(2-Amino-1-hydroxyethyl)phosphonate

Details

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Internal ID ffce77bf-b6ca-44af-950d-c7c570bcc407
Taxonomy Organic acids and derivatives > Organic phosphonic acids and derivatives > Organic phosphonic acids
IUPAC Name (2-amino-1-hydroxyethyl)phosphonic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C2H8NO4P/c3-1-2(4)8(5,6)7/h2,4H,1,3H2,(H2,5,6,7)
InChI Key RTTXIBKRJFIBBG-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C2H8NO4P
Molecular Weight 141.06 g/mol
Exact Mass 141.01909473 g/mol
Topological Polar Surface Area (TPSA) 104.00 Ų
XlogP -5.30
Atomic LogP (AlogP) -1.56
H-Bond Acceptor 3
H-Bond Donor 4
Rotatable Bonds 2

Synonyms

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1-hydroxy-2-aminoethylphosphonic acid
115511-00-7
41744-58-5
1-Hydroxy-2-aminoethylphosphonate
(2-amino-1-hydroxyethyl)phosphonate
C05678
SCHEMBL44349
CHEBI:631
AKOS006339616
(2-amino-1-hydroxyethyl)phosphonicacid
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-Amino-1-hydroxyethyl)phosphonate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.8876 88.76%
Caco-2 - 0.9589 95.89%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Lysosomes 0.5129 51.29%
OATP2B1 inhibitior - 0.8555 85.55%
OATP1B1 inhibitior + 0.9828 98.28%
OATP1B3 inhibitior + 0.9344 93.44%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9679 96.79%
P-glycoprotein inhibitior - 0.9825 98.25%
P-glycoprotein substrate - 0.9634 96.34%
CYP3A4 substrate - 0.7483 74.83%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6886 68.86%
CYP3A4 inhibition - 0.9423 94.23%
CYP2C9 inhibition - 0.9229 92.29%
CYP2C19 inhibition - 0.9270 92.70%
CYP2D6 inhibition - 0.9328 93.28%
CYP1A2 inhibition - 0.9380 93.80%
CYP2C8 inhibition - 0.9949 99.49%
CYP inhibitory promiscuity - 0.9878 98.78%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.6087 60.87%
Eye corrosion + 0.7593 75.93%
Eye irritation - 0.7279 72.79%
Skin irritation - 0.7182 71.82%
Skin corrosion - 0.7948 79.48%
Ames mutagenesis - 0.5102 51.02%
Human Ether-a-go-go-Related Gene inhibition - 0.7970 79.70%
Micronuclear + 0.5700 57.00%
Hepatotoxicity - 0.7695 76.95%
skin sensitisation - 0.8617 86.17%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity + 0.5052 50.52%
Acute Oral Toxicity (c) III 0.6189 61.89%
Estrogen receptor binding - 0.8573 85.73%
Androgen receptor binding - 0.9012 90.12%
Thyroid receptor binding - 0.8074 80.74%
Glucocorticoid receptor binding - 0.8638 86.38%
Aromatase binding - 0.9195 91.95%
PPAR gamma - 0.8251 82.51%
Honey bee toxicity - 0.5108 51.08%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity - 0.9592 95.92%

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 93.17% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.29% 96.09%
CHEMBL3230 O95977 Sphingosine 1-phosphate receptor Edg-6 84.80% 94.01%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 84.23% 92.86%
CHEMBL1782 P14324 Farnesyl diphosphate synthase 80.78% 92.38%

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 440756
LOTUS LTS0231111
wikiData Q27105321