(2-Aminoethyl)phosphonic acid

Details

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Internal ID f035d226-c303-4c0e-983c-b0b71b989adf
Taxonomy Organic acids and derivatives > Organic phosphonic acids and derivatives > Organic phosphonic acids
IUPAC Name 2-aminoethylphosphonic acid
SMILES (Canonical) C(CP(=O)(O)O)N
SMILES (Isomeric) C(CP(=O)(O)O)N
InChI InChI=1S/C2H8NO3P/c3-1-2-7(4,5)6/h1-3H2,(H2,4,5,6)
InChI Key QQVDJLLNRSOCEL-UHFFFAOYSA-N
Popularity 365 references in papers

Physical and Chemical Properties

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Molecular Formula C2H8NO3P
Molecular Weight 125.06 g/mol
Exact Mass 125.02418011 g/mol
Topological Polar Surface Area (TPSA) 83.60 Ų
XlogP -4.80
Atomic LogP (AlogP) -0.88
H-Bond Acceptor 2
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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2041-14-7
2-aminoethylphosphonic acid
Ciliatine
Phosphonoethylamine
AMINOETHYLPHOSPHONIC ACID
Phosphonic acid, (2-aminoethyl)-
(2-Aminoethane)phosphonic acid
beta-Aminoethylphosphonic acid
NSC-133837
AH00YJQ334
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-Aminoethyl)phosphonic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7824 78.24%
Caco-2 - 0.5775 57.75%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.8714 87.14%
Subcellular localzation Lysosomes 0.5596 55.96%
OATP2B1 inhibitior - 0.8607 86.07%
OATP1B1 inhibitior + 0.9739 97.39%
OATP1B3 inhibitior + 0.9438 94.38%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9546 95.46%
P-glycoprotein inhibitior - 0.9759 97.59%
P-glycoprotein substrate - 0.9855 98.55%
CYP3A4 substrate - 0.7709 77.09%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6886 68.86%
CYP3A4 inhibition - 0.8310 83.10%
CYP2C9 inhibition - 0.9272 92.72%
CYP2C19 inhibition - 0.9284 92.84%
CYP2D6 inhibition - 0.9442 94.42%
CYP1A2 inhibition - 0.9100 91.00%
CYP2C8 inhibition - 0.9905 99.05%
CYP inhibitory promiscuity - 0.9718 97.18%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5700 57.00%
Carcinogenicity (trinary) Non-required 0.5951 59.51%
Eye corrosion + 0.8520 85.20%
Eye irritation + 0.7402 74.02%
Skin irritation - 0.6216 62.16%
Skin corrosion + 0.6246 62.46%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7452 74.52%
Micronuclear + 0.5900 59.00%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.8702 87.02%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity + 0.5652 56.52%
Acute Oral Toxicity (c) III 0.6834 68.34%
Estrogen receptor binding - 0.8885 88.85%
Androgen receptor binding - 0.9362 93.62%
Thyroid receptor binding - 0.8701 87.01%
Glucocorticoid receptor binding - 0.8686 86.86%
Aromatase binding - 0.9405 94.05%
PPAR gamma - 0.8330 83.30%
Honey bee toxicity - 0.6529 65.29%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity - 0.9883 98.83%

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
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 92.09% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.47% 96.09%
CHEMBL3230 O95977 Sphingosine 1-phosphate receptor Edg-6 89.26% 94.01%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 80.41% 92.86%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.16% 89.34%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 339
LOTUS LTS0013798
wikiData Q421682