Butylamine
Relevant Data
Food Additives Approved in the United States:
Food Additives Approved by WHO:
General Information
| Chemical name | Butylamine |
| CAS number | 109-73-9 |
| COE number | 524 |
| JECFA number | 1582 |
| Flavouring type | substances |
| FL No. | 11.003 |
| Mixture | No |
| Purity of the named substance at least 95% unless otherwise specified | |
| Reference body | EFSA |
From webgate.ec.europa.eu
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 8007 |
| IUPAC Name | butan-1-amine |
| InChI | InChI=1S/C4H11N/c1-2-3-4-5/h2-5H2,1H3 |
| InChI Key | HQABUPZFAYXKJW-UHFFFAOYSA-N |
| Canonical SMILES | CCCCN |
| Molecular Formula | C4H11N |
| Wikipedia | butylamine |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 73.139 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 2 |
| Complexity | 13.1 |
| CACTVS Substructure Key Fingerprint | A A A D c c B i A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A H A A Q A A A A C A D B A A Q C A A B A A A A A A A A A A A A A A A A A A A A A A I A A A A A A A A A A g A A A A A A A E A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A = = |
| Topological Polar Surface Area | 26.0 |
| Monoisotopic Mass | 73.089 |
| Exact Mass | 73.089 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 5 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Isotope Atom Count | 0 |
| Covalently-Bonded Unit Count | 1 |
From Pubchem
Food Additives Biosynthesis/Degradation
ADMET Predicted Profile --- Classification
| Model | Result | Probability |
|---|---|---|
| Absorption | ||
| Blood-Brain Barrier | BBB+ | 0.9587 |
| Human Intestinal Absorption | HIA+ | 1.0000 |
| Caco-2 Permeability | Caco2+ | 0.8242 |
| P-glycoprotein Substrate | Non-substrate | 0.6145 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.9077 |
| Non-inhibitor | 0.9415 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.7416 |
| Distribution | ||
| Subcellular localization | Lysosome | 0.9589 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8673 |
| CYP450 2D6 Substrate | Substrate | 0.6591 |
| CYP450 3A4 Substrate | Non-substrate | 0.7738 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.6954 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9072 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.7098 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.8807 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9245 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.8873 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8976 |
| Non-inhibitor | 0.8477 | |
| AMES Toxicity | Non AMES toxic | 0.9317 |
| Carcinogens | Carcinogens | 0.5632 |
| Fish Toxicity | Low FHMT | 0.6493 |
| Tetrahymena Pyriformis Toxicity | Low TPT | 0.8366 |
| Honey Bee Toxicity | High HBT | 0.5232 |
| Biodegradation | Ready biodegradable | 0.8994 |
| Acute Oral Toxicity | II | 0.7614 |
| Carcinogenicity (Three-class) | Non-required | 0.7465 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -0.5405 | LogS |
| Caco-2 Permeability | 1.3795 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 2.2694 | LD50, mol/kg |
| Fish Toxicity | 2.4625 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -0.6039 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic nitrogen compounds |
| Class | Organonitrogen compounds |
| Subclass | Amines |
| Intermediate Tree Nodes | Primary amines |
| Direct Parent | Monoalkylamines |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Organopnictogen compound - Hydrocarbon derivative - Primary aliphatic amine - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as monoalkylamines. These are organic compounds containing an primary aliphatic amine group. |
From ClassyFire
Targets
- General Function:
- Drug binding
- Specific Function:
- Secreted aspartic peptidases (SAPs) are a group of ten acidic hydrolases considered as key virulence factors. These enzymes supply the fungus with nutrient amino acids as well as are able to degrade the selected host's proteins involved in the immune defense. Induces host inflammatory cytokine production in a proteolytic activity-independent way. Plays a role in tissue damage during superficial infection. Moreover, acts toward human hemoglobin though limited proteolysis to generate a variety of antimicrobial hemocidins, enabling to compete with the other microorganisms of the same physiological niche using the microbicidal peptides generated from the host protein.
- Gene Name:
- SAP2
- Uniprot ID:
- P0DJ06
- Molecular Weight:
- 42315.655 Da
From T3DB