Palmityl-glutinopallal

Details

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Internal ID ae159935-0627-4dac-9b4e-afa3d5c7c177
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name methyl (1R,4R,7R,8R)-11-hexadecanoyloxy-5-propan-2-ylidene-2,12-dioxapentacyclo[8.3.0.01,3.04,7.08,10]tridecane-8-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C32H50O6/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-25(33)37-29-31-20-30(31,28(34)35-4)24-19-23(22(2)3)26(24)27-32(31,38-27)21-36-29/h24,26-27,29H,5-21H2,1-4H3/t24-,26+,27?,29?,30+,31?,32-/m1/s1
InChI Key DWLMKNGTFCUNKN-JOSAHTOSSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C32H50O6
Molecular Weight 530.70 g/mol
Exact Mass 530.36073931 g/mol
Topological Polar Surface Area (TPSA) 74.40 Ų
XlogP 8.20
Atomic LogP (AlogP) 7.04
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 16

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Palmityl-glutinopallal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9904 99.04%
Caco-2 - 0.6960 69.60%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.7322 73.22%
OATP2B1 inhibitior - 0.7194 71.94%
OATP1B1 inhibitior + 0.8705 87.05%
OATP1B3 inhibitior + 0.9719 97.19%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior + 0.9432 94.32%
P-glycoprotein inhibitior + 0.7669 76.69%
P-glycoprotein substrate + 0.6399 63.99%
CYP3A4 substrate + 0.6514 65.14%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8635 86.35%
CYP3A4 inhibition - 0.7085 70.85%
CYP2C9 inhibition - 0.6392 63.92%
CYP2C19 inhibition - 0.7353 73.53%
CYP2D6 inhibition - 0.9040 90.40%
CYP1A2 inhibition - 0.7402 74.02%
CYP2C8 inhibition + 0.5153 51.53%
CYP inhibitory promiscuity - 0.8259 82.59%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5166 51.66%
Eye corrosion - 0.9806 98.06%
Eye irritation - 0.8548 85.48%
Skin irritation - 0.7100 71.00%
Skin corrosion - 0.9368 93.68%
Ames mutagenesis - 0.7423 74.23%
Human Ether-a-go-go-Related Gene inhibition - 0.4743 47.43%
Micronuclear - 0.5400 54.00%
Hepatotoxicity - 0.5458 54.58%
skin sensitisation - 0.7852 78.52%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.7561 75.61%
Acute Oral Toxicity (c) III 0.5115 51.15%
Estrogen receptor binding + 0.7641 76.41%
Androgen receptor binding + 0.7624 76.24%
Thyroid receptor binding - 0.6325 63.25%
Glucocorticoid receptor binding + 0.5501 55.01%
Aromatase binding + 0.5397 53.97%
PPAR gamma + 0.5883 58.83%
Honey bee toxicity - 0.8322 83.22%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.7989 79.89%
Fish aquatic toxicity + 0.9832 98.32%

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 99.15% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.82% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.62% 99.17%
CHEMBL2581 P07339 Cathepsin D 93.64% 98.95%
CHEMBL340 P08684 Cytochrome P450 3A4 91.96% 91.19%
CHEMBL5255 O00206 Toll-like receptor 4 91.19% 92.50%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 90.91% 95.50%
CHEMBL221 P23219 Cyclooxygenase-1 90.84% 90.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.08% 94.45%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 89.04% 89.34%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.04% 97.25%
CHEMBL299 P17252 Protein kinase C alpha 87.31% 98.03%
CHEMBL2996 Q05655 Protein kinase C delta 86.68% 97.79%
CHEMBL4227 P25090 Lipoxin A4 receptor 86.60% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.74% 99.23%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 85.09% 92.86%
CHEMBL230 P35354 Cyclooxygenase-2 84.05% 89.63%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 83.86% 94.33%
CHEMBL255 P29275 Adenosine A2b receptor 83.02% 98.59%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 82.46% 100.00%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 82.41% 95.17%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.33% 92.62%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 81.22% 96.90%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 80.71% 97.29%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 80.54% 98.75%
CHEMBL5028 O14672 ADAM10 80.47% 97.50%

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 139585652
LOTUS LTS0004081
wikiData Q77484481