Putrescine

Details

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Internal ID b1c0faa6-06ff-4625-9f3b-08b18c945ac7
Taxonomy Organic nitrogen compounds > Organonitrogen compounds > Amines > Primary amines > Monoalkylamines
IUPAC Name butane-1,4-diamine
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C4H12N2/c5-3-1-2-4-6/h1-6H2
InChI Key KIDHWZJUCRJVML-UHFFFAOYSA-N
Popularity 16,539 references in papers

Physical and Chemical Properties

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Molecular Formula C4H12N2
Molecular Weight 88.15 g/mol
Exact Mass 88.100048391 g/mol
Topological Polar Surface Area (TPSA) 52.00 Ų
XlogP -0.90
Atomic LogP (AlogP) -0.32
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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putrescine
1,4-butanediamine
110-60-1
butane-1,4-diamine
tetramethylenediamine
Butylenediamine
Putrescin
1,4-Butylenediamine
Tetramethyldiamine
1,4-Tetramethylenediamine
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Putrescine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8885 88.85%
Caco-2 + 0.9313 93.13%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.8857 88.57%
Subcellular localzation Lysosomes 0.8762 87.62%
OATP2B1 inhibitior - 0.8682 86.82%
OATP1B1 inhibitior + 0.9810 98.10%
OATP1B3 inhibitior + 0.9538 95.38%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9489 94.89%
P-glycoprotein inhibitior - 0.9840 98.40%
P-glycoprotein substrate - 0.9687 96.87%
CYP3A4 substrate - 0.8392 83.92%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.5429 54.29%
CYP3A4 inhibition - 0.9111 91.11%
CYP2C9 inhibition - 0.9071 90.71%
CYP2C19 inhibition - 0.9084 90.84%
CYP2D6 inhibition - 0.9497 94.97%
CYP1A2 inhibition - 0.9045 90.45%
CYP2C8 inhibition - 0.9882 98.82%
CYP inhibitory promiscuity - 0.8704 87.04%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5700 57.00%
Carcinogenicity (trinary) Non-required 0.6203 62.03%
Eye corrosion + 0.9958 99.58%
Eye irritation + 0.9208 92.08%
Skin irritation + 0.8719 87.19%
Skin corrosion + 0.9932 99.32%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6856 68.56%
Micronuclear - 0.8800 88.00%
Hepatotoxicity - 0.7750 77.50%
skin sensitisation + 0.4857 48.57%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.8209 82.09%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity + 0.5378 53.78%
Acute Oral Toxicity (c) II 0.7692 76.92%
Estrogen receptor binding - 0.9188 91.88%
Androgen receptor binding - 0.8267 82.67%
Thyroid receptor binding - 0.8418 84.18%
Glucocorticoid receptor binding - 0.7812 78.12%
Aromatase binding - 0.9139 91.39%
PPAR gamma - 0.8898 88.98%
Honey bee toxicity - 0.9311 93.11%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity - 0.9191 91.91%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 28183.8 nM
28183.8 nM
Potency
Potency
via CMAUP
via CMAUP

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4581 P52732 Kinesin-like protein 1 88.26% 93.18%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.97% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 85.97% 87.45%
CHEMBL3492 P49721 Proteasome Macropain subunit 83.72% 90.24%
CHEMBL3038469 P24941 CDK2/Cyclin A 81.97% 91.38%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.52% 91.11%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.93% 97.21%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.27% 96.95%

Cross-Links

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PubChem 1045
NPASS NPC309330
ChEMBL CHEMBL46257
LOTUS LTS0238763
wikiData Q410190