9 Results for "

intraperitoneal toxicity

" in MedChemExpress (MCE) Product Catalog:
Products (9)

9 Results for "intraperitoneal toxicity" in MCE Product Catalog:

Cat. No.: HY-152261
CAS No.: 2891709-58-1
Purity:  99.2%
Research Areas:  

Cancer

MS6105 is a PROTAC degrader targeting LDHA and LDHB, with DC50 values of 38 nM and 74 nM for degrading LDHA and LDHB in PANC-1 cells, respectively, and no hook effect is observed at high concentrations. MS6105 inhibits the proliferation of pancreatic cancer cells, and no obvious toxicity is observed after intraperitoneal administration in mice. MS6105 can be used for pancreatic cancer-related research .
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Cat. No.: HY-N4031
CAS No.: 82375-29-9
Humantenine is a highly toxic indole alkaloid from Gelsemium elegans (Gardn. & Champ.) Benth. that binds to RNA m6A modification regulatory proteins (ALKBH5, METTL). Humantenine stably binds via hydrogen bonding and hydrophobic interactions and disrupts the m6A methylation level of target genes, thereby impairing the expression of intestinal epithelial cell tight junction and cytoskeleton-related genes, causing intestinal barrier dysfunction and significant intestinal cytotoxicity. The intraperitoneal injection LD50 values of Humantenine are <1 mg/kg in mice, 1.2 mg/kg in male rats and 1.5 mg/kg in female rats, respectively. Species differences exist in the metabolism of Humantenine in human, porcine, goat and rat liver microsomes, and demethylation, dehydrogenation and oxidation occur in liver microsomes .
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Cat. No.: HY-125290
CAS No.: 2275601-87-9
Purity:  99.50%
Target:  

CDK DYRK

Research Areas:  

Cancer

MU1210 (compound 12f), a chemical probe, is an inhibitor of CDC-like kinases Clk1, Clk2, and Clk4 (with IC50 values of 8, 20, and 12 nM respectively), with IC50 for HIPK1 and DYRK2 are 187 and 1309 nM. MU1210 also has favorable pharmacokinetic characteristics (in mice, 10 mg/kg, intraperitoneal injection: Cmax=1.24 μM, T1/2=58 minutes; no acute toxicity observed) .
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Cat. No.: HY-W012663
CAS No.: 106-69-4
Research Areas:  

Others

1,2,6-Hexanetriol, a polyol, is an intermediate for wetting agents, solvents, and pharmaceuticals with excellent moisturizing property. 1,2,6-Hexanetriol is a humectant and plasticizer for hydrophilic films. 1,2,6-Hexanetriol has no significant toxicity in rats, rabbits, and dogs via oral (16 mL/kg), intraperitoneal (10 g/kg) and intravenous (5.6 mL/kg) routes. 1,2,6-Hexanetriol can be used for the cosmetics and resin industries .
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Cat. No.: HY-N11732
CAS No.: 36375-21-0
O-Demethylrotenone is a rotenone (HY-B1756) derivative and a photodegradation product of rotenone that induces acute intraperitoneal toxicity. The acute intraperitoneal LD50 of O-Demethylrotenone in Mus musculus is 8.0 mg/kg .
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Cat. No.: HY-167108
CAS No.: 91635-05-1
Target:  

Drug Derivative

Research Areas:  

Endocrinology

3-Glyoxyloylcoumarin is a Coumarin (HY-N0709) derivative with moderate to low acute toxicity. 3-Glyoxyloylcoumarin is applicable to studies on urinary system toxicity .
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Cat. No.: HY-N18254
CAS No.: 86500-43-8
Hokbusine A is a diterpenic alkaloid and C19 norditerpenoid (aconitine-type) alkaloid that can be found in the roots of Aconitum napellus L. (Swiss variety) and Aconitum jaluense .Hokbusine A exhibits low acute toxicity in ddY mice via intraperitoneal administration, with an LD50 value greater than 1 mg/kg .
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Cat. No.: HY-N21836
CAS No.: 76551-64-9
Category:  

Microorganisms Antibiotics

Target:  

Parasite Fungal

Partricin A is an antimicrobial agent with affinity for ergosterol and cholesterol. Partricin A inhibits growth of fungal species and Trichomonas vaginalis. Partricin A induces hemolysis of rat erythrocytes. Partricin A causes acute toxicity in mice via intraperitoneal or intravenous administration. Partricin A serves as a starting material for synthesis of semisynthetic amide derivatives. Partricin A can be used for the research of fungal infections, trichomonas vaginalis infection .
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Cat. No.: HY-W072994
CAS No.: 1338-02-9
Target:  

Fungal Insecticide

Research Areas:  

Infection

Copper naphthenate is an organocopper compound with the properties of a fungicide, preservative, oil-borne protectant, and toxicant. Copper naphthenate increases serum and urine copper levels in exposed populations, causes skin irritation, and induces intraperitoneal toxicity in rats. Copper naphthenate inhibits the growth of decay fungi and molds on moso bamboo, kills the free-living stages of Ichthyophthirius multifiliis, and controls wood-boring insects and termites .
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