(Tetrahydropyran-4-yl)methyl+tosylate
Catalog Number:
(EM8.02304.0025)
Catalog Number:
(76002-126)
Supplier:
Enzo Life Sciences
Description:
Dnmt inhibitor
Supplier:
AMBEED, INC
Description:
4-[(Methylcarbamoyl)amino]benzeneboronic acid, pinacol ester 98%
Supplier:
AMBEED, INC
Description:
Madecassoside ≥98%
Supplier:
Thermo Scientific Chemicals
Description:
MDL: MFCD00148896
Notes: Transition interval: pH 5.2 (yellow-green) to pH 6.8 (purple)
Supplier:
Adipogen
Description:
Key constituent of St. John's wort. Shows properties of potential pharmacological interest, including antibacterial, anti-malarial, anti-inflammatory, anti-cancer and anti-angiogenic effects. Anti-depressant and anxiolytic compound. Specific activator of TRPC6 channels. Inhibits the re-uptake of neurotransmitters in synapses (serotonin, norepinephrine, dopamine, GABA, glutamate). Activator of the pregnane X receptor (PXR). Regulates expression of the cytochrome P450 CYP3A4 and CYP2C9 and hepatic drugs metabolism. Potential anti-Alzheimer compound. Potent SIRT1 (sirtuin 1) and SIRT2 (sirtuin 2) inhibitor.
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Supplier:
AAT BIOQUEST INC
Description:
Among the ratiometric calcium indicators, Fura-2 and Indo-1 are most commonly used.
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Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 042183-5G , MDL Number: MFCD06656460
Supplier:
Matrix Scientific
Description:
MF=C17H25N3O5S MW=383.47 CAS=96036-03-2 MDL=MFCD00864966 1G
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 041614-5G , MDL Number: MFCD00797872
Catalog Number:
(89151-486)
Supplier:
Enzo Life Sciences
Catalog Number:
(76483-472)
Supplier:
AAT BIOQUEST INC
Description:
It is a cell-permeable version of calcein blue.
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Supplier:
TCI America
Description:
CAS Number: 1006-94-6
MDL Number: MFCD00005674 Molecular Formula: C9H9NO Molecular Weight: 147.18 Purity/Analysis Method: >99.0% (GC) Form: Crystal Boiling point (°C): 178 Melting point (°C): 55 Storage Temperature: 0-10°C
Supplier:
Adipogen
Description:
JNJ-38158471 is a well tolerated, orally available, highly selective VEGFR-2 inhibitor with an IC(50) of 40nM. It also inhibits closely related tyrosine kinases such as Ret (IC(50) of 180nM) and Kit (C50 of 500nM). It has no significant activity (<gt/>1µM) against VEGFR-1 and VEGFR-3.
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