Trichothec-9-en-8-one,13-epoxy-4-hydroxy-, crotonate

Details

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Internal ID ffc5d21c-0645-4ee7-a7fc-18f84c4e8328
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Trichothecenes
IUPAC Name [(12R)-1,2,5-trimethyl-4-oxospiro[8-oxatricyclo[7.2.1.02,7]dodec-5-ene-12,2'-oxirane]-11-yl] (E)-but-2-enoate
SMILES (Canonical) CC=CC(=O)OC1CC2C3(C1(C4(CC(=O)C(=CC4O2)C)C)C)CO3
SMILES (Isomeric) C/C=C/C(=O)OC1CC2[C@@]3(C1(C4(CC(=O)C(=CC4O2)C)C)C)CO3
InChI InChI=1S/C19H24O5/c1-5-6-16(21)24-14-8-15-19(10-22-19)18(14,4)17(3)9-12(20)11(2)7-13(17)23-15/h5-7,13-15H,8-10H2,1-4H3/b6-5+/t13?,14?,15?,17?,18?,19-/m1/s1
InChI Key LJWZOKOFCBPNAG-JGVKRIKOSA-N
Popularity 23 references in papers

Physical and Chemical Properties

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Molecular Formula C19H24O5
Molecular Weight 332.40 g/mol
Exact Mass 332.16237386 g/mol
Topological Polar Surface Area (TPSA) 65.10 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.35
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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Trichothecine
CCRIS 6650
NSC 92492
NSC-92492
6379-69-7
12,13-Epoxy-4-hydroxytrichothec-9-en-8-one crotonate
12,13-Epoxy-4-((1-oxo-2-butenyl)oxy)trichothec-9-en-8-one
Trichothec-9-en-8-one, 12,13-epoxy-4-hydroxy-, crotonate
[4beta(Z)]-12,13-Epoxy-4-[(1-oxo-2-butenyl)oxy]trichothec-9-en-8-one
NSC92492
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Trichothec-9-en-8-one,13-epoxy-4-hydroxy-, crotonate

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 + 0.7584 75.84%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.7180 71.80%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8535 85.35%
OATP1B3 inhibitior + 0.9390 93.90%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.5878 58.78%
P-glycoprotein inhibitior - 0.6096 60.96%
P-glycoprotein substrate - 0.6658 66.58%
CYP3A4 substrate + 0.6573 65.73%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8916 89.16%
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 - 0.5959 59.59%
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 - 0.9701 97.01%
Skin irritation - 0.6324 63.24%
Skin corrosion - 0.9363 93.63%
Ames mutagenesis - 0.9600 96.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4017 40.17%
Micronuclear - 0.5000 50.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.7642 76.42%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.7383 73.83%
Acute Oral Toxicity (c) IV 0.3962 39.62%
Estrogen receptor binding + 0.7652 76.52%
Androgen receptor binding + 0.6281 62.81%
Thyroid receptor binding - 0.5530 55.30%
Glucocorticoid receptor binding - 0.5358 53.58%
Aromatase binding - 0.5214 52.14%
PPAR gamma + 0.5596 55.96%
Honey bee toxicity - 0.7287 72.87%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5900 59.00%
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 96.38% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.06% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.49% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.95% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.86% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.77% 94.45%
CHEMBL3714130 P46095 G-protein coupled receptor 6 86.60% 97.36%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.46% 99.23%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.91% 92.94%
CHEMBL3401 O75469 Pregnane X receptor 81.62% 94.73%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.79% 97.09%
CHEMBL340 P08684 Cytochrome P450 3A4 80.23% 91.19%

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.
Trichosanthes kirilowii

Cross-Links

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PubChem 49789068
NPASS NPC75684