Phalloidine (>80%)

CAS: 17466-45-4

Ref. TR-P294523

Produktinformation

• Name: Phalloidine (>80%)
• Synonyme: Cyclo[L-alanyl-D-threonyl-L-cysteinyl-(4S)-4-hydroxy-L-prolyl-L-alanyl-2-mercapto-L-tryptophyl-(4R)-4,5-dihydroxy-L-leucyl] Cyclic (3?6)-thioether, 18,9-(Iminoethaniminoethaniminoethaniminomethano)-17H-pyrrolo[1',2':5,6][1,5,8,11]thiatriazacyclopentadecino[15,14-b]indole Cyclic Peptide Derivative, NSC 523214, Phalloidin, Amanita phalloides, Phalloidin, 29-(2,3-dihydroxy-2-methylpropyl)-2-hydroxy-23-(1-hydroxyethyl)-6,26-dimethyl-1,2,3,3a,5,6,8,9,10,15-decahydro-17H-18,9-(epiminoethanoiminoethanoiminoethanoiminomethano)pyrrolo[1',2':5,6][1,5,8,11]thiatriazacyclopentadecino[15,14-b]indole-4,7,19,22,25,28,31(18H)-heptone, (2S,3aS,6S,9S,18R,23R,26S,29S)-29-[(2R)-2,3-dihydroxy-2-methylpropyl]-2-hydroxy-23-[(1S)-1-hydroxyethyl]-6,26-dimethyl-1,2,3,3a,5,6,8,9,10,15-decahydro-17H-18,9-(epiminoethanoiminoethanoiminoethanoiminomethano)pyrrolo[1',2':5,6][1,5,8,11]thiatriazacyclopentadecino[15,14-b]indole-4,7,19,22,25,28,31(18H)-heptone
• CAS: 17466-45-4

Beschreibung

Applications Phalloidin is an F-actin stabilizing toxin and aids cytoskeletal deorganization in WPMY-1 cells. Phalloidin belongs to a class of toxins called phallotoxins, which are found in the death cap mushroom
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Wang, Y., et al.: Br. J. Pharmacol., 173, 3342-3358 (2016);

• Marke: TRC

Chemische Eigenschaften

• Molekulargewicht: 788.87
• Formel: C₃₅H₄₈N₈O₁₁S
• Reinheit: >80%
• Farbe/Form: Neat
• InChl: InChI=1S/C35H48N8O11S/c1-15-27(47)38-22-10-20-19-7-5-6-8-21(19)41-33(20)55-13-24(34(53)43-12-18(46)9-25(43)31(51)37-15)40-32(52)26(17(3)45)42-28(48)16(2)36-30(50)23(39-29(22)49)11-35(4,54)14-44/h5-8,15-18,22-26,41,44-46,54H,9-14H2,1-4H3,(H,36,50)(H,37,51)(H,38,47)(H,39,49)(H,40,52)(H,42,48)/t15-,16-,17-,18-,22-,23-,24?,25-,26+,35+/m0/s1
• InChI Key: InChIKey=KPKZJLCSROULON-QKGLWVMZSA-N
• SMILES: C[C@@H]1NC(=O)[C@H](C[C@@](C)(O)CO)NC(=O)[C@@H]2Cc3c([nH]c4ccccc34)SC[C@H](NC(=O)[C@@H]([C@H](C)O)NC1=O)C(=O)N1C[C@@H](O)C[C@H]1C(=O)N[C@@H](C)C(=O)N2