Distearyl phosphate

Details

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Internal ID 8bc5d421-3d37-414b-899c-36da01fa374f
Taxonomy Organic acids and derivatives > Organic phosphoric acids and derivatives > Phosphate esters > Alkyl phosphates > Dialkyl phosphates
IUPAC Name dioctadecyl hydrogen phosphate
SMILES (Canonical) CCCCCCCCCCCCCCCCCCOP(=O)(O)OCCCCCCCCCCCCCCCCCC
SMILES (Isomeric) CCCCCCCCCCCCCCCCCCOP(=O)(O)OCCCCCCCCCCCCCCCCCC
InChI InChI=1S/C36H75O4P/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-35-39-41(37,38)40-36-34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h3-36H2,1-2H3,(H,37,38)
InChI Key FRXGWNKDEMTFPL-UHFFFAOYSA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C36H75O4P
Molecular Weight 603.00 g/mol
Exact Mass 602.54029787 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 16.60
Atomic LogP (AlogP) 13.64
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 36

Synonyms

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Dioctadecyl hydrogen phosphate
di-n-Octadecyl phosphate
Dioctadecyl phosphate
Distearyl acid phosphate
Dioctadecyl orthophosphate
Phosphoric acid, dioctadecyl ester
Phosphated stearyl alcohol
UNII-47N7586GSW
47N7586GSW
NSC 2681
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Distearyl phosphate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8121 81.21%
Caco-2 - 0.7509 75.09%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.8429 84.29%
Subcellular localzation Mitochondria 0.7130 71.30%
OATP2B1 inhibitior - 0.8523 85.23%
OATP1B1 inhibitior + 0.9569 95.69%
OATP1B3 inhibitior + 0.9382 93.82%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.4788 47.88%
P-glycoprotein substrate - 0.9584 95.84%
CYP3A4 substrate - 0.5850 58.50%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.7895 78.95%
CYP3A4 inhibition - 0.8934 89.34%
CYP2C9 inhibition - 0.8511 85.11%
CYP2C19 inhibition - 0.8483 84.83%
CYP2D6 inhibition - 0.9086 90.86%
CYP1A2 inhibition - 0.8826 88.26%
CYP2C8 inhibition - 0.9141 91.41%
CYP inhibitory promiscuity - 0.9140 91.40%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6400 64.00%
Carcinogenicity (trinary) Non-required 0.6305 63.05%
Eye corrosion + 0.9653 96.53%
Eye irritation - 0.5000 50.00%
Skin irritation - 0.7029 70.29%
Skin corrosion + 0.9704 97.04%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6252 62.52%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.6138 61.38%
skin sensitisation - 0.7158 71.58%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.8261 82.61%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.7605 76.05%
Acute Oral Toxicity (c) III 0.6151 61.51%
Estrogen receptor binding + 0.7029 70.29%
Androgen receptor binding - 0.5644 56.44%
Thyroid receptor binding + 0.6356 63.56%
Glucocorticoid receptor binding - 0.6424 64.24%
Aromatase binding + 0.5327 53.27%
PPAR gamma + 0.7193 71.93%
Honey bee toxicity - 0.9114 91.14%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity + 0.6098 60.98%
Fish aquatic toxicity + 0.9571 95.71%

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 98.42% 97.29%
CHEMBL3230 O95977 Sphingosine 1-phosphate receptor Edg-6 96.38% 94.01%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 95.97% 85.94%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 94.90% 92.86%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.62% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.53% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.10% 99.17%
CHEMBL2885 P07451 Carbonic anhydrase III 89.77% 87.45%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 88.56% 100.00%
CHEMBL1075162 Q13304 Uracil nucleotide/cysteinyl leukotriene receptor 88.54% 80.33%
CHEMBL1907 P15144 Aminopeptidase N 88.23% 93.31%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 88.15% 96.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 88.01% 92.08%
CHEMBL4040 P28482 MAP kinase ERK2 86.69% 83.82%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 85.65% 95.17%
CHEMBL230 P35354 Cyclooxygenase-2 84.34% 89.63%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 83.97% 80.78%
CHEMBL3401 O75469 Pregnane X receptor 83.76% 94.73%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 82.75% 91.81%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 82.56% 90.24%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 82.10% 94.33%

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.
Angelica dahurica

Cross-Links

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PubChem 76433
NPASS NPC265470