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CAS 137734-07-7

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methyl (2S)-2-({[(2S,3S,4S,5R,6R)-6-{[(2S,3R,4S,5S,6S)-6-{[(1S)-1-benzyl-2-methoxy-2-oxoethyl]carbamoyl}-2-{[(3S,4aR,6aR,6bS,8aS,11S,12aR,14aR,14bS)-11-{[(1S)-1-benzyl-2-methoxy-2-oxoethyl]carbamoyl}-4,4,6a,6b,8a,11,14b-heptamethyl-14-oxo-1,2,3,4,4a,5,6,6

Description:
The chemical substance known as methyl (2S)-2-({[(2S,3S,4S,5R,6R)-6-{[(2S,3R,4S,5S,6S)-6-{[(1S)-1-benzyl-2-methoxy-2-oxoethyl]carbamoyl}-2-{[(3S,4aR,6aR,6bS,8aS,11S,12aR,14aR,14bS)-11-{[(1S)-1-benzyl-2-methoxy-2-oxoethyl]carbamoyl}-4,4,6a,6b,8a,11,14b-heptamethyl-14-oxo-1,2,3,4,4a,5,6,6... (CAS 137734-07-7) is a complex organic compound characterized by its intricate stereochemistry and multiple functional groups. It features a methyl group, various chiral centers, and multiple benzyl and methoxy substituents, indicating potential biological activity. The presence of carbamoyl groups suggests it may participate in hydrogen bonding, influencing its solubility and reactivity. This compound is likely to exhibit significant pharmacological properties, given its structural complexity, which may include interactions with biological targets. Its synthesis and characterization would require advanced techniques in organic chemistry, particularly in stereochemical analysis, to ensure the correct configuration of its numerous chiral centers. Overall, this substance exemplifies the intricate nature of organic molecules and their potential applications in medicinal chemistry.
Formula:C72H95N3O19
InChI:InChI=1/C72H95N3O19/c1-67(2)48-26-29-72(7)58(47(76)37-42-43-38-69(4,31-30-68(43,3)32-33-71(42,72)6)66(87)75-46(63(86)90-10)36-41-24-18-13-19-25-41)70(48,5)28-27-49(67)91-65-57(53(80)52(79)56(93-65)60(83)74-45(62(85)89-9)35-40-22-16-12-17-23-40)94-64-54(81)50(77)51(78)55(92-64)59(82)73-44(61(84)88-8)34-39-20-14-11-15-21-39/h11-25,37,43-46,48-58,64-65,77-81H,26-36,38H2,1-10H3,(H,73,82)(H,74,83)(H,75,87)/t43-,44-,45-,46-,48-,49-,50-,51-,52-,53-,54+,55-,56-,57+,58+,64-,65-,68+,69-,70-,71+,72+/m0/s1
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