4-Aminobutanal

Details

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Internal ID d9854de4-a165-4372-934d-cf560162d01b
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Alpha-hydrogen aldehydes
IUPAC Name 4-aminobutanal
SMILES (Canonical) C(CC=O)CN
SMILES (Isomeric) C(CC=O)CN
InChI InChI=1S/C4H9NO/c5-3-1-2-4-6/h4H,1-3,5H2
InChI Key DZQLQEYLEYWJIB-UHFFFAOYSA-N
Popularity 305 references in papers

Physical and Chemical Properties

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Molecular Formula C4H9NO
Molecular Weight 87.12 g/mol
Exact Mass 87.068413911 g/mol
Topological Polar Surface Area (TPSA) 43.10 Ų
XlogP -0.90
Atomic LogP (AlogP) -0.08
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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4-aminobutyraldehyde
4390-05-0
Butanal, 4-amino-
gamma-aminobutyraldehyde
4-amino-butyraldehyde
Butyraldehyde, 4-amino-
CHEBI:17769
4-amino-butanal
Butanal, 4-amino- (9CI)
GTPL6606
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-Aminobutanal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9931 99.31%
Caco-2 + 0.8089 80.89%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Lysosomes 0.8292 82.92%
OATP2B1 inhibitior - 0.8625 86.25%
OATP1B1 inhibitior + 0.9587 95.87%
OATP1B3 inhibitior + 0.9536 95.36%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.9535 95.35%
P-glycoprotein inhibitior - 0.9849 98.49%
P-glycoprotein substrate - 0.9364 93.64%
CYP3A4 substrate - 0.7509 75.09%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4004 40.04%
CYP3A4 inhibition - 0.8829 88.29%
CYP2C9 inhibition - 0.9184 91.84%
CYP2C19 inhibition - 0.9259 92.59%
CYP2D6 inhibition - 0.9333 93.33%
CYP1A2 inhibition - 0.6863 68.63%
CYP2C8 inhibition - 0.9868 98.68%
CYP inhibitory promiscuity - 0.9170 91.70%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.7061 70.61%
Eye corrosion + 0.9927 99.27%
Eye irritation + 0.8532 85.32%
Skin irritation + 0.7544 75.44%
Skin corrosion + 0.9761 97.61%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7325 73.25%
Micronuclear - 0.8100 81.00%
Hepatotoxicity - 0.7875 78.75%
skin sensitisation - 0.8370 83.70%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity - 0.6889 68.89%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity + 0.5973 59.73%
Acute Oral Toxicity (c) II 0.4804 48.04%
Estrogen receptor binding - 0.9485 94.85%
Androgen receptor binding - 0.9076 90.76%
Thyroid receptor binding - 0.8650 86.50%
Glucocorticoid receptor binding - 0.8405 84.05%
Aromatase binding - 0.8440 84.40%
PPAR gamma - 0.8024 80.24%
Honey bee toxicity - 0.8964 89.64%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity - 0.9932 99.32%

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
CHEMBL4581 P52732 Kinesin-like protein 1 88.73% 93.18%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.20% 96.09%
CHEMBL3492 P49721 Proteasome Macropain subunit 85.40% 90.24%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.66% 95.56%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.10% 89.34%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.79% 99.17%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 118
LOTUS LTS0204686
wikiData Q27073754