beta-Alanine betaine

Details

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Internal ID fbe38060-5e30-417f-b6ad-ac8e4e2f1364
Taxonomy Organic nitrogen compounds > Organonitrogen compounds > Quaternary ammonium salts > Tetraalkylammonium salts
IUPAC Name 3-(trimethylazaniumyl)propanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H13NO2/c1-7(2,3)5-4-6(8)9/h4-5H2,1-3H3
InChI Key ACZVSMNFVFBOTM-UHFFFAOYSA-N
Popularity 12 references in papers

Physical and Chemical Properties

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Molecular Formula C6H13NO2
Molecular Weight 131.17 g/mol
Exact Mass 131.094628657 g/mol
Topological Polar Surface Area (TPSA) 40.10 Ų
XlogP 0.40
Atomic LogP (AlogP) -1.17
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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Propiobetaine
3-(trimethylazaniumyl)propanoate
6458-06-6
beta-Homobetaine
beta-Alaninebetaine
3-(trimethylammonio)propanoate
beta-Homobetain
beta-Homobetain [German]
N,N,N-trimethyl-beta-alanine
beta-Alanine, trimethyl betaine
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of beta-Alanine betaine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.9265 92.65%
Caco-2 + 0.8353 83.53%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.6159 61.59%
OATP2B1 inhibitior - 0.8388 83.88%
OATP1B1 inhibitior + 0.9512 95.12%
OATP1B3 inhibitior + 0.9435 94.35%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9518 95.18%
P-glycoprotein inhibitior - 0.9711 97.11%
P-glycoprotein substrate - 0.9837 98.37%
CYP3A4 substrate - 0.7396 73.96%
CYP2C9 substrate + 0.6001 60.01%
CYP2D6 substrate - 0.8307 83.07%
CYP3A4 inhibition - 0.9857 98.57%
CYP2C9 inhibition - 0.9467 94.67%
CYP2C19 inhibition - 0.9596 95.96%
CYP2D6 inhibition - 0.9621 96.21%
CYP1A2 inhibition - 0.8569 85.69%
CYP2C8 inhibition - 0.9836 98.36%
CYP inhibitory promiscuity - 0.9957 99.57%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5000 50.00%
Carcinogenicity (trinary) Non-required 0.7107 71.07%
Eye corrosion + 0.7695 76.95%
Eye irritation + 0.9906 99.06%
Skin irritation + 0.5979 59.79%
Skin corrosion + 0.6994 69.94%
Ames mutagenesis - 0.5154 51.54%
Human Ether-a-go-go-Related Gene inhibition - 0.7902 79.02%
Micronuclear - 0.8300 83.00%
Hepatotoxicity - 0.7875 78.75%
skin sensitisation - 0.8677 86.77%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity - 0.7778 77.78%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity + 0.4759 47.59%
Acute Oral Toxicity (c) III 0.6294 62.94%
Estrogen receptor binding - 0.9465 94.65%
Androgen receptor binding - 0.9266 92.66%
Thyroid receptor binding - 0.9182 91.82%
Glucocorticoid receptor binding - 0.9355 93.55%
Aromatase binding - 0.8803 88.03%
PPAR gamma - 0.8164 81.64%
Honey bee toxicity - 0.9761 97.61%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity - 0.8588 85.88%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.17% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.26% 99.17%
CHEMBL2581 P07339 Cathepsin D 83.02% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.40% 94.45%

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.
Armeria maritima
Limonium vulgare

Cross-Links

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PubChem 441440
LOTUS LTS0209088
wikiData Q27103917