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You Searched For: (2'Z,3'E)-6-Bromoindirubin-3'-oxime


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(2'Z,3'E)-6-Bromoindirubin-3'-oxime ≥98%

Supplier: Enzo Life Sciences
Description: Inibitor of phosphoinositide-dependent kinase 1 and GSK

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(2'Z,3'E)-6-Bromoindirubin-3'-oxime ≥95.0% (by HPLC)

Supplier: TCI America
Description: CAS Number: 667463-62-9 MDL Number: MFCD08705318 Molecular Formula: C16H10BrN3O2 Molecular Weight: 356.18 Purity/Analysis Method: <gt/>95.0% (HPLC) Form: Crystal Melting point (°C): 300 Storage Temperature: 0-10°C

SDS Certificates

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(2'Z,3'E)-6-Bromoindirubin-3'-oxime 97%

Supplier: Thermo Scientific Chemicals
Description: 6-Bromoindirubin-3'-oxime, 97%. Solid.

SDS Certificates

Image Unavailable-77157-076

(2'Z,3'E)-6-Bromoindirubin-3'-oxime 98%

Supplier: AMBEED, INC
Description: (2Z,3E)-6'-Bromo-3-(hydroxyimino)-[2,3'-biindolinylidene]-2'-one, Purity: 98%, CAS Number: 667463-62-9, Appearance: Form: Crystal - Powder/Colour: Yellow red - Deep yellow red - Deep red, Storage: Keep in dark place, Inert atmosphere, 2-8 C, Size: 10mg

Image Unavailable-102516-098

(2'Z,3'E)-6-Bromoindirubin-3'-oxime ≥98% (by NMR)

Supplier: Adipogen
Description: Phosphoinositide-dependent kinase 1 (PDK1) inhibitor. Potent, reversible and ATP-competitive glycogen synthase kinase-3alpha/beta (GSK-3alpha/beta) inhibitor. JAK/STAT3 signaling inhibitor. Apoptosis inducer. Potent antiproliferative agent in malignant lymphoid cell. Antimetastatic agent. Potent chemosensitizing agent fighting TRAIL resistant cancer cells.

Small Business Enterprise

Image Unavailable-102988-838

(2'Z,3'E)-6-Bromoindirubin-3'-oxime ≥99% (by NMR)

Supplier: Adipogen
Description: Potent, reversible and ATP-competitive glycogen synthase kinase-3alpha/beta (GSK-3alpha/beta) inhibitor. JAK/STAT3 signaling inhibitor. Phosphoinositide-dependent kinase 1 (PDK1) inhibitor. Anticancer compound. Potent antiproliferative agent. Suppresses metastasis. Apoptosis inducer. Sustains pluripotency and self-renewal of human and mouse embryonic stem cells (ESCs) by activation of the Wnt signaling pathway. Anti-leishmanial (IC50 = 0.150µM). Proto-oncogene tyrosine-protein kinase receptor RET inhibitor (IC50=0.51µM). Inhibits HIV-1 transcription and protects against Tat induced neurotoxicity.

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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
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