905579-51-3

  • Product Name:Pevonedistat
  • Molecular Formula:C21H25N5O4S
  • Molecular Weight:443.527
  • Appearance:White Solid
Inquiry

Product Details

pd_meltingpoint:161-163 °C

Appearance:White Solid

Purity:99%

Pevonedistat 905579-51-3 In Stock

  • Molecular Formula:C21H25N5O4S
  • Molecular Weight:443.527
  • Appearance/Colour:White Solid 
  • Melting Point:161-163 °C 
  • Boiling Point:721.0±70.0 °C at 760 mmHg 
  • PKA:9.35±0.70(Predicted) 
  • Flash Point:389.9±35.7 °C 
  • PSA:140.74000 
  • Density:1.6±0.1 g/cm3 
  • LogP:3.91690 

Sulfamic acid [(1S,2S,4R)-4-[4-[[(1S)-2,3-dihydro-1H-inden-1-yl]amino]-7H-pyrrolo[2,3-d]pyrimidin-7-yl]-2-hydroxycyclopentyl]methyl ester(Cas 905579-51-3) Usage

Description

MLN4924 (905579-51-3) is a potent and selective NEDD8-activating enzyme (NAE) inhibitor.1?It disrupts cullin-RING ligase-mediated protein turnover leading to apoptosis in human tumor cells. Suppresses the growth of human tumor xenografts in mice.2?Upregulates PD-L1 expression and enhances the efficacy of immune checkpoint blockade in glioblastoma.3?Modulates tumor microenvironment.4?Cell permeable.

Chemical Properties

White Solid

Uses

A potent and selective inhibitor of NAE.

Enzyme inhibitor

This first-in-class small molecule inhibitor (FW = 443.52 g/mol; CAS 905579-51-3; Solubility = 10 mg/mL DMSO), also named MLN4924 and [(1S,2S,4R)-4-[4-[[(1S)-2,3-dihydro-1H-inden-1-yl]amino]-7H-pyrrolo[2,3- d]pyrimidin-7-yl]-2-hydroxycyclopentyl]sulfamate methyl ester, targets Nedd8 activating enzyme, or NAE (IC50 = 4.7 nM), with much weaker action against UAE (IC50 = 1.5 μM), SAE (IC50 = 8.2 μM), and UBA6 (IC50 = 1.8 μM). In most cancer cells, pevonedistat treatment results in the induction of DNA re-replication, resulting in DNA damage and cell death. MLN4924 also exhibits an alternative mechanism of action. Treatment of activated B cell-like (ABC) diffuse large B-cell lymphoma (DLBCL) cells with pevonedistat resulted in rapid accumulation of pIkBa, decrease in nuclear p65 content, reduction of transcriptional activity of NF-kB (or nuclear factor k-light-chain-enhancer of activated B cells), and G1 arrest, ultimately resulting in apoptosis induction, events consistent with potent NF-kB pathway inhibition. Treatment of germinal-center B cell-like (GCB) DLBCL cells resulted in an increase in cellular Cdt-1 and accumulation of cells in S-phase, consistent with cells undergoing DNA rereplication. Pevonedistat also inhibits Vpx/Vpr-induced SAMHD1 degradation by inhibiting the neddylation of E3 ubiquitin-ligase and blocking SIVmac replication in myeloid cells, therebyindicating the potential efficacy of inhibiting neddylation as an antiretroviral strategy

References

1) Soucy, et al. (2009), An inhibitor of NEDD8-activating enzyme as a new approach to treat cancer. Nature 458 732 2) Milhollen, et al. (2010) MLN4924, a NEDD8-activating enzyme inhibitor, is active in diffuse large B-cell lymphoma models: rationale for treatment of NF-(kappa)B-dependent lymphoma. Blood, 116 1515 3) Zhou et al. (2019) Neddylation inhibition upregulates PD-L1 expression and enhances the efficacy of immune checkpoint blockade in glioblastoma; Int. J. Cancer, 145 763 4) Zhou et al. (2019) Neddylation: a novel modulator of the tumor microenvironment; Mol. Cancer 18 77

 

905579-51-3 Relevant articles

Preparation of Sulfamates and Sulfamides Using a Selective Sulfamoylation Agent

Wang, Hai-Ming,Xiong, Chao-Dong,Chen, Xiao-Qu,Hu, Chun,Wang, Dong-Yu

supporting information, p. 2595 - 2599 (2021/05/05)

Sulfamates and sulfamides are prevalent ...

Catalytic Sulfamoylation of Alcohols with Activated Aryl Sulfamates

Rapp, Peter B.,Murai, Koichi,Ichiishi, Naoko,Leahy, David K.,Miller, Scott J.

supporting information, p. 168 - 174 (2019/12/30)

We report a new catalytic method for alc...

Process Development and GMP Production of a Potent NAE Inhibitor Pevonedistat

Armitage, Ian,Elliott, Eric L.,Hicks, Frederick,Langston, Marianne,McCarron, Ashley,McCubbin, Quentin J.,Obrien, Erin,Stirling, Matt,Zhu, Lei

, p. 1299 - 1307 (2015/09/28)

A practical synthesis of a novel NEDD8-a...

PREPARATION METHOD OF MLN4924 AS AN E1 ACTIVATING INHIBITOR

-

, (2013/02/28)

The present invention relates to a metho...

905579-51-3 Process route

tert-butyl {[((1S,2S,4R)-4-{4-[(1R)-2,3-dihydro-1H-inden-1-ylamino]-7H-pyrrolo[2,3-d]pyrimidin-7-yl}-2-hydroxycyclopentyl)methoxy]sulfonyl}carbamate
945950-17-4

tert-butyl {[((1S,2S,4R)-4-{4-[(1R)-2,3-dihydro-1H-inden-1-ylamino]-7H-pyrrolo[2,3-d]pyrimidin-7-yl}-2-hydroxycyclopentyl)methoxy]sulfonyl}carbamate

MLN4924
905579-51-3

MLN4924

Conditions
Conditions Yield
tert-butyl {[((1S,2S,4R)-4-{4-[(1R)-2,3-dihydro-1H-inden-1-ylamino]-7H-pyrrolo[2,3-d]pyrimidin-7-yl}-2-hydroxycyclopentyl)methoxy]sulfonyl}carbamate; With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 0.25h;
With sodium hydrogencarbonate; In methanol; for 0.166667h;
58%
(1S,2S,4R)-2-{[(Aminosulfonyl)oxy]methyl}-4-{4-[(1S)-2,3-dihydro-1H-inden-1-ylamino]-7H-pyrrolo[2,3-d]pyrimidin-7-yl}cyclopentyl acetate

(1S,2S,4R)-2-{[(Aminosulfonyl)oxy]methyl}-4-{4-[(1S)-2,3-dihydro-1H-inden-1-ylamino]-7H-pyrrolo[2,3-d]pyrimidin-7-yl}cyclopentyl acetate

((1S,2S,4R)-4-(4-(((S)-2,3-dihydro-1H-inden-1-yl)amino)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-2-hydroxycyclopentyl)-methyl sulfamate
905579-51-3

((1S,2S,4R)-4-(4-(((S)-2,3-dihydro-1H-inden-1-yl)amino)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-2-hydroxycyclopentyl)-methyl sulfamate

Conditions
Conditions Yield
With methanol; ammonia; at 20 ℃; for 120h;
90%

905579-51-3 Upstream products

  • 1189-71-5
    1189-71-5

    isocyanate de chlorosulfonyle

  • 905580-90-7
    905580-90-7

    (1S,2S,4R)-4-{4-[(1S)-2,3-dihydro-1H-inden-1-ylamino]-7H-pyrrolo[2,3-d]pyrimidin-7-yl}-2-(hydroxymethyl)-cyclopentanol

  • 1281922-74-4
    1281922-74-4

    6-(tert-butyldiphenylsilanyloxymethyl)-2,2-dimethyltetrahydrocyclopenta[1,3]dioxol-4-one

  • 1281922-76-6
    1281922-76-6

    6-(tert-butyldiphenylsilanyloxymethyl)-2,2-dimethyltetrahydrocyclopenta[1,3]dioxol-4-ol