5-Aminopentanal

Details

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Internal ID d68fe4e0-3a1f-4c11-8c6a-923d803ef833
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Alpha-hydrogen aldehydes
IUPAC Name 5-aminopentanal
SMILES (Canonical) C(CCN)CC=O
SMILES (Isomeric) C(CCN)CC=O
InChI InChI=1S/C5H11NO/c6-4-2-1-3-5-7/h5H,1-4,6H2
InChI Key SZBGXBOFCGNPEU-UHFFFAOYSA-N
Popularity 46 references in papers

Physical and Chemical Properties

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Molecular Formula C5H11NO
Molecular Weight 101.15 g/mol
Exact Mass 101.084063974 g/mol
Topological Polar Surface Area (TPSA) 43.10 Ų
XlogP -0.60
Atomic LogP (AlogP) 0.31
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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Pentanal, 5-amino-
14049-15-1
5-Amino-pentanal
CHEBI:31130
5-Azanylpentanal
5-Aminovaleraldehyde
Valeraldehyde, 5-amino-
7AC7RQZ8BZ
SCHEMBL97690
CHEMBL2261443
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 5-Aminopentanal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9825 98.25%
Caco-2 + 0.8530 85.30%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Lysosomes 0.7976 79.76%
OATP2B1 inhibitior - 0.8614 86.14%
OATP1B1 inhibitior + 0.9528 95.28%
OATP1B3 inhibitior + 0.9517 95.17%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.9531 95.31%
P-glycoprotein inhibitior - 0.9873 98.73%
P-glycoprotein substrate - 0.9396 93.96%
CYP3A4 substrate - 0.7471 74.71%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4004 40.04%
CYP3A4 inhibition - 0.8910 89.10%
CYP2C9 inhibition - 0.9281 92.81%
CYP2C19 inhibition - 0.9264 92.64%
CYP2D6 inhibition - 0.9057 90.57%
CYP1A2 inhibition - 0.5837 58.37%
CYP2C8 inhibition - 0.9855 98.55%
CYP inhibitory promiscuity - 0.8764 87.64%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6300 63.00%
Carcinogenicity (trinary) Non-required 0.6985 69.85%
Eye corrosion + 0.9457 94.57%
Eye irritation + 0.7623 76.23%
Skin irritation + 0.7556 75.56%
Skin corrosion + 0.9625 96.25%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6659 66.59%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.8125 81.25%
skin sensitisation - 0.8020 80.20%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity - 0.8333 83.33%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.5580 55.80%
Acute Oral Toxicity (c) II 0.4750 47.50%
Estrogen receptor binding - 0.9285 92.85%
Androgen receptor binding - 0.8838 88.38%
Thyroid receptor binding - 0.8524 85.24%
Glucocorticoid receptor binding - 0.8028 80.28%
Aromatase binding - 0.8008 80.08%
PPAR gamma - 0.8038 80.38%
Honey bee toxicity - 0.9011 90.11%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity - 0.9741 97.41%

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 89.39% 93.18%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.61% 96.09%
CHEMBL3038469 P24941 CDK2/Cyclin A 84.21% 91.38%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.43% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.37% 95.56%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.61% 89.34%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.15% 91.11%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.65% 90.24%

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.
Hippobroma longiflora
Lycopodiella cernua

Cross-Links

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PubChem 443849
LOTUS LTS0023370
wikiData Q27114159