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1. (Article ID: 12470)
Melero CP, Medarde M, San Feliciano A
A short review on cardiotonic steroids and their aminoguanidine analogues
Molecules 5(1) (2000)
51-81
A short review on cardiotonic steroids and their analogues is presented. The natural, semisynthetic and synthetic derivatives, as well as their mechanism of action and structure-activity relationships are shown, with a special reference to aminoguanidine derivatives.
structure-activity relationships, digitalis glycosides analogues, inotropic activity, Na+, K+-ATPase, aminoguanidine analogues
Publication DOI: 10.3390/50100051Journal NLM ID: 100964009Publisher: Basel, Switzerland: MDPI
Correspondence: medarde
gugu.usal.es
Institutions: Departamento de Química Farmacéutica, Facultad de Farmacia, Salamanca, Spain
The publication contains the following compound(s):
- Compound ID: 32361
Structure type: monomer
Compound class: glycoside
- Compound ID: 32362
|
b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Digp3Me-(1-3)-Subst
Subst = digitalis-like aglycon |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 32363
|
b-D-Glcp-(1-6)-b-D-Glcp-(1-4)-b-D-Digp3Me-(1-3)-Subst
Subst = digitalis-like aglycon |
Show graphically |
Structure type: oligomer
Compound class: glycoside
- Compound ID: 22306
|
b-D-Digp-(1-4)-b-D-Digp-(1-4)-b-D-Digp-(1-3)-Subst
Subst = digoxigenin = SMILES O=C1OCC([C@H]2CC{14}[C@]3(O)[C@]4([H])CC[C@]5([H])C{3}[C@@H](O)CC[C@]5(C)[C@@]4([H])C{12}[C@@H](O)[C@]23C)=C1 |
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Structure type: oligomer
Trivial name: digoxin
Compound class: saponin glycoside, glycoside, triterpenoid glycoside, cardiac glycoside
Reference(s) to other database(s): CCSD:
3412, CBank-STR:3871, GenDB:MK530410
- Compound ID: 32354
|
b-D-Digp4Me-(1-4)-b-D-Digp-(1-4)-b-D-Digp-(1-3)-Subst
Subst = digoxigenin = SMILES O=C1OCC([C@H]2CC{14}[C@]3(O)[C@]4([H])CC[C@]5([H])C{3}[C@@H](O)CC[C@]5(C)[C@@]4([H])C{12}[C@@H](O)[C@]23C)=C1 |
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Structure type: oligomer
Trivial name: methyldigoxin
Compound class: glycoside, cardiac glycoside
- Compound ID: 32355
|
a-L-Rhap-(1-3)-Subst
Subst = ouabagenin = SMILES O{3}[C@H]1C{1}[C@@H](O)[C@]2({23}CO)[C@@H]3[C@H]({14}[C@@]4(O)CC[C@H](C5=CC(OC5)=O)[C@@]4(C)C{11}[C@H]3O)CC{5}[C@]2(O)C1 |
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Structure type: oligomer
Trivial name: ouabain
Compound class: glycoside
- Compound ID: 32356
|
b-D-Glcp-(1-4)-a-L-Rhap-(1-3)-Subst
Subst = hellebrigenin = SMILES O{3}[C@H]1CC[C@]2(C=O)[C@H]3CC[C@]4(C)[C@@H](C5=COC(C=C5)=O)CC{14}[C@]4(O)[C@@H]3CC{5}[C@]2(O)C1 |
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Structure type: oligomer
Trivial name: hellebrine
Compound class: glycoside
- Compound ID: 32357
|
b-D-Glcp-(1-4)-b-D-Digp3Ac-(1-3)-Subst
Subst = digitoxigenin = SMILES O{3}[C@H]1CC[C@]2(C)[C@@]3([H])CC[C@]4(C)[C@@H](C(CO5)=CC5=O)CC{14}[C@]4(O)[C@]3([H])CC[C@@]([H])2C1 |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 32358
|
b-D-Glcp-(1-4)-b-D-Digp3Me-(1-3)-Subst
Subst = acovenosigenin = SMILES O{3}[C@H]1C{1}[C@H](O)[C@]2(C)[C@@]3([H])CC[C@]4(C)[C@@H](C(CO5)=CC5=O)CC{14}[C@]4(O)[C@]3([H])CC[C@@]([H])2C1 |
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Structure type: oligomer
Trivial name: acobioside A
Compound class: glycoside
- Compound ID: 32359
|
b-D-Glcp-(1-6)-b-D-Glcp-(1-4)-b-D-Digp3Me-(1-3)-Subst14Ac
Subst = acovenosigenin = SMILES O{3}[C@H]1C{1}[C@H](O)[C@]2(C)[C@@]3([H])CC[C@]4(C)[C@@H](C(CO5)=CC5=O)CC{14}[C@]4(O)[C@]3([H])CC[C@@]([H])2C1 |
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Structure type: oligomer
Trivial name: 14-O-acetylacovenioside C
Compound class: glycoside
- Compound ID: 32360
Structure type: monomer
Compound class: glycoside
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