[(1R,2S,6R,10S,11R,13S,15R)-13-acetyloxy-1,6-dihydroxy-4,12,12,15-tetramethyl-5-oxo-8-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl]methyl decanoate

Details

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Internal ID 783e9be6-52af-4e62-bd5d-5173704d8349
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Tigliane and ingenane diterpenoids > Phorbol esters
IUPAC Name [(1R,2S,6R,10S,11R,13S,15R)-13-acetyloxy-1,6-dihydroxy-4,12,12,15-tetramethyl-5-oxo-8-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl]methyl decanoate
SMILES (Canonical) CCCCCCCCCC(=O)OCC1=CC2C3C(C3(CC(C2(C4C=C(C(=O)C4(C1)O)C)O)C)OC(=O)C)(C)C
SMILES (Isomeric) CCCCCCCCCC(=O)OCC1=C[C@H]2[C@H]3[C@](C3(C)C)(C[C@H]([C@@]2([C@@H]4C=C(C(=O)[C@]4(C1)O)C)O)C)OC(=O)C
InChI InChI=1S/C32H48O7/c1-7-8-9-10-11-12-13-14-26(34)38-19-23-16-24-27-29(5,6)31(27,39-22(4)33)17-21(3)32(24,37)25-15-20(2)28(35)30(25,36)18-23/h15-16,21,24-25,27,36-37H,7-14,17-19H2,1-6H3/t21-,24+,25-,27-,30-,31+,32-/m1/s1
InChI Key HISKSQNGCRXRPV-AIPLTYTCSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C32H48O7
Molecular Weight 544.70 g/mol
Exact Mass 544.34000387 g/mol
Topological Polar Surface Area (TPSA) 110.00 Ų
XlogP 5.40
Atomic LogP (AlogP) 5.22
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 11

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)-13-acetyloxy-1,6-dihydroxy-4,12,12,15-tetramethyl-5-oxo-8-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl]methyl decanoate

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 - 0.7426 74.26%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.7949 79.49%
OATP2B1 inhibitior - 0.7215 72.15%
OATP1B1 inhibitior + 0.8530 85.30%
OATP1B3 inhibitior + 0.9454 94.54%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.7275 72.75%
BSEP inhibitior + 0.9721 97.21%
P-glycoprotein inhibitior + 0.7918 79.18%
P-glycoprotein substrate + 0.5638 56.38%
CYP3A4 substrate + 0.6956 69.56%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9177 91.77%
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 + 0.6042 60.42%
CYP inhibitory promiscuity - 0.8202 82.02%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6814 68.14%
Eye corrosion - 0.9912 99.12%
Eye irritation - 0.9060 90.60%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9512 95.12%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6463 64.63%
Micronuclear - 0.7400 74.00%
Hepatotoxicity - 0.5107 51.07%
skin sensitisation - 0.8543 85.43%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity + 0.5587 55.87%
Acute Oral Toxicity (c) III 0.3728 37.28%
Estrogen receptor binding + 0.7892 78.92%
Androgen receptor binding + 0.7062 70.62%
Thyroid receptor binding - 0.5213 52.13%
Glucocorticoid receptor binding + 0.7446 74.46%
Aromatase binding + 0.7310 73.10%
PPAR gamma + 0.5869 58.69%
Honey bee toxicity - 0.8403 84.03%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.8345 83.45%
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 98.42% 96.09%
CHEMBL2996 Q05655 Protein kinase C delta 97.90% 97.79%
CHEMBL299 P17252 Protein kinase C alpha 97.29% 98.03%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.84% 97.25%
CHEMBL2581 P07339 Cathepsin D 94.42% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 93.89% 89.63%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.80% 91.11%
CHEMBL3045 P05771 Protein kinase C beta 91.70% 97.63%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.60% 99.17%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 89.75% 100.00%
CHEMBL5255 O00206 Toll-like receptor 4 89.65% 92.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.61% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.78% 99.23%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.44% 97.09%
CHEMBL4794 Q8NER1 Vanilloid receptor 85.43% 98.97%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 82.18% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.63% 94.45%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.35% 100.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.19% 93.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.05% 89.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.00% 100.00%

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 cornigera

Cross-Links

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PubChem 24813122
NPASS NPC170212
LOTUS LTS0010445
wikiData Q105028990