Trichothecolone acetate

Details

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Internal ID bd67c923-fd55-4c0a-b0f3-f3c871f65485
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Trichothecenes
IUPAC Name [(1S,2R,7R,9R,11R,12S)-1,2,5-trimethyl-4-oxospiro[8-oxatricyclo[7.2.1.02,7]dodec-5-ene-12,2'-oxirane]-11-yl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H22O5/c1-9-5-12-15(3,7-11(9)19)16(4)13(21-10(2)18)6-14(22-12)17(16)8-20-17/h5,12-14H,6-8H2,1-4H3/t12-,13-,14-,15+,16-,17+/m1/s1
InChI Key UGISZOXYFHGCSR-IKIFYQGPSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H22O5
Molecular Weight 306.40 g/mol
Exact Mass 306.14672380 g/mol
Topological Polar Surface Area (TPSA) 65.10 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.79
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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4-O-Acetyltrichothecolone
Acetyltrichothecolone
YY7B0P0407
UNII-YY7B0P0407
4682-54-6
Trichothec-9-en-8-one, 4-(acetyloxy)-12,13-epoxy-, (4beta)-
CHEBI:223048
Q27896836
(4.BETA.)-4-(ACETYLOXY)-12,13-EPOXYTRICHOTHEC-9-EN-8-ONE
TRICHOTHEC-9-EN-8-ONE, 4-(ACETYLOXY)-12,13-EPOXY-, (4.BETA.)-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Trichothecolone acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9822 98.22%
Caco-2 + 0.6892 68.92%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7180 71.80%
OATP2B1 inhibitior - 0.8607 86.07%
OATP1B1 inhibitior + 0.8666 86.66%
OATP1B3 inhibitior + 0.9390 93.90%
MATE1 inhibitior - 0.6600 66.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.5958 59.58%
P-glycoprotein inhibitior - 0.7262 72.62%
P-glycoprotein substrate - 0.7777 77.77%
CYP3A4 substrate + 0.6388 63.88%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8912 89.12%
CYP3A4 inhibition - 0.7777 77.77%
CYP2C9 inhibition - 0.9004 90.04%
CYP2C19 inhibition - 0.8918 89.18%
CYP2D6 inhibition - 0.9530 95.30%
CYP1A2 inhibition - 0.7810 78.10%
CYP2C8 inhibition - 0.7450 74.50%
CYP inhibitory promiscuity - 0.8667 86.67%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6386 63.86%
Eye corrosion - 0.9863 98.63%
Eye irritation - 0.8987 89.87%
Skin irritation - 0.6324 63.24%
Skin corrosion - 0.9363 93.63%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6292 62.92%
Micronuclear - 0.5000 50.00%
Hepatotoxicity + 0.5408 54.08%
skin sensitisation - 0.7642 76.42%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.8311 83.11%
Acute Oral Toxicity (c) IV 0.3962 39.62%
Estrogen receptor binding + 0.7086 70.86%
Androgen receptor binding + 0.6122 61.22%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.6330 63.30%
Aromatase binding - 0.5847 58.47%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.7480 74.80%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9912 99.12%

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 95.22% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.01% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.22% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.31% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.02% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.82% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.16% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.84% 94.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.51% 97.09%
CHEMBL2581 P07339 Cathepsin D 84.31% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.89% 89.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.82% 92.94%
CHEMBL3714130 P46095 G-protein coupled receptor 6 83.35% 97.36%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.80% 93.04%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.62% 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.
There are no matching plants.

Cross-Links

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PubChem 20841657
LOTUS LTS0126365
wikiData Q27896836