2-(Acetyloxy)-3-carboxy-N,N,N-trimethylpropan-1-aminium

Details

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Internal ID 3b0ed8a3-c946-4a6a-8586-d36a6e51d28d
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters > Acyl carnitines
IUPAC Name (2-acetyloxy-3-carboxypropyl)-trimethylazanium
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H17NO4/c1-7(11)14-8(5-9(12)13)6-10(2,3)4/h8H,5-6H2,1-4H3/p+1
InChI Key RDHQFKQIGNGIED-UHFFFAOYSA-O
Popularity 1,074 references in papers

Physical and Chemical Properties

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Molecular Formula C9H18NO4+
Molecular Weight 204.24 g/mol
Exact Mass 204.12358306 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP -0.30
Atomic LogP (AlogP) 0.10
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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7559-18-4
2-(acetyloxy)-3-carboxy-N,N,N-trimethylpropan-1-aminium
RefChem:1061414
DTXCID50196881
[2-(ACETYLOXY)-3-CARBOXYPROPYL]TRIMETHYLAZANIUM
SCHEMBL3259109
CHEMBL1625375
ALBB-032444
AKOS024284761
ST079275
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-(Acetyloxy)-3-carboxy-N,N,N-trimethylpropan-1-aminium

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.9924 99.24%
Caco-2 + 0.5494 54.94%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.9286 92.86%
Subcellular localzation Mitochondria 0.6450 64.50%
OATP2B1 inhibitior - 0.8549 85.49%
OATP1B1 inhibitior + 0.9587 95.87%
OATP1B3 inhibitior + 0.9448 94.48%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9504 95.04%
P-glycoprotein inhibitior - 0.9546 95.46%
P-glycoprotein substrate - 0.9304 93.04%
CYP3A4 substrate - 0.6279 62.79%
CYP2C9 substrate + 0.6023 60.23%
CYP2D6 substrate - 0.8405 84.05%
CYP3A4 inhibition - 0.8818 88.18%
CYP2C9 inhibition - 0.9236 92.36%
CYP2C19 inhibition - 0.9025 90.25%
CYP2D6 inhibition - 0.9355 93.55%
CYP1A2 inhibition - 0.9367 93.67%
CYP2C8 inhibition - 0.9366 93.66%
CYP inhibitory promiscuity - 0.9761 97.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.6288 62.88%
Eye corrosion - 0.8482 84.82%
Eye irritation + 0.9760 97.60%
Skin irritation - 0.7695 76.95%
Skin corrosion - 0.8561 85.61%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7916 79.16%
Micronuclear - 0.8300 83.00%
Hepatotoxicity - 0.7343 73.43%
skin sensitisation - 0.9120 91.20%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity - 0.7556 75.56%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity + 0.6270 62.70%
Acute Oral Toxicity (c) III 0.7060 70.60%
Estrogen receptor binding - 0.9218 92.18%
Androgen receptor binding - 0.8224 82.24%
Thyroid receptor binding - 0.8388 83.88%
Glucocorticoid receptor binding - 0.6921 69.21%
Aromatase binding - 0.8514 85.14%
PPAR gamma - 0.8955 89.55%
Honey bee toxicity - 0.9261 92.61%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.7755 77.55%
Fish aquatic toxicity - 0.8444 84.44%

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
CHEMBL2581 P07339 Cathepsin D 95.22% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.03% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.16% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.21% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 85.77% 97.21%

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.
Sagittaria sagittifolia

Cross-Links

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PubChem 2
NPASS NPC46294