CAS 1397-89-3
:Amphotéricine B
Description :
Amphotéricine B est un agent antifongique polyène principalement utilisé pour traiter des infections fongiques graves, en particulier celles causées par des espèces de Candida et d'Aspergillus. Il est dérivé de la bactérie Streptomyces nodosus et est connu pour sa capacité à se lier à l'ergostérol, un composant clé des membranes cellulaires fongiques, entraînant une rupture de la membrane cellulaire et finalement la mort cellulaire. Amphotéricine B se caractérise par sa couleur brun jaunâtre et est généralement administré par voie intraveineuse en raison de sa faible biodisponibilité orale. Il a un poids moléculaire relativement élevé et est soluble dans le diméthylsulfoxyde (DMSO) et d'autres solvants organiques, mais peu soluble dans l'eau. Le médicament est connu pour ses effets secondaires potentiels, notamment la néphrotoxicité et les réactions liées à l'infusion, ce qui nécessite une surveillance attentive pendant le traitement. Amphotéricine B est souvent utilisé dans des cas graves où d'autres traitements antifongiques peuvent être inefficaces, ce qui en fait une option critique dans la gestion des infections fongiques invasives.
Formule :C47H73NO17
InChI :InChI=1/C47H73NO17/c1-27-17-15-13-11-9-7-5-6-8-10-12-14-16-18-34(64-46-44(58)41(48)43(57)30(4)63-46)24-38-40(45(59)60)37(54)26-47(61,65-38)25-33(51)22-36(53)35(52)20-19-31(49)21-32(50)23-39(55)62-29(3)28(2)42(27)56/h5-18,27-38,40-44,46,49-54,56-58,61H,19-26,48H2,1-4H3,(H,59,60)/b6-5+,9-7+,10-8+,13-11+,14-12+,17-15+,18-16+/t27-,28-,29-,30+,31+,32+,33-,34-,35+,36+,37-,38-,40+,41-,42+,43+,44-,46-,47+/m0/s1
Code InChI :InChIKey=APKFDSVGJQXUKY-INPOYWNPSA-N
SMILES :C(O)(=O)[C@H]1[C@]2(O[C@@](O)(C[C@@H]1O)C[C@@H](O)C[C@@H](O)[C@H](O)CC[C@@H](O)C[C@@H](O)CC(=O)O[C@@H](C)[C@H](C)[C@H](O)[C@@H](C)\C=C\C=C\C=C\C=C\C=C\C=C\C=C\[C@H](O[C@H]3[C@@H](O)[C@@H](N)[C@H](O)[C@@H](C)O3)C2)[H]
Synonymes :- (1R,3S,5R,6R,9R,11R,15S,16R,17R,18S,19E,21E,23E,25E,27E,29E,31E,33R,35S,36R,37S)-33-[(3-Amino-3,6-dideoxy-b-D-mannopyranosyl)oxy]-1,3,5,6,9,11,17,37-octahydroxy-15,16,18-trimethyl-13-oxo-14,39-dioxabicyclo[33.3.1]nonatriaconta-19,21,23,25,27,29,31-heptaene-36-carboxylicacid
- (1R,3S,5R,6R,9R,11R,15S,16R,17R,18S,19E,21E,23E,25E,27E,29E,31E,33R,35S,36R,37S)-33-[(3-Amino-3,6-dideoxy-β-<span class="text-smallcaps">D</span>-mannopyranosyl)oxy]-1,3,5,6,9,11,17,37-octahydroxy-15,16,18-trimethyl-13-oxo-14,39-dioxabicyclo[33.3.1]nonatriaconta-19,21,23,25,27,29,31-heptaene-36-carboxylic acid
- (1R,3S,5R,6R,9R,11R,15S,16R,17R,18S,19E,21E,23E,25E,27E,29E,31E,33R,35S,36R,37S)-33-[(3-Amino-3,6-dideoxy-β-D-mannopyranosyl)oxy]-1,3,5,6,9,11,17,37-octahydroxy-15,16,18-trimethyl-13-oxo-14,39-dioxabicyclo[33.3.1]nonatriaconta-19,21,23,25,27,29,31-heptaene-36-carboxylic acid
- (1R,3S,5R,6R,9R,11R,15S,16R,17R,18S,19E,21E,23E,25E,27E,29E,31E,33R,35S,36R,37S)-33-[(3-amino-3,6-dideoxy-beta-D-mannopyranosyl)oxy]-1,3,5,6,9,11,17,37-octahydroxy-15,16,18-trimethyl-13-oxo-14,39-dioxabicyclo[33.3.1]nonatriaconta-19,21,23,25,27,29,31-heptaene-36-carboxylic acid
- 14,39-Dioxabicyclo[33.3.1]nonatriaconta-19,21,23,25,27,29,31-heptaene-36-carboxylic acid, 33-[(3-amino-3,6-dideoxy-β-<span class="text-smallcaps">D</span>-mannopyranosyl)oxy]-1,3,5,6,9,11,17,37-octahydroxy-15,16,18-trimethyl-13-oxo-, (1R,3S,5R,6R,9R,11R,15S,16R,17R,18S,19E,21E,23E,25E,27E,29E,31E,33R,35S,36R,37S)-
- 14,39-Dioxabicyclo[33.3.1]nonatriaconta-19,21,23,25,27,29,31-heptaene-36-carboxylic acid, 33-[(3-amino-3,6-dideoxy-β-D-mannopyranosyl)oxy]-1,3,5,6,9,11,17,37-octahydroxy-15,16,18-trimethyl-13-oxo-, (1R,3S,5R,6R,9R,11R,15S,16R,17R,18S,19E,21E,23E,25E,27E,29E,31E,33R,35S,36R,37S)-
- 14,39-Dioxabicyclo[33.3.1]nonatriaconta-19,21,23,25,27,29,31-heptaene-36-carboxylicacid, 33-[(3-amino-3,6-dideoxy-b-D-mannopyranosyl)oxy]-1,3,5,6,9,11,17,37-octahydroxy-15,16,18-trimethyl-13-oxo-,(1R,3S,5R,6R,9R,11R,15S,16R,17R,18S,19E,21E,23E,25E,27E,29E,31E,33R,35S,36R,37S)-
- Abelcet
- Abelecet
- AmBisome
- Ampho-Moronal
- Amphocin
- Amphozone
- Apothecon
- Fungilin
- Fungizona
- Fungizone
- Halizon
- Kalsome 10
- LNS-AmB
- Ns 718
- Nsc 527017
- amfotericina B
- amphotericine B
- Amphotericin B
- 17,37-octahydroxy-15,16,18-trimethyl-13-oxo-(1r-(1r*,3s*,5r*,6r*,9r*,11r*,15s*
- 14,39-dioxabicyclo(33.3.1)nonatriaconta-19,21,23,25,27,29,31-heptaene-36-carbo
- AMPHOTERICIN B, STREPTOMYCES NODOSUS
- AMPHOTERICIN B, STREPTOMYCES SPECIES
- FUNGIZONE(R)
- AMPHOTERCIN B
- amphotericineb
- AMPHOTERICIN B SOLUBILIZED
- 33-((3-amino-3,6-dideoxy-beta-d-mannopyranosyl)oxy)-1,3,5,6,9,11,-xylicaci
- 33-[(3-amino-3,6-dideoxy-beta-d-mannopyranosyl)oxy]-1,3,5,6,9,11,17,37-octahydroxy-15,16,18-trimethyl-13-oxo-14,39-dioxabicyclo[33.3.1]nonatriaconta-19,21,23,25,27,29,31-heptaene-36-carboxylic acid
- AMPHOTERICIN B, SOLUBLE
- amphomoronal
- ,16r*,17r*,18s*,19e,21e,23e,25e-27e,29e,31e,33r*,35s*,36r*,37s*))-
- Voir plus de synonymes
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Amphotericin B, 250 μg/mL in distilled water, sterile-filtered
CAS :<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Amphotericin B, Streptomyces nodosus
CAS :<p>Amphotericin B, Streptomyces nodosus, 1397-89-3, is a polyene with antibiotic properties which alters cell membrane permeability, leading to lysis and cell death. Learn more.</p>Formule :C47H73NO17Masse moléculaire :924.09AMPHOTERICIN B FOR PEAK IDENTIFICATION CRS
CAS :AMPHOTERICIN B FOR PEAK IDENTIFICATION CRSFormule :C47H73NO17Masse moléculaire :924.079AMPHOTERICIN B FOR MICROBIOLOGICAL ASSAY CRS
CAS :AMPHOTERICIN B FOR MICROBIOLOGICAL ASSAY CRSFormule :C47H73NO17Masse moléculaire :924.079SECOND INTERNATIONAL STANDARD FOR AMPHOTERICIN B
CAS :SECOND INTERNATIONAL STANDARD FOR AMPHOTERICIN BFormule :C47H73NO17Masse moléculaire :924.079Amphotericin B
CAS :Antibiotics nesoiFormule :C47H73NO17Couleur et forme :Yellow Orange PowderMasse moléculaire :923.48785Amphotericin B
CAS :Amphotericin B (NSC-527017) is a polyene antifungal agent with broad-spectrum activity against many fungal species.Formule :C47H73NO17Degré de pureté :99.75% - ≥98%Couleur et forme :Deep Yellow Prisms Or Needles From N N-Dimethylformamide Physical Description Bright Yellow Powder (Ntp 1992)Masse moléculaire :924.08AmphotericinB
CAS :Formule :C47H73NO17Degré de pureté :95%Couleur et forme :SolidMasse moléculaire :924.0790Amphotericin B
CAS :Formule :C47H73NO17Degré de pureté :≥ 750μg/mg (C47H73NO17, dried basis)Couleur et forme :Yellow to dark yellow or orange powderMasse moléculaire :924.10Amphotericin B, Ph. Eur. grade
CAS :Formule :C47H73NO17Degré de pureté :≤ 2.0% (at 383nm)Couleur et forme :Yellow or orange powderMasse moléculaire :924.10Amphotericin B
CAS :Amphotericin BFormule :C47H73NO17Couleur et forme : yellow powderMasse moléculaire :924.07902g/molAmphotericin B
CAS :Formule :C47H73NO17Degré de pureté :>80.0%(HPLC)Couleur et forme :White to Light orange to Yellow powder to crystalMasse moléculaire :924.09Amphotericin B
CAS :Produit contrôléFormule :C47H73NO17Couleur et forme :NeatMasse moléculaire :924.08Amphotericin B (85%)
CAS :Formule :C47H73NO17Degré de pureté :85%Couleur et forme :YellowMasse moléculaire :924.08Amphotericin B - Bio-X ™
CAS :<p>Amphotericin B is a macrocycle antibiotic with very potent antifungal effects and resistance very rarely occurs. Amphotericin B is a polyene antifungal that binds to fungal cell membrane, i.e., ergosterol disrupts the membrane permeability leading to leakage of intracellular components. It is often used as an alternative therapy for leishmaniasis and to treat severe mycoses including: systemic Candida, Cryptococcus, blastomycosis, and histoplasmosis.</p>Formule :C47H73NO17Degré de pureté :Min. 75.0%Couleur et forme :PowderMasse moléculaire :924.08 g/molAmphotericin B, Antibiotic for Culture Media Use Only
CAS :Amphotericin B is a macrocycle antibiotic first isolated from Streptomyces nodosus. Its antifungal activity is exerted by interacting with the fungal membrane, mainly ergosterol, and inducing pore formation. The increase in membrane permeability causes loss of ions and cell death. The C-2 hydroxyl residue of the mycosamine carbohydrate moiety in the structure seems to have a major role in binding to ergosterol. It is used in cell culture to prevent growth of microbial contaminants, such as yeast and fungi. It is recommended by the WHO and CDC as an antifungal component for VTM at a concentration of 250ug/ml.Formule :C47H73NO17Degré de pureté :Min. 80.0 Area-%Masse moléculaire :924.08 g/mol












