| Weight | 368.342 g/mol |
|---|---|
| Formula | C16H20N2O8 |
| Hydrogen Acceptors | 8 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 9 |
Disuccinimidyl suberate (68526-60-3, 68528-80-3)
DSIS · NHS-SA · N-hydroxysuccinimide suberic acid ester
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- In(III), Tl(III) and V(IV) tris-chelates of the heterocyclic dithiolene and diselenolene ligands 1,3-dithiole-2-thione-4,5-dithiolate (dmit), 1,2-dithiole-3-thione-4,5-dithiolate (dmt) and 1,3-diselenole-2-selone-4,5-diselenolate (dsis). Crystal and molecular structure of (Bu4N)2 [V(dmt)3] (Inorganica Chimica Acta, 1987)
- The dynamic stabilizing innersole system (DSIS): The management of hyperpronation in children (Journal of Foot & Ankle Surgery, 1995)
- Spectroscopic and electrical properties of [Cu4(dmit)3]2 and [Cu4(dsis)3]2 cluster anion complexes and their oxidized species (dmit=4,5-dimercapto-1,3-dithiole-2-thionate; dsis=4,5-di(hydroseleno)-1,3-diselenole-2-selonate) (Inorganica Chimica Acta, 1991)
- Disuccinimidyl suberate cross-linked ricin does not inhibit cell-free protein synthesis (Biochemical and Biophysical Research Communications, 1982)
- Effective Synthesis of 1,3-Diselenole-2-selone-4,5-diselenolate (dsis) and its Utilization for the Synthesis of Selenocycle-fused Tetraselenafulvalene (TSF) Derivatives (Synthesis, 2001)
- DSIS - a database system with interrelational semantics (Very Large Data Bases, 1981)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - DSIS
- NHS-SA
- N-hydroxysuccinimide suberic acid ester
- 1,1'-((1,8-dioxo-1,8-octanediyl)bis(oxy))bis-2,5-pyrrolidinedione
-
SMILESC1CC(=O)N(C1=O)OC(=O)CCCCCCC(=O)ON2C(=O)CCC2=O
-
InChIKeyZWIBGKZDAWNIFC-UHFFFAOYSA-N
- Pubchem - Disuccinimidyl suberate
- Wikipedia - Disuccinimidyl suberate
Disuccinimidyl suberate (DSS) is a biochemical tool used as protein cross-linking agent.
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Disuccinimidyl suberate
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