4-aminobutylazanium;chloride

Details

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Internal ID 5750a1fc-3367-4fce-b14f-406dc7964889
Taxonomy Organic nitrogen compounds > Organonitrogen compounds > Amines > Primary amines > Monoalkylamines
IUPAC Name 4-aminobutylazanium;chloride
SMILES (Canonical) C(CCN)C[NH3+].[Cl-]
SMILES (Isomeric) C(CCN)C[NH3+].[Cl-]
InChI InChI=1S/C4H12N2.ClH/c5-3-1-2-4-6;/h1-6H2;1H
InChI Key BPHGMWVJJCWDPB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C4H13ClN2
Molecular Weight 124.61 g/mol
Exact Mass 124.0767261 g/mol
Topological Polar Surface Area (TPSA) 53.70 Ų
XlogP 0.00
Atomic LogP (AlogP) -4.03
H-Bond Acceptor 1
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-aminobutylazanium;chloride

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7425 74.25%
Caco-2 + 0.9313 93.13%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.8676 86.76%
OATP2B1 inhibitior - 0.8682 86.82%
OATP1B1 inhibitior + 0.9745 97.45%
OATP1B3 inhibitior + 0.9509 95.09%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.9489 94.89%
P-glycoprotein inhibitior - 0.9840 98.40%
P-glycoprotein substrate - 0.8799 87.99%
CYP3A4 substrate - 0.7792 77.92%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7242 72.42%
CYP3A4 inhibition - 0.8213 82.13%
CYP2C9 inhibition - 0.8220 82.20%
CYP2C19 inhibition - 0.8242 82.42%
CYP2D6 inhibition - 0.8980 89.80%
CYP1A2 inhibition - 0.8405 84.05%
CYP2C8 inhibition - 0.9632 96.32%
CYP inhibitory promiscuity - 0.8467 84.67%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5500 55.00%
Carcinogenicity (trinary) Non-required 0.5604 56.04%
Eye corrosion + 0.8682 86.82%
Eye irritation + 0.9208 92.08%
Skin irritation + 0.7145 71.45%
Skin corrosion + 0.9156 91.56%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6856 68.56%
Micronuclear - 0.8400 84.00%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation - 0.6578 65.78%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.5328 53.28%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.5218 52.18%
Acute Oral Toxicity (c) II 0.6261 62.61%
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 - 0.9135 91.35%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity - 0.8677 86.77%

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 91.52% 93.18%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.97% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 87.04% 87.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.83% 91.11%
CHEMBL3492 P49721 Proteasome Macropain subunit 85.75% 90.24%
CHEMBL3038469 P24941 CDK2/Cyclin A 83.16% 91.38%

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.
Canavalia gladiata
Glycine max
Hordeum vulgare
Panax ginseng
Phyllanthus emblica

Cross-Links

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PubChem 85247068
NPASS NPC28081