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Propacetamol (hydrochloride)

Propacetamol (hydrochloride)

Item no.	HY-108292-50mg
Manufacturer	MedChem Express
CASRN	66532-86-3
Amount	50 mg
Quantity options	100 mg 10 mM/1 mL 10 mg 1 ea 250 mg 50 mg 5 mg
Category	Inhibitors & Compound Libraries Small Molecules
Type	Inhibitor
Specific against	other
Purity	99.89
Citations	[1]Ewan D McNicol, et al. Single dose intravenous paracetamol or intravenous propacetamol for postoperative pain. Cochrane Database Syst Rev.\|[2]Tsai MS, et al. Kaempferol protects against propacetamol-induced acute liver injury through CYP2E1 inactivation, UGT1A1 activation, and attenuation of oxidative stress, inflammation and apoptosis in mice. Toxicol Lett. 2018 Jun 15;290:97-109.
Smiles	O=C(OC1=CC=C(NC(C)=O)C=C1)CN(CC)CC.[H]Cl
ECLASS 10.1	32160490
ECLASS 11.0	32160490
UNSPSC	12000000
Shipping Condition	Room temperature
Available
Manufacturer - Type	Reference compound
Manufacturer - Applications	Cancer-programmed cell death
Manufacturer - Targets	Others
Shipping Temperature	Room Temperature
Storage Conditions	4°C (Powder, stored under nitrogen, away from moisture)
Molecular Weight	300.79
Product Description	Propacetamol hydrochloride is an analgesic agent, can be used in induction of acute liver injury. Propacetamol hydrochloride acts function through CYP2E1 inactivation, UGT1A1 activation, and attenuation of oxidative stress. Propacetamol hydrochloride also is a precursor form of paracetamol. Propacetamol hydrochloride can be used in postoperative pain, acute trauma and gastrointestinal disorders[1].
Manufacturer - Research Area	Cancer
Solubility	DMSO : 25 mg/mL (ultrasonic; warming; heat to 80°C)\|H2O : 250 mg/mL (ultrasonic)
Manufacturer - Pathway	Others
Clinical information	Launched

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HY-108292-50mg-safety-datasheet.pdf