Chemical Formula: C24H34O9
Chemical Formula C24H34O9
Found 92 metabolite its formula value is C24H34O9
T2 Toxin
T2 Toxin is isolated from Fusarium species and Trichoderma lignorum. T2 Toxin is an important mycotoxin occurring naturally in various agricultural products. Isolated from Fusarium subspecies and Trichoderma lignorum. Important mycotoxin occurring naturally in various agricultural products D009676 - Noxae > D011042 - Poisons > D014255 - Trichothecenes D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins T-2 Toxin (T-2 Mycotoxin) is a toxic trichothecene mycotoxin produced by various Fusarium species in feedstuffs and cereal grains, LD50 values of T-2 Toxin in mice and rats are 5.2 and 1.5 mg/kg BWa,respectively [1]. T-2 Toxin (T-2 Mycotoxin) can be transformed into a variety of metabolite, the typical metabolites of T-2 toxin in animals are HT-2 toxin and T-2-triol, which are hydrolysates[1]. T-2 Toxin (T-2 Mycotoxin) is an inhibitor of protein synthesis resulting from binding peptidyltransferase, which is an integral part of the 60s ribosomal subunit. T-2 Toxin (T-2 Mycotoxin) inhibits the synthesis of DNA and RNA, interferes with the metabolism of membrane phospholipids, and increases the level of liver lipid peroxides[1]. T-2 Toxin (T-2 Mycotoxin) induces apoptosis in the immune system, gastrointestinal tissues, and fetal tissues[2].
8-Pentanoylneosolaniol
8-Pentanoylneosolaniol is produced by Fusarium sporotrichioides. D009676 - Noxae > D011042 - Poisons > D014255 - Trichothecenes D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins Production by Fusarium sporotrichioides
Cardivin C
A germacranolide isolated from the aerial parts of Carpesium divaricatum. It exhibits cytotoxicity against the human tumor cells, A-549 (nonsmall cell lung), SK-OV-3 (ovary), SK-MEL-2 (skin), XF-498 (central nervous system) and HCT-15 (colon).
12,13-Epoxy-trichothec-9-ene-3a,4b,8,15-tetrol 4,15-diacetate 8-isovalerate
2-[2,6-bis(3-methylbut-2-enyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2-hydroxyacetic acid
6beta,9beta-diacetoxypulchellin-2-O-<2-methylbutyrate>
1alpha,6-diacetoxy-11beta-hydroxy-16(S)-hydroxymethyl-6,7-seco-ent-kauran-15-one-7,20-olide|taihangexcisoidesin B
4-O-acetyl-6beta-acetoxy-9beta-hydroxypulchellin-2-O-<2-methylbutyrate>
4-O-acetyl-6beta-acetoxy-9beta-hydroxypulchellin-2-O-isovalerate
(12R)-6alpha,19-diacetoxy-1beta,12-epoxy-4alpha,18-dihydroxy-neo-clerod-13-en-15,16-olide|ajugaciliatin G
10beta,11alpha-diacetoxy-8alpha-(2-methylbutanoyloxy)-2beta-hydroxyslov-3-enolide
2beta,5-epoxy-5,10beta-dihydroxy-6alpha-isobutyloxy-9beta-angeloyloxy-germacran-8alpha,12-olide|ineupatolide A
2beta,5-epoxy-6alpha,10beta-dihydroxy-5alpha-2-methylbutyloxy-9beta-isobutyloxy-germacran-8alpha,12-olide|ineupatolide B
13alpha,20beta-diacetoxy-5alpha,7beta,9alpha,10beta-tetrahydroxy-2alpha,20-epoxy-11(15->1)-abeotaxa-11,15-diene|4alpha,13alpha-diacetoxy-2alpha,20-epoxy-11(15->1)abeotaxa-11,15-diene-5alpha,7beta,9alpha,10beta-tetraol
2-[2,6-bis(3-methylbut-2-enyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2-hydroxyacetic acid
4β,15-Diacetoxy-8α-(3-methylbutyryloxy)-12,13-epoxytrichothec-9-en-3α-ol
D009676 - Noxae > D011042 - Poisons > D014255 - Trichothecenes D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins T-2 Toxin (T-2 Mycotoxin) is a toxic trichothecene mycotoxin produced by various Fusarium species in feedstuffs and cereal grains, LD50 values of T-2 Toxin in mice and rats are 5.2 and 1.5 mg/kg BWa,respectively [1]. T-2 Toxin (T-2 Mycotoxin) can be transformed into a variety of metabolite, the typical metabolites of T-2 toxin in animals are HT-2 toxin and T-2-triol, which are hydrolysates[1]. T-2 Toxin (T-2 Mycotoxin) is an inhibitor of protein synthesis resulting from binding peptidyltransferase, which is an integral part of the 60s ribosomal subunit. T-2 Toxin (T-2 Mycotoxin) inhibits the synthesis of DNA and RNA, interferes with the metabolism of membrane phospholipids, and increases the level of liver lipid peroxides[1]. T-2 Toxin (T-2 Mycotoxin) induces apoptosis in the immune system, gastrointestinal tissues, and fetal tissues[2]. T 2 Toxin. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=21259-20-1 (retrieved 2024-09-06) (CAS RN: 21259-20-1). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
T-2 TOXIN
A trichothecene mycotoxin produced by fungi of the genus Fusarium. It is a common contaminant in food and feedstuffs of cereal origin and is known to cause a range of toxic effects in humans and animals. D009676 - Noxae > D011042 - Poisons > D014255 - Trichothecenes D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins CONFIDENCE Reference Standard (Level 1)
2-[2,6-bis(3-methylbut-2-enyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2-hydroxyacetic acid_major
2-[2,6-bis(3-methylbut-2-enyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2-hydroxyacetic acid_89.4\\%
8-Pentanoylneosolaniol
D009676 - Noxae > D011042 - Poisons > D014255 - Trichothecenes D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins
[4-(?-D-Glucopyranosyloxy)-2,6-bis(3-methyl-2-buten-1-yl)phenyl](hydroxy)acetic acid
2-[[2,2-Bis[[(1-oxoallyl)oxy]methyl]butoxy]methyl]-2-ethyl-1,3-propanediyl diacrylate
Phthalic anhydride,fumaric acid,tricyclodecanedimethanol polymer
T-2 Mycotoxin
D009676 - Noxae > D011042 - Poisons > D014255 - Trichothecenes D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins
[(2R,4S,10R,11S)-11-acetyloxy-2-(acetyloxymethyl)-10-hydroxy-1,5-dimethylspiro[8-oxatricyclo[7.2.1.02,7]dodec-5-ene-12,2-oxirane]-4-yl] 3-methylbutanoate
D009676 - Noxae > D011042 - Poisons > D014255 - Trichothecenes D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins
Ajugaciliatin G
A diterpene lactone isolated from the whole plants of Ajuga ciliata.
Insariotoxin
Insariotoxin has been reported in Fusarium tricinctum
14-(acetyloxy)-16-formyl-2,3-dihydroxy-4,9,13,16-tetramethyl-5-oxo-6-oxatricyclo[11.3.0.0³,⁷]hexadec-8-en-12-yl acetate
4,9-bis(acetyloxy)-5-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl 3-methylbutanoate
(1's,2r,2'r,4'r,7'r,9'r,10'r,11's)-11'-(acetyloxy)-2'-[(acetyloxy)methyl]-10'-hydroxy-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-4'-yl 3-methylbutanoate
8,10-dihydroxy-6,10-dimethyl-3-methylidene-4-[(2-methylpropanoyl)oxy]-2,5-dioxo-octahydrocyclodeca[b]furan-11-yl 2-methylbut-2-enoate
(1r,1's,2s,6r,6's,7's,9's,10's)-2-(acetyloxy)-7'-hydroxy-10'-(hydroxymethyl)-5,5-dimethyl-2',11'-dioxo-3'-oxaspiro[cyclohexane-1,5'-tricyclo[7.2.1.0¹,⁶]dodecan]-6-ylmethyl acetate
12-(acetyloxy)-2,3-dihydroxy-4,9,13,18-tetramethyl-5-oxo-6,17-dioxatetracyclo[11.5.0.0³,⁷.0¹⁶,¹⁸]octadec-8-en-14-yl acetate
2-(acetyloxy)-4a,6,10a-trihydroxy-4,4,7,11b-tetramethyl-9-oxo-1h,2h,3h,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-1-yl acetate
(1r,2s,4ar,6ar,7s,10ar,11as,11bs)-2-(acetyloxy)-4a,7,10a-trihydroxy-4,4,7,11b-tetramethyl-9-oxo-1h,2h,3h,5h,6h,6ah,11h,11ah-phenanthro[3,2-b]furan-1-yl acetate
(1's,2r,2'r,4's,7'r,9'r,10'r,11's)-11'-(acetyloxy)-2'-[(acetyloxy)methyl]-10'-hydroxy-1',5'-dimethyl-8'-oxaspiro[oxirane-2,12'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-en-4'-yl pentanoate
(1r,2s,4ar,6s,6as,7r,10ar,11as,11bs)-2-(acetyloxy)-4a,6,10a-trihydroxy-4,4,7,11b-tetramethyl-9-oxo-1h,2h,3h,5h,6h,6ah,7h,11h,11ah-phenanthro[3,2-b]furan-1-yl acetate
ajugamarin c1
{"Ingredient_id": "HBIN014978","Ingredient_name": "ajugamarin c1","Alias": "NA","Ingredient_formula": "C24H34O9","Ingredient_Smile": "CC1CC(C2(C(C1(C)CC(C3=CC(=O)OC3)O)C(CCC24CO4)O)COC(=O)C)OC(=O)C","Ingredient_weight": "466.5 g/mol","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "804","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "12136682","DrugBank_id": "NA"}