Sapinsignoid D

Details

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Internal ID b6d64ef8-d1c1-4dbf-837e-e954b3b75b3f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Tigliane and ingenane diterpenoids > Phorbol esters
IUPAC Name [(1R,2S,6R,10S,11R,12S,13S,15R)-12-(acetyloxymethyl)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,15-trimethyl-5-oxo-13-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] (3E,5E)-tetradeca-3,5-dienoate
SMILES (Canonical) CCCCCCCCC=CC=CCC(=O)OC12CC(C3(C(C1C2(C)COC(=O)C)C=C(CC4(C3C=C(C4=O)C)O)CO)O)C
SMILES (Isomeric) CCCCCCCC/C=C/C=C/CC(=O)O[C@@]12C[C@H]([C@]3([C@H]([C@@H]1[C@@]2(C)COC(=O)C)C=C(C[C@]4([C@H]3C=C(C4=O)C)O)CO)O)C
InChI InChI=1S/C36H52O8/c1-6-7-8-9-10-11-12-13-14-15-16-17-30(39)44-35-20-25(3)36(42)28(31(35)33(35,5)23-43-26(4)38)19-27(22-37)21-34(41)29(36)18-24(2)32(34)40/h13-16,18-19,25,28-29,31,37,41-42H,6-12,17,20-23H2,1-5H3/b14-13+,16-15+/t25-,28+,29-,31-,33-,34-,35+,36-/m1/s1
InChI Key UYPOIYOXALXFNN-UFANGNBOSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C36H52O8
Molecular Weight 612.80 g/mol
Exact Mass 612.36621861 g/mol
Topological Polar Surface Area (TPSA) 130.00 Ų
XlogP 5.40
Atomic LogP (AlogP) 5.31
H-Bond Acceptor 8
H-Bond Donor 3
Rotatable Bonds 14

Synonyms

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CHEMBL2042143

2D Structure

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2D Structure of Sapinsignoid D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9664 96.64%
Caco-2 - 0.8097 80.97%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7227 72.27%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8249 82.49%
OATP1B3 inhibitior + 0.9410 94.10%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6119 61.19%
BSEP inhibitior + 0.9755 97.55%
P-glycoprotein inhibitior + 0.7905 79.05%
P-glycoprotein substrate + 0.6129 61.29%
CYP3A4 substrate + 0.7156 71.56%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9209 92.09%
CYP3A4 inhibition - 0.7683 76.83%
CYP2C9 inhibition + 0.6560 65.60%
CYP2C19 inhibition - 0.8660 86.60%
CYP2D6 inhibition - 0.9229 92.29%
CYP1A2 inhibition - 0.9039 90.39%
CYP2C8 inhibition + 0.6944 69.44%
CYP inhibitory promiscuity - 0.8805 88.05%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6912 69.12%
Eye corrosion - 0.9910 99.10%
Eye irritation - 0.9181 91.81%
Skin irritation + 0.4897 48.97%
Skin corrosion - 0.9531 95.31%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7399 73.99%
Micronuclear - 0.7400 74.00%
Hepatotoxicity - 0.6108 61.08%
skin sensitisation - 0.9137 91.37%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity + 0.6356 63.56%
Acute Oral Toxicity (c) III 0.4829 48.29%
Estrogen receptor binding + 0.7863 78.63%
Androgen receptor binding + 0.7553 75.53%
Thyroid receptor binding + 0.5488 54.88%
Glucocorticoid receptor binding + 0.7822 78.22%
Aromatase binding + 0.6603 66.03%
PPAR gamma + 0.6087 60.87%
Honey bee toxicity - 0.8105 81.05%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.8031 80.31%
Fish aquatic toxicity + 0.9813 98.13%

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 98.35% 96.09%
CHEMBL299 P17252 Protein kinase C alpha 96.22% 98.03%
CHEMBL2581 P07339 Cathepsin D 95.63% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.58% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.29% 97.25%
CHEMBL2996 Q05655 Protein kinase C delta 94.19% 97.79%
CHEMBL1937 Q92769 Histone deacetylase 2 93.24% 94.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.42% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.86% 94.45%
CHEMBL230 P35354 Cyclooxygenase-2 88.38% 89.63%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 87.97% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.69% 95.56%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 87.50% 96.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 86.49% 93.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.23% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.11% 86.33%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.77% 97.29%
CHEMBL325 Q13547 Histone deacetylase 1 84.75% 95.92%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.67% 97.09%
CHEMBL5255 O00206 Toll-like receptor 4 84.45% 92.50%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.85% 100.00%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 83.13% 96.90%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 82.40% 92.08%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 81.45% 91.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.28% 99.23%

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.
Falconeria insignis

Cross-Links

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PubChem 57408646
LOTUS LTS0007323
wikiData Q105281792