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TSAT (Tris-(succinimidyl)aminotriacetate) ≥99% (by NMR), Sigma-Aldrich®

Catalog Number: (102599-126)
Supplier: Chem Impex International
Description: Crosslinking agent for compounds carrying an amino group
Image Unavailable-AA42348-KV

Tetrahydrofuran-[D₈] (100% D) (Isotopic) for NMR spectroscopy

Catalog Number: (AA42348-KV)
Supplier: Thermo Scientific Chemicals
Description: MDL: MFCD00044238

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Image Unavailable-102987-714

Diphenyliodonium hexafluorophosphate

Supplier: Adipogen
Description: Catalyst for the photochemical polymerization of various monomers.

Image Unavailable-80603-772

Tris(hydroxypropyl)phosphine ≥80% (by 31P-NMR), Calbiochem®, Millipore®

Catalog Number: (80603-772)
Supplier: MilliporeSigma
Description: THP, a water-soluble, neutral, and odorless disulfide reducing agent that is more stable and effective than DTT.

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Image Unavailable-AAA36470-14

Chloroform-[D₁] (99.8% D) (Isotopic) +1% v/v TMS for NMR spectroscopy

Supplier: Thermo Scientific Chemicals
Description: MDL: MFCD00000827

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Image Unavailable-AA42280-06

1,2-Dichlorobenzene-[D₄] (99% D) (Isotopic) for NMR spectroscopy

Catalog Number: (AA42280-06)
Supplier: Thermo Scientific Chemicals
Description: MDL: MFCD00037106

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Image Unavailable-AA42342-06

Pyridine-[D₅] (99.5% D) (Isotopic) + 0.05% v/v TMS for NMR spectroscopy

Supplier: Thermo Scientific Chemicals
Description: MDL: MFCD00044639 Beilstein Registry No.: 114377

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Image Unavailable-89150-880

DETA NONOate (NOC-18) ≥97% (by 1H-NMR)

Supplier: Enzo Life Sciences
Description: Nitric oxide (NO) donor.

Image Unavailable-102516-178

GW1929 ≥98% (by NMR)

Supplier: Adipogen
Description: Potent and subtype-selective (<gt/>1'000-fold) PPARgamma agonist. Angiogenesis inhibitor. Apoptosis inhibitor. Anti-inflammatory. Anti-hyperglycemic and anti-hyperlipidemic agent. Antidiabetic. The glucose-lowering effect in rats is 100-fold more potent than that of troglitazone.

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Image Unavailable-102515-948

MK-571 sodium salt ≥97% (by NMR)

Supplier: Adipogen
Description: Selective leukotriene LTD4 receptor antagonist. Potent MRP1 inhibitor. Antinociceptive.

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Image Unavailable-102516-224

Paprotrain ≥98% (by NMR)

Catalog Number: (102516-224)
Supplier: Adipogen
Description: Cell permeable and reversible kinesin-specific MKLP-2 (mitotic kinesin-like protein 2) inhibitor. Inhibits the recruitment of the chromosome passenger proteins survivin and aurora B to the central spindle during anaphase chromosome segregation. Moderate DYRK1A inhibitor (IC50= 5.5 µM). Lead compound.

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Image Unavailable-101322-296

Dimethyl sulfoxide-[D₆] (99.9% D) for NMR spectroscopy

Supplier: Cambridge Isotope Labs Inc
Description: Dimethyl sulfoxide-[D₆] (99.9% D) for NMR spectroscopy

Image Unavailable-102987-842

Ageladine A trifluoracetate ≥98% (by NMR)

Catalog Number: (102987-842)
Supplier: Adipogen
Description: Non-toxic, pH-sensitive fluorescent dye (blue-green range) for live imaging of pH alteration in acidic organelles, vesicles, cells, tissue and even small whole animals over several days without side effects. Stronger fluorescent intensity under acidic conditions and barely detectable in alkaline solutions (wide range from pH 4 to pH 8). Highly cell/membrane permeable. Trapped within the cells and acidic organelles through hydrophobic interactions with the inner side of the membranes. Barely metabolized and long-term stable, thus slow photobleaching. Angiogenesis inhibitor. Inhibitor of matrix metalloproteinases MMP-1,-2,-8,-9,-12,-13. TYK2, DYRK2,Dyrk1A, YSK4 and RPS6KA1/2 inhibitor.
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.

Product Image-89147-480

Purvalanol A ≥99% (by NMR)

Supplier: Enzo Life Sciences
Description: Inhibitor of human CDK1 (IC50=4nM), CDK2/cyclin A (IC50=70nM), Cdc2/cyclin B, CDK2/cyclin E (IC50=35nM), CDK4/cyclin D1 (IC50=850nM) as well as CDK5/p35 (IC50=75nM). More membrane permeable than purvalanol B.

Image Unavailable-AA42347-09

1,1,2,2-Tetrachloroethane-[D₂] (99.6% D) (Isotopic) for NMR spectroscopy

Supplier: Thermo Scientific Chemicals
Description: MDL: MFCD00037672

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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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