Terracinolide H

Details

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Internal ID 449a9e52-e8a4-4e85-b98f-892ca83ca749
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Hexacarboxylic acids and derivatives
IUPAC Name [(1R,2R,3R,4R,6R,8S,9E,12S,13S,14R,15S)-4,6,12,13-tetraacetyloxy-15-butan-2-yloxy-3-hydroxy-4,8,11,11-tetramethyl-7,18-dioxo-19-oxatricyclo[13.4.0.02,6]nonadec-9-en-14-yl] 2-methylpropanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C38H56O15/c1-13-21(5)51-37-17-15-26(43)49-31(37)27-30(45)36(12,52-24(8)41)18-38(27,53-25(9)42)29(44)20(4)14-16-35(10,11)32(48-23(7)40)28(47-22(6)39)33(37)50-34(46)19(2)3/h14,16,19-21,27-28,30-33,45H,13,15,17-18H2,1-12H3/b16-14+/t20-,21?,27+,28-,30+,31+,32+,33+,36+,37-,38+/m0/s1
InChI Key YAWDIXVIMRZNCX-VOJHQUFTSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C38H56O15
Molecular Weight 752.80 g/mol
Exact Mass 752.36192108 g/mol
Topological Polar Surface Area (TPSA) 204.00 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.48
H-Bond Acceptor 15
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

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CHEMBL2074671

2D Structure

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2D Structure of Terracinolide H

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9432 94.32%
Caco-2 - 0.8200 82.00%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7101 71.01%
OATP2B1 inhibitior - 0.8578 85.78%
OATP1B1 inhibitior + 0.8087 80.87%
OATP1B3 inhibitior + 0.8067 80.67%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.9933 99.33%
P-glycoprotein inhibitior + 0.8667 86.67%
P-glycoprotein substrate + 0.6474 64.74%
CYP3A4 substrate + 0.6994 69.94%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8751 87.51%
CYP3A4 inhibition - 0.7335 73.35%
CYP2C9 inhibition - 0.8060 80.60%
CYP2C19 inhibition - 0.7450 74.50%
CYP2D6 inhibition - 0.9550 95.50%
CYP1A2 inhibition - 0.8063 80.63%
CYP2C8 inhibition + 0.6028 60.28%
CYP inhibitory promiscuity - 0.9107 91.07%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6369 63.69%
Eye corrosion - 0.9854 98.54%
Eye irritation - 0.8987 89.87%
Skin irritation - 0.6181 61.81%
Skin corrosion - 0.8845 88.45%
Ames mutagenesis + 0.5263 52.63%
Human Ether-a-go-go-Related Gene inhibition - 0.3992 39.92%
Micronuclear - 0.8600 86.00%
Hepatotoxicity + 0.5843 58.43%
skin sensitisation - 0.8151 81.51%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.7074 70.74%
Acute Oral Toxicity (c) III 0.4841 48.41%
Estrogen receptor binding + 0.7840 78.40%
Androgen receptor binding + 0.7283 72.83%
Thyroid receptor binding + 0.5770 57.70%
Glucocorticoid receptor binding + 0.7929 79.29%
Aromatase binding + 0.6815 68.15%
PPAR gamma + 0.7442 74.42%
Honey bee toxicity - 0.6568 65.68%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9292 92.92%

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 98.77% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.24% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.15% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.86% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.63% 86.33%
CHEMBL2581 P07339 Cathepsin D 93.07% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 92.73% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.68% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.34% 85.14%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 88.94% 96.77%
CHEMBL340 P08684 Cytochrome P450 3A4 88.26% 91.19%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.08% 92.62%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 86.79% 94.80%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 86.75% 98.75%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 86.71% 95.71%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.83% 100.00%
CHEMBL5028 O14672 ADAM10 82.91% 97.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.78% 89.00%
CHEMBL3922 P50579 Methionine aminopeptidase 2 82.72% 97.28%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.36% 97.09%
CHEMBL230 P35354 Cyclooxygenase-2 80.92% 89.63%

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 dendroides
Euphorbia segetalis

Cross-Links

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PubChem 70697248
LOTUS LTS0061658
wikiData Q105345633