Nouveaux produits
  1. Cat.No. Nom du produit Informations
  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. Nom du produit Informations
  2. GC32804 HUHS015 A PCA-1 inhibitor HUHS015
  3. GC91632 Verrucarin H

    Verrucarin H is a macrocyclic trichothecene mycotoxin that has been found in M. verrucaria.

    Verrucarin H
  4. GC79707 ST1072

    ST1072 is an inhibitor of CerS4 and CerS6.

    ST1072
  5. GC62861 BAY-298 BAY-298 est un antagoniste du récepteur de l'hormone lutéinisante (LH-R) actif et sélectif par voie orale avec des IC50 de 96 nM, 23 nM et 78 nM pour hLH (LH humaine) et rLH (LH de rat) et cLH (LH de singe cynomolgus), respectivement . BAY-298
  6. GC45339 3-Oxocholic Acid A secondary bile acid 3-Oxocholic Acid
  7. GC10278 Sucralose artificial sweetener and sugar substitute Sucralose
  8. GN10470 Eriodictyol Eriodictyol
  9. GN10200 Salvianolic acid C Salvianolic acid C is a cytochrome inhibitor with anti-inflammatory and antioxidant activities. Salvianolic acid C inhibits CYP2C8 (Ki=4.82μM) and CYP2J2 (Ki=5.75μM) activities. Salvianolic acid C
  10. GC16116 Costunolide Costunolide is a multi-target NF-κB inhibitor with diverse biological activities. Costunolide
  11. GC44616 PGPC

    PGPC is an oxidized phospholipid that can be formed under conditions of oxidative stress.

    PGPC

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