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. GC45339 3-Oxocholic Acid A secondary bile acid 3-Oxocholic Acid
  3. GC10278 Sucralose artificial sweetener and sugar substitute Sucralose
  4. GN10470 Eriodictyol Eriodictyol
  5. 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
  6. GC16116 Costunolide Costunolide is a multi-target NF-κB inhibitor with diverse biological activities. Costunolide
  7. GC44616 PGPC

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

    PGPC
  8. GC20125 Testosterone enanthate Testosterone enanthateis an androgen that enhances male muscle mass and strength within a short period of time. Testosterone enanthate
  9. GC11587 Ochratoxin A endoplasmic reticulum ATP-dependent calcium pump activator Ochratoxin A
  10. GC19393 S107 S107 is a RyR-selective 1,4-benzothiazepine derivative that stabilizes RyR2 channels by enhancing the binding affinity of calstabin2 to mutant and/or PKA-phosphorylated channels. S107
  11. GC63589 NSC668394 NSC668394 is a potent ezrin (Thr567) phosphorylation inhibitor, with a Kd of 12.59 μM. NSC668394 inhibit ezrin T567 phosphorylation caused by PKCΙ primarily via their binding to ezrin. NSC668394 can be used to prevent tumor metastasis. NSC668394

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