[(1R,2S,6R,10S,11R,13S,15R)-8-(acetyloxymethyl)-1,6-dihydroxy-4,12,12,15-tetramethyl-5-oxo-13-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] (Z)-octadec-9-enoate

Details

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Internal ID 9196bbfb-ddf1-4d8c-b109-aabc7e0dcd23
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Tigliane and ingenane diterpenoids > Phorbol esters
IUPAC Name [(1R,2S,6R,10S,11R,13S,15R)-8-(acetyloxymethyl)-1,6-dihydroxy-4,12,12,15-tetramethyl-5-oxo-13-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] (Z)-octadec-9-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C40H62O7/c1-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-34(42)47-39-25-29(3)40(45)32(35(39)37(39,5)6)24-31(27-46-30(4)41)26-38(44)33(40)23-28(2)36(38)43/h14-15,23-24,29,32-33,35,44-45H,7-13,16-22,25-27H2,1-6H3/b15-14-/t29-,32+,33-,35-,38-,39+,40-/m1/s1
InChI Key FRLZOANJBWVXPT-LWDNIVNZSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C40H62O7
Molecular Weight 654.90 g/mol
Exact Mass 654.44955431 g/mol
Topological Polar Surface Area (TPSA) 110.00 Ų
XlogP 8.80
Atomic LogP (AlogP) 8.12
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 18

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1R,2S,6R,10S,11R,13S,15R)-8-(acetyloxymethyl)-1,6-dihydroxy-4,12,12,15-tetramethyl-5-oxo-13-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] (Z)-octadec-9-enoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9845 98.45%
Caco-2 - 0.8055 80.55%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.7949 79.49%
OATP2B1 inhibitior - 0.5757 57.57%
OATP1B1 inhibitior + 0.8007 80.07%
OATP1B3 inhibitior + 0.9454 94.54%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7275 72.75%
BSEP inhibitior + 0.9633 96.33%
P-glycoprotein inhibitior + 0.7700 77.00%
P-glycoprotein substrate + 0.5701 57.01%
CYP3A4 substrate + 0.7046 70.46%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9212 92.12%
CYP3A4 inhibition - 0.7812 78.12%
CYP2C9 inhibition + 0.8458 84.58%
CYP2C19 inhibition - 0.8764 87.64%
CYP2D6 inhibition - 0.9253 92.53%
CYP1A2 inhibition - 0.8930 89.30%
CYP2C8 inhibition + 0.6611 66.11%
CYP inhibitory promiscuity - 0.8202 82.02%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6814 68.14%
Eye corrosion - 0.9912 99.12%
Eye irritation - 0.9063 90.63%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9512 95.12%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6787 67.87%
Micronuclear - 0.7400 74.00%
Hepatotoxicity - 0.5441 54.41%
skin sensitisation - 0.8543 85.43%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity + 0.5131 51.31%
Acute Oral Toxicity (c) III 0.3728 37.28%
Estrogen receptor binding + 0.8152 81.52%
Androgen receptor binding + 0.7274 72.74%
Thyroid receptor binding - 0.5172 51.72%
Glucocorticoid receptor binding + 0.7329 73.29%
Aromatase binding + 0.6508 65.08%
PPAR gamma + 0.6368 63.68%
Honey bee toxicity - 0.8314 83.14%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.8900 89.00%
Fish aquatic toxicity + 0.9942 99.42%

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 97.94% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 97.01% 99.17%
CHEMBL230 P35354 Cyclooxygenase-2 96.81% 89.63%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.30% 91.11%
CHEMBL299 P17252 Protein kinase C alpha 96.17% 98.03%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.92% 97.25%
CHEMBL2581 P07339 Cathepsin D 95.43% 98.95%
CHEMBL2996 Q05655 Protein kinase C delta 94.59% 97.79%
CHEMBL5255 O00206 Toll-like receptor 4 90.79% 92.50%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 90.38% 100.00%
CHEMBL1937 Q92769 Histone deacetylase 2 88.50% 94.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.05% 86.33%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 87.91% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.18% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.75% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.10% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.88% 97.09%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.81% 93.00%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 84.20% 92.08%
CHEMBL4227 P25090 Lipoxin A4 receptor 83.76% 100.00%
CHEMBL3045 P05771 Protein kinase C beta 82.45% 97.63%
CHEMBL325 Q13547 Histone deacetylase 1 82.13% 95.92%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 81.90% 82.38%
CHEMBL221 P23219 Cyclooxygenase-1 81.87% 90.17%

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.
Euphorbia fischeriana

Cross-Links

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PubChem 11534767
LOTUS LTS0116827
wikiData Q105000251