Demanyl phosphate

Details

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Internal ID 7d46dce3-d737-4bad-a464-24c99abad9c5
Taxonomy Organic acids and derivatives > Organic phosphoric acids and derivatives > Phosphate esters > Phosphoethanolamines
IUPAC Name 2-(dimethylamino)ethyl dihydrogen phosphate
SMILES (Canonical) CN(C)CCOP(=O)(O)O
SMILES (Isomeric) CN(C)CCOP(=O)(O)O
InChI InChI=1S/C4H12NO4P/c1-5(2)3-4-9-10(6,7)8/h3-4H2,1-2H3,(H2,6,7,8)
InChI Key BLHVJAAEHMLMOI-UHFFFAOYSA-N
Popularity 32 references in papers

Physical and Chemical Properties

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Molecular Formula C4H12NO4P
Molecular Weight 169.12 g/mol
Exact Mass 169.05039486 g/mol
Topological Polar Surface Area (TPSA) 70.00 Ų
XlogP -3.80
Atomic LogP (AlogP) -0.34
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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6909-62-2
Phosphodimethylethanolamine
2-(dimethylamino)ethyl dihydrogen phosphate
N,N-dimethylethanolamine phosphate
Phosphoric acid, mono(2-(dimethylamino)ethyl) ester
N,N-Dimethylaminoethanol Phosphate (~70%)
R2680E432U
Phosphoric acid, mono[2-(dimethylamino)ethyl] ester
Panclar
P-DMEA
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Demanyl phosphate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7997 79.97%
Caco-2 + 0.5220 52.20%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.5756 57.56%
OATP2B1 inhibitior - 0.8545 85.45%
OATP1B1 inhibitior + 0.9615 96.15%
OATP1B3 inhibitior + 0.9441 94.41%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9824 98.24%
P-glycoprotein inhibitior - 0.9819 98.19%
P-glycoprotein substrate - 0.9713 97.13%
CYP3A4 substrate + 0.5468 54.68%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4072 40.72%
CYP3A4 inhibition - 0.9160 91.60%
CYP2C9 inhibition - 0.8434 84.34%
CYP2C19 inhibition - 0.8484 84.84%
CYP2D6 inhibition - 0.9132 91.32%
CYP1A2 inhibition - 0.8747 87.47%
CYP2C8 inhibition - 0.9962 99.62%
CYP inhibitory promiscuity - 0.9762 97.62%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Non-required 0.6026 60.26%
Eye corrosion - 0.5654 56.54%
Eye irritation + 0.7814 78.14%
Skin irritation - 0.6851 68.51%
Skin corrosion - 0.6062 60.62%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6321 63.21%
Micronuclear - 0.5500 55.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.8406 84.06%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity + 0.5553 55.53%
Acute Oral Toxicity (c) III 0.5993 59.93%
Estrogen receptor binding - 0.8709 87.09%
Androgen receptor binding - 0.7806 78.06%
Thyroid receptor binding - 0.7700 77.00%
Glucocorticoid receptor binding - 0.8941 89.41%
Aromatase binding - 0.8978 89.78%
PPAR gamma - 0.9122 91.22%
Honey bee toxicity - 0.5245 52.45%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.8500 85.00%
Fish aquatic toxicity - 0.8036 80.36%

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 93.84% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 93.58% 97.29%
CHEMBL3230 O95977 Sphingosine 1-phosphate receptor Edg-6 92.32% 94.01%
CHEMBL3401 O75469 Pregnane X receptor 84.31% 94.73%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 81.57% 91.71%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 81.03% 93.10%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 80.17% 80.78%

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 151438
LOTUS LTS0175247
wikiData Q27114746