New Products
  1. Cat.No. Product Name Information
  2. GC28246 2-(Methylthio)-7,8-dihydroquinazolin-5(6H)-one

    2-(Methylthio)-7,8-dihydroquinazolin-5(6H)-one is a compound featuring a saturated ring fused to an aromatic (hetero)cyclic ring.

    2-(Methylthio)-7,8-dihydroquinazolin-5(6H)-one
  3. GK10050 JC-1 Mitochondrial Membrane Potential Assay Kit JC-1 Mitochondrial Membrane Potential Assay Kit
  4. GC28245 JNJ-26489112

    JNJ-26489112 is a CNS-active agent and inhibitor of voltage-gated Na+ channels and N-type Ca2+ channels with broad-spectrum anticonvulsant activity in rodents and can be used to study neurological disorders.

    JNJ-26489112
  5. GC28244 HALOFUGINONE LACTATE

    HALOFUGINONE LACTATE is a halogenated derivative of febrifugine, a natural quinazolinone-containing compound found in the Chinese herb D. febrifuga.

    HALOFUGINONE LACTATE
  6. GC28243 Sulcardine 2HCl

    Sulcardine 2HCl is a multi-ion channel blocker with antiarrhythmic effects that blocks the properties of hERG and hNav1.5 channels and can be used to study atrial fibrillation and ventricular arrhythmias.

    Sulcardine 2HCl
  7. GC28242 Anisodine

    Anisodine is an inhibitor of muscarinic acetylcholine receptors (mAChR) with neuroprotective activity, used in research on multiple myeloma and metastatic breast cancer.

    Anisodine
  8. GC28241 Selinexor HCl

    Selinexor HCl (1393477-72-9 free base) is an oral selective XPO1 (XPO1/CRM1) inhibitor that induces cell cycle arrest and apoptosis in tumor cells by blocking the transport of tumor suppressor proteins from the nucleus to the cytoplasm, thereby promoting their accumulation within the nucleus.

    Selinexor HCl
  9. GC28239 VRT-325

    VRT-325 is a CFTR modulator with the ability to promote ΔF508-CFTR folding and endoplasmic reticulum trafficking.

    VRT-325
  10. GC28240 Ivacaftor-D9

    Ivacaftor-D9 is transmembrane conductance regulator (CFTR) channel activator, is used potentially for the treatment of cystic fibrosis.

    Ivacaftor-D9
  11. GC28238 P7-2302

    P7-2302 inhibits PDE7 and PDE4B with IC50 values of 0.18 nM and 77.3 nM, respectively. It also inhibits the efflux of P-gp and BCRP (breast cancer resistance protein) and shows low uptake in rat brains.

    P7-2302

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  1. Cat.No. Product Name Information
  2. GC16608 ARCA Anti-Reverse Cap Analog (ARCA) is a modified cap analog in which the 3' OH group (closer to m7G) is replaced with -OCH3. ARCA
  3. GC45380 Aminooxyacetic Acid Aminooxyacetic Acid, an inhibitor of GABA-t, is also inhibited CBS and CSE with an IC50s of 8.5 and 1.1 µM. Aminooxyacetic Acid
  4. GC38376 Coniferaldehyde Coniferaldehyde is a natural phenolic compound with potent anti-inflammatory activity. Coniferaldehyde
  5. GC19546 AMG-510 racemate AMG-510 is the first KRAS G12C inhibitor in clinical development and leads to the regression of KRAS G12C tumors[1,3]. AMG-510 racemate
  6. GC35261 Aflatoxin B1 Aflatoxin B1, as a class of carcinogenic mycotoxins produced by Aspergillus fungi, always lead to the development of hepatocellular carcinoma (HCC) in humans and animals. Aflatoxin B1
  7. GC63718 N-Acetyl-Ser-Asp-Lys-Pro acetate N-Acetyl-Ser-Asp-Lys-Pro acetate is an endogenous tetrapeptide secreted by bone marrow, which is a specific substrate for the N-terminal site of angiotensin-converting enzyme (ACE). N-Acetyl-Ser-Asp-Lys-Pro acetate
  8. GC33889 N-Acetyl-Ser-Asp-Lys-Pro N-Acetyl-Ser-Asp-Lys-Pro is an endogenous tetrapeptide secreted by bone marrow, which is a specific substrate for the N-terminal site of angiotensin-converting enzyme (ACE). N-Acetyl-Ser-Asp-Lys-Pro
  9. GC16797 Escitalopram Oxalate Selective 5-HT reuptake inhibitor Escitalopram Oxalate
  10. GC13161 Escitalopram Serotonin reuptake inhibitor Escitalopram
  11. GC34214 Adalimumab (Anti-Human TNF-alpha, Human Antibody) Adalimumab (Anti-Human TNF-alpha, Human Antibody) is one of the leading therapies for the treatment of rheumatoid arthritis. Adalimumab (Anti-Human TNF-alpha, Human Antibody)

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