12-Deoxyphorbaldehyde-13-hexadecanoate

Details

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Internal ID 910ba966-b5f0-40d9-a164-ab776e478c3e
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-formyl-1,6-dihydroxy-4,12,12,15-tetramethyl-5-oxo-13-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] hexadecanoate
SMILES (Canonical) CCCCCCCCCCCCCCCC(=O)OC12CC(C3(C(C1C2(C)C)C=C(CC4(C3C=C(C4=O)C)O)C=O)O)C
SMILES (Isomeric) CCCCCCCCCCCCCCCC(=O)O[C@@]12C[C@H]([C@]3([C@H]([C@@H]1C2(C)C)C=C(C[C@]4([C@H]3C=C(C4=O)C)O)C=O)O)C
InChI InChI=1S/C36H56O6/c1-6-7-8-9-10-11-12-13-14-15-16-17-18-19-30(38)42-35-22-26(3)36(41)28(31(35)33(35,4)5)21-27(24-37)23-34(40)29(36)20-25(2)32(34)39/h20-21,24,26,28-29,31,40-41H,6-19,22-23H2,1-5H3/t26-,28+,29-,31-,34-,35+,36-/m1/s1
InChI Key NFTGKFBSWRGMSO-IEIRSVMLSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C36H56O6
Molecular Weight 584.80 g/mol
Exact Mass 584.40768950 g/mol
Topological Polar Surface Area (TPSA) 101.00 Ų
XlogP 8.50
Atomic LogP (AlogP) 7.20
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 16

Synonyms

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CHEMBL3953142
CHEBI:69821
12-Deoxyphorbaldehyde-13-hexadecacetate
Q27138162
[(1R,2S,6R,10S,11R,13S,15R)-8-formyl-1,6-dihydroxy-4,12,12,15-tetramethyl-5-oxo-13-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] hexadecanoate

2D Structure

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2D Structure of 12-Deoxyphorbaldehyde-13-hexadecanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9838 98.38%
Caco-2 - 0.7797 77.97%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.7177 71.77%
OATP2B1 inhibitior - 0.8599 85.99%
OATP1B1 inhibitior + 0.8238 82.38%
OATP1B3 inhibitior + 0.9011 90.11%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.7666 76.66%
P-glycoprotein inhibitior + 0.7109 71.09%
P-glycoprotein substrate + 0.5551 55.51%
CYP3A4 substrate + 0.6801 68.01%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9116 91.16%
CYP3A4 inhibition - 0.5626 56.26%
CYP2C9 inhibition + 0.7874 78.74%
CYP2C19 inhibition - 0.7113 71.13%
CYP2D6 inhibition - 0.9242 92.42%
CYP1A2 inhibition - 0.8367 83.67%
CYP2C8 inhibition + 0.5566 55.66%
CYP inhibitory promiscuity - 0.8094 80.94%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6816 68.16%
Eye corrosion - 0.9912 99.12%
Eye irritation - 0.9123 91.23%
Skin irritation + 0.5407 54.07%
Skin corrosion - 0.9392 93.92%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6784 67.84%
Micronuclear - 0.7200 72.00%
Hepatotoxicity - 0.5282 52.82%
skin sensitisation - 0.7827 78.27%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity + 0.4829 48.29%
Acute Oral Toxicity (c) II 0.3540 35.40%
Estrogen receptor binding + 0.7022 70.22%
Androgen receptor binding + 0.7037 70.37%
Thyroid receptor binding - 0.5546 55.46%
Glucocorticoid receptor binding + 0.6868 68.68%
Aromatase binding + 0.6564 65.64%
PPAR gamma + 0.5698 56.98%
Honey bee toxicity - 0.8825 88.25%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.8095 80.95%
Fish aquatic toxicity + 0.9952 99.52%

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 97.13% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.23% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 93.29% 89.63%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.95% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.86% 97.25%
CHEMBL299 P17252 Protein kinase C alpha 91.76% 98.03%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.22% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.26% 86.33%
CHEMBL5255 O00206 Toll-like receptor 4 88.19% 92.50%
CHEMBL2996 Q05655 Protein kinase C delta 88.11% 97.79%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.78% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.62% 94.45%
CHEMBL325 Q13547 Histone deacetylase 1 86.01% 95.92%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 85.97% 93.00%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 85.23% 100.00%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 84.85% 85.94%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.31% 99.23%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 83.33% 82.38%
CHEMBL4227 P25090 Lipoxin A4 receptor 83.08% 100.00%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 82.82% 91.24%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.40% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.10% 97.09%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 80.37% 96.00%

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 fischeri

Cross-Links

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PubChem 11671494
NPASS NPC232665
LOTUS LTS0254893
wikiData Q27138162