1-Diethoxyphosphorylhexane

Details

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Internal ID ec7826cc-4c08-4eca-89fc-bb4653344436
Taxonomy Organic acids and derivatives > Organic phosphonic acids and derivatives > Phosphonic acid diesters > Dialkyl alkylphosphonates
IUPAC Name 1-diethoxyphosphorylhexane
SMILES (Canonical) CCCCCCP(=O)(OCC)OCC
SMILES (Isomeric) CCCCCCP(=O)(OCC)OCC
InChI InChI=1S/C10H23O3P/c1-4-7-8-9-10-14(11,12-5-2)13-6-3/h4-10H2,1-3H3
InChI Key VVUJWLDQIIFQHI-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C10H23O3P
Molecular Weight 222.26 g/mol
Exact Mass 222.13848159 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 2.50
Atomic LogP (AlogP) 3.83
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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Diethyl hexylphosphonate
16165-66-5
Hexylphosphonic acid diethyl ester
PAE(sub 6)
Phosphonic acid, hexyl-, diethyl ester
BRN 1771540
AI3-18566
Phosphonic acid, P-hexyl-, diethyl ester
4-04-00-03560 (Beilstein Handbook Reference)
Hexylphosphonic acid diethyl
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1-Diethoxyphosphorylhexane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9763 97.63%
Caco-2 + 0.8789 87.89%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.5908 59.08%
OATP2B1 inhibitior - 0.8445 84.45%
OATP1B1 inhibitior + 0.9561 95.61%
OATP1B3 inhibitior + 0.9458 94.58%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8783 87.83%
P-glycoprotein inhibitior - 0.9280 92.80%
P-glycoprotein substrate - 0.9444 94.44%
CYP3A4 substrate - 0.5439 54.39%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7861 78.61%
CYP3A4 inhibition - 0.8992 89.92%
CYP2C9 inhibition - 0.8818 88.18%
CYP2C19 inhibition - 0.8637 86.37%
CYP2D6 inhibition - 0.9194 91.94%
CYP1A2 inhibition - 0.8591 85.91%
CYP2C8 inhibition - 0.9522 95.22%
CYP inhibitory promiscuity - 0.8780 87.80%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Non-required 0.5868 58.68%
Eye corrosion + 0.9667 96.67%
Eye irritation + 0.9198 91.98%
Skin irritation - 0.7223 72.23%
Skin corrosion - 0.8339 83.39%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7397 73.97%
Micronuclear - 0.7400 74.00%
Hepatotoxicity + 0.6433 64.33%
skin sensitisation - 0.7209 72.09%
Respiratory toxicity - 0.9444 94.44%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.8907 89.07%
Acute Oral Toxicity (c) IV 0.6345 63.45%
Estrogen receptor binding - 0.8485 84.85%
Androgen receptor binding - 0.6262 62.62%
Thyroid receptor binding - 0.7466 74.66%
Glucocorticoid receptor binding - 0.8867 88.67%
Aromatase binding - 0.7860 78.60%
PPAR gamma - 0.7482 74.82%
Honey bee toxicity - 0.5426 54.26%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.7737 77.37%
Fish aquatic toxicity + 0.9463 94.63%

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 96.50% 97.29%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 95.09% 92.86%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.25% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 89.38% 92.08%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 86.96% 91.81%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.64% 99.17%
CHEMBL3230 O95977 Sphingosine 1-phosphate receptor Edg-6 86.26% 94.01%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 85.95% 100.00%
CHEMBL2581 P07339 Cathepsin D 85.82% 98.95%
CHEMBL1907 P15144 Aminopeptidase N 85.73% 93.31%
CHEMBL3401 O75469 Pregnane X receptor 85.37% 94.73%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 84.59% 85.94%
CHEMBL4040 P28482 MAP kinase ERK2 82.30% 83.82%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 82.15% 90.24%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.86% 97.25%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.77% 96.95%
CHEMBL230 P35354 Cyclooxygenase-2 80.63% 89.63%

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.
Senna alexandrina

Cross-Links

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PubChem 85311
NPASS NPC39249