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Chemical Structure| 2179-57-9 Chemical Structure| 2179-57-9
Chemical Structure| 2179-57-9

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Diallyl disulfide is an active compound in garlic oil that inhibits human squalene monooxygenase, with an IC50 of 400 μM for squalene epoxidation. It exhibits significant anti-inflammatory, antioxidant, antidepressant, and anti-tumor activities. It can inhibit human squalene monooxygenase and exhibits anti-tumor activity, which is enhanced when combined with miR-200b and miR-22.

Synonyms: DADS; NSC 29228; Garlicin

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

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Product Details of Diallyl disulfide

CAS No. :2179-57-9
Formula : C6H10S2
M.W : 146.27
SMILES Code : C=CCSSCC=C
Synonyms :
DADS; NSC 29228; Garlicin
English Name :Diallyldisulfide
MDL No. :MFCD00008656
InChI Key :PFRGXCVKLLPLIP-UHFFFAOYSA-N
Pubchem ID :16590

Safety of Diallyl disulfide

Application In Synthesis of Diallyl disulfide

* 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 [ 2179-57-9 ]

[ 2179-57-9 ] Synthesis Path-Downstream   1~8

  • 1
  • [ 2179-57-9 ]
  • [ 62488-53-3 ]
  • [ 592-88-1 ]
  • [ 2050-87-5 ]
  • [ 2444-49-7 ]
YieldReaction ConditionsOperation in experiment
1: 9.7 % Chromat. 2: 3 % Chromat. 3: 0.47 % Chromat. 4: 0.7 % Chromat. at 50℃; for 168h; Further byproducts given;
  • 2
  • [ 539-86-6 ]
  • [ 62488-53-3 ]
  • [ 2179-57-9 ]
  • [ 2050-87-5 ]
  • [ 80028-57-5 ]
YieldReaction ConditionsOperation in experiment
1: 0.03 g 2: 0.01 g 3: 0.015 g 4: 0.008 g In chloroform-d1 at 25℃; for 144h;
  • 3
  • [ 539-86-6 ]
  • [ 62488-53-3 ]
  • [ 2179-57-9 ]
  • [ 2050-87-5 ]
  • [ 80028-57-5 ]
  • [ 92285-00-2 ]
  • [ 92284-99-6 ]
YieldReaction ConditionsOperation in experiment
at 37℃; for 48h; other temperatures, other times;
  • 4
  • [ 267219-51-2 ]
  • [ 2179-57-9 ]
  • [ 869113-67-7 ]
YieldReaction ConditionsOperation in experiment
46% With triethylamine at 60℃; for 8h;
  • 5
  • [ 110-81-6 ]
  • [ 150-60-7 ]
  • [ 2179-57-9 ]
  • [ 624-92-0 ]
  • [ 629-19-6 ]
  • [ 20333-39-5 ]
  • [ 2179-60-4 ]
  • [ 30453-31-7 ]
  • [ 2179-59-1 ]
  • [ 72437-63-9 ]
  • [ 21230-16-0 ]
  • [ 27657-11-0 ]
  • [ 2179-58-0 ]
  • [ 699-10-5 ]
  • [ 68794-86-5 ]
YieldReaction ConditionsOperation in experiment
With tricyclohexylphosphine In dimethyl sulfoxide at 20℃;
  • 6
  • [ 2179-57-9 ]
  • [ 629-19-6 ]
  • [ 2179-59-1 ]
YieldReaction ConditionsOperation in experiment
With copper dichloride In acetonitrile at 25℃;
  • 7
  • [ 877399-50-3 ]
  • [ 2179-57-9 ]
  • C16H25N3O2S [ No CAS ]
  • 8
  • [ 2179-57-9 ]
  • [ 20362-54-3 ]
  • [ 2833773-00-3 ]
YieldReaction ConditionsOperation in experiment
With hexaethylphosphoric triamide In acetonitrile at 20℃; for 3h;
 

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