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1.
(
Organism ID:
10317)
Ascochyta
caulina
(
NCBI TaxID 565413
,
species name lookup
)
Taxonomic group:
fungi
Phylum:
Ascomycota
The following compound(s) are assigned to this organism:
Compound ID:
17716
b-D-Glcp1N-(1-2)-Subst Subst = 2,4,7-triamino-5-hydroxy-octane-1,8-dioic acid = SMILES N{2}[C@H]({1}C(O)=O)C{4}[C@@H](N){5}[C@H](O)C{7}[C@H](N){8}C(O)=O
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Structure type:
monomer ; 398 [M+H]+
Trivial name:
ascaulitoxin
Reference(s) to other database(s):
PubChem: 102462860
Phytochemistry
1998, "Ascaulitoxin, a phytotoxic bis-amino acid N-glucoside from Ascochyta caulina"
CSDB ID 40531
(all data & tools)
Compound ID:
17717
b-D-Glcp1NAc2Ac3Ac4Ac6Ac-(1-2)-Subst Subst = 2,4,7-triamino-5-hydroxy-octane-1,8-dioic acid = SMILES N{2}[C@H]({1}C(O)=O)C{4}[C@@H](N){5}[C@H](O)C{7}[C@H](N){8}C(O)=O
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Structure type:
monomer ; 571.208969
C24H33N3O13
Phytochemistry
1998, "Ascaulitoxin, a phytotoxic bis-amino acid N-glucoside from Ascochyta caulina"
CSDB ID 40785
(all data & tools)
Compound ID:
17718
b-D-Glcp1N2Ac3Ac4Ac6Ac-(1-2)-Subst7Ac Subst = 2,4,7-triamino-5-hydroxy-octane-1,8-dioic acid = SMILES N{2}[C@H]({1}C(O)=O)C{4}[C@@H](N){5}[C@H](O)C{7}[C@H](N){8}C(O)=O
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Structure type:
monomer ; 571.204681
C24H33N3O13
Phytochemistry
1998, "Ascaulitoxin, a phytotoxic bis-amino acid N-glucoside from Ascochyta caulina"
CSDB ID 40786
(all data & tools)
Compound ID:
17719
b-D-Glcp1NAc2Ac3Ac4Ac6Ac-(1-2)-Subst7Ac Subst = 2,4,7-triamino-5-hydroxy-octane-1,8-dioic acid = SMILES N{2}[C@H]({1}C(O)=O)C{4}[C@@H](N){5}[C@H](O)C{7}[C@H](N){8}C(O)=O
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Structure type:
monomer ; 529.185326
C22H31N3O12
Phytochemistry
1998, "Ascaulitoxin, a phytotoxic bis-amino acid N-glucoside from Ascochyta caulina"
CSDB ID 40787
(all data & tools)
Compound ID:
18911
b-D-Glcp-(1-2)-Subst Subst = 2,4,7-triamino-5-hydroxyoctandoic acid = SMILES N{2}C(CC(N)C(O)CC(N)C(=O)O)C(=O)O
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Structure type:
monomer
Trivial name:
ascaulitoxin
Compound class:
N-glycoside
Analytical Methods
2010, "A new GC-MS method for the analysis of ascaulitoxin, its aglycone and 4-aminoproline from culture filtrates of Ascochyta caulina"
CSDB ID 43994
(all data & tools)
Compound ID:
18912
Subst1-(1-7)-+ | Subst1-(1-4)-+ | | | Subst1-(1-6)-+ | | | | | Subst1-(1-3)-+ | | | | | | | Subst1-(1-2)-b-D-Glcp-(1-2)-Subst-(1-1)-Subst1 | | | Subst1-(1-4)-+ | | | | Subst1-(1-5)-+ | | Subst1-(1-8)-+ Subst = 2,4,7-triamino-5-hydroxyoctandoic acid = SMILES N{2}C(C{4}C(N){5}C(O)C{7}C(N){8}C(=O)O){1}C(=O)O; Subst1 = trimethylsilanol = SMILES C[Si](C)(C){1}O
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Structure type:
monomer
Analytical Methods
2010, "A new GC-MS method for the analysis of ascaulitoxin, its aglycone and 4-aminoproline from culture filtrates of Ascochyta caulina"
CSDB ID 43995
(all data & tools)
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