[2-(4-chlorophenyl)quinolin-4-yl]-(2-piperidyl)methanol

[2-(4-chlorophenyl)quinolin-4-yl]-(2-piperidyl)methanol Structure
CAS No.
5428-80-8
Chemical Name:
[2-(4-chlorophenyl)quinolin-4-yl]-(2-piperidyl)methanol
Synonyms
Vacquinol-1;CS-2185;NSC13316;NSC-13316;NSC 13316;Vacquinol-1(NSC13316);NSC 13316;NSC13316;NSC-13316;VACQUINOL 1;VACQUINOL1;4-Quinolinemethanol,2-(4-chlorophenyl)-a-2-piperidinyl-;[2-(4-chlorophenyl)quinolin-4-yl]-(2-piperidyl)methanol;4-Quinolinemethanol, 2-(4-chlorophenyl)-α-2-piperidinyl-
CBNumber:
CB51254607
Molecular Formula:
C21H21ClN2O
Molecular Weight:
352.86
MOL File:
5428-80-8.mol
Modify Date:
2023/6/8 9:02:17

[2-(4-chlorophenyl)quinolin-4-yl]-(2-piperidyl)methanol Properties

Melting point 198-199.5 °C
Boiling point 551.4±50.0 °C(Predicted)
Density 1.244±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMF: 10 mg/ml; DMF:PBS(pH 7.2)(1:1): 0.5 mg/ml; DMSO: 1 mg/ml; Ethanol: 0.25 mg/ml
form A crystalline solid
pka 13.22±0.20(Predicted)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H317-H319
Precautionary statements  P280-P305+P351+P338
HS Code  2933499090
NFPA 704
0
2 0

[2-(4-chlorophenyl)quinolin-4-yl]-(2-piperidyl)methanol Chemical Properties,Uses,Production

Description

Vacquinols are a new class of quinine-derivatives that stimulate death in glioblastoma cells by massive macropinocytotic vacuolization, ATP depletion, and cytoplasmic membrane rupture. A key effector of vacquinols is MAPK kinase 4 (MKK4). Vacquinol-1 is an activator of MKK4-dependent macropinocytotic cell death in glioblastoma cells. It induces ATP depletion in glioblastoma cells (IC50 = 3.14 μM at 1 day) without affecting fibroblasts, embryonic stem cells, or osteosarcoma cells. Vacquinol-1 is orally bioavailable with good brain penetrance and excellent pharmacokinetics. Oral administration of vacquinol-1 (20 mg/kg once daily for five days) substantially impairs the growth of engrafted glioblastoma cell tumors in mice and prolongs survival.

Uses

Vacquinol-1 is in the vacquinol class of quinine derivatives that stimulate death in glioblastoma cells through massive macropinocytotic vacuolization, ATP depletion and eventual cytoplasmic membrane rupture.

[2-(4-chlorophenyl)quinolin-4-yl]-(2-piperidyl)methanol Preparation Products And Raw materials

Raw materials

Preparation Products

5428-80-8([2-(4-chlorophenyl)quinolin-4-yl]-(2-piperidyl)methanol)Related Search:

[2-(4-chlorophenyl)quinolin-4-yl]-(2-piperidyl)methanol 4-Quinolinemethanol,2-(4-chlorophenyl)-a-2-piperidinyl- NSC 13316 NSC 13316;NSC13316;NSC-13316;VACQUINOL 1;VACQUINOL1 NSC13316 NSC-13316 CS-2185 4-Quinolinemethanol, 2-(4-chlorophenyl)-α-2-piperidinyl- Vacquinol-1 Vacquinol-1(NSC13316) 5428-80-8 C21H23Cl3N2O building block