CAS 64202-81-9
:(8R,9R,12R,13R,14R,16R)-19-amino-13-hydroxy-8,14-dimethoxy-4,10,12,16-tetramethyl-3,20,22-trioxo-2-azabicyclo[16.3.1]docosa-1(21),4,6,10,18-pentaen-9-yl carbamate
Description:
The chemical substance with the name "(8R,9R,12R,13R,14R,16R)-19-amino-13-hydroxy-8,14-dimethoxy-4,10,12,16-tetramethyl-3,20,22-trioxo-2-azabicyclo[16.3.1]docosa-1(21),4,6,10,18-pentaen-9-yl carbamate" and CAS number "64202-81-9" is a complex organic compound characterized by its intricate bicyclic structure and multiple functional groups. It features a unique arrangement of stereocenters, which contributes to its potential biological activity. The presence of amino, hydroxy, and methoxy groups suggests that it may exhibit polar characteristics, influencing its solubility and reactivity. The compound's trioxo and carbamate functionalities indicate potential for interactions with biological macromolecules, making it of interest in medicinal chemistry. Its specific stereochemistry and functional groups may also play a crucial role in its pharmacological properties, including enzyme inhibition or receptor binding. Overall, this compound represents a fascinating example of synthetic organic chemistry with potential applications in drug development or biochemical research.
Formula:C28H39N3O8
InChI:InChI=1/C28H39N3O8/c1-14-10-18-23(29)20(32)13-19(25(18)34)31-27(35)15(2)8-7-9-21(37-5)26(39-28(30)36)17(4)12-16(3)24(33)22(11-14)38-6/h7-9,12-14,16,21-22,24,26,33H,10-11,29H2,1-6H3,(H2,30,36)(H,31,35)/b9-7+,15-8-,17-12+/t14-,16-,21-,22-,24-,26-/m1/s1
Synonyms:- (10E)-19-amino-13-hydroxy-8,14-dimethoxy-4,10,12,16-tetramethyl-3,20,22-trioxo-2-azabicyclo[16.3.1]docosa-1(21),4,6,10,18-pentaen-9-yl carbamate
- Ipi-493
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Found 6 products.
IPI-493
CAS:<p>IPI-493 is a bioactive chemical.</p>Formula:C28H39N3O8Purity:>99.99%Color and Shape:SolidMolecular weight:545.6217-Amino Geldanamycin-13C,15N2
CAS:Controlled Product<p>Applications The labelled active metabolite of 17-(Allylamino)geldanamycin (17AAG).<br>References Kamal, A., et al.: Nature, 425, 407 (2003), Goetz, M., et al.: J. Clin. Oncol., 23, 1078 (2005), Bagatell, R., et al.: Clin. Cancer Res., 13, 1783 (2007), Burger, A., et al.: Cancer Lett., 245, 11 (2007),<br></p>Formula:CC27H3915N2NO8Color and Shape:NeatMolecular weight:548.60417-Amino Geldanamycin
CAS:Controlled Product<p>Applications The active metabolite of 17-(Allylamino)geldanamycin (17AAG).<br>References Kamal, A., et al.: Nature, 425, 407 (2003), Goetz, M., et al.: J. Clin. Oncol., 23, 1078 (2005), Bagatell, R., et al.: Clin. Cancer Res., 13, 1783 (2007), Burger, A., et al.: Cancer Lett., 245, 11 (2007),<br></p>Formula:C28H39N3O8Color and Shape:NeatMolecular weight:545.6217-Aminogeldanamycin
CAS:<p>Inhibits chaperone protein Hsp90; antineoplastic</p>Formula:C28H39N3O8Purity:Min. 95%Color and Shape:PowderMolecular weight:545.62 g/mol




