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Vitamin B12 test kit

ZSTK474

Cat. No.: OB0225LY-0462
Appearance: Solid
Purity: ≥99%
Identity: Confirmed by NMR and HPLC.
Size:
ZSTK474

Product Overview

Description: ZSTK474 is a novel oral small molecule inhibitor targeting the PI3K signaling pathway with antitumor activity that inhibits the proliferation and survival of tumor cells.
Synonym: 475110-96-4; ZSTK-474; 4,4'-(6-(2-(Difluoromethyl)-1H-benzo[d]imidazol-1-yl)-1,3,5-triazine-2,4-diyl)dimorpholine; 2-(2-Difluoromethylbenzimidazol-1-yl)-4,6-dimorpholino-1,3,5-triazine; 2-(2-Difluoromethylbenzimidazol-1-yl)-4,6-bis(morpholino)-1,3,5-triazine; 4,4''-(6-(2-(Difluoromethyl)-1H-benzo[d]imidazol-1-yl)-1,3,5-triazine-2,4-diyl)dimorpholine
CAS No.: 475110-96-4
Compound CID: 11647372
Formula: C19H21F2N7O2
Formula Weight: 417.41

Specification

Relative Density: 1.57 g/cm3
Stability: 3 years in powder form.
Storage: Storage at -20°C.
Applications: ZSTK474 can be used to study the role of the PI3K/AKT signaling pathway in cancer or to evaluate its anti-tumor potential during the development of new drugs.

Library Information

Targets: PI3K
Receptors: PI3Kα; PI3Kβ; PI3Kγ; PI3Kδ
Pathways: PI3K/Akt/mTOR signaling; Autophagy
Plate Number: AOCL-6
Plate Location: h9
Empty Location: a1-h1; a12-h12
Container: 96-well plate
Formulation: 10 mM DMSO
DMSO Max Solubility: 8.75 mg/mL; 20.96 mM
Water Max Solubility: <1 mg/mL (insoluble or slightly soluble)
Ethanol Max Solubility: <1 mg/mL (insoluble or slightly soluble)
ALogP: 3.366
HBA_Count: 6
HBD_Count: 0
Rotatable Bond: 4
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