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KM mouse

" in MedChemExpress (MCE) Product Catalog:

6

Inhibitors & Agonists

2

Inhibitory Antibodies

1

Click Chemistry

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-151229

    DETC-Me; DDTC-Me; Diethyldithiocarbamic acid methyl ester

    Aldehyde Dehydrogenase (ALDH) Metabolic Disease
    S-Methyl-N,N-diethylthiolcarbamate (DETC-Me; DDTC-Me) is the active metabolite of the aldehyde dehydrogenase inhibitor disulfiram (HY-B0240). It is produced by the methylation of the disulfiram metabolite diethyldithiocarbamate in mouse liver microsomes. S-Methyl-N,N-diethylthiolcarbamate (DETC-Me; DDTC-Me) inhibits rat liver low Km aldehyde dehydrogenase (ALDH) (ID50=15.5 mg/kg). When administered at a dose of 20.6 mg/kg, it decreases mean arterial pressure (MAP) and increases heart rate in rats during ethanol stimulation.
    S-Methyl-N,N-diethylthiolcarbamate
  • HY-W010617

    Biochemical Assay Reagents Inflammation/Immunology
    2-Cyclohexen-1-ol is a biochemical reagent. 2-Cyclohexen-1-ol is the oxidation substrate of mouse aldo-keto reductase AKR1C12, with a Km of 1080 μM and a Kcat of 13 min -1, showing low catalytic efficiency .
    2-Cyclohexen-1-ol
  • HY-168214

    Potassium Channel Neurological Disease
    Kv7.2/Kv7.3 agonist 1 (Compound 16) is an orally active agonist for KV7.2/7.3 channel (KCNQ2/3) with an EC50 of 1.03 μM. Kv7.2/Kv7.3 agonist 1 exhibits analgesic efficacy in mice chronic constriction injury (CCI) model and mice Streptozotocin (HY-13753)-induced diabetic peripheral neuropathic pain (DPNP) model, with ED50 of 12.02 and 9.63 mg/kg .
    Kv7.2/Kv7.3 agonist 1
  • HY-P991756

    CD44 Cancer
    Anti-Mouse CD44 Antibody (KM703) recognizes mouse CD44. CD44 is the main receptor for hyaluronan (HA). Anti-Mouse CD44 Antibody (KM703) does not recognize the HA binding site of CD44. Anti-Mouse CD44 Antibody (KM703) is a non-HA-blocking antibody. Recommend Isotype Controls: Rat IgG2a kappa, Isotype Control (HY-P990679) .
    Anti-Mouse CD44 Antibody (KM703)
  • HY-113798

    Thymidylate Synthase Antifolate Cancer
    ICI 198583 is a thymidylate synthase (TS) inhibitor with a Ki value of 10 nM for both mouse and human TS. ICI 198583 serves as a substrate for folylpolyglutamate synthetase (FPGS) with a Km of 40 μM. ICI 198583 exerts persistent, dose-dependent inhibition on thymidylate synthase flux in mice. ICI 198583 is applicable to relevant research on leukemia .
    ICI 198583
  • HY-180551

    PROTACs RET Trk Receptor Endocrinology Cancer
    ZW-6-052 (compound 20), the derivative of ZW-18-116 (HY-180550), is a dual-target PROTAC degrader for the oncoproteins TRKA and RET. ZW-6-052 induces degradation of TMP3-TRKA in KM12 mouse xenograft models. ZW-6-052 can be used for RET or TRKA-derived cancer research, such as thyroid, lung, and colon cancers .
    ZW-6-052

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