Isotrichodermin

Details

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Internal ID bac3b9c1-ab10-4fdd-96d0-554d9d7a9380
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Trichothecenes
IUPAC Name [(1R,2R,10R)-1,2,5-trimethylspiro[8-oxatricyclo[7.2.1.02,7]dodec-5-ene-12,2'-oxirane]-10-yl] acetate
SMILES (Canonical) CC1=CC2C(CC1)(C3(CC(C(C34CO4)O2)OC(=O)C)C)C
SMILES (Isomeric) CC1=CC2[C@](CC1)([C@]3(C[C@H](C(C34CO4)O2)OC(=O)C)C)C
InChI InChI=1S/C17H24O4/c1-10-5-6-15(3)13(7-10)21-14-12(20-11(2)18)8-16(15,4)17(14)9-19-17/h7,12-14H,5-6,8-9H2,1-4H3/t12-,13?,14?,15+,16-,17?/m1/s1
InChI Key OZXJPPYWZVBMGW-WIAGQQCESA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C17H24O4
Molecular Weight 292.40 g/mol
Exact Mass 292.16745924 g/mol
Topological Polar Surface Area (TPSA) 48.10 Ų
XlogP 1.80
Atomic LogP (AlogP) 2.61
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Isotrichodermin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9801 98.01%
Caco-2 + 0.8635 86.35%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7175 71.75%
OATP2B1 inhibitior - 0.8596 85.96%
OATP1B1 inhibitior + 0.8906 89.06%
OATP1B3 inhibitior + 0.9611 96.11%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.5425 54.25%
P-glycoprotein inhibitior - 0.7527 75.27%
P-glycoprotein substrate - 0.8350 83.50%
CYP3A4 substrate + 0.6458 64.58%
CYP2C9 substrate - 0.8155 81.55%
CYP2D6 substrate - 0.8496 84.96%
CYP3A4 inhibition - 0.9220 92.20%
CYP2C9 inhibition - 0.8866 88.66%
CYP2C19 inhibition - 0.8928 89.28%
CYP2D6 inhibition - 0.9330 93.30%
CYP1A2 inhibition - 0.6046 60.46%
CYP2C8 inhibition - 0.6568 65.68%
CYP inhibitory promiscuity - 0.8743 87.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6345 63.45%
Eye corrosion - 0.9879 98.79%
Eye irritation - 0.9327 93.27%
Skin irritation - 0.6024 60.24%
Skin corrosion - 0.9408 94.08%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6206 62.06%
Micronuclear - 0.6000 60.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.7963 79.63%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity + 0.6554 65.54%
Acute Oral Toxicity (c) IV 0.6496 64.96%
Estrogen receptor binding + 0.5972 59.72%
Androgen receptor binding + 0.6868 68.68%
Thyroid receptor binding + 0.6712 67.12%
Glucocorticoid receptor binding - 0.5258 52.58%
Aromatase binding - 0.6470 64.70%
PPAR gamma + 0.6467 64.67%
Honey bee toxicity - 0.7818 78.18%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5955 59.55%
Fish aquatic toxicity + 0.9816 98.16%

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 96.70% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.30% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.88% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.53% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.11% 100.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.61% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.56% 94.45%
CHEMBL2581 P07339 Cathepsin D 82.49% 98.95%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.78% 94.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.51% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.09% 89.00%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 81.04% 94.08%
CHEMBL5028 O14672 ADAM10 80.78% 97.50%
CHEMBL3922 P50579 Methionine aminopeptidase 2 80.47% 97.28%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.11% 95.50%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 102515367
LOTUS LTS0245783
wikiData Q104253956