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Chemical Structure| 6892-68-8 Chemical Structure| 6892-68-8
Chemical Structure| 6892-68-8

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DTE is a sulfur containing sugar derived from the corresponding 4-carbon monosaccharide erythrose and is an epimer of dithiothreitol (DTT).

Synonyms: Dithioerythritol; Cleland’s reagent

4.5 *For Research Use Only! Not for Human Use. We Do Not Sell to Patients.

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Product Citations

Product Citations

Kumpati, Greeshma P ; Ronayne, Conor T ; Johnson, Joseph L ; Gardner, Zachary S ; Singh, Anuj K ; Iyer, Ananth , et al.

Abstract: Glutathione transferase (GSTP1 and GSTM2) are tractable targets for anticancer drug development. In this work, a series of 6-(7-nitro-2,1,3-benzoxadiazol-4-ylthio)hexanol (NBDHEX) based analogues were designed, synthesized, and evaluated both theoretically and experimentally as GSTP1 and GSTM2 inhibitors. Among the synthesized compounds, 3h showed selective inhibition toward GSTP1 while 5b showed selective inhibition of GSTM2. Compounds 5b and 5c exhibited stronger potency while compound 3h showed slightly lower potency against the tested cancer cells than its parent molecule . Comprehensive biological studies were conducted on the effect of 3h, 5b and 5c towards breast cancer MDA-MB-231 and pancreatic MiaPaCa-2 cell lines revealed that 3h, 5b and 5c could activate pathway and induce cell . Furthermore in vivo experiments using NSG mice demonstrated that 5b significantly reduced tumor growth when administered in combination with , effectively overcoming resistance in the MiaPaCa-2 cell model through targeted inhibition of GSTM2. These findings suggests that, 5b could become a promising candidate for further development as a potential antitumor agent in cancer therapy.

Keywords: anticancer agents ; oxidative stress ; GSTP1 ; GSTM2 ; ; resistance

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Product Details of DTE

CAS No. :6892-68-8
Formula : C4H10O2S2
M.W : 154.25
SMILES Code : SC[C@H](O)[C@H](O)CS
Synonyms :
Dithioerythritol; Cleland’s reagent
English Name :trans-1,4-Dimercaptobutane-2,3-diol
MDL No. :MFCD00063750
InChI Key :VHJLVAABSRFDPM-ZXZARUISSA-N
Pubchem ID :439352

Safety of DTE

Application In Synthesis of DTE

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 6892-68-8 ]

[ 6892-68-8 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 6892-68-8 ]
  • [ 138-59-0 ]
  • [ 35661-39-3 ]
  • [ 14704-31-5 ]
  • (1R,2S,3S,4S,5R)-2-[4-(Biphenyl-3-ylmethylsulfanyl)-2,3-dihydroxy-butylsulfanyl]-3,4,5-trihydroxy-cyclohexanecarboxylic acid ((S)-1-carbamoyl-ethyl)-amide [ No CAS ]
  • 2
  • [ 6892-68-8 ]
  • [ 138-59-0 ]
  • [ 35661-39-3 ]
  • [ 42877-95-2 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
Multistep reaction;
  • 3
  • [ 6892-68-8 ]
  • [ 138-59-0 ]
  • [ 14704-31-5 ]
  • [ 71989-14-5 ]
  • (S)-3-({(1R,2S,3S,4S,5R)-2-[4-(Biphenyl-3-ylmethylsulfanyl)-2,3-dihydroxy-butylsulfanyl]-3,4,5-trihydroxy-cyclohexanecarbonyl}-amino)-succinamic acid [ No CAS ]
  • 4
  • [ 6892-68-8 ]
  • [ 138-59-0 ]
  • [ 14704-31-5 ]
  • [ 71989-18-9 ]
  • (S)-4-({(1R,2S,3S,4S,5R)-2-[4-(Biphenyl-3-ylmethylsulfanyl)-2,3-dihydroxy-butylsulfanyl]-3,4,5-trihydroxy-cyclohexanecarbonyl}-amino)-4-carbamoyl-butyric acid [ No CAS ]
  • 5
  • [ 6892-68-8 ]
  • [ 138-59-0 ]
  • [ 71989-14-5 ]
  • [ 42877-95-2 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
Multistep reaction;
  • 6
  • [ 6892-68-8 ]
  • [ 138-59-0 ]
  • [ 71989-18-9 ]
  • [ 42877-95-2 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
Multistep reaction;
 

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