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Merck
CN

SML4495

TTD, Cys-Interactome Capture Probe

≥98% (HPLC)

Synonym(s):

11-((Prop-2-yn-1-yloxy)methyl)-5,10-ethanothianthrene-5,10-diium tetrafluoroborate, TTD

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About This Item

Empirical Formula (Hill Notation):
C18H16OS2·B2F8
Molecular Weight:
486.06
UNSPSC Code:
12352200
Assay:
≥98% (HPLC)
Form:
powder
Storage condition:
desiccated
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Quality Segment

assay

≥98% (HPLC)

form

powder

storage condition

desiccated

color

white to beige

solubility

DMSO: 2 mg/mL, clear

storage temp.

-10 to -25°C

Biochem/physiol Actions

TTD (Thianthrenium Dication) is a cell-permeable, bench-stable precursor that redefines live-cell PPI mapping by generating the reactive alkenyl thianthrenium species in situ. TTD’s mechanism operates via a rapid, stepwise chemical cascade: immediate deprotonation (t1/2 ≈ 3 s) facilitates cysteine-selective Michael addition (86% intracellular site-selectivity), followed by intramolecular thianthrene displacement to yield a highly reactive episulfonium intermediate. This intermediate undergoes nucleophilic ring-opening by proximal amino acids to secure stable ethylene-linked inter- and intra-protein cross-links. A critical design innovation is the integration of a bioorthogonal alkyne handle that enables affinity enrichment of low-abundance targets without elongating the inter-residue bridge, thereby preserving precise short-distance restraints (4–23 Å) essential for high-resolution modeling. Fully compatible with live-cell protocols (1 hour labeling) and exhibiting no acute cytotoxicity, TTD enables high-fidelity structural characterization of complex interaction interfaces in their native environment, revealing previously unreported protein−protein interactions (PPIs).

Disclaimer

Hygroscopic, Store with desiccant


Pictograms

Exclamation mark

Signal Word

Warning

Hazard Codes

Precautionary Statements

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable



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