MDL | MFCD00149764 |
---|---|
Molecular Weight | 42.39 (anhydrous basis) |
Molecular Formula | LiCl·xH2O |
SMILES | [Li]Cl.O |
Lithium chloride hydrate, an orally active mood stabilizer, is a potent virus inhibitor and effective immunomodulatory agent. Lithium chloride hydrate has antidepressant activity by inhibiting GSK3β and promoting neurogenesis. Lithium chloride hydrate alleviates cognition dysfunction and the symptoms of acute mania and depression. Lithium chloride hydrate can also be used for research of virus infection and Alzheimer's disease [1] [2] [3] .
GSK-3β |
Lithium chloride hydrate (5 and 20 mM, 36 h) inhibits cytopathy and IBV replication in IBV Beaudette-infected BHK cells
[1]
.
Lithium chloride hydrate (5 and 20 mM, 36 h) inhibits IBV-induced BHK cell apoptosis and inflammation
[1]
.
Lithium chloride hydrate (1 mg/mL) improves the efficiency of induced pluripotent stem cell-derived neurospheres
[4]
.
Lithium chloride hydrate (1.2 mM, 72 h) protects PC12 cells from Morphine (HY-P1701)-induced apoptosis
[5]
.
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
RT-PCR [1]
Cell Line: | BHK cells |
Concentration: | 5 and 20 mM |
Incubation Time: | 36 h |
Result: |
Blocked the expression of NF-κB, NLRP3, TNF-α, and IL-1β.
Blocked levels of Caspase-3, Bax and increased Bcl-2 level. |
Lithium chloride hydrate (60 mg/kg, i.p., twice a day) improves Sevoflurane (SEV)-induced memory impairment in rats
[2]
.
Lithium chloride hydrate (150 mg/kg, p.o., every other day) stimulates bone formation in extraction socket repair in rats
[5]
.
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Animal Model: | Rats [5] |
Dosage: | 150 mg/kg |
Administration: | Oral administration (p.o.), every other day |
Result: |
Produced greater proportion of newly formed bone (NB).
Lowered the rate of TRAP-stained cells. |
Animal Model: | Sevoflurane-induced memory impairment rats [2] |
Dosage: | 60 mg/kg |
Administration: | Intraperitoneal injection (i.p.), twice a day. |
Result: |
Reduced escape latency, increased time in the objective quadrant and raised platform crossings.
Suppresses SEV-induced oxidative stress reduces and reduced SEV-induced apoptosis in the hippocampus. |
Room temperature in continental US; may vary elsewhere.
Please store the product under the recommended conditions in the Certificate of Analysis.