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1.
(
Organism ID:
12440)
Arthrinium
phaeospermum
(
NCBI TaxID 112178
,
species name lookup
)
Taxonomic group:
fungi
Phylum:
Ascomycota
The following compound(s) are assigned to this organism:
Compound ID:
21147
Subst1-(1-3)-+ | Subst-(1-6)-b-D-Manp-(1-4)-a-D-Sugp Subst = (2E,4Z,6E)-8-hydroxydeca-2,4,6-trienoic acid = SMILES CCC(O)/C=C/C=C\C=C\{1}C(=O)O; Subst1 = 7-hydroxy-8,14-dimethylhexadeca-2E,4E,8E,10E-tetraenoic acid = SMILES CCC(C)CC/C=C/C=C(C)/{7}C(O)C/C=C/C=C/{1}C(=O)O; Sug = Glc 1O,1C-derivative with 3,5-dihydroxybenzyl alcohol 1O,2C = SMILES OC[C@H]3O[C@]2(OCc1cc(O)cc(O)c12)[C@H](O){3}[C@@H](O){4}[C@@H]3O
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Structure type:
monomer
Trivial name:
papulacandin B
Compound class:
glycoside
Reference(s) to other database(s):
GTC:G53406VG
Helvetica Chimica Acta
1977, "On the structure of papulacandin B, a new antibiotic with antifungal activity"
CSDB ID 47343
(all data & tools)
The Journal of Antibiotics
1980, "Papulacandins, a new family of antibiotics with antifungal activity. Structures of papulacandins A, B, C and D"
CSDB ID 47345
(all data & tools)
Compound ID:
21148
Subst1-(1-3)-+ | Subst-(1-6)-b-D-Manp-(1-4)-a-D-Sugp Subst = 2E,4E-decadienoic acid = SMILES CCCCC/C=C/C=C/{1}C(=O)O; Subst1 = 7-hydroxy-8,14-dimethylhexadeca-2E,4E,8E,10E-tetraenoic acid = SMILES CCC(C)CC/C=C/C=C(C)/{7}C(O)C/C=C/C=C/{1}C(=O)O; Sug = Glc 1O,1C-derivative with 3,5-dihydroxybenzyl alcohol 1O,2C = SMILES OC[C@H]3O[C@]2(OCc1cc(O)cc(O)c12)[C@H](O){3}[C@@H](O){4}[C@@H]3O
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Structure type:
monomer
C47H66O16
Trivial name:
papulacandin A
Compound class:
glycoside
Reference(s) to other database(s):
GTC:G53406VG
The Journal of Antibiotics
1980, "Papulacandins, a new family of antibiotics with antifungal activity. Structures of papulacandins A, B, C and D"
CSDB ID 47344
(all data & tools)
Compound ID:
21149
Subst1-(1-3)-+ | Subst-(1-6)-b-D-Manp-(1-4)-a-D-Sugp Subst = (2E,4E,6E)-8-hydroxydeca-2,4,6-trienoic acid = SMILES CCC(O)/C=C/C=C/C=C/{1}C(=O)O; Subst1 = 7-hydroxy-8,14-dimethylhexadeca-2E,4E,8E,10E-tetraenoic acid = SMILES CCC(C)CC/C=C/C=C(C)/{7}C(O)C/C=C/C=C/{1}C(=O)O; Sug = Glc 1O,1C-derivative with 3,5-dihydroxybenzyl alcohol 1O,2C = SMILES OC[C@H]3O[C@]2(OCc1cc(O)cc(O)c12)[C@H](O){3}[C@@H](O){4}[C@@H]3O
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Structure type:
monomer
Trivial name:
papulacandin C
Compound class:
glycoside
The Journal of Antibiotics
1980, "Papulacandins, a new family of antibiotics with antifungal activity. Structures of papulacandins A, B, C and D"
CSDB ID 47346
(all data & tools)
Compound ID:
20764
Subst-(1-6)-b-D-Galp-(1-4)-a-D-Sugp-(3-1)-Subst1 Subst = 2E,4E-decadienoic acid = SMILES CCCCC/C=C/C=C/{1}C(=O)O; Sug = Glc 1O,1C-derivative with 3,5-dihydroxybenzyl alcohol 1O,2C = SMILES OC[C@H]3O[C@]2(OCc1cc(O)cc(O)c12)[C@H](O){3}[C@@H](O){4}[C@@H]3O; Subst1 = 7-hydroxy-8,14-dimethylhexadeca-2E,4E,8E,10E-tetraenoic acid = SMILES CCC(C)CC/C=C/C=C(C)/{7}C(O)C/C=C/C=C/{1}C(=O)O
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Structure type:
oligomer
Trivial name:
papulacandin A
Compound class:
glycoside, papulacandin
Trends in Food Science and Technology
2021, "Fungal glycosides: Structure and biological function"
CSDB ID 51484
(all data & tools)
Compound ID:
20765
Subst-(1-6)-b-D-Galp-(1-4)-a-D-Sugp-(3-1)-Subst1 Subst = (2E,4Z,6E)-8-hydroxydeca-2,4,6-trienoic acid = SMILES CCC(O)/C=C/C=C\C=C\{1}C(=O)O; Sug = Glc 1O,1C-derivative with 3,5-dihydroxybenzyl alcohol 1O,2C = SMILES OC[C@H]3O[C@]2(OCc1cc(O)cc(O)c12)[C@H](O){3}[C@@H](O){4}[C@@H]3O; Subst1 = 7-hydroxy-8,14-dimethylhexadeca-2E,4E,8E,10E-tetraenoic acid = SMILES CCC(C)CC/C=C/C=C(C)/{7}C(O)C/C=C/C=C/{1}C(=O)O
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Structure type:
oligomer
Trivial name:
papulacandin B
Compound class:
glycoside, papulacandin
Trends in Food Science and Technology
2021, "Fungal glycosides: Structure and biological function"
CSDB ID 51485
(all data & tools)
Compound ID:
20766
Subst-(1-6)-b-D-Galp-(1-4)-a-D-Sugp-(3-1)-Subst1 Subst = (2E,4E,6E)-8-hydroxydeca-2,4,6-trienoic acid = SMILES CCC(O)/C=C/C=C/C=C/{1}C(=O)O; Sug = Glc 1O,1C-derivative with 3,5-dihydroxybenzyl alcohol 1O,2C = SMILES OC[C@H]3O[C@]2(OCc1cc(O)cc(O)c12)[C@H](O){3}[C@@H](O){4}[C@@H]3O; Subst1 = 7-hydroxy-8,14-dimethylhexadeca-2E,4E,8E,10E-tetraenoic acid = SMILES CCC(C)CC/C=C/C=C(C)/{7}C(O)C/C=C/C=C/{1}C(=O)O
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Structure type:
oligomer
Trivial name:
papulacandin C
Compound class:
glycoside, papulacandin
Trends in Food Science and Technology
2021, "Fungal glycosides: Structure and biological function"
CSDB ID 51486
(all data & tools)
Compound ID:
20767
a-D-Sugp-(3-1)-Subst Sug = Glc 1O,1C-derivative with 3,5-dihydroxybenzyl alcohol 1O,2C = SMILES OC[C@H]3O[C@]2(OCc1cc(O)cc(O)c12)[C@H](O){3}[C@@H](O){4}[C@@H]3O; Subst = 7-hydroxy-8,14-dimethylhexadeca-2E,4E,8E,10E-tetraenoic acid = SMILES CCC(C)CC/C=C/C=C(C)/{7}C(O)C/C=C/C=C/{1}C(=O)O
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Structure type:
monomer
Trivial name:
papulacandin D
Compound class:
glycoside, papulacandin
Trends in Food Science and Technology
2021, "Fungal glycosides: Structure and biological function"
CSDB ID 51487
(all data & tools)
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