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D3514

Sigma-Aldrich

4,4′-Diisothiocyanatostilben-2,2′-Disulfonsäure Dinatriumsalz Hydrat

≥80% (elemental analysis), powder

Synonym(e):

DIDS, Dinatrium-4,4′-diisothiocyanatostilben-2,2′-disulfonat

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About This Item

Empirische Formel (Hill-System):
C16H8N2Na2O6S4 · xH2O
CAS-Nummer:
Molekulargewicht:
498.48 (anhydrous basis)
Beilstein:
8179433
MDL-Nummer:
UNSPSC-Code:
12352200
PubChem Substanz-ID:
NACRES:
NA.25

Qualität

for analytical purposes

Assay

≥80% (elemental analysis)

Form

powder

Eignung der Reaktion

reagent type: cross-linking reagent

Farbe

yellow

Löslichkeit

0.1 M potassium bicarbonate: 50 mg/mL

Lagertemp.

2-8°C

SMILES String

[Na+].[Na+].[O-]S(=O)(=O)c1cc(ccc1\C=C\c2ccc(cc2S([O-])(=O)=O)N=C=S)N=C=S

InChI

1S/C16H10N2O6S4.2Na/c19-27(20,21)15-7-13(17-9-25)5-3-11(15)1-2-12-4-6-14(18-10-26)8-16(12)28(22,23)24;;/h1-8H,(H,19,20,21)(H,22,23,24);;/q;2*+1/p-2/b2-1+;;

InChIKey

GEPAYBXVXXBSKP-SEPHDYHBSA-L

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Anwendung

A negatively charged homobifunctional cross-linking reagent. The isothiocyanate groups react with primary amines at pH 9.0-10.0.
4,4′-Diisothiocyanatostilbene-2,2′-disulfonic acid disodium salt hydrate has been used:
  • as band3 protein inhibitor in rabbits(19)
  • for the inhibition of bicarbonate transporters in brain slice tissue(20)
  • as HCO3-/Cl- exchanger (anion exchanger) in embryos(21)

Biochem./physiol. Wirkung

A specific inhibitor of cellular anion permeability used in cell transport studies.
4,4′-Diisothiocyanatostilbene-2,2′-disulfonic acid is an anionic alkylating agent containing isothiocyanate residue. It is a negatively charged homobifunctional cross-linking reagent. 4,4′-Diisothiocyanatostilbene-2,2′-disulfonic acid is a specific inhibitor of cellular anion permeability used in cell transport studies. The isothiocyanate groups react with primary amines at pH 9.0-10.0. 4,4′-Diisothiocyanatostilbene-2,2′-disulfonic acid alkylates lysine residues and inhibits apoptosis indirectly by targeting membrane based anion transporters.In addition, it also inhibits calcium transport in vesicles.

Piktogramme

Health hazardExclamation mark

Signalwort

Danger

Gefahreneinstufungen

Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Die Dokumentenbibliothek aufrufen

DIDS (4, 4'-Diisothiocyanatostilbene-2, 2'-disulfonate) directly inhibits caspase activity in HeLa cell lysates
Benitez-Rangel E, et al.
Cell death discovery, 1, 15037-15037 (2015)
Narongrit Thongon et al.
Pflugers Archiv : European journal of physiology, 468(11-12), 1809-1821 (2016-11-21)
Hypomagnesemia is the most concerned side effect of proton pump inhibitors (PPIs) in chronic users. However, the mechanism of PPIs-induced systemic Mg2+ deficit is currently unclear. The present study aimed to elucidate the direct effect of short-term and long-term PPIs
Michael Kittl et al.
International journal of molecular sciences, 20(14) (2019-07-18)
Many cell types express an acid-sensitive outwardly rectifying (ASOR) anion current of an unknown function. We characterized such a current in BV-2 microglial cells and then studied its interrelation with the volume-sensitive outwardly rectifying (VSOR) Cl- current and the effect
Akihiro Kamikawa et al.
American journal of physiology. Cell physiology, 311(5), C808-C819 (2016-08-26)
The Cl- secretion via Ca2+-activated Cl- channel (CaCC) is critical for fluid secretion in exocrine glands like the salivary gland. Also in the mammary gland, it has been hypothesized that CaCC plays an important role in the secretion of Cl-
Nuclease activity of the MutS homologue MutS2 from Thermus thermophilus is confined to the Smr domain
Fukui K, et al.
Nucleic Acids Research, 35(3), 850-860 (2007)

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