP2D6 substrate - 0.7976 79.76%
CYP3A4 inhibition - 0.8300 83.00%
CYP2C9 inhibition - 0.8372 83.72%
CYP2C19 inhibition - 0.8486 84.86%
CYP2D6 inhibition - 0.9251 92.51%
CYP1A2 inhibition - 0.6615 66.15%
CYP2C8 inhibition - 0.9703 97.03%
CYP inhibitory promiscuity - 0.6682 66.82%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.5700 57.00%
Carcinogenicity (trinary) Non-required 0.6373 63.73%
Eye corrosion + 0.6423 64.23%
Eye irritation + 0.9886 98.86%
Skin irritation + 0.5639 56.39%
Skin corrosion - 0.5773 57.73%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7747 77.47%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.5010 50.10%
skin sensitisation - 0.7647 76.47%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity - 0.9111 91.11%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.6030 60.30%
Acute Oral Toxicity (c) II 0.5479 54.79%
Estrogen receptor binding - 0.8328 83.28%
Androgen receptor binding - 0.8940 89.40%
Thyroid receptor binding - 0.8111 81.11%
Glucocorticoid receptor binding - 0.6918 69.18%
Aromatase binding - 0.7500 75.00%
PPAR gamma - 0.8266 82.66%
Honey bee toxicity - 0.6384 63.84%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity - 0.8824 88.24%

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
CHEMBL226 P30542 Adenosine A1 receptor 83.38% 95.93%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.05% 96.09%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 80.61% 86.92%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.59% 91.11%

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.
Cardiospermum halicacabum
Vicia sativa

Cross-Links

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PubChem 5316227
NPASS NPC257956