Satratoxin H 12'-acetate

Details

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Internal ID dc9688bd-68e6-4dc4-a85c-cb7e642c6cef
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Trichothecenes
IUPAC Name [(6R,14R,15S,16R,19Z,27R)-23-(1-hydroxyethyl)-9,15-dimethyl-3,18-dioxospiro[4,12,17,24-tetraoxapentacyclo[21.3.1.113,16.06,11.06,15]octacosa-1,9,19,21-tetraene-14,2'-oxirane]-27-yl] acetate
SMILES (Canonical) CC1=CC2C3(CC1)COC(=O)C=C4CCOC(C4OC(=O)C)(C=CC=CC(=O)OC5C3(C6(CO6)C(C5)O2)C)C(C)O
SMILES (Isomeric) CC1=CC2[C@@]3(CC1)COC(=O)C=C4CCOC([C@@H]4OC(=O)C)(C=C/C=C\C(=O)O[C@H]5[C@]3([C@@]6(CO6)C(C5)O2)C)C(C)O
InChI InChI=1S/C31H38O10/c1-18-8-11-29-16-36-26(35)14-21-9-12-37-30(19(2)32,27(21)39-20(3)33)10-6-5-7-25(34)41-22-15-24(40-23(29)13-18)31(17-38-31)28(22,29)4/h5-7,10,13-14,19,22-24,27,32H,8-9,11-12,15-17H2,1-4H3/b7-5-,10-6?,21-14?/t19?,22-,23?,24?,27-,28-,29-,30?,31-/m1/s1
InChI Key YFKYOBAFGWNPSA-WENWRFNUSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C31H38O10
Molecular Weight 570.60 g/mol
Exact Mass 570.24649740 g/mol
Topological Polar Surface Area (TPSA) 130.00 Ų
XlogP 1.40
Atomic LogP (AlogP) 2.64
H-Bond Acceptor 10
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Satratoxin H 12'-acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9347 93.47%
Caco-2 - 0.7848 78.48%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.8178 81.78%
OATP2B1 inhibitior - 0.8600 86.00%
OATP1B1 inhibitior + 0.8435 84.35%
OATP1B3 inhibitior + 0.9481 94.81%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6271 62.71%
BSEP inhibitior + 0.9862 98.62%
P-glycoprotein inhibitior + 0.8494 84.94%
P-glycoprotein substrate + 0.7760 77.60%
CYP3A4 substrate + 0.7087 70.87%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8874 88.74%
CYP3A4 inhibition - 0.9375 93.75%
CYP2C9 inhibition - 0.8910 89.10%
CYP2C19 inhibition - 0.9235 92.35%
CYP2D6 inhibition - 0.9455 94.55%
CYP1A2 inhibition - 0.7437 74.37%
CYP2C8 inhibition + 0.5385 53.85%
CYP inhibitory promiscuity - 0.9568 95.68%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5570 55.70%
Eye corrosion - 0.9882 98.82%
Eye irritation - 0.9317 93.17%
Skin irritation - 0.5390 53.90%
Skin corrosion - 0.9294 92.94%
Ames mutagenesis - 0.6737 67.37%
Human Ether-a-go-go-Related Gene inhibition - 0.3778 37.78%
Micronuclear - 0.6000 60.00%
Hepatotoxicity + 0.5701 57.01%
skin sensitisation - 0.8640 86.40%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.6654 66.54%
Acute Oral Toxicity (c) I 0.5213 52.13%
Estrogen receptor binding + 0.8220 82.20%
Androgen receptor binding + 0.7516 75.16%
Thyroid receptor binding + 0.5358 53.58%
Glucocorticoid receptor binding + 0.8470 84.70%
Aromatase binding + 0.7169 71.69%
PPAR gamma + 0.6488 64.88%
Honey bee toxicity - 0.6006 60.06%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9808 98.08%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.11% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.76% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.44% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.03% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.70% 94.45%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 93.69% 98.75%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 91.82% 94.80%
CHEMBL1994 P08235 Mineralocorticoid receptor 91.44% 100.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 90.76% 96.77%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.37% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.86% 89.00%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 89.78% 96.47%
CHEMBL2581 P07339 Cathepsin D 89.18% 98.95%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 89.04% 95.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.74% 99.23%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.47% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.13% 86.33%
CHEMBL4208 P20618 Proteasome component C5 85.73% 90.00%
CHEMBL340 P08684 Cytochrome P450 3A4 84.99% 91.19%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.14% 92.62%
CHEMBL5852 Q96P65 Pyroglutamylated RFamide peptide receptor 82.69% 85.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.44% 95.89%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 81.11% 95.71%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.11% 97.14%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.45% 93.04%
CHEMBL5028 O14672 ADAM10 80.42% 97.50%
CHEMBL245 P20309 Muscarinic acetylcholine receptor M3 80.39% 97.53%

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.
There are no matching plants.

Cross-Links

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PubChem 139584517
LOTUS LTS0173022
wikiData Q77370695