Physordinose D

Details

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Internal ID 562c862d-7113-488b-8071-a58ed9ccd3dd
Taxonomy Lipids and lipid-like molecules > Saccharolipids
IUPAC Name [(2R,3R,4S,5R,6R)-2-[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-(2-methylpropoxy)oxan-3-yl] dodecanoate
SMILES (Canonical) CCCCCCCCCCCC(=O)OC1C(C(C(OC1OC2(C(C(C(O2)CO)O)O)CO)CO)O)OCC(C)C
SMILES (Isomeric) CCCCCCCCCCCC(=O)O[C@@H]1[C@H]([C@@H]([C@H](O[C@@H]1O[C@]2([C@H]([C@@H]([C@H](O2)CO)O)O)CO)CO)O)OCC(C)C
InChI InChI=1S/C28H52O12/c1-4-5-6-7-8-9-10-11-12-13-21(32)38-25-24(36-16-18(2)3)22(33)19(14-29)37-27(25)40-28(17-31)26(35)23(34)20(15-30)39-28/h18-20,22-27,29-31,33-35H,4-17H2,1-3H3/t19-,20-,22-,23-,24+,25-,26+,27-,28+/m1/s1
InChI Key APUQGTNFGFBPEX-ZRVLSRDKSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C28H52O12
Molecular Weight 580.70 g/mol
Exact Mass 580.34587709 g/mol
Topological Polar Surface Area (TPSA) 185.00 Ų
XlogP 3.90
Atomic LogP (AlogP) 0.76
H-Bond Acceptor 12
H-Bond Donor 6
Rotatable Bonds 19

Synonyms

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CHEMBL1173479

2D Structure

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2D Structure of Physordinose D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7011 70.11%
Caco-2 - 0.8299 82.99%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Mitochondria 0.8445 84.45%
OATP2B1 inhibitior - 0.5737 57.37%
OATP1B1 inhibitior + 0.8381 83.81%
OATP1B3 inhibitior + 0.9212 92.12%
MATE1 inhibitior - 0.9812 98.12%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.5935 59.35%
P-glycoprotein inhibitior - 0.4607 46.07%
P-glycoprotein substrate - 0.6060 60.60%
CYP3A4 substrate + 0.6284 62.84%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8963 89.63%
CYP3A4 inhibition - 0.7625 76.25%
CYP2C9 inhibition - 0.8293 82.93%
CYP2C19 inhibition - 0.8397 83.97%
CYP2D6 inhibition - 0.9317 93.17%
CYP1A2 inhibition - 0.8877 88.77%
CYP2C8 inhibition - 0.6238 62.38%
CYP inhibitory promiscuity - 0.9267 92.67%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6802 68.02%
Eye corrosion - 0.9890 98.90%
Eye irritation - 0.9059 90.59%
Skin irritation - 0.7879 78.79%
Skin corrosion - 0.9568 95.68%
Ames mutagenesis - 0.8279 82.79%
Human Ether-a-go-go-Related Gene inhibition - 0.4216 42.16%
Micronuclear - 0.8800 88.00%
Hepatotoxicity - 0.6875 68.75%
skin sensitisation - 0.9114 91.14%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.5717 57.17%
Acute Oral Toxicity (c) III 0.5486 54.86%
Estrogen receptor binding + 0.6494 64.94%
Androgen receptor binding + 0.5570 55.70%
Thyroid receptor binding - 0.6352 63.52%
Glucocorticoid receptor binding - 0.5988 59.88%
Aromatase binding + 0.6104 61.04%
PPAR gamma + 0.5373 53.73%
Honey bee toxicity - 0.8352 83.52%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5020 50.20%
Fish aquatic toxicity + 0.8680 86.80%

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 98.27% 96.09%
CHEMBL2581 P07339 Cathepsin D 97.67% 98.95%
CHEMBL299 P17252 Protein kinase C alpha 97.20% 98.03%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.85% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 96.08% 99.17%
CHEMBL5255 O00206 Toll-like receptor 4 95.00% 92.50%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 94.91% 92.86%
CHEMBL230 P35354 Cyclooxygenase-2 94.36% 89.63%
CHEMBL2996 Q05655 Protein kinase C delta 94.30% 97.79%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 92.98% 97.29%
CHEMBL1293316 Q9HBX9 Relaxin receptor 1 92.85% 82.50%
CHEMBL3359 P21462 Formyl peptide receptor 1 90.44% 93.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.79% 96.00%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 88.00% 91.24%
CHEMBL226 P30542 Adenosine A1 receptor 87.91% 95.93%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.70% 94.45%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 87.18% 85.94%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 86.85% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 86.21% 94.73%
CHEMBL4227 P25090 Lipoxin A4 receptor 86.09% 100.00%
CHEMBL2885 P07451 Carbonic anhydrase III 84.66% 87.45%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 83.38% 96.47%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 83.19% 92.08%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 81.12% 96.90%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.02% 92.62%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.49% 94.33%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 80.06% 96.21%

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.
Physalis sordida

Cross-Links

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PubChem 46872117
NPASS NPC185419
ChEMBL CHEMBL1173479
LOTUS LTS0088571
wikiData Q104916556