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Vitamin B12 test kit

CYC-116

Cat. No.: 0225LY-0658
Appearance: Solid
Purity: ≥97%
Identity: Confirmed by NMR, and HPLC.
Size:
CYC-116
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Product Overview

Description: CYC116 is a potent Aurora A and B inhibitor (Ki: 8.0/9.2 nM) in Phase 1 trials that also targets VEGFR2 (Ki: 44 nM), while showing no activity against PKA, Akt, PKC, or Plk1 and demonstrating 50-fold higher potency over CDKs.
Synonym: 693228-63-6; 4-methyl-5-(2-(4-morpholinophenylamino)pyrimidin-4-yl)thiazol-2-amine; 4-methyl-5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]-1,3-thiazol-2-amine; 4-methyl-5-(2-((4-morpholinophenyl)amino)pyrimidin-4-yl)thiazol-2-amine; 2-Pyrimidinamine,4-(2-amino-4-methyl-5-thiazolyl)-N-[4-(4-morpholinyl)phenyl]-; 4-(2-amino-4-methyl-1,3-thiazol-5-yl)-N-[4-(morpholin-4-yl)phenyl]pyrimidin-2-amine
CAS No.: 693228-63-6
Compound CID: 6420138
Formula: C18H20N6OS
Formula Weight: 368.46

Specification

Targets&IC50: Aurora A: 8 nM(Ki); Aurora B: 9.2 nM(Ki)
Relative Density: 1.355 g/cm3
Stability: 3 years in powder form.
Storage: Storage at -20°C.
Applications: CYC-116 can be used in kinase research to evaluate the dual inhibition of Aurora kinases and VEGFR.

Library Information

Target: FLT; VEGFR; Aurora kinase; CDK; S6 Kinase
Receptor: Aurora A; Aurora B; CDK2/CyclinE; CDK9/CyclinT; FLT3; p70 S6K; VEGFR2
Pathways: Chromatin/Epigenetic; Cell cycle/Checkpoint; PI3K/Akt/mTOR signaling; Angiogenesis; MAPK; Tyrosine kinase/adaptors
Plate Number: AOCL-9
Plate Location: e4
Empty Location: a1-h1; a12-h12
Container: 96-well plate
Formulation: 10mM DMSO
DMSO Max Solubility: 13.4 mg/mL; 36.37 mM
Water Max Solubility: <1 mg/mL (insoluble or slightly soluble)
Ethanol Max Solubility: <1 mg/mL (insoluble or slightly soluble)
ALogP: 2.743
HBA_Count: 4
HBD_Count: 2
Rotatable Bond: 4
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