HT-2 Toxin

Details

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Internal ID e5c005d6-a7a8-44af-9d40-74d350bfd90f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Trichothecenes
IUPAC Name [(1S,2R,4S,7R,9R,10R,11S,12S)-2-(acetyloxymethyl)-10,11-dihydroxy-1,5-dimethylspiro[8-oxatricyclo[7.2.1.02,7]dodec-5-ene-12,2'-oxirane]-4-yl] 3-methylbutanoate
SMILES (Canonical) CC1=CC2C(CC1OC(=O)CC(C)C)(C3(C(C(C(C34CO4)O2)O)O)C)COC(=O)C
SMILES (Isomeric) CC1=C[C@@H]2[C@](C[C@@H]1OC(=O)CC(C)C)([C@]3([C@@H]([C@H]([C@H]([C@@]34CO4)O2)O)O)C)COC(=O)C
InChI InChI=1S/C22H32O8/c1-11(2)6-16(24)29-14-8-21(9-27-13(4)23)15(7-12(14)3)30-19-17(25)18(26)20(21,5)22(19)10-28-22/h7,11,14-15,17-19,25-26H,6,8-10H2,1-5H3/t14-,15+,17+,18+,19+,20+,21+,22-/m0/s1
InChI Key PNKLMTPXERFKEN-MLXHEQMXSA-N
Popularity 229 references in papers

Physical and Chemical Properties

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Molecular Formula C22H32O8
Molecular Weight 424.50 g/mol
Exact Mass 424.20971797 g/mol
Topological Polar Surface Area (TPSA) 115.00 Ų
XlogP 0.40
Atomic LogP (AlogP) 1.12
H-Bond Acceptor 8
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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26934-87-2
Toxin HT 2
HT 2 Toxin
NC6C26RM46
CHEBI:138861
12,13-Epoxytrichothec-9-ene-3-alpha,4-beta,8-alpha,15-tetrol 15-acetate 8-isovalerate
NSC-278571
[(1S,2R,4S,7R,9R,10R,11S,12S)-2-(acetyloxymethyl)-10,11-dihydroxy-1,5-dimethylspiro[8-oxatricyclo[7.2.1.02,7]dodec-5-ene-12,2'-oxirane]-4-yl] 3-methylbutanoate
3,4-dihydroxy-15-acetoxy-8-(3-methylbutyryloxy)-12,13-epoxy-delta9-trichothecene
15-Acetoxy-3,4-dihydroxy-8-(3-methylbutyryloxy)-12,13-epoxy delta9-trichothecene
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of HT-2 Toxin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8595 85.95%
Caco-2 - 0.6900 69.00%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7734 77.34%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8512 85.12%
OATP1B3 inhibitior + 0.9141 91.41%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.7955 79.55%
P-glycoprotein inhibitior - 0.5482 54.82%
P-glycoprotein substrate - 0.5684 56.84%
CYP3A4 substrate + 0.6685 66.85%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8454 84.54%
CYP3A4 inhibition - 0.9581 95.81%
CYP2C9 inhibition - 0.8248 82.48%
CYP2C19 inhibition - 0.8189 81.89%
CYP2D6 inhibition - 0.9193 91.93%
CYP1A2 inhibition - 0.8438 84.38%
CYP2C8 inhibition - 0.6478 64.78%
CYP inhibitory promiscuity - 0.8943 89.43%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6522 65.22%
Eye corrosion - 0.9862 98.62%
Eye irritation - 0.9209 92.09%
Skin irritation - 0.6874 68.74%
Skin corrosion - 0.9349 93.49%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5842 58.42%
Micronuclear - 0.6100 61.00%
Hepatotoxicity + 0.5519 55.19%
skin sensitisation - 0.7844 78.44%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity + 0.8254 82.54%
Acute Oral Toxicity (c) I 0.8085 80.85%
Estrogen receptor binding + 0.7594 75.94%
Androgen receptor binding + 0.6431 64.31%
Thyroid receptor binding - 0.5854 58.54%
Glucocorticoid receptor binding + 0.7108 71.08%
Aromatase binding + 0.6513 65.13%
PPAR gamma + 0.6177 61.77%
Honey bee toxicity - 0.7344 73.44%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6305 63.05%
Fish aquatic toxicity + 0.9782 97.82%

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 98.39% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.38% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.17% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.71% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.10% 97.09%
CHEMBL3401 O75469 Pregnane X receptor 89.33% 94.73%
CHEMBL221 P23219 Cyclooxygenase-1 88.65% 90.17%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 86.61% 94.80%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.41% 97.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.11% 89.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 84.72% 97.21%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 84.48% 96.47%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 82.54% 98.75%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 82.24% 94.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.12% 96.00%
CHEMBL4005 P42336 PI3-kinase p110-alpha subunit 81.62% 97.47%
CHEMBL5028 O14672 ADAM10 81.20% 97.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.15% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.33% 100.00%
CHEMBL3437 Q16853 Amine oxidase, copper containing 80.07% 94.00%

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 10093830
LOTUS LTS0092038
wikiData Q27896911