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Catalog: | HY-B0433A |
Brand: | MCE |
CAS: | 6119-47-7 |
MDL | MFCD00151248 |
---|---|
Molecular Weight | 396.91 |
Molecular Formula | C20H29ClN2O4 |
SMILES | COC1=CC2=C(N=CC=C2[C@H]([C@@]3([H])[N@](C[C@@H]4C=C)CC[C@@]4([H])C3)O)C=C1.Cl.O.O |
Quinine hydrochloride dihydrate (Qualaquin) is an orally active and can be used in anti-malarial studies. Quinine hydrochloride dihydrate is a potassium channel inhibitor that inhibits WT mouse Slo3 (K Ca 5.1) channel currents evoked by voltage pulses to +100 mV with an IC 50 of 169 μM [1] [2] .
Quinine hydrochloride dihydrate (150 μM, 30 min) inhibits the proliferation and cytostatic effects of DENV (Dengue virus) in human hepatocarcinoma HepG2 cell line
[1]
.
Quinine hydrochloride dihydrate (37.5-150 μM, 24 hours) significantly reduces viral DENV RNA and protein levels in a dose-dependent manner in human hepatocarcinoma HepG2 cell line
[1]
.
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Cell Proliferation Assay [1]
Cell Line: | Human hepatocarcinoma cell line(HepG2) |
Concentration: | 150 μM |
Incubation Time: | 30 min |
Result: | Inhibited DENV virus replication with 19% yield compared to untreated. Reduced DENV-positive cells from 23.28% to 12.05% in a dose-dependent manner. |
Quinine hydrochloride dihydrate (oral gavage, 12 or 15 mg/kg, every week, 16 weeks) has some tumor suppressing effect on skin cancer in Swiss albino mice
[2]
.
Quinine hydrochloride dihydrate (oral gavage, 10 mg/kg, everyday, 8 weeks) causes a decrease in the antioxidant defense system of rat testicular tissue such as SOD, CAT and GSH enzyme activity in male adult albino rats
[3]
.
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Animal Model: | Swiss albino mice 7-8-weeks (weighing 24 g) [2] |
Dosage: | Swiss albino mice 7-8-weeks (weighing 24 g) [2] |
Administration: | Oral gavage; every week; 16 weeks |
Result: | Resulted in a significant reduction in tumor size and weight at 12 mg/kg and little effect at higher dose of 15 mg/kg. |
NCT Number | Sponsor | Condition | Start Date | Phase |
---|---|---|---|---|
NCT02630472 | University of Pennsylvania |
Rhinitis|Sinusitis
|
October 2015 | Phase 1|Phase 2 |
NCT00785213 | Mutual Pharmaceutical Company, Inc.|Cetero Research, San Antonio |
Healthy
|
September 2008 | Phase 1 |
NCT00785551 | Mutual Pharmaceutical Company, Inc. |
Healthy|Renal Impairment
|
November 2007 | Phase 1 |
NCT00727272 | Mutual Pharmaceutical Company, Inc. |
Healthy
|
February 2004 | Phase 1 |
NCT00726895 | Mutual Pharmaceutical Company, Inc. |
Healthy
|
May 2004 | Phase 1 |
NCT00806078 | Mutual Pharmaceutical Company, Inc. |
Healthy
|
July 2007 | Phase 1 |
NCT00000706 | National Institute of Allergy and Infectious Diseases (NIAID) |
HIV Infections
|
Not Applicable | |
NCT00785486 | Mutual Pharmaceutical Company, Inc. |
Healthy
|
March 2007 | Phase 1 |
NCT00785980 | Mutual Pharmaceutical Company, Inc. |
Healthy
|
September 2008 | Phase 1 |
NCT00726414 | Mutual Pharmaceutical Company, Inc. |
Healthy
|
December 2005 | Phase 1 |
Solid
Room temperature in continental US; may vary elsewhere.
4°C, sealed storage, away from moisture
* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
DMSO : ≥ 100 mg/mL ( 251.95 mM )
H 2 O : 20 mg/mL ( 50.39 mM ; Need ultrasonic)
* "≥" means soluble, but saturation unknown.
Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
---|
1 mM | 2.5195 mL | 12.5973 mL | 25.1946 mL |
5 mM | 0.5039 mL | 2.5195 mL | 5.0389 mL |
10 mM | 0.2519 mL | 1.2597 mL | 2.5195 mL |
Add each solvent one by one: PBS
Solubility: 2.6 mg/mL (6.55 mM); Clear solution; Need ultrasonic and warming and heat to 60°C
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