| Identification | Back Directory |  [Name]
  (9H-fluoren-9-yl)Methyl ((S)-1-(((S)-1-(((3R,4S,5S)-1-((S)-2-((1R,2R)-3-(((1S,2R)-1-hydroxy-1-phenylpropan-2-yl)aMino)-1-Methoxy-2-Methyl-3-oxopropyl)pyrrolidin-1-yl)-3-Methoxy-5-Methyl-1-oxoheptan-4-yl)(Methyl)aMino)-3-Methyl-1-oxobutan-2-yl)aMino)-3-Met |  [CAS]
  474645-26-6 |  [Synonyms]
  Fmoc-MMAE Fmoc-DL-N(Me)Val-DL-Val-Unk ((S)-1 - ((S)-1 - (((3R,4S,5S)-1 - ((S)-2 - ((1R,2 (9H-fluoren-9-yl)Methyl ((S)-1-(((S)-1-(((3R,4S,5S)-1-((S)-2-((1R,2R)-3-(((1S,2R)-1-hydroxy-1-phenylpropan-2-yl)aMino)-1-Methoxy-2-Methyl-3-oxopropyl)pyrrolidin-1-yl)-3-Methoxy-5-Methyl-1-oxoheptan-4-yl)(Methyl)aMino)-3-Methyl-1-oxobutan-2-yl)aMino)-3-Met L-Valinamide, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methyl-L-valyl-N-[(1S,2R)-4-[(2S)-2-[(1R,2R)-3-[[(1R,2S)-2-hydroxy-1-methyl-2-phenylethyl]amino]-1-methoxy-2-methyl-3-oxopropyl]-1-pyrrolidinyl]-2-methoxy-1-[(1S)-1-methylpropyl]-4-oxobutyl]-N-methyl- (9CI) (9H-fluoren-9-yl)methyl ((S)-1-(((S)-1-(((3R,4S,5S)-1-((S)-2-((1R,2R)-3-(((1S,2R)-1-hydroxy-1-phenylpropan-2-yl)amino)-1-methoxy-2-methyl-3-oxopropyl)pyrrolidin-1-yl)-3-methoxy-5-methyl-1-oxoheptan-4-yl)(methyl)amino)-3-methyl-1-oxobutan-2-yl)amino)-3-methyl-1-oxobutan-2-yl)(methyl)carbamate |  [Molecular Formula]
  C54H77N5O9 |  [MDL Number]
  MFCD28386986 |  [MOL File]
  474645-26-6.mol |  [Molecular Weight]
  940.22 |  
 | Chemical Properties | Back Directory |  [Boiling point ]
  1036.4±65.0 °C(Predicted) |  [density ]
  1.148±0.06 g/cm3(Predicted) |  [storage temp. ]
  4°C, stored under nitrogen   ,unstable in solution, ready to use. |  [solubility ]
  DMSO : ≥ 45 mg/mL (47.86 mM) |  [form ]
  Solid |  [pka]
  13.66±0.20(Predicted) |  [color ]
  White to off-white |  
 | Hazard Information | Back Directory |  [Uses]
  Fmoc-MMAE is a protective group-conjugated monomethyl auristatin E (MMAE), which is a potent tubulin inhibitor. Fmoc-MMAE can be used in the synthesis of ADC[1]. |  [IC 50]
  Auristatin |  [storage]
  4°C, stored under nitrogen   ,unstable in solution, ready to use. |  [References]
  [1] Pan D, et al. An antibody-drug conjugate targeting a GSTA glycosite-signature epitope of MUC1 expressed by non-small cell lung cancer. Cancer Med. 2020;9(24):9529-9540. DOI:10.1002/cam4.3554 |  
  
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