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Medchemexpress LLC Bay 61-3606 dihydrochloride | 648903-57-5 | MFCD08276916 | 99.5% | 463.32 g·mol^-1 | C20H20Cl2N6O3 | 10 MG
SDP

Catalog No. 5000286672
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BAY 61-3606 dihydrochloride is a potent, ATP-competitive, reversible, and highly selective inhibitor of spleen tyrosine kinase (Syk), provided as the dihydrochloride salt for research use. It is intended for biochemical and cell-based studies of kinase signaling and apoptosis, and has reported biochemical potency (Ki = 7.5 nM; IC50 ≈ 10 nM) and high purity for reliable experimental results.

  • High biochemical potency (Ki = 7.5 nM; IC50 ≈ 10 nM).
  • High reported purity (≈99.5%).
  • Provided as dihydrochloride salt suitable for cell-based assays.
  • Characterized by COA, HNMR, and LC-MS documentation.
  • Useful for studying Syk-dependent signaling and apoptosis.

Catalog No. 50-002-86672 Supplier Medchemexpress LLC Supplier No. HY1498510MG
May include imposed supplier surcharges.
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BAY 61-3606 dihydrochloride is a potent, ATP-competitive, reversible, and highly selective inhibitor of spleen tyrosine kinase (Syk), provided as the dihydrochloride salt for research use. It is intended for biochemical and cell-based studies of kinase signaling and apoptosis, and has reported biochemical potency (Ki = 7.5 nM; IC50 ≈ 10 nM) and high purity for reliable experimental results.

  • High biochemical potency (Ki = 7.5 nM; IC50 ≈ 10 nM).
  • High reported purity (≈99.5%).
  • Provided as dihydrochloride salt suitable for cell-based assays.
  • Characterized by COA, HNMR, and LC-MS documentation.
  • Useful for studying Syk-dependent signaling and apoptosis.

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